Fuu‐jen Tsai
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Fuu‐jen Tsaibiology Degrees
Biology
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Genetics
#840
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#933
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Biology
Fuu‐jen Tsai's Degrees
- PhD Genetics Stanford University
- Masters Biotechnology National Taiwan University
- Bachelors Life Science National Taiwan University
Why Is Fuu‐jen Tsai Influential?
(Suggest an Edit or Addition)Fuu‐jen Tsai's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
- ERK promotes tumorigenesis by inhibiting FOXO3a via MDM2-mediated degradation (2008) (653)
- IKKβ Suppression of TSC1 Links Inflammation and Tumor Angiogenesis via the mTOR Pathway (2007) (636)
- Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians (2011) (581)
- Erk Associates with and Primes GSK-3β for Its Inactivation Resulting in Upregulation of β-Catenin (2005) (494)
- Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds (2005) (425)
- Meta-analysis identifies common variants associated with body mass index in East Asians (2012) (372)
- Erk associates with and primes GSK-3beta for its inactivation resulting in upregulation of beta-catenin. (2005) (343)
- The crosstalk of mTOR/S6K1 and Hedgehog pathways. (2012) (333)
- Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations (2012) (264)
- An in vivo evaluation of a biodegradable genipin-cross-linked gelatin peripheral nerve guide conduit material. (2005) (190)
- Pompe Disease in Infants: Improving the Prognosis by Newborn Screening and Early Treatment (2009) (188)
- Identification of type 2 diabetes loci in 433,540 East Asian individuals (2019) (188)
- Down-regulation of myeloid cell leukemia-1 through inhibiting Erk/Pin 1 pathway by sorafenib facilitates chemosensitization in breast cancer. (2008) (177)
- Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. (2014) (163)
- Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis (2012) (158)
- Functional genomic analysis identified epidermal growth factor receptor activation as the most common genetic event in oral squamous cell carcinoma. (2009) (156)
- Genome-wide association study of diabetic retinopathy in a Taiwanese population. (2011) (134)
- Resveratrol-induced autophagy and apoptosis in cisplatin-resistant human oral cancer CAR cells: A key role of AMPK and Akt/mTOR signaling. (2017) (129)
- Identification of over-expressed proteins in oral squamous cell carcinoma (OSCC) patients by clinical proteomic analysis. (2007) (126)
- Vascular endothelial growth factor gene-460 C/T polymorphism is a biomarker for prostate cancer. (2003) (120)
- Current developments of computer-aided drug design (2010) (115)
- A novel single nucleotide polymorphism in ERCC6 gene is associated with oral cancer susceptibility in Taiwanese patients. (2008) (115)
- Osteopontin increases lung cancer cells migration via activation of the alphavbeta3 integrin/FAK/Akt and NF-kappaB-dependent pathway. (2009) (113)
- Long-term prognosis of patients with infantile-onset Pompe disease diagnosed by newborn screening and treated since birth. (2015) (101)
- Subunit 6 of the COP9 signalosome promotes tumorigenesis in mice through stabilization of MDM2 and is upregulated in human cancers. (2011) (95)
- IGF-II/mannose-6-phosphate receptor signaling induced cell hypertrophy and atrial natriuretic peptide/BNP expression via Galphaq interaction and protein kinase C-alpha/CaMKII activation in H9c2 cardiomyoblast cells. (2008) (94)
- Plumbagin suppresses endothelial progenitor cell-related angiogenesis in vitro and in vivo (2019) (94)
- Later-onset Pompe disease: early detection and early treatment initiation enabled by newborn screening. (2011) (94)
- Vascular endothelial growth factor gene polymorphisms in age-related macular degeneration. (2008) (90)
- Puerariae radix isoflavones and their metabolites inhibit growth and induce apoptosis in breast cancer cells. (2009) (90)
- Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
- Asymmetric chitosan membrane containing collagen I nanospheres for skin tissue engineering. (2009) (88)
- Ligand-Based Dual Target Drug Design for H1N1: Swine Flu- A Preliminary First Study (2009) (85)
- Inhibitory effect of alpinate Oxyphyllae fructus extracts on Ang II-induced cardiac pathological remodeling-related pathways in H9c2 cardiomyoblast cells (2013) (84)
- Emodin inhibits the growth of hepatoma cells: finding the common anti-cancer pathway using Huh7, Hep3B, and HepG2 cells. (2010) (83)
- Association of tumour necrosis factor alpha −308 gene polymorphism with primary open-angle glaucoma in Chinese (2003) (83)
- Phosphorylation of PDHA by AMPK Drives TCA Cycle to Promote Cancer Metastasis (2020) (82)
- Casticin inhibits human prostate cancer DU 145 cell migration and invasion via Ras/Akt/NF-κB signaling pathways. (2019) (82)
- Structure-Based and Ligand-Based Drug Design for HER 2 Receptor (2010) (82)
- Molecular analysis of thiopurine S-methyltransferase alleles in South-east Asian populations. (2002) (82)
- Birthmarks and congenital skin lesions in Chinese newborns. (1993) (81)
- Ethylene glycol induces calcium oxalate crystal deposition in Malpighian tubules: a Drosophila model for nephrolithiasis/urolithiasis. (2011) (81)
- The proline form of p53 codon 72 polymorphism is associated with endometriosis. (2002) (79)
- Detecting multiple lysosomal storage diseases by tandem mass spectrometry--a national newborn screening program in Taiwan. (2014) (79)
- Akt mediates 17β-estradiol and/or estrogen receptor-α inhibition of LPS-induced tumor necresis factor-α expression and myocardial cell apoptosis by suppressing the JNK1/2-NFκB pathway (2009) (79)
- Analysis of urinary nucleosides as potential tumor markers in human colorectal cancer by high performance liquid chromatography/electrospray ionization tandem mass spectrometry. (2009) (78)
- High-density lipoprotein ameliorates palmitic acid-induced lipotoxicity and oxidative dysfunction in H9c2 cardiomyoblast cells via ROS suppression (2019) (78)
- Carthamus tinctorius L. prevents LPS-induced TNFalpha signaling activation and cell apoptosis through JNK1/2-NFkappaB pathway inhibition in H9c2 cardiomyoblast cells. (2010) (78)
- Talin‐1 overexpression defines high risk for aggressive oral squamous cell carcinoma and promotes cancer metastasis (2011) (78)
- Anti-apoptotic and pro-survival effects of exercise training on hypertensive hearts. (2012) (78)
- Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (77)
- Oxidative DNA damage in pterygium. (2005) (76)
- Soya-cerebroside reduces IL-1β-induced MMP-1 production in chondrocytes and inhibits cartilage degradation: implications for the treatment of osteoarthritis (2019) (75)
- Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions. (2002) (75)
- The A2A adenosine receptor rescues the urea cycle deficiency of Huntington's disease by enhancing the activity of the ubiquitin-proteasome system. (2009) (72)
- Mesenchymal Stem Cell Insights: Prospects in Cardiovascular Therapy (2014) (71)
- CXCL10/IP-10 is a biomarker and mediator for Kawasaki disease. (2015) (71)
- Preparation, characterisation and activity of the inclusion complex of paeonol with β-cyclodextrin. (2010) (71)
- Epigallocatechin gallate sensitizes cisplatin‐resistant oral cancer CAR cell apoptosis and autophagy through stimulating AKT/STAT3 pathway and suppressing multidrug resistance 1 signaling (2017) (70)
- RANKL increases migration of human lung cancer cells through intercellular adhesion molecule‐1 up‐regulation (2011) (70)
- Association of phospholipase A2 receptor 1 polymorphisms with idiopathic membranous nephropathy in Chinese patients in Taiwan (2010) (70)
- Fisetin and rutin as 3C protease inhibitors of enterovirus A71. (2012) (69)
- Glucocerebroside reduces endothelial progenitor cell-induced angiogenesis (2019) (69)
- Endothelin‐1 promotes MMP‐13 production and migration in human chondrosarcoma cells through FAK/PI3K/Akt/mTOR pathways (2012) (69)
- Japanese encephalitis virus down-regulates thioredoxin and induces ROS-mediated ASK1-ERK/p38 MAPK activation in human promonocyte cells. (2010) (69)
- Tetramethylpyrazine reverses high-glucose induced hypoxic effects by negatively regulating HIF-1α induced BNIP3 expression to ameliorate H9c2 cardiomyoblast apoptosis (2020) (68)
- Interleukin gene polymorphisms in age-related macular degeneration. (2008) (68)
- Association between transforming growth factor-beta1 gene C-509T and T869C polymorphisms and rheumatic heart disease. (2004) (66)
- YC-1 induces G0/G1 phase arrest and mitochondria-dependent apoptosis in cisplatin-resistant human oral cancer CAR cells (2017) (65)
- iSMART: An Integrated Cloud Computing Web Server for Traditional Chinese Medicine for Online Virtual Screening, de novo Evolution and Drug Design (2011) (64)
- Skp2-Mediated RagA Ubiquitination Elicits a Negative Feedback to Prevent Amino-Acid-Dependent mTORC1 Hyperactivation by Recruiting GATOR1. (2015) (64)
- AKT1 Inhibits Epithelial-to-Mesenchymal Transition in Breast Cancer through Phosphorylation-Dependent Twist1 Degradation. (2016) (64)
- A traditional Chinese herbal antilithic formula, Wulingsan, effectively prevents the renal deposition of calcium oxalate crystal in ethylene glycol-fed rats (2008) (64)
- Dopamine receptor D2 gene polymorphisms are associated in Taiwanese children with Tourette syndrome. (2005) (62)
- The roles of human sucrose nonfermenting protein 2 homologue in the tumor-promoting functions of Rsf-1. (2008) (62)
- Vascular endothelial growth factor gene-460 C/T polymorphism is a biomarker for oral cancer. (2005) (62)
- Kaempferol inhibits enterovirus 71 replication and internal ribosome entry site (IRES) activity through FUBP and HNRP proteins. (2011) (62)
- The TGFbeta1 gene codon 10 polymorphism contributes to the genetic predisposition to high myopia. (2006) (61)
- Eccentric cardiac hypertrophy was induced by long‐term intermittent hypoxia in rats (2007) (60)
- Peptide biomarker discovery for identification of methicillin-resistant and vancomycin-intermediate Staphylococcus aureus strains by MALDI-TOF. (2012) (59)
- Personalized medicine: A paradigm shift in healthcare (2013) (59)
- Rsf-1, a Chromatin Remodeling Protein, Induces DNA Damage and Promotes Genomic Instability* (2010) (59)
- Prognostic Significance of the Proline Form of p53 Codon 72 Polymorphism in Nasopharyngeal Carcinoma (2002) (59)
- Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: identification of five novel mutations. (2002) (58)
- Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots. (2001) (58)
- A Novel Strategy for Designing the Selective PPAR Agonist by the “Sum of Activity” Model (2010) (58)
- Leptin increases motility and integrin up‐regulation in human prostate cancer cells (2011) (58)
- Vitamin D receptor gene polymorphisms are associated with risk of Hashimoto's thyroiditis in Chinese patients in Taiwan (2006) (57)
- Potent Inhibitor Design Against H1N1 Swine Influenza: Structure-based and Molecular Dynamics Analysis for M2 Inhibitors from Traditional Chinese Medicine Database (2011) (57)
- Distributions of p53 codon 72 polymorphism in bladder cancer – proline form is prominent in invasive tumor (2000) (56)
- Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference (2016) (56)
- Interleukin‐4 gene, but not the interleukin‐1 beta gene polymorphism, is associated with oral cancer (2005) (56)
- Transforming growth factor-beta1 increases cell migration and beta1 integrin up-regulation in human lung cancer cells. (2009) (56)
- Analysis of urinary nucleosides as helper tumor markers in hepatocellular carcinoma diagnosis. (2009) (55)
- Risk of epilepsy in type 1 diabetes mellitus: a population-based cohort study (2016) (55)
- Resveratrol inhibited the metastatic behaviors of cisplatin-resistant human oral cancer cells via phosphorylation of ERK/p-38 and suppression of MMP-2/9. (2021) (54)
- Activation of insulin-like growth factor II receptor induces mitochondrial-dependent apoptosis through G(alpha)q and downstream calcineurin signaling in myocardial cells. (2009) (54)
- Evaluation of the poly(ADP‐ribose) polymerase‐1 gene variants in Alzheimer's disease (2010) (53)
- Urinary Nucleosides as Biomarkers of Breast, Colon, Lung, and Gastric Cancer in Taiwanese (2013) (53)
- Investigation into Potent Inflammation Inhibitors from Traditional Chinese Medicine (2011) (53)
- Identification of eight novel mutations of the acid α-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II (2008) (53)
- P53 gene mutation spectrum and the relationship between gene mutation and protein levels in pterygium. (2005) (52)
- Sclera-related gene polymorphisms in high myopia (2009) (52)
- Probiotic-fermented purple sweet potato yogurt activates compensatory IGF‑IR/PI3K/Akt survival pathways and attenuates cardiac apoptosis in the hearts of spontaneously hypertensive rats. (2013) (51)
- T allele for VEGF gene-460 polymorphism at the 5'-untranslated region: association with a higher susceptibility to endometriosis. (2004) (51)
- TRAF6 Restricts p53 Mitochondrial Translocation, Apoptosis, and Tumor Suppression. (2016) (51)
- Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations. (2006) (50)
- Metformin triggers the intrinsic apoptotic response in human AGS gastric adenocarcinoma cells by activating AMPK and suppressing mTOR/AKT signaling (2019) (50)
- Relationship between polymorphisms of nucleotide excision repair genes and oral cancer risk in Taiwan: evidence for modification of smoking habit. (2007) (50)
- Kaempferol inhibits angiogenic ability by targeting VEGF receptor-2 and downregulating the PI3K/AKT, MEK and ERK pathways in VEGF-stimulated human umbilical vein endothelial cells. (2018) (50)
- HLA-E gene polymorphism associated with susceptibility to Kawasaki disease and formation of coronary artery aneurysms. (2009) (50)
- Association Analysis of γ2 Subunit of γ-Aminobutyric Acid Type A Receptor Polymorphisms with Febrile Seizures (2003) (49)
- Soya-cerebroside inhibits VEGF-facilitated angiogenesis in endothelial progenitor cells (2020) (49)
- An Overview of Concepts for Cancer Stem Cells (2011) (49)
- Interleukin (IL)‐1β, IL‐1 receptor antagonist, IL‐6, IL‐8, IL‐10, and tumor necrosis factor α gene polymorphisms in patients with febrile seizures (2010) (48)
- Association of TNF-α gene polymorphisms with systemic lupus erythematosus in Taiwanese patients (2009) (48)
- Schwann Cell Migration Induced by Earthworm Extract via Activation of PAs and MMP2/9 Mediated through ERK1/2 and p38 (2011) (48)
- Characteristics of community-acquired methicillin-resistant Staphylococcus aureus in infants and children without known risk factors. (2002) (48)
- Timing of Applying Electrical Stimulation Is an Important Factor Deciding the Success Rate and Maturity of Regenerating Rat Sciatic Nerves (2010) (48)
- In silico pharmacology suggests ginger extracts may reduce stroke risks. (2011) (47)
- Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndrome. (2007) (47)
- Distributions of p53 codon 72 polymorphism in primary open angle glaucoma (2002) (47)
- Overexpression of a chromatin remodeling factor, RSF-1/HBXAP, correlates with aggressive oral squamous cell carcinoma. (2011) (47)
- Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. (2017) (46)
- No association of vitamin D receptor gene start codon fok 1 polymorphisms in Chinese patients with systemic lupus erythematosus. (2002) (46)
- Collagen type 3 alpha 1 polymorphism and risk of pelvic organ prolapse (2008) (46)
- Cyclooxygenase 2 expression in pterygium (2007) (46)
- Lipopolysaccharide upregulates uPA, MMP-2 and MMP-9 via ERK1/2 signaling in H9c2 cardiomyoblast cells (2009) (46)
- PP2A mediates diosmin p53 activation to block HA22T cell proliferation and tumor growth in xenografted nude mice through PI3K-Akt-MDM2 signaling suppression. (2012) (46)
- Glutathione S-transferase M1*null genotype but not myeloperoxidase promoter G-463A polymorphism is associated with higher susceptibility to endometriosis. (2004) (46)
- p53 Gene Codon 72 Polymorphism but Not Tumor Necrosis Factor-α Gene Is Associated with Prostate Cancer (2004) (46)
- Toll-like receptor gene polymorphisms are associated with susceptibility to graves' ophthalmopathy in Taiwan males (2010) (46)
- Screening from the World's Largest TCM Database Against H1N1 Virus (2011) (45)
- Garlic Oil Alleviates MAPKs- and IL-6-mediated Diabetes-related Cardiac Hypertrophy in STZ-induced DM Rats (2010) (45)
- Th1 and Th2 cytokines are elevated in HCV-infected SVR(-) patients treated with interferon-alpha. (2009) (45)
- Association of genetic polymorphisms of MK, IL-4, p16, p21, p53 genes and human gastric cancer in Taiwan. (2005) (45)
- Interleukin 4, interleukin 6 and interleukin 10 polymorphisms in children with acute and chronic immune thrombocytopenic purpura (2005) (44)
- Association of IL‐1Ra gene polymorphism, but no association of IL‐1β and IL‐4 gene polymorphisms, with Kawasaki disease (2005) (44)
- Urokinase gene 3'-UTR T/C polymorphism is associated with urolithiasis. (2002) (44)
- Amorphous copolyesters based on 1,3/1,4-cyclohexanedimethanol: Synthesis, characterization and properties (2008) (44)
- Interleukin‐4 gene intron‐3 polymorphism is associated with transitional cell carcinoma of the urinary bladder (2005) (44)
- Use of electrical stimulation at different current levels to promote recovery after peripheral nerve injury in rats. (2009) (43)
- Association of the lumican gene functional 3'-UTR polymorphism with high myopia. (2010) (43)
- Bufalin induces G2/M phase arrest and triggers autophagy via the TNF, JNK, BECN-1 and ATG8 pathway in human hepatoma cells. (2013) (43)
- Kaempferol induces ATM/p53-mediated death receptor and mitochondrial apoptosis in human umbilical vein endothelial cells. (2016) (43)
- Contribution of matrix metalloproteinases-1 genotypes to gastric cancer susceptibility in Taiwan (2017) (43)
- Polymorphism for Transforming Growth Factor Beta 1-509 (TGF-B1-509): Association with Endometriosis (2005) (43)
- Polymorphism of Angiotensin-1 Converting Enzyme Gene and Kawasaki Disease (2004) (43)
- Proteomic analysis of up‐regulated proteins in human promonocyte cells expressing severe acute respiratory syndrome coronavirus 3C‐like protease (2007) (43)
- Overnight orthokeratology is comparable with atropine in controlling myopia (2014) (42)
- Prognostic impact of allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia patients with internal tandem duplication of FLT3. (2013) (42)
- Histone acetylation is essential for ANG‐II‐induced IGF‐IIR gene expression in H9c2 cardiomyoblast cells and pathologically hypertensive rat heart (2012) (42)
- Association of XPD polymorphisms with prostate cancer in Taiwanese patients. (2007) (42)
- Inhibition of enterovirus 71 infections and viral IRES activity by Fructus gardeniae and geniposide. (2013) (42)
- Increased prevalence of interleukin-1 receptor antagonist gene polymorphism in patients with chronic rhinosinusitis. (2006) (42)
- Oral Lactobacillus reuteri GMN-32 treatment reduces blood glucose concentrations and promotes cardiac function in rats with streptozotocin-induced diabetes mellitus (2013) (42)
- Chromosome 3p12.3-p14.2 and 3q26.2-q26.32 Are Genomic Markers for Prognosis of Advanced Nasopharyngeal Carcinoma (2009) (42)
- Hypoxia-induced compensatory effect as related to Shh and HIF-1α in ischemia embryo rat heart (2008) (42)
- Mutation analysis of Wilson disease in Taiwan and description of six new mutations (1998) (42)
- Association of p53 and p21(CDKN1A/WAF1/CIP1) polymorphisms with oral cancer in Taiwan patients. (2007) (41)
- Discovery of potent inhibitors for phosphodiesterase 5 by virtual screening and pharmacophore analysis (2009) (41)
- 3-O-methyldopa levels in newborns: Result of newborn screening for aromatic l-amino-acid decarboxylase deficiency. (2016) (40)
- Cytogenetic study of workers exposed to chromium compounds. (2000) (39)
- Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI. (2016) (39)
- Two novel mutations of the glycine receptor gene in a Taiwanese hyperekplexia family (2004) (38)
- Protective effect of Flos carthami extract against ethylene glycol-induced urolithiasis in rats (2012) (38)
- Characterization of trans‐ and cis‐cleavage activity of the SARS coronavirus 3CLpro protease: basis for the in vitro screening of anti‐SARS drugs (2004) (38)
- Matrix metalloproteinase-9 polymorphism and risk of pelvic organ prolapse in Taiwanese women. (2010) (38)
- A novel genetic variant of BMP2K contributes to high myopia (2009) (38)
- Association of the Neuronal Nicotinic Acetylcholine Receptor Subunit α4 Polymorphisms with Febrile Convulsions (2003) (38)
- Mutation analysis of Taiwanese Wilson disease patients. (2006) (38)
- The molecular mechanism of contrast-induced nephropathy (CIN) and its link to in vitro studies on iodinated contrast media (CM) (2018) (37)
- Characteristics of Chinese herbal medicine usage and its effect on survival of lung cancer patients in Taiwan. (2018) (37)
- Estrogen receptor α dinucleotide repeat and cytochrome P450c17α gene polymorphisms are associated with susceptibility to endometriosis (2005) (37)
- p21 gene codon 31 polymorphism is associated with bladder cancer. (2002) (37)
- Screening assay of very long chain fatty acids in human plasma with multiwalled carbon nanotube-based surface-assisted laser desorption/ionization mass spectrometry. (2010) (37)
- Interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis. (2001) (37)
- Severe acute respiratory syndrome coronavirus papain-like protease suppressed alpha interferon-induced responses through downregulation of extracellular signal-regulated kinase 1-mediated signalling pathways. (2011) (37)
- MUC4 gene polymorphisms associate with endometriosis development and endometriosis-related infertility (2011) (37)
- Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review. (2011) (37)
- S100A8 Is Identified as a Biomarker of HPV18-Infected Oral Squamous Cell Carcinomas by Suppression Subtraction Hybridization, Clinical Proteomics Analysis, and Immunohistochemistry Staining (2007) (36)
- Mutant BRAF induces DNA strand breaks, activates DNA damage response pathway, and up-regulates glucose transporter-1 in nontransformed epithelial cells. (2012) (36)
- Pterygium and genetic polymorphism of DNA double strand break repair gene Ku70. (2007) (36)
- Association of interleukin‐I beta and receptor antagonist gene polymorphisms with late onset Alzheimer's disease in Taiwan Chinese (2005) (36)
- β-catenin plays a key role in metastasis of human hepatocellular carcinoma. (2011) (36)
- Rapid screening assay of congenital adrenal hyperplasia by measuring 17α‐hydroxyprogesterone with high‐performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots (2002) (36)
- Enhancement of rhubarb extract solubility and bioactivity by 2-hydroxypropyl-β-cyclodextrin. (2013) (36)
- Association of GABRG2 polymorphisms with idiopathic generalized epilepsy. (2007) (36)
- Effects of insulin replacement on cardiac apoptotic and survival pathways in streptozotocin‐induced diabetic rats (2009) (36)
- Personalized medicine in Type 2 Diabetes (2014) (35)
- Approaches towards fighting the COVID-19 pandemic (Review) (2020) (35)
- Association between COL3A1 collagen gene exon 31 polymorphism and risk of floppy mitral valve/mitral valve prolapse. (2004) (35)
- Efficacy of epigallocatechin-3-gallate and Amla (Emblica officinalis) extract for the treatment of diabetic-uremic patients. (2011) (35)
- Growth hormone (GH) deficiency in patients with β-thalassemia major and the efficacy of recombinant GH treatment (2003) (35)
- IGF-II/mannose 6-phosphate receptor activation induces metalloproteinase-9 matrix activity and increases plasminogen activator expression in H9c2 cardiomyoblast cells. (2008) (34)
- p38α MAPK mediates 17β‐estradiol inhibition of MMP‐2 and ‐9 expression and cell migration in human lovo colon cancer cells (2012) (34)
- Phosphorylation of cofilin-1 by ERK confers HDAC inhibitor resistance in hepatocellular carcinoma cells via decreased ROS-mediated mitochondria injury (2017) (34)
- Breech deformation complex in neonates. (2000) (34)
- Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A). (2013) (34)
- Interleukin‐10 gene –627 allele variants, not interleukin‐I beta gene and receptor antagonist gene polymorphisms, are associated with atopic bronchial asthma (2003) (34)
- IL-10 and TNF-alpha promoter polymorphisms in susceptibility to systemic lupus erythematosus in Taiwan. (2010) (33)
- Correlation of p21 gene codon 31 polymorphism and TNF‐α gene polymorphism with nasopharyngeal carcinoma (2002) (33)
- Combinational treatment of all-trans retinoic acid (ATRA) and bisdemethoxycurcumin (BDMC)-induced apoptosis in liver cancer Hep3B cells. (2019) (33)
- p53 Expression in Pterygium by Immunohistochemical Analysis: A Series Report of 127 Cases and Review of the Literature (2005) (33)
- Type I IFN induced IL1-Ra expression in hepatocytes is mediated by activating STAT6 through the formation of STAT2: STAT6 heterodimer (2008) (33)
- Disease association of the interleukin-18 promoter polymorphisms in Taiwan Chinese systemic lupus erythematosus patients (2007) (33)
- Estrogen receptor α (ESR1) over-expression mediated apoptosis in Hep3B cells by binding with SP1 proteins. (2013) (33)
- Key Features for Designing Phosphodiesterase-5 Inhibitors (2010) (33)
- Polymorphisms for interleukin‐4 (IL‐4) –590 promoter, IL‐4 intron3, and tumor necrosis factor alpha –308 promoter: Non‐association with endometriosis (2002) (33)
- P-coumaric acid regulates exon 12 splicing of the ATP7B gene by modulating hnRNP A1 protein expressions (2015) (33)
- Rsf‐1, a chromatin remodelling protein, interacts with cyclin E1 and promotes tumour development (2013) (33)
- Cardiac Fas Receptor‐dependent Apoptotic Pathway in Obese Zucker Rats (2007) (32)
- Appearance of acanthosis nigricans may precede obesity: An involvement of the insulin/IGF receptor signaling pathway (2013) (32)
- Role of ERK signaling in the neuroprotective efficacy of magnesium sulfate treatment during focal cerebral ischemia in the gerbil cortex. (2010) (32)
- Prenatal diagnosis of Apert syndrome (1998) (32)
- Relation of vitamin D receptor FokI start codon polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal women in Taiwan (2002) (32)
- CCN6 enhances ICAM‐1 expression and cell motility in human chondrosarcoma cells (2012) (32)
- Estrogen receptor alpha dinucleotide repeat and cytochrome P450c17alpha gene polymorphisms are associated with susceptibility to endometriosis. (2005) (32)
- Enterovirus infection is associated with an increased risk of childhood type 1 diabetes in Taiwan: a nationwide population-based cohort study (2014) (32)
- Calcitonin Receptor Gene Polymorphism: A Possible Genetic Marker for Patients with Calcium Oxalate Stones (2001) (32)
- Identification of Urinary Metabolite Biomarkers of Type 2 Diabetes Nephropathy Using an Untargeted Metabolomic Approach. (2018) (32)
- Polymorphisms in the DNA repair gene XRCC1 and associations with systemic lupus erythematosus risk in the Taiwanese Han Chinese population (2009) (32)
- Genetic mutation profile of isovaleric acidemia patients in Taiwan. (2007) (32)
- Neuron Regeneration and Proliferation Effects of Danshen and Tanshinone IIA (2010) (31)
- Interleukin-1β gene and receptor antagonist gene polymorphisms in patients with calcium oxalate stones (2001) (31)
- Anti-allergic activity of grapeseed extract (GSE) on RBL-2H3 mast cells (2012) (31)
- Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency. (2000) (31)
- Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures. (2002) (31)
- Proliferation‐ and migration‐enhancing effects of ginseng and ginsenoside Rg1 through IGF‐I‐ and FGF‐2‐signaling pathways on RSC96 Schwann cells (2009) (31)
- Pterostilbene modulates the suppression of multidrug resistance protein 1 and triggers autophagic and apoptotic mechanisms in cisplatin-resistant human oral cancer CAR cells via AKT signaling (2018) (31)
- p21 gene codon 31 arginine/serine polymorphism: Non‐association with endometriosis (2001) (31)
- Androgen receptor trinucleotide polymorphism in endometriosis. (2001) (31)
- Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B (2010) (31)
- Current concepts regarding developmental mechanisms in diabetic retinopathy in Taiwan (2016) (31)
- Usefulness of Machine Learning-Based Detection and Classification of Cardiac Arrhythmias With 12-Lead Electrocardiograms. (2020) (31)
- Association of E-Cadherin Gene 3’-UTR C/T Polymorphism with Calcium Oxalate Stone Disease (2003) (30)
- Association of interleukin-1beta (IL1B) polymorphisms with Graves' ophthalmopathy in Taiwan Chinese patients. (2010) (30)
- Association of toll-like receptor 9 gene polymorphism in Chinese patients with systemic lupus erythematosus in Taiwan (2011) (30)
- Association analysis between Tourette's syndrome and dopamine D1 receptor gene in Taiwanese children (2004) (30)
- Poly(ethylene terephthalate) copolymers that contain 5-tert-butylisophthalic acid and 1-3/1-4-cyclohexanedimethanol : Synthesis, characterization, and properties (2007) (30)
- Mitochondria DNA deletion and copy numbers of cumulus cells associated with in vitro fertilization outcomes. (2010) (30)
- Genetic variations within the PSORS1 region affect Kawasaki disease development and coronary artery aneurysm formation (2013) (30)
- Uncaria rhynchophylla upregulates the expression of MIF and cyclophilin A in kainic acid-induced epilepsy rats: A proteomic analysis. (2010) (30)
- H3 ubiquitination by NEDD4 regulates H3 acetylation and tumorigenesis (2017) (30)
- Lack of association of genetic polymorphisms in the interleukin-1beta, interleukin-1 receptor antagonist, interleukin-4, and interleukin-10 genes with risk of rheumatic heart disease in Taiwan Chinese. (2005) (30)
- Proinflammatory cytokine gene polymorphisms among Hashimoto's thyroiditis patients (2006) (30)
- Association analysis of gamma 2 subunit of gamma- aminobutyric acid type A receptor polymorphisms with febrile seizures. (2003) (30)
- Vascular endothelial growth factor gene polymorphism is associated with calcium oxalate stone disease (2003) (30)
- Anti-apoptotic and pro-survival effect of protocatechuic acid on hypertensive hearts. (2014) (29)
- Increased incidence of Parkinsonism among Chinese with β-glucosidase mutation in central Taiwan (2013) (29)
- Human lymphocyte antigen B‐associated transcript 2, 3, and 5 polymorphisms and haplotypes are associated with susceptibility of Kawasaki disease and coronary artery aneurysm (2010) (29)
- Leu27IGF2 plays an opposite role to IGF1 to induce H9c2 cardiomyoblast cell apoptosis via Galphaq signaling. (2009) (29)
- Tumor necrosis factor alpha, CYP 17, urokinase, and interleukin 10 gene polymorphisms in postmenopausal women: correlation to bone mineral density and susceptibility to osteoporosis. (2005) (29)
- Single nucleotide polymorphism rs2229634 in the ITPR3 gene is associated with the risk of developing coronary artery aneurysm in children with Kawasaki disease (2010) (29)
- Shape memory effects of poly(ethylene terephthalate-co-ethylene succinate) random copolymers (2008) (29)
- Resistance to irinotecan (CPT-11) activates epidermal growth factor receptor/nuclear factor kappa B and increases cellular metastasis and autophagy in LoVo colon cancer cells. (2014) (29)
- Release of paeonol-β-CD complex from thermo-sensitive poly(N-isopropylacrylamide) hydrogels. (2010) (29)
- Interleukin (IL)-12 receptor beta1 codon 378 G homozygote and allele, but not IL-1 (beta-511 promoter, 3953 exon 5, receptor antagonist), IL-2 114, IL-4-590 intron 3, IL-8 3'-UTR 2767, and IL-18 105, are associated with higher susceptibility to leiomyoma. (2007) (29)
- Development of a high-resolution melting method for the screening of Wilson disease-related ATP7B gene mutations. (2010) (29)
- Cytokine (IL-6) and chemokine (IL-8) gene polymorphisms among rheumatoid arthritis patients in Taiwan. (2008) (29)
- Polymorphisms of interleukin 1 gene IL1RN are associated with Tourette syndrome. (2010) (29)
- The association between fibromyalgia and polymorphism of monoamine oxidase A and interleukin-4 (2006) (28)
- Normal values of inner canthal distance, interpupillary distance and palpebral fissure length in normal Chinese children in Taiwan. (2000) (28)
- Effect of bis(hydroxymethyl) alkanoate curcuminoid derivative MTH-3 on cell cycle arrest, apoptotic and autophagic pathway in triple-negative breast adenocarcinoma MDA-MB-231 cells: An in vitro study (2017) (28)
- Impact of plasminogen activator inhibitor-1 gene polymorphisms on primary membranous nephropathy. (2008) (28)
- GABA tea prevents cardiac fibrosis by attenuating TNF-alpha and Fas/FasL-mediated apoptosis in streptozotocin-induced diabetic rats. (2014) (28)
- An Emerging Translational Model to Screen Potential Medicinal Plants for Nephrolithiasis, an Independent Risk Factor for Chronic Kidney Disease (2014) (28)
- Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA (2014) (28)
- T homozygote and allele of epidermal growth factor receptor 2073 gene polymorphism are associated with higher susceptibility to endometriosis and leiomyomas. (2005) (28)
- A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings. (2010) (28)
- RSC96 Schwann Cell Proliferation and Survival Induced by Dilong through PI3K/Akt Signaling Mediated by IGF-I (2011) (28)
- Depsipeptide (FK228) inhibits growth of human prostate cancer cells. (2008) (27)
- Interleukin-1 Receptor Antagonist Gene Polymorphism in Chinese Patients with Systemic Lupus Erythematosus (2002) (27)
- Nerve Regeneration Potential of Protocatechuic Acid in RSC96 Schwann Cells by Induction of Cellular Proliferation and Migration through IGF-IR-PI3K-Akt Signaling. (2015) (27)
- Protective effect of Danggui (Radix Angelicae Sinensis) on angiotensin II-induced apoptosis in H9c2 cardiomyoblast cells (2014) (27)
- Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay. (2010) (27)
- Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in Taiwan. (2010) (27)
- Activation of estrogen receptors with E2 downregulates peroxisome proliferator-activated receptor γ in hepatocellular carcinoma. (2013) (27)
- Dung-shen (Codonopsis pilosula) attenuated the cardiac-impaired insulin-like growth factor II receptor pathway on myocardial cells. (2013) (27)
- Pterygium and genetic polymorphisms of the DNA repair enzymes XRCC1, XPA, and XPD (2010) (27)
- HTRA1 POLYMORPHISM IN DRY AND WET AGE-RELATED MACULAR DEGENERATION (2008) (27)
- No association of vitamin D receptor gene BsmI polymorphisms with calcium oxalate stone formation. (2001) (27)
- Angiotensin I-converting enzyme ACE 2350*G and ACE-240*T-related genotypes and alleles are associated with higher susceptibility to endometriosis. (2005) (27)
- Aloe‐emodin suppressed NMDA‐induced apoptosis of retinal ganglion cells through regulation of ERK phosphorylation (2007) (26)
- Enzyme replacement therapy for mucopolysaccharidosis VI—experience in Taiwan (2010) (26)
- Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients. (2008) (26)
- Association of Interleukin 1β and Receptor Antagonist Gene Polymorphisms with Primary Open-Angle Glaucoma (2003) (26)
- Suppression of Plasminogen Activators and the MMP-2/-9 Pathway by a Zanthoxylum avicennae Extract to Inhibit the HA22T Human Hepatocellular Carcinoma Cell Migration and Invasion Effects in Vitro and in Vivo via Phosphatase 2A Activation (2013) (26)
- The contribution of XRCC6/Ku70 to hepatocellular carcinoma in Taiwan. (2013) (26)
- New analytical method for investigating the antioxidant power of food extracts on the basis of their electron-donating ability: comparison to the ferric reducing/antioxidant power (FRAP) assay. (2010) (26)
- Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses. (2010) (26)
- JNK suppression is essential for 17β-Estradiol inhibits prostaglandin E2-Induced uPA and MMP-9 expressions and cell migration in human LoVo colon cancer cells (2011) (26)
- Association between angiotensin I-converting enzyme gene insertion/deletion polymorphism and mitral valve prolapse syndrome. (2003) (26)
- Tumor necrosis factor-alpha-308 promoter and p53 codon 72 gene polymorphisms in women with leiomyomas. (2004) (26)
- Network analysis and mechanisms of action of Chinese herb-related natural compounds in lung cancer cells. (2019) (26)
- Chinese Herbal Medicine Treatment Improves the Overall Survival Rate of Individuals with Hypertension among Type 2 Diabetes Patients and Modulates In Vitro Smooth Muscle Cell Contractility (2015) (26)
- Earthworm extracts facilitate PC12 cell differentiation and promote axonal sprouting in peripheral nerve injury. (2010) (26)
- The differential regulation of microRNAs is associated with oral cancer. (2017) (25)
- Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease (2019) (25)
- Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency. (2008) (25)
- Characterization of in vitro and in vivo bioactivity of a ferulic acid-2-Hydroxypropyl-β-cyclodextrin inclusion complex. (2019) (25)
- Interleukin-1beta and interleukin-1 receptor antagonist gene polymorphism in postmenopausal women: correlation to bone mineral density and susceptibility to osteoporosis. (2003) (25)
- Interleukin‐1‐β gene, but not the interleukin‐1 receptor antagonist gene, is associated with graves' disease (2005) (25)
- Levels of retinol-binding protein 4 and uric acid in patients with type 2 diabetes mellitus. (2009) (25)
- Endothelin-1 enhances cell migration through COX-2 up-regulation in human chondrosarcoma. (2013) (25)
- Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia (2009) (25)
- Association between angiotensin I-converting enzyme gene insertion/deletion polymorphism and risk of rheumatic heart disease. (2004) (25)
- Lack of association between pro‐inflammatory cytokine (IL‐6, IL‐8 and TNF‐α) gene polymorphisms and Graves’ disease (2005) (25)
- Transformation of 5-D itch scale and numerical rating scale in chronic hemodialysis patients (2017) (25)
- Monotherapy with meropenem versus combination therapy with ceftazidime plus amikacin as empirical therapy for neutropenic fever in children with malignancy. (2003) (25)
- Correlation between TGF‐β1 expression and proteomic profiling induced by severe acute respiratory syndrome coronavirus papain‐like protease (2012) (25)
- Pigment epithelium-derived factor gene Met72Thr polymorphism is associated with increased risk of wet age-related macular degeneration. (2008) (25)
- Unbalanced reciprocal translocations at amniocentesis. (2011) (24)
- STAT2*C related genotypes and allele but not TLR4 and CD40 gene polymorphisms are associated with higher susceptibility for asthma (2009) (24)
- Influence of interleukin 18 promoter polymorphisms in susceptibility to Kawasaki disease in Taiwan. (2008) (24)
- Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia (2008) (24)
- Inhibition of DNA methyltransferase 1 increases nuclear receptor subfamily 4 group A member 1 expression and decreases blood glucose in type 2 diabetes (2016) (24)
- Growth-Promoting Effects of Quercetin on Peripheral Nerves in Rats (2011) (24)
- Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21‐year period (2018) (24)
- Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995–2012 (2016) (24)
- Artificial neural network-based study can predict gastric cancer staging. (2008) (24)
- Lupeol suppresses migration and invasion via p38/MAPK and PI3K/Akt signaling pathways in human osteosarcoma U-2 OS cells (2019) (24)
- A codon 31ser-arg polymorphism of the WAF-1/CIP-1/p21/tumour suppressor gene in Chinese primary open-angle glaucoma. (2004) (24)
- Lack of association of interleukin‐6 and interleukin‐8 gene polymorphisms in Chinese patients with systemic lupus erythematosus (2006) (24)
- Effect of IL-6 C-572G polymorphism on idiopathic membranous nephropathy risk in a han chinese population (2010) (24)
- Inhibition of HSF2 SUMOylation via MEL18 upregulates IGF-IIR and leads to hypertension-induced cardiac hypertrophy. (2017) (24)
- Interleukin‐18 gene 105A/C genetic polymorphism is associated with the susceptibility of Kawasaki disease (2009) (24)
- Möbius syndrome in a male with XX/XY mosaicism (2013) (24)
- Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series (2016) (24)
- The Yang-Tonifying Herbal Medicine Cynomorium songaricum Extends Lifespan and Delays Aging in Drosophila (2012) (23)
- Muscarinic acetylcholine receptor 3 is dominant in myopia progression. (2012) (23)
- The contribution of caveolin-1 genotype and phenotype to hepatocellular carcinoma. (2013) (23)
- Apicidin-Resistant HA22T Hepatocellular Carcinoma Cells strongly activated the Wnt/β-Catenin Signaling Pathway and MMP-2 Expression via the IGF-IR/PI3K/Akt Signaling Pathway Enhancing Cell Metastatic Effect (2013) (23)
- Rapid modifications of N-substitution in iminosugars: development of new β-glucocerebrosidase inhibitors and pharmacological chaperones for Gaucher disease. (2013) (23)
- Rhubarb inhibits hepatocellular carcinoma cell metastasis via GSK-3-β activation to enhance protein degradation and attenuate nuclear translocation of β-catenin. (2013) (23)
- Genetic Variation in N-Methyl-D-Aspartate Receptor Subunit NR3A but Not NR3B Influences Susceptibility to Alzheimer’s Disease (2009) (23)
- Slow, progressive myopathy in neonatally treated patients with infantile-onset Pompe disease: a muscle magnetic resonance imaging study (2016) (23)
- Insulin‐like growth factor‐II gene polymorphism is associated with primary open angle glaucoma (2003) (23)
- XRCC4 codon 247*A and XRCC4 promoter −1394*T related genotypes but not XRCC4 intron 3 gene polymorphism are associated with higher susceptibility for endometriosis (2008) (23)
- Herbal Supplement Ameliorates Cardiac Hypertrophy in Rats with CCl4-Induced Liver Cirrhosis (2012) (23)
- Association of Vascular Endothelial Growth Factor C–634 G Polymorphism in Taiwanese Children With Kawasaki Disease (2008) (23)
- Genistein suppresses the isoproterenol-treated H9c2 cardiomyoblast cell apoptosis associated with P-38, Erk1/2, JNK, and NFκB signaling protein activation. (2013) (23)
- Electrical stimulation improves peripheral nerve regeneration in streptozotocin-induced diabetic rats (2012) (23)
- Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan. (2001) (23)
- Association analysis between Tourette's syndrome and two dopamine genes (DAT1, DBH) in Taiwanese children (2013) (22)
- Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea. (2010) (22)
- Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians (2017) (22)
- PTPRD silencing by DNA hypermethylation decreases insulin receptor signaling and leads to type 2 diabetes (2015) (22)
- Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene. (2012) (22)
- Glutathione S-transferase M1 gene null genotype and gastric cancer risk in Taiwan. (2005) (22)
- Association of Interleukin-10 A-592C Polymorphism in Taiwanese Children with Kawasaki Disease (2009) (22)
- The coexistence of nocturnal sustained hypoxia and obesity additively increases cardiac apoptosis. (2008) (22)
- BMPR1B Up-Regulation via a miRNA Binding Site Variation Defines Endometriosis Susceptibility and CA125 Levels (2013) (22)
- A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay. (2008) (22)
- Mechanisms governing the protective effect of 17β-estradiol and estrogen receptors against cardiomyocyte injury (2011) (22)
- Lack of association of interleukin-1ß gene polymorphisms in Chinese patients with systemic lupus erythematosus (2002) (22)
- Inhibitory effect of Angelica sinensis extract in the presence of 2-hydroxypropyl-β-cyclodextrin. (2014) (22)
- Urinary Proteomics for the Early Diagnosis of Diabetic Nephropathy in Taiwanese Patients (2018) (22)
- Lack of evidence for the association of tumor necrosis factor-alpha gene promoter polymorphism with calcium oxalate stone and bladder cancer patients (2001) (22)
- A novel titanium dioxide-polydimethylsiloxane plate for phosphopeptide enrichment and mass spectrometry analysis. (2014) (22)
- Potential effects of allyl isothiocyanate on inhibiting cellular proliferation and inducing apoptotic pathway in human cisplatin-resistant oral cancer cells. (2020) (22)
- Estrogen receptor beta gene haplotype is associated with pelvic organ prolapse. (2008) (22)
- Paeoniae alba Radix Promotes Peripheral Nerve Regeneration (2011) (22)
- Association of E-Cadherin Gene 3’-UTR C/T Polymorphism with Primary Open Angle Glaucoma (2005) (22)
- Association between copy number variation of complement component C4 and Graves' disease (2011) (22)
- The AluI Calcitonin Receptor Gene Polymorphism (TT) Is Associated with Low Bone Mineral Density and Susceptibility to Osteoporosis in Postmenopausal Women (2003) (22)
- A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan. (2001) (21)
- Interleukin-1-beta gene, but not the interleukin-1 receptor antagonist gene, is associated with Graves' disease. (2005) (21)
- Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan (2017) (21)
- Alpinate Oxyphyllae Fructus (Alpinia Oxyphylla Miq) Extracts Inhibit Angiotensin-II Induced Cardiac Apoptosis in H9c2 Cardiomyoblast Cells (2013) (21)
- Effect of antiretroviral therapy use and adherence on the risk of hyperlipidemia among HIV-infected patients, in the highly active antiretroviral therapy era (2017) (21)
- Nonassociation of Interleukin 4 Intron 3 and 590 Promoter Polymorphisms with Bronchopulmonary Dysplasia for Ventilated Preterm Infants (2005) (21)
- Penile length of normal boys in Taiwan. (2006) (21)
- p53 codon 72 proline/arginine polymorphism and autoimmune thyroid diseases (2008) (21)
- Estrogen receptor thymine-adenine dinucleotide repeat polymorphism is associated with susceptibility to leiomyoma. (2003) (21)
- Glutathione S-transferase M1 gene but not insulin-like growth factor-2 gene or epidermal growth factor gene is associated with prostate cancer. (2005) (21)
- Urokinase gene 3′‐UTR T/C polymorphism is associated with oral cancer (2004) (21)
- Effect of Chinese herbal medicine on stroke patients with type 2 diabetes. (2017) (21)
- Oxidized ApoC1 on MALDI-TOF and glycated-ApoA1 band on gradient gel as potential diagnostic tools for atherosclerotic vascular disease. (2013) (21)
- Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes. (2009) (21)
- E4BP4 is a cardiac survival factor and essential for embryonic heart development (2010) (21)
- Association of interleukin 1beta and receptor antagonist gene polymorphisms with primary open-angle glaucoma. (2003) (21)
- Drug design for Influenza A virus subtype H1N1 (2010) (21)
- Gelsolin (GSN) induces cardiomyocyte hypertrophy and BNP expression via p38 signaling and GATA-4 transcriptional factor activation (2014) (21)
- Estrogen receptor alpha polymorphism is associated with pelvic organ prolapse risk (2008) (20)
- Progesterone receptor polymorphism is associated with pelvic organ prolapse risk (2009) (20)
- The association between polymorphisms of B7 molecules (CD80 and CD86) and Graves' ophthalmopathy in a Taiwanese population. (2011) (20)
- A novel interaction between interferon-inducible protein p56 and ribosomal protein L15 in gastric cancer cells. (2011) (20)
- Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses. (2010) (20)
- Karyotypic evolution of a novel cervid satellite DNA family isolated by microdissection from the Indian muntjac Y-chromosome (2005) (20)
- Oridonin, A natural diterpenoid, protected NGF-differentiated PC12 cells against MPP+- and kainic acid-induced injury. (2019) (20)
- Dangshen (Codonopsis pilosula) activates IGF-I and FGF-2 pathways to induce proliferation and migration effects in RSC96 Schwann cells. (2010) (20)
- Aloe-emodin metabolites protected N-methyl-d-aspartate-treated retinal ganglion cells by Cu-Zn superoxide dismutase. (2007) (20)
- Association of TAP2 gene polymorphisms in Chinese patients with rheumatoid arthritis (2004) (20)
- ZAK induces MMP-2 activity via JNK/p38 signals and reduces MMP-9 activity by increasing TIMP-1/2 expression in H9c2 cardiomyoblast cells (2009) (20)
- Novel use of biodegradable casein conduits for guided peripheral nerve regeneration (2011) (20)
- Prediction of stone disease by discriminant analysis and artificial neural networks in genetic polymorphisms: a new method (2003) (20)
- Lipolysis-stimulating peptide-VHVV ameliorates high fat diet induced hepatocyte apoptosis and fibrosis (2014) (20)
- The comparison between capillary blood sampling and arterial blood sampling in an NICU. (2002) (20)
- Endometriosis: Polymorphisms for Interleukin-1β (IL-1β)-511 Promoter, IL-1β Exon 5, and IL-1 Receptor Antagonist: Nonassociation with Endometriosis (2001) (20)
- Genetic variations of MUC17 are associated with endometriosis development and related infertility (2015) (20)
- Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation. (2001) (20)
- Contribution of personalized Cyclin D1 genotype to triple negative breast cancer risk (2014) (20)
- Outcome of early-treated type III Gaucher disease patients. (2014) (19)
- Intraventricular fetus in fetu: report of one case. (1993) (19)
- Growth Hormone (GH) Receptor C.1319 G>T Polymorphism, But Not Exon 3 Retention or Deletion Is Associated With Better First-Year Growth Response to GH Therapy in Patients With GH Deficiency (2007) (19)
- Association between genetic polymorphisms of the NPHS1 gene and membranous glomerulonephritis in the Taiwanese population. (2010) (19)
- Chinese herbal medicine therapy and the risk of overall mortality for patients with liver cancer who underwent surgical resection in Taiwan. (2019) (19)
- Short-term versus long-term intermittent hypobaric hypoxia on cardiac fibrosis and Fas death receptor dependent apoptotic pathway in rat hearts. (2008) (19)
- Genetic variability in copper-transporting P-type adenosine triphosphatase (ATP7B) is associated with Alzheimer's disease in a Chinese population. (2013) (19)
- Androgen Receptor Trinucleotide Polymorphism in Leiomyoma (2004) (19)
- Distribution of oxidation enzyme eNOS and myeloperoxidase in primary open angle glaucoma (2005) (19)
- Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly. (2010) (19)
- Prediction of survival in surgical unresectable lung cancer by artificial neural networks including genetic polymorphisms and clinical parameters (2003) (19)
- Interleukin-18 gene polymorphism, but not interleukin-2 gene polymorphism, is associated with rheumatoid arthritis (2007) (19)
- Polymorphism of XRCC1 codon arg 399 Gln is associated with higher susceptibility to endometriosis. (2007) (19)
- Effects of Chinese herbal medicine on hyperlipidemia and the risk of cardiovascular disease in HIV-infected patients in Taiwan. (2018) (19)
- The lack of association between febrile convulsions and polymorphisms in SCN1A (2003) (19)
- Mass spectroscopic characteristics of low molecular weight proteins extracted from calcium oxalate stones: preliminary study (2008) (19)
- Sensitivity of allyl isothiocyanate to induce apoptosis via ER stress and the mitochondrial pathway upon ROS production in colorectal adenocarcinoma cells (2020) (19)
- Melamine-induced urolithiasis in a Drosophila model. (2012) (19)
- S100A8 is identified as a biomarker of HPV18-infected oral squamous cell carcinomas by suppression subtraction hybridization, clinical proteomics analysis, and immunohistochemistry staining. (2007) (19)
- Association of Genes on Chromosome 6, GRIK2, TMEM217 and TMEM63B (Linked to MRPL14) with Diabetic Retinopathy (2012) (19)
- Urinary cytidine as an adjunct biomarker to improve the diagnostic ratio for gastric cancer in Taiwanese patients. (2014) (18)
- Binding interaction of SARS coronavirus 3CLpro protease with vacuolar‐H+ ATPase G1 subunit (2005) (18)
- A water-based topical Chinese traditional medicine (Zicao) for wound healing developed using 2-hydroxypropyl-β-cyclodextrin. (2018) (18)
- Han ethnicity-specific type 2 diabetic treatment from traditional Chinese medicine? (2013) (18)
- Applications of meridian electrical conductance for renal colic: a prospective study. (2009) (18)
- Cytochrome P450c17α 5′-untranslated region *T/C polymorphism in endometriosis (2004) (18)
- Mutation in the FGFR2 gene in a Taiwanese patient with Beare–Stevenson cutis gyrata syndrome (2002) (18)
- Association analysis of dopaminergic gene variants (Comt, Drd4 And Dat1) with Alzheimer s disease. (2012) (18)
- Pharmacogenetics of dipeptidyl peptidase 4 inhibitors in a Taiwanese population with type 2 diabetes (2017) (18)
- Association between fibrillin-1 gene exon 15 and 27 polymorphisms and risk of mitral valve prolapse. (2003) (18)
- Up-regulation of ribosome biogenesis by MIR196A2 genetic variation promotes endometriosis development and progression (2016) (18)
- A/C polymorphism in the interleukin-18 coding region among Taiwanese systemic lupus erythematosus patients (2008) (18)
- Epidermal growth factor receptor (EGFR) gene Bsr I polymorphism is associated with systemic lupus erythematosus (2004) (18)
- Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association (2000) (18)
- Lumbrokinase from earthworm extract ameliorates second‐hand smoke‐induced cardiac fibrosis (2015) (18)
- Mesenchymal Stem Cell Insights: Prospects in Hematological Transplantation (2013) (18)
- Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus. (2010) (17)
- Mass Spectrometry-Based Proteomic Study Makes High-Density Lipoprotein a Biomarker for Atherosclerotic Vascular Disease (2015) (17)
- Association study of cyclooxygenase 2 single nucleotide polymorphisms and childhood acute lymphoblastic leukemia in Taiwan. (2010) (17)
- Androgen receptor (AR) gene microsatellite polymorphism in postmenopausal women: correlation to bone mineral density and susceptibility to osteoporosis. (2003) (17)
- The proliferation and migration effects of huangqi on RSC96 Schwann cells. (2009) (17)
- Arginine and proline alleles of the p53 gene are associated with different locations of gastric cancer. (2005) (17)
- Taohe Chengqi Tang ameliorates acute liver injury induced by carbon tetrachloride in rats. (2010) (17)
- Brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms in febrile seizures (2004) (17)
- A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non‐syndromic craniosynostosis (2000) (17)
- The Relationship between Stasis-Stagnation Constitution and Peripheral Arterial Disease in Patients with Type 2 Diabetes (2014) (17)
- Vascular Endothelial Growth Factor Gene 460 Polymorphism Is Associated With Pterygium Formation in Female Patients (2008) (17)
- Earlier and higher dosing of alglucosidase alfa improve outcomes in patients with infantile-onset Pompe disease: Evidence from real-world experiences (2020) (17)
- Balanced reciprocal translocations detected at amniocentesis. (2010) (17)
- Quercetin is increased in heat-processed Cuscuta campestris seeds, which enhances the seed's anti-inflammatory and anti-proliferative activities (2011) (17)
- Puerarin accelerates peripheral nerve regeneration. (2011) (17)
- Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling. (2010) (17)
- Effects of Chinese herbal medicine therapy on survival and hepatic outcomes in patients with hepatitis C virus infection in Taiwan. (2019) (17)
- Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots. (2002) (17)
- BTNL2 gene polymorphisms may be associated with susceptibility to Kawasaki disease and formation of coronary artery lesions in Taiwanese children (2010) (17)
- X-ray repair cross-complementing group 4 (XRCC4) promoter -1394( *)T-related genotype, but not XRCC4 codon 247/intron 3 or xeroderma pigmentosum group D codon 312, 751/promoter -114, polymorphisms are correlated with higher susceptibility to myoma. (2008) (17)
- Simple fabrication of hydrophobic surface target for increased sensitivity and homogeneity in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis of peptides, phosphopeptides, carbohydrates and proteins. (2013) (17)
- Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review. (2008) (17)
- JAK-1 rs2780895 C-related genotype and allele but not JAK-1 rs10789166, rs4916008, rs2780885, rs17127114, and rs3806277 are associated with higher susceptibility to asthma. (2011) (16)
- Identification of biomarkers to improve diagnostic sensitivity of sporadic colorectal cancer in patients with low preoperative serum carcinoembryonic antigen by clinical proteomic analysis. (2011) (16)
- Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8. (2010) (16)
- BNIP3 induces IL6 and calcineurin/NFAT3 hypertrophic-related pathways in H9c2 cardiomyoblast cells (2010) (16)
- Dilong: Role in Peripheral Nerve Regeneration (2011) (16)
- Rare diseases: A mysterious puzzle (2013) (16)
- Relaxant and vasoprotective effects of ginger extracts on porcine coronary arteries. (2018) (16)
- Lose Weight with Traditional Chinese Medicine? Potential Suppression of Fat Mass and Obesity-Associated Protein (2011) (16)
- Inhibition of cardiac hypertrophy by probiotic-fermented purple sweet potato yogurt in spontaneously hypertensive rat hearts. (2012) (16)
- Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation. (2008) (16)
- Search for Novel Remedies to Augment Radiation Resistance of Inhabitants of Fukushima and Chernobyl Disasters: Identifying DNA Repair Protein XRCC4 Inhibitors (2011) (16)
- COMPLEMENT FACTOR H VARIANT INCREASES THE RISK FOR EARLY AGE-RELATED MACULAR DEGENERATION (2008) (16)
- Rapid screening assay of trimethylaminuria in urine with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. (2007) (16)
- Association between urokinase-plasminogen activator gene T4065C polymorphism and risk of mitral valve prolapse. (2004) (16)
- Genetic polymorphisms of the DNA repair gene UNG are associated with the susceptibility of rheumatoid arthritis (2012) (16)
- Smith-Magenis syndrome with bilateral vesicoureteral reflux: a case report. (2002) (16)
- RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia (2011) (16)
- Osteocalcin gene HindIII C/T polymorphism is a biomarker for prostate cancer and responsiveness to hormone therapy. (2003) (16)
- CYP17 gene promoter allelic variant is not associated with prostate cancer. (2003) (16)
- The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions (2002) (16)
- Apicidin-resistant HA22T hepatocellular carcinoma cells massively promote pro-survival capability via IGF-IR/PI3K/Akt signaling pathway activation (2013) (15)
- Insertion/deletion mutations of type I oculocutaneous albinism in Chinese patients from Taiwan (1999) (15)
- Relation of BsmI Vitamin D Receptor Gene Polymorphism to Bone Mineral Density and Occurrence of Osteoporosis in Postmenopausal Chinese Women in Taiwan (2001) (15)
- Nonketotic hyperglycinemia: A case report and brief review (2012) (15)
- Major histocompatibility complex class I chain-related gene polymorphisms: associated with susceptibility to Kawasaki disease and coronary artery aneurysms. (2011) (15)
- Association of Promoter Genetic Variants in Interleukin‐10 and Kawasaki Disease With Coronary Artery Aneurysms (2014) (15)
- Effects of Chinese Herbal Medicines on the Risk of Overall Mortality, Readmission, and Reoperation in Hip Fracture Patients (2019) (15)
- Limb-body wall complex in one fetus of a dizygotic twin pregnancy conceived by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review. (2009) (15)
- Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study (2017) (15)
- Computational screening and QSAR analysis for design of AMP-activated protein kinase agonist (2010) (15)
- Sorting nexin 24 genetic variation associates with coronary artery aneurysm severity in Kawasaki disease patients (2013) (15)
- G/T polymorphism in the interleukin-2 exon 1 region among Han Chinese systemic lupus erythematosus patients in Taiwan. (2008) (15)
- Association between GRIN3A Gene Polymorphism in Kawasaki Disease and Coronary Artery Aneurysms in Taiwanese Children (2013) (15)
- Simultaneous detection of diagnostic biomarkers of alkaptonuria, ornithine carbamoyltransferase deficiency, and neuroblastoma disease by high-performance liquid chromatography/tandem mass spectrometry. (2013) (15)
- Attenuation of Magnesium Sulfate on CoCl₂-Induced Cell Death by Activating ERK1/2/MAPK and Inhibiting HIF-1α via Mitochondrial Apoptotic Signaling Suppression in a Neuronal Cell Line. (2015) (15)
- Protective effects and network analysis of natural compounds obtained from Radix dipsaci, Eucommiae cortex, and Rhizoma drynariae against RANKL-induced osteoclastogenesis in vitro. (2019) (15)
- Rs 6313 polymorphism in 5‐hydroxytryptamine receptor 2A gene association with polysymptomatic primary nocturnal enuresis (2010) (15)
- Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly. (2011) (15)
- Effects of commercial citrate‐containing juices on urolithiasis in a Drosophila model (2013) (15)
- Association study between Tourette's syndrome and polymorphisms of noradrenergic genes (ADRA2A, ADRA2C). (2007) (15)
- The relationship of salivary and cord blood cortisol inpreterm infants (2011) (15)
- Blocking the DNA Repair System by Traditional Chinese Medicine? (2011) (15)
- The comparison of CHCA solvent compositions for improving LC-MALDI performance and its application to study the impact of aflatoxin B1 on the liver proteome of diabetes mellitus type 1 mice (2017) (14)
- Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. (2011) (14)
- Garlic oil attenuates the cardiac apoptosis in hamster-fed with hypercholesterol diet. (2013) (14)
- A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error (2005) (14)
- Suppression of TLR-4-related inflammatory pathway and anti-fibrosis effects of probiotic-fermented purple sweet potato yogurt in hearts of spontaneously hypertensive rats. (2013) (14)
- Gene polymorphisms of adiponectin and leptin receptor are associated with early onset of type 2 diabetes mellitus in the Taiwanese population (2012) (14)
- E-Cadherin Gene 3′-UTR C/T Polymorphism Is Associated with Prostate Cancer (2005) (14)
- Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population (2014) (14)
- Kidney stone distribution caused by melamine and cyanuric acid in rats. (2014) (14)
- Mutation of IVS2 -12A/C>G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency. (2003) (14)
- XRCC1 399*Arg-related genotype and allele, but not XRCC1 His107Arg, XRCC1 Trp194Arg, KCNQ2, AT1R, and hOGG1 polymorphisms, are associated with higher susceptibility of endometriosis (2012) (14)
- De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure. (2011) (14)
- 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization. (2009) (14)
- Cytochrome P450c17alpha 5'-untranslated region *T/C polymorphism in endometriosis. (2004) (14)
- Biomedicine brings the future nearer (2011) (14)
- Association of interleukin‐18 gene polymorphism with asthma in Chinese patients (2008) (14)
- Three novel beta-galactosidase gene mutations in Han Chinese patients with GM1 gangliosidosis are correlated with disease severity (2010) (14)
- Null type of glutathione S-transferase M1 polymorphism is associated with early onset pterygium. (2004) (14)
- Drug Design for the Influenza A Virus Subtype H1N1 (2009) (14)
- Concomitant exencephaly and limb defects associated with pentalogy of Cantrell. (2008) (14)
- Comparison of Oral and Subcutaneous Iron Chelation Therapies in the Prevention of Major Endocrinopathies in β-Thalassemia Major Patients (2006) (14)
- Herbal supplement attenuation of cardiac fibrosis in rats with CCl₄-induced liver cirrhosis. (2014) (14)
- TUMOR NECROSIS FACTOR-α GENE POLYMORPHISMS IN AGE-RELATED MACULAR DEGENERATION (2010) (14)
- Association of interleukin-18 gene polymorphisms with calcium oxalate kidney stone disease (2010) (14)
- Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataract. (2013) (14)
- Myelination arrest demonstrated using magnetic resonance imaging in a child with type I GM1 gangliosidosis. (1998) (13)
- Association between polymorphism of interleukin-1β-511 promoter and susceptibility to febrile convulsions in Taiwanese children (2007) (13)
- Association between Ataxia Telangiectasia Mutated gene polymorphisms and childhood leukemia in Taiwan. (2011) (13)
- Dual Effect of a Polymorphism in the Macrophage Migration Inhibitory Factor Gene Is Associated with New-Onset Graves Disease in a Taiwanese Chinese Population (2014) (13)
- Craniofacial dysmorphism, what is your diagnosis? (2012) (13)
- Drug design for hemagglutinin: Screening and molecular dynamics from traditional Chinese medicine database (2011) (13)
- Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation. (2008) (13)
- Disease association of the CD103 polymorphisms in Taiwan Chinese Graves' ophthalmopathy patients. (2010) (13)
- Induction of the Mitochondria Apoptosis Pathway by Phytohemagglutinin Erythroagglutinating in Human Lung Cancer Cells (2011) (13)
- Interleukin-1β Exon 5 and Interleukin-1 Receptor Antagonist in Children With Immune Thrombocytopenic Purpura (2007) (13)
- Association of IL12B polymorphisms with susceptibility to Graves ophthalmopathy in a Taiwan Chinese population (2012) (13)
- Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019) (2020) (13)
- Lumbrokinase attenuates side-stream-smoke-induced apoptosis and autophagy in young hamster hippocampus: correlated with eNOS induction and NFκB/iNOS/COX-2 signaling suppression. (2013) (13)
- Dracorhodin perchlorate enhances wound healing via β-catenin, ERK/p38, and AKT signaling in human HaCaT keratinocytes (2021) (13)
- Association of rheumatoid arthritis risk with EGFR genetic polymorphisms in Taiwan’s Han Chinese population (2012) (13)
- Novel quinazolinone MJ-33 induces AKT/mTOR-mediated autophagy-associated apoptosis in 5FU-resistant colorectal cancer cells (2020) (13)
- Amino acid concentrations in cerebrospinal fluid in children with acute lymphoblastic leukemia undergoing chemotherapy. (2005) (13)
- Simultaneous determination of components released from dental composite resins in human saliva by liquid chromatography/multiple‐stage ion trap mass spectrometry (2012) (13)
- Effects of Chinese herbal medicines on dementia risk in patients with sleep disorders in Taiwan. (2020) (13)
- Enhancement of AG1024-induced H9c2 cardiomyoblast cell apoptosis via the interaction of IGF2R with Galpha proteins and its downstream PKA and PLC-beta modulators by IGF-II. (2009) (13)
- Effect of exercise training on calpain systems in lean and obese Zucker rats (2008) (13)
- Reduction of TLR4 mRNA stability and protein expressions through inhibiting cytoplasmic translocation of HuR transcription factor by E₂ and/or ERα in LPS-treated H9c2 cardiomyoblast cells. (2014) (13)
- IL‐2 gene C/T polymorphism is associated with prostate cancer (2006) (13)
- Lack of association between interleukin-4 gene polymorphisms and autoimmune thyroid diseases amongst Taiwanese Chinese (2007) (12)
- Angiotensin II type 1 receptor gene adenine/cytosine1166 polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese. (2002) (12)
- Relationships among Height, Weight, Body Mass Index, and Age in Taiwanese Children with Different Types of Mucopolysaccharidoses (2019) (12)
- CYP17 and tumor necrosis factor-α gene polymorphisms are associated with risk of oral cancer in Chinese patients in Taiwan (2005) (12)
- Cardiac hypertrophy-related pathways in obesity. (2014) (12)
- Mutation analysis of the tumor suppressor gene PPP2R1B in human cervical cancer. (2007) (12)
- Effects of Tamm-Horsfall Protein and Albumin on the Inhibition of Free Radicals (2001) (12)
- Detection of a homozygous D645E mutation of the acid α‐glucosidase gene and glycogen deposition in tissues in a second‐trimester fetus with infantile glycogen storage disease type II (2004) (12)
- Novel susceptibility genes associated with diabetic cataract in a Taiwanese population (2013) (12)
- Association of the C-285T and A5954G polymorphisms in the DNA repair gene OGG1 with the susceptibility of rheumatoid arthritis (2012) (12)
- Toll-like receptor 9 SNPs are susceptible to the development and progression of membranous glomerulonephritis: 27 years follow-up in Taiwan (2013) (12)
- Urine proteome analysis by C18 plate–matrix-assisted laser desorption/ionization time-of-flight mass spectrometry allows noninvasive differential diagnosis and prediction of diabetic nephropathy (2018) (12)
- Single nucleotide polymorphisms at the PRR3, ABCF1, and GNL1 genes in the HLA class I region are associated with Graves' ophthalmopathy in a gender-dependent manner. (2014) (12)
- T allele for VEGF-460 Gene Polymorphism at 5′-Untranslated Region is Associated with Higher Susceptibility of Leiomyoma (2008) (12)
- Protective effects of valproic acid on 6‐hydroxydopamine‐induced neuroinjury (2020) (12)
- Expression of protein kinase C isoforms in cancerous breast tissue and adjacent normal breast tissue. (2012) (12)
- Single-nucleotide polymorphisms in chromosome 3p14.1- 3p14.2 are associated with susceptibility of Type 2 diabetes with cataract (2010) (12)
- Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan. (2002) (12)
- Association of TLR7 and TSHR copy number variation with Graves’ disease and Graves’ ophthalmopathy in Chinese population in Taiwan (2014) (12)
- Lack of association of genetic polymorphisms in the interleukin-1beta, interleukin-1 receptor antagonist, interleukin-4 and interleukin-10 genes with mitral valve prolapse in Taiwan Chinese. (2003) (12)
- Effects of Growth Hormone Treatment on Height, Weight, and Obesity in Taiwanese Patients with Prader‐Willi Syndrome (2008) (12)
- The Effect of Elephantopus scaber L. on Liver Regeneration after Partial Hepatectomy (2013) (12)
- Rare rearrangements: A “jumping satellite” in one family and autosomal location of the SRY gene in an XX male (2009) (12)
- Effects of cytokine and cytokine receptor gene variation on high anti-HB titers: following up on Taiwan's neonatal hepatitis B immunization program. (2012) (11)
- Serological surveillance and IL-10 genetic variants on anti-HBs titers: hepatitis B vaccination 20 years after neonatal immunization in Taiwan. (2011) (11)
- Association of the nicotinic receptor beta 2 subunit and febrile seizures. (2004) (11)
- Association of an A allele for interleukin-10 -627 gene promoter polymorphism with higher susceptibility to endometriosis. (2003) (11)
- Class 1 integrons and plasmid-mediated multiple resistance genes of the Campylobacter species from pediatric patient of a university hospital in Taiwan (2017) (11)
- Effect of Chinese Herbal Medicine Therapy on Overall and Cancer Related Mortality in Patients With Advanced Nasopharyngeal Carcinoma in Taiwan (2021) (11)
- Novel K6-K14 keratin fusion enhances cancer stemness and aggressiveness in oral squamous cell carcinoma (2019) (11)
- Autosomal dominant inherited oculo-auriculo-vertebral spectrum: report of one family. (1993) (11)
- Interleukin-2 receptor beta (IL-2R beta)-627*C homozygote but not IL-12R beta 1 codon 378 or IL-18 105 polymorphism is associated with higher susceptibility to endometriosis. (2005) (11)
- Effects of yam and diosgenin on calpain systems in skeletal muscle of ovariectomized rats. (2008) (11)
- EFFECTS OF DEEP-SEA WATER ON CARDIAC ABNORMALITY IN HIGH-CHOLESTEROL DIETARY MICE (2012) (11)
- Citrus medica var. sarcodactylis (Foshou) activates fibroblast growth factor-2 signaling to induce migration of RSC96 Schwann cells. (2014) (11)
- Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p (2007) (11)
- Interleukin-2 receptor β (IL-2Rβ)-627*C homozygote but not IL-12Rβ1 codon 378 or IL-18 105 polymorphism is associated with higher susceptibility to endometriosis (2005) (11)
- Gadolinium chloride elicits apoptosis in human osteosarcoma U-2 OS cells through extrinsic signaling, intrinsic pathway and endoplasmic reticulum stress. (2016) (11)
- Alpinia Oxyphylla Miquel Fruit Extract Activates MAPK-mediated Signaling of PAs and MMP2/9 to Induce Schwann Cell Migration and Nerve Regeneration (2014) (11)
- Genetic analysis of chromosome 22q11.2 markers in congenital heart disease (2003) (11)
- Association between vitamin‐D receptor gene FokI polymorphism and Graves' disease among Taiwanese Chinese (2007) (11)
- Albuterol as an adjunctive treatment to enzyme replacement therapy in infantile-onset Pompe disease☆ (2017) (11)
- Akt mediates 17 -estradiol and/or estrogen receptor- inhibition of LPS-induced tumor necresis factor- expression and myocardial cell apoptosis by suppressing the JNK1/2-NF B pathway (2009) (11)
- MUC2 polymorphisms are associated with endometriosis development and infertility: a case-control study (2012) (11)
- Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18. (2010) (11)
- The association of −627 interleukin-10 promoter polymorphism in Chinese patients with systemic lupus erythematosus (2007) (11)
- Measurement of ear length in neonates, infants and preschool children in Taiwan. (2002) (11)
- Chimerin 2 genetic polymorphisms are associated with non-proliferative diabetic retinopathy in Taiwanese type 2 diabetic patients. (2014) (11)
- Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: data from the hunter outcome survey (HOS) (2018) (11)
- Rheumatoid arthritis is associated with rs17337023 polymorphism and increased serum level of the EGFR protein (2017) (11)
- Diversity of the CYP21A2 gene: a 6.2-kb TaqI fragment and a 3.2-kb TaqI fragment mistaken as CYP21A1P. (2006) (11)
- Cytokine polymorphisms and chronic lung disease in small preterm infants (2004) (11)
- Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array comparative genomic hybridization in pregnancy with abnormal ultrasound findings detected in late second and third trimesters. (2010) (11)
- Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization. (2010) (11)
- Characteristics of Chinese herbal medicine usage in ischemic heart disease patients among type 2 diabetes and their protection against hydrogen peroxide-mediated apoptosis in H9C2 cardiomyoblasts (2017) (10)
- High Protein Diet and Huntington's Disease (2015) (10)
- Thymic stromal lymphopoietin gene promoter polymorphisms and expression levels in Graves’ disease and Graves’ ophthalmopathy (2012) (10)
- Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method (2002) (10)
- Early prediction of severe acute pancreatitis by urinary β-2 microglobulin/saposin B peak ratios on MALDI-TOF. (2015) (10)
- Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients (2001) (10)
- Mutation analysis of Crouzon syndrome in Taiwanese patients (2006) (10)
- A randomized, double-blind, placebo-controlled trial of a Chinese herbal Sophora flower formula in patients with symptomatic haemorrhoids: a preliminary study. (2013) (10)
- Association of STAT4 polymorphisms with susceptibility to primary membranous glomerulonephritis and renal failure. (2011) (10)
- Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation. (2001) (10)
- Clinical manifestation and carbamazepine treatment of patients with paroxysmal kinesigenic choreoathetosis. (2005) (10)
- Attenuated Cardiac Mitochondrial-Dependent Apoptotic Effects by Li-Fu Formula in Hamsters Fed with a Hypercholesterol Diet (2011) (10)
- Congenital generalized lipodystrophy in Taiwan. (2019) (10)
- Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4. (2011) (10)
- Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester. (2012) (10)
- Identification of contributing genes of Huntington’s disease by machine learning (2020) (10)
- Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2‐13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high‐density oligonucleotide array‐a recognizable syndrome (2010) (10)
- Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype (2006) (10)
- No association of interleukin-4 gene polymorphisms in Chinese patients with rheumatoid arthritis in Taiwan. (2002) (10)
- Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis. (2009) (10)
- A novel PIGA mutation in a Taiwanese family with early-onset epileptic encephalopathy (2018) (10)
- Association between urokinase gene 3'-UTR T/C polymorphism and Chinese patients with rheumatoid arthritis in Taiwan. (2004) (10)
- Amino acids with basic amino side chain accelerate the pro-oxidant ability of polyphenolic compounds (2012) (10)
- Lack of association between transient receptor potential cation channel 6 polymorphisms and primary membranous glomerulonephritis (2010) (10)
- Zanthoxylum avicennae extracts inhibit cell proliferation through protein phosphatase 2A activation in HA22T human hepatocellular carcinoma cells in vitro and in vivo. (2012) (10)
- Activation of snail and EMT-like signaling via the IKKαβ/NF-κB pathway in Apicidin-resistant HA22T hepatocellular carcinoma cells. (2013) (9)
- Diosmin induces cell apoptosis through protein phosphatase 2A activation in HA22T human hepatocellular carcinoma cells and blocks tumour growth in xenografted nude mice (2012) (9)
- Prominent vacuolation of the eyelid levator muscle in an early‐treated child with infantile‐onset Pompe disease (2014) (9)
- Miller Fisher syndrome possibly related to mycoplasma pneumoniae infection: report of one case. (2004) (9)
- Matched unrelated bone marrow transplantation without splenectomy for a child with Gaucher disease caused by homozygosity of the L444P mutation, who also suffered from schizencephaly. (2007) (9)
- Genetic screening of the makorin ring finger 3 gene in girls with idiopathic central precocious puberty (2016) (9)
- Association between angiotensinogen gene M235T polymorphism and mitral valve prolapse syndrome in Taiwan Chinese. (2002) (9)
- Disruption of IGF-1R signaling by a novel quinazoline derivative, HMJ-30, inhibits invasiveness and reverses epithelial-mesenchymal transition in osteosarcoma U-2 OS cells (2018) (9)
- A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings. (2011) (9)
- Hematopoietically expressed homeobox gene is associated with type 2 diabetes in KK Cg-Ay/J mice and a Taiwanese Han Chinese population (2018) (9)
- Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18. (2010) (9)
- Association Between Genetic Polymorphism of the MIF Gene and Colorectal Cancer in Taiwan (2015) (9)
- Loss of Response Gene to Complement 32 (RGC-32) in Diabetic Mouse Retina Is Involved in Retinopathy Development (2018) (9)
- Novel human pathological mutations. Gene symbol: COMP. Disease: pseudoachondroplasia. (2009) (9)
- Long, Noncoding RNA SRA Induces Apoptosis of β-Cells by Promoting the IRAK1/LDHA/Lactate Pathway (2021) (9)
- Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis. (2009) (9)
- Mutation analysis of type II Gaucher disease in five Taiwanese children: identification of two novel mutations. (2001) (9)
- Rapid fabrication of functionalized plates for peptides, glycopeptides and protein purification and mass spectrometry analysis. (2016) (9)
- Genetic Architecture Associated with Familial Short Stature. (2020) (9)
- Novel hemagglutinin inhibitors for H1N1 influenza virus screening from TCM database (2011) (9)
- Evaluation of Transforming Growth Factor and Vascular Endothelial Growth Factor Polymorphisms in Taiwan Chinese Patients with Pterygium (2008) (9)
- Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation (2014) (9)
- Genetic susceptibility to idiopathic membranous nephropathy in high-prevalence Area, Taiwan (2014) (9)
- Multilocus genetic risk score for diabetic retinopathy in the Han Chinese population of Taiwan (2018) (9)
- Transient hypogammaglobulinemia of infancy presenting as Staphylococcus aureus sepsis with deep neck infection. (2005) (9)
- Transporter Associated with Antigen Processing Gene 1 Codon 333 and Codon 637 Polymorphisms are Associated with Primary Open-Angle Glaucoma (2004) (9)
- Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene. (2010) (9)
- Filamin B Loss‐of‐Function Mutation in Dimerization Domain Causes Autosomal‐Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies (2017) (9)
- Alternative Splicing in Acad8 Resulting a Mitochondrial Defect and Progressive Hepatic Steatosis in Mice (2011) (9)
- Significant association of caveolin-1 single nucleotide polymorphisms with childhood leukemia in Taiwan. (2013) (9)
- Genetic polymorphisms of the DNA repair geneMPG may be associated with susceptibility to rheumatoid arthritis (2011) (8)
- Genetic impacts on thermostability of onco-lncRNA HOTAIR during the development and progression of endometriosis (2021) (8)
- Evaluation of TNF-α and IL-1β polymorphisms in Taiwan Chinese patients with pterygium (2005) (8)
- Proteomic analysis of chondrocytes exposed to pressure. (2010) (8)
- Potential Genitourinary Toxicity and Lithogenic Effect of Ractopamine (2015) (8)
- Lack of association of genetic variants for diabetic retinopathy in Taiwanese patients with diabetic nephropathy (2020) (8)
- Th1 and Th2 cytokines are elevated in HCV-infected SVR( ) patients treated with interferon-a (2009) (8)
- Resveratrol Pretreatment Ameliorates Concanavalin A-Induced Advanced Renal Glomerulosclerosis in Aged Mice through Upregulation of Sirtuin 1-Mediated Klotho Expression (2020) (8)
- Arginine form of p21 gene codon 31 is less prominent in patients with calcium oxalate stone (2001) (8)
- Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis. (2011) (8)
- Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings. (2010) (8)
- Drug design for mPGES-1 from traditional Chinese medicine database: A screening, docking, QSAR, molecular dynamics, and pharmacophore mapping study (2011) (8)
- Two novel polymorphisms (c954T>C and c1038A>G) in exon8 of NPHS2 gene identified in Taiwan Chinese. (2001) (8)
- Lack of association of tumor necrosis factor alpha gene polymorphism in patients with rheumatoid arthritis in central Taiwan (2003) (8)
- Clinical analysis of a dysentery outbreak in Taichung. (2000) (8)
- Androgen receptor gene polymorphism and rheumatoid arthritis in Taiwan. (2006) (8)
- Down regulation of IGF-I and IGF-IR gene expression in right atria tissue of ventricular septal defect infants with right atria hypoxemia. (2007) (8)
- Association Between SRC‐1 Gene Polymorphisms and Coronary Artery Aneurysms Formation in Taiwanese Children With Kawasaki Disease (2014) (8)
- A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys. (2009) (8)
- Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes. (2012) (8)
- Prenatal diagnosis of partial monosomy 1q (1q42.3-qter) associated with hydrocephalus and corpus callosum agenesis. (2010) (8)
- Variants in ZNRD1 Gene Predict HIV-1/AIDS Disease Progression in a Han Chinese Population in Taiwan (2013) (8)
- Pro‐inflammation and pro‐fibrosis factors were highly induction in heart tissues of carotid arteries balloon‐injured animal model (2012) (8)
- Improved final predicted height with the injection of leuprolide in children with earlier puberty: A retrospective cohort study (2017) (8)
- Zanthoxylum avicennae extracts induce cell apoptosis through protein phosphatase 2A activation in HA22T human hepatocellular carcinoma cells and block tumor growth in xenografted nude mice. (2011) (8)
- Immunoglobulin E and matrix metalloproteinase-9 in patients with different stages of coronary artery diseases. (2007) (8)
- Association of CD4 Enhancer Gene Polymorphisms with Rheumatoid Arthritis and Systemic Lupus Erythematosus in Taiwan (2008) (8)
- Matrix metalloproteinase 14 modulates diabetes and Alzheimer’s disease cross-talk: a meta-analysis (2018) (8)
- TAP1 gene AccI polymorphism is associated with atopic bronchial asthma (2003) (8)
- Interleukin-1beta exon 5 and interleukin-1 receptor antagonist in children with immune thrombocytopenic purpura. (2007) (8)
- Association of interleukin-16 polymorphisms with graves' disease in a Taiwanese population. (2014) (8)
- Prenatal diagnosis of concomitant Wolf–Hirschhorn syndrome and split hand‐foot malformation associated with partial monosomy 4p (4p16.1→pter) and partial trisomy 10q (10q25.1→qter) (2008) (8)
- β-Sitosterol-2-hydroxypropyl-β-cyclodextrin inclusion complex: Characterization and inhibitory effect on adipogenesis in 3T3-L1 pre-adipocytes (2018) (8)
- Study of Baicalin toward COVID-19 Treatment: In silico Target Analysis and in vitro Inhibitory Effects on SARS-CoV-2 Proteases (2021) (8)
- Dung-Shen Downregulates the Synergistic Apoptotic Effects of Angiotensin II Plus Leu 27-IGF II on Cardiomyoblasts. (2014) (8)
- The cuttable C-related genotype and allele for the E-cadherin 3-UTR Pml I polymorphism are associated with higher susceptibility to endometriosis (2005) (8)
- Qi deficiency is associated with depression in chronic hemodialysis patients. (2017) (8)
- Isovaleric acidemia diagnosed promptly by tandem mass spectrometry: report of one case. (2004) (7)
- SHSST-cyclodextrin complex inhibits TGF-β/Smad3/CTGF to a greater extent than silymarin in a rat model of carbon tetrachloride-induced liver injury. (2015) (7)
- Prenatal diagnosis of dyssegmental dysplasia. A case report. (1999) (7)
- Effects of Casein Kinase 2 Alpha 1 Gene Expression on Mice Liver Susceptible to Type 2 Diabetes Mellitus and Obesity (2020) (7)
- Association of CYP17 gene polymorphism and rheumatoid arthritis in Chinese patients in central Taiwan (2005) (7)
- Screening from TCM Database@Taiwan and QSAR model for identifying HER2 inhibitors (2011) (7)
- No association of p53 codon 72 and p21 codon 31 polymorphisms in Taiwan Chinese patients with pterygium (2004) (7)
- Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele (2001) (7)
- There Is No Evidence of Difference in Polymorphisms in the IL-1 β-511 Promoter and IL-1Ra Gene Between Asthmatic and Healthy Groups (2004) (7)
- Low-density lipoprotein (LDL) apheresis reduces atherogenic and oxidative markers in uremic patients with hyperlipidemia (2011) (7)
- Cytochrome P450c17α (CYP17) gene polymorphism is not associated with leiomyoma susceptibility (2002) (7)
- A More Diverse Cervical Microbiome Associates with Better Clinical Outcomes in Patients with Endometriosis: A Pilot Study (2022) (7)
- Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer. (2011) (7)
- Transparent Copolyester/Organoclay Nanocomposites Prepared by In Situ Intercalation Polymerization: Synthesis, Characterization, and Properties (2011) (7)
- Polymorphisms of TAP1 transporter genes in Chinese patients with systemic lupus erythematosus in Taiwan (2004) (7)
- In Silico De Novo Curcuminoid Derivatives From the Compound Library of Natural Products Research Laboratories Inhibit COVID-19 3CLpro Activity (2020) (7)
- Aberrant transcripts of FHIT, TSG101 and PTEN/MMAC1 genes in normal peripheral mononuclear cells. (2000) (7)
- Lack of association between transforming growth factor-beta1 gene polymorphisms and mitral valve prolapse in Taiwan Chinese. (2002) (7)
- Association study in Taiwanese girls with precocious puberty (2011) (7)
- Effects of sodium citrate on melamine-cyanuric acid mixture-induced urolithiasis in rats. (2013) (7)
- Coronary artery aneurysms occurrence risk analysis between Kawasaki disease and LRP1B gene in Taiwanese children (2014) (7)
- Identification and characterization of a new type of asymmetrical dicentric chromosome derived from a single maternal chromosome 18 (2008) (7)
- Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21. (2010) (7)
- Cantharidin decreased viable cell number in human osteosarcoma U-2 OS cells through G2/M phase arrest and induction of cell apoptosis (2019) (7)
- Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization. (2011) (7)
- Prenatal 3‐dimensional sonographic and MRI findings in omphalocele–exstrophy–imperforate anus–spinal defects complex (2008) (7)
- Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome. (2010) (7)
- Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings. (2011) (7)
- A Novel Nonsense Mutation of the Sedlin Gene in a Family with Spondyloepiphyseal Dysplasia Tarda (2002) (7)
- Association of MRC-1 and IL-28B with the treatment outcome of hepatitis C: a case control study (2014) (7)
- Long-term effects of enzyme replacement therapy for Taiwanese patients with mucopolysaccharidosis IVA. (2019) (7)
- Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus (2010) (7)
- Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy. (2010) (7)
- Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease (2001) (7)
- High levels of circulating endothelial progenitor cells in patients with diabetic retinopathy are positively associated with ARHGAP22 expression (2018) (6)
- Interleukin-1β gene polymorphisms in Taiwanese patients with gout (2005) (6)
- 3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: report of one case. (1999) (6)
- Molecular pathways related to the longevity promotion and cognitive improvement of Cistanche tubulosa in Drosophila. (2017) (6)
- Correlation of oestrogen receptor gene polymorphism with gouty arthritis (2006) (6)
- Key features for designing M2 proton channel anti swine flu inhibitors (2011) (6)
- NT5C2 methylation regulatory interplay between DNMT1 and insulin receptor in type 2 diabetes (2020) (6)
- FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome (2010) (6)
- Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features. (2010) (6)
- The NBS1 Genetic Polymorphisms and the Risk of the Systemic Lupus Erythematosus in Taiwanese Patients (2010) (6)
- Genetic risk score for risk prediction of diabetic nephropathy in Han Chinese type 2 diabetes patients (2019) (6)
- Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits (2007) (6)
- Limb-body wall complex with craniofacial defects after ovarian stimulation. (2008) (6)
- Carboxamide analog ITR-284 evokes apoptosis and inhibits migration ability in human lung adenocarcinoma A549 cells. (2017) (6)
- Genetic epidemiological study doesn't support GLA IVS4+919G>A variant is a significant mutation in Fabry disease. (2017) (6)
- Sister chromatid exchange in Chinese newborn infants treated with phototherapy for more than five days. (1998) (6)
- Increased expression of glucose transporter 3 in gerbil brains following magnesium sulfate treatment and focal cerebral ischemic injury (2010) (6)
- Interleukin-1 receptor antagonist gene polymorphism in Taiwanese patients with gout. (2005) (6)
- Prenatal ultrasound demonstration of limb-body wall complex with megacystis. (2011) (6)
- Causal Relationship between Adiponectin and Diabetic Retinopathy: A Mendelian Randomization Study in an Asian Population (2020) (6)
- Low ambient temperatures correlate with increased risk of hypoglycemia in patients with type 2 diabetes (2020) (6)
- Urokinase Gene 3′-UTR T/C Polymorphism Is Associated with Malignancy and ESRD in Idiopathic Membranous Nephropathy (2014) (6)
- Decreased overall mortality rate with Chinese herbal medicine usage in patients with decompensated liver cirrhosis in Taiwan (2020) (6)
- Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine (2015) (6)
- Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system. (2008) (6)
- Turner Syndrome with Pseudodicentric Y Chromosome Mosaicism (2002) (6)
- Association between MYH9 gene polymorphisms and membranous glomerulonephritis patients in Taiwan (2013) (6)
- Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis. (2009) (6)
- Distributions of p 53 codon 72 polymorphism in primary open angle glaucoma (2002) (6)
- Molecular aspects of Dravet syndrome patients in Taiwan. (2013) (6)
- Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population (2019) (6)
- CCY-1a-E2 induces G2/M phase arrest and apoptotic cell death in HL-60 leukemia cells through cyclin-dependent kinase 1 signaling and the mitochondria-dependent caspase pathway. (2016) (5)
- Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review. (2009) (5)
- NFκB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 → qter) (2008) (5)
- Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity (1999) (5)
- Deletion of exon 4 in the N-acetylgalactosamine-4-sulfatase gene in a Taiwanese patient with mucopolysaccharidosis type VI. (2015) (5)
- Prenatal diagnosis of 46,XX,DER(13;21)(Q10;Q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites. (2009) (5)
- Association of adenosine triphosphate-binding cassette transporter A1 gene polymorphism with lipid profiles and early-onset type 2 diabetes (2014) (5)
- Trisomy 13 mosaicism associated with cyclopia and cystic hygroma. (2009) (5)
- Effect of p53 codon 72 polymorphism on p53 protein expression in pterygium (2005) (5)
- Molecular analysis of Taiwanese patients with 3-hydroxy-3-methylglutaryl CoA lyase deficiency. (2009) (5)
- Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22. (2010) (5)
- Persistent cloaca presenting with a perineal cyst: Prenatal ultrasound and magnetic resonance imaging findings. (2012) (5)
- Urokinase gene 3'-UTR T/C polymorphism is not associated with bladder cancer (2004) (5)
- Genetic variants of glutamate receptor gene family in Taiwanese Kawasaki disease children with coronary artery aneurysms (2014) (5)
- Auditory brainstem responses in term neonates treated with gentamicin. (1992) (5)
- Chromosome 3 p 12 . 3p 14 . 2 and 3 q 26 . 2q 26 . 32 Are Genomic Markers for Prognosis of Advanced Nasopharyngeal Carcinoma (2009) (5)
- Genome-wide and candidate gene association analyses identify a 14-SNPs combination for hypertension in patients with type 2 diabetes. (2020) (5)
- Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester. (2010) (5)
- Effect of adiponectin level and genetic variation of its receptors on diabetic retinopathy (2019) (5)
- Evaluation of TNF-alpha and IL-1beta polymorphisms in Taiwan Chinese patients with pterygium. (2005) (5)
- Polymorphism and protein expression of MUTYH gene for risk of rheumatoid arthritis (2017) (5)
- Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism. (2009) (5)
- Functional independence of Taiwanese patients with mucopolysaccharidoses (2019) (5)
- Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review. (2009) (5)
- Molecular diagnosis of patients with β-thalassemia major in central Taiwan by amplified created restriction site analysis (1998) (5)
- Structure-based and ligand-based drug design for microsomal prostaglandin E synthase-1 inhibitors (2011) (5)
- Data supporting the angiotensin II activates MEL18 to deSUMOylate HSF2 for hypertension-related heart failure (2017) (5)
- Tumor necrosis factor-α and interleukin-4 gene polymorphisms in Chinese patients with gout (2007) (5)
- Effects of Chinese herbal medicines on the occurrence of diabetic retinopathy in type 2 diabetes patients and protection of ARPE-19 retina cells by inhibiting oxidative stress (2017) (5)
- Insulin-like growth factor II gene Apa I polymorphism is not associated with endometriosis susceptibility (2004) (5)
- Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21 --> q11.23 by array comparative genomic hybridization. (2010) (5)
- Comparison of oral and subcutaneous iron chelation therapies in the prevention of major endocrinopathies in beta-thalassemia major patients. (2006) (5)
- Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data. (1999) (5)
- Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB (2014) (5)
- IGF-II and MMP9 as surgical repair indicators of ventricular septal defects. (2011) (5)
- Marked improvement in febrile infection-related epilepsy syndrome after lidocaine plus MgSO4 treatment in a 12-year-old girl (2016) (5)
- Identification of a polymorphism (D366H) in the endoglin gene in Chinese. (2000) (5)
- Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation. (2010) (5)
- Association Analysis of Polymorphisms in Lumican Gene and Systemic Lupus Erythematosus in a Taiwan Chinese Han Population (2011) (5)
- Chinese Herbal Medicine Therapy Reduces the Risks of Overall and Anemia-Related Mortalities in Patients With Aplastic Anemia: A Nationwide Retrospective Study in Taiwan (2021) (5)
- Association of Genetic Variations in X‐Ray Repair Cross‐Complementing Group 1 and Tourette Syndrome (2012) (5)
- Effect of Flos carthami Extract and α 1-Adrenergic Antagonists on the Porcine Proximal Ureteral Peristalsis (2014) (5)
- The polymorphisms of codon 727 and 52 of thyroid-stimulating hormone receptor gene are not associated with mitral valve prolapse syndrome in Taiwan Chinese. (2002) (4)
- Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization. (2010) (4)
- Self-injurious behavior associated with trisomy 9p (9p13.1 --> p24.3). (2011) (4)
- Novel mutations in the cartilage oligomeric matrix protein gene identified in two Taiwanese patients with pseudoachondroplasia and multiple epiphyseal dysplasia. (2017) (4)
- Pathological characterization of a malformed umbilical cord associated with body stalk anomaly. (2011) (4)
- Association of glutathione S-transferase P1 (GSTP1) polymorphism with Tourette syndrome in Taiwanese patients. (2014) (4)
- Association Between XRCC3 Thr241Met SNP and Systemic Lupus Erythematosus in Han Chinese Patients in Taiwan, and a Meta‐Analysis of Healthy Populations (2014) (4)
- Mutant EXT1 in Taiwanese Patients with Multiple Hereditary Exostoses (2014) (4)
- Integrated Chinese Herbal Medicine Therapy Improves the Survival of Patients With Ovarian Cancer (2019) (4)
- Next-generation sequencing analysis reveals that MTH-3, a novel curcuminoid derivative, suppresses the invasion of MDA-MB-231 triple-negative breast adenocarcinoma cells (2021) (4)
- Proliferative effects of Chishao on Schwann cells are FGF-uPA, and ERK- and JNK-dependent. (2009) (4)
- The application of (-)-epigallocatechin gallate in preparation of an antioxidant dialysate. (2012) (4)
- Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele (2008) (4)
- Identification of one novel homozygous mutation in the NPR2 gene in a patient from Taiwan with acromesomelic dysplasia Maroteaux type. (2017) (4)
- Association between the TAP2 gene codon 665 polymorphism and Graves' Disease (2006) (4)
- Late onset of biliopleural fistula following percutaneous transhepatic biliary drainage: a case report (2018) (4)
- Dystonin/BPAG1 modulates diabetes and Alzheimer’s disease cross-talk: a meta-analysis (2019) (4)
- Association of toll-like receptor 4 gene polymorphisms with primary membranous nephropathy in a high prevalence renal disease area in Taiwan. (2010) (4)
- Fetal alcohol syndrome with Arnold-Chiari malformation: report of one case. (1998) (4)
- Effects of Chinese herbal medicines on the occurrence of diabetic retinopathy in type 2 diabetes patients and protection of ARPE-19 retina cells by inhibiting oxidative stress. (2017) (4)
- UNSTABLE Hb PERTH IN A TAIWANESE SUBJECT: A T → C SUBSTITUTION AT CODON 32 OF THE β-GLOBIN GENE CREATES AN MspI SITE (2002) (4)
- Chylous ascites: report of one case. (1995) (4)
- A codon 31 ser–arg polymorphism of the WAF-1/CIP-1/p21/ tumour suppressor gene in Chinese primary open-angle glaucoma (2004) (4)
- Mitochondrial Dysfunction as a Novel Target for Neuroprotective Nutraceuticals in Ocular Diseases (2020) (4)
- No association between TAP1 DpnII polymorphism and bronchopulmonary dysplasia. (2005) (4)
- No association of urokinase gene 3'-UTR polymorphism with bronchopulmonary dysplasia for ventilated preterm infants. (2004) (4)
- Leu 27 IGF 2 plays an opposite r ole to IGF 1 to induce H 9 c 2 cardiomyoblast cell apoptosis via G a q signaling (2009) (4)
- Association of poly(ADP-ribose) polymerase-1 polymorphism with Tourette syndrome (2013) (4)
- Molecular diagnosis of Apert syndrome in Chinese patients. (1999) (4)
- Evaluation of Oral Antiretroviral Drugs in Mice With Metabolic and Neurologic Complications (2018) (4)
- The Role of 99m Tc-ECD Brain SPECT in Differentiating Tourrette's Syndrome from Chronic Tic Disorder (2003) (4)
- Human gene mutations. Gene symbol: GLA. Disease: Fabry disease. (2007) (4)
- Report of clinical bone age assessment using deep learning for an Asian population in Taiwan (2021) (4)
- Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant Osteopetrosis. (2016) (4)
- Prenatal evaluation with magnetic resonance imaging of a giant blind ectopic ureter associated with a duplex kidney (2008) (4)
- Insulin-like growth factors II exon 9 and E-cadherin-Pml I but not myeloperoxidase promoter-463, urokinase-ApaL I nor xeroderma pigmentosum polymorphisms are associated with higher susceptibility to leiomyoma. (2010) (4)
- Reduction in imiglucerase dosage causes immediate rise of chitotriosidase activity in patients with Gaucher disease. (2010) (3)
- Drug discovery for DNA break repair system by screening from TCM database and molecular dynamics approach (2011) (3)
- The p38 and NFκB signaling protein activation involved in glycitein protective effects on isoproterenol-treated H9c2 cardiomyoblast cells (2013) (3)
- An R223P mutation in EXT2 gene causes hereditary multiple exostoses. (2000) (3)
- Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency. (2001) (3)
- Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (3)
- Complementary Chinese Herbal Medicine Therapy Improves Survival in Patients With Pemphigus: A Retrospective Study From a Taiwan-Based Registry (2020) (3)
- Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling. (2010) (3)
- The involvement of insulin receptor genotypes in pre- and co-obese acanthosis Nigricans children and adolescent. (2010) (3)
- Genetic variations in the CεmX domain of human membrane-bound IgE (2010) (3)
- The impact of polymorphisms in STAT6 on treatment outcome in HCV infected Taiwanese Chinese (2013) (3)
- Does Chronic Cola Consumption Increase Urinary Stone Risk? Evidence from the Drosophila Model of Urolithiasis (2015) (3)
- Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis. (2010) (3)
- Investigation of neurochemical techniques for assessment of nerve regeneration within polymer guides (2012) (3)
- Greig cephalopolysyndactyly syndrome in a family. (2006) (3)
- The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma. (2009) (3)
- Inhaled nitric oxide in persistent pulmonary hypertension of the newborn: four-year experience in a single medical center. (2002) (3)
- Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis (2003) (3)
- Rotavirus associated with poliomyelitis-like syndrome. (1998) (3)
- MALDI-TOF mass spectrometry analysis of small molecular weight compounds (under 10 KDa) as biomarkers of rat hearts undergoing arecoline challenge (2013) (3)
- Establishment of a Novel Temozolomide Resistant Subline of Glioblastoma Multiforme Cells and Comparative Transcriptome Analysis With Parental Cells (2021) (3)
- Rapid diagnosis of common aneuploidies by quantitative fluorescent polymerase chain reaction. (1999) (3)
- MBD4 gene is associated with rheumatoid arthritis in Chinese patients in Taiwan (2010) (3)
- Genomic interrogation of familial short stature contributes to the discovery of the pathophysiological mechanisms and pharmaceutical drug repositioning (2019) (3)
- Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty. (2021) (3)
- C-Reactive Protein Gene Variants and Their Serum Levels in Early Adult-onset Type 2 Diabetes Mellitus (2019) (3)
- Proliferative effects of chishao on injured peripheral neurons. (2010) (3)
- Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome. (2010) (3)
- Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers. (2002) (3)
- The role of genotype/phenotype at apurinic/apyrimidinic endonuclease Rs1130409 in renal cell carcinoma (2020) (3)
- Genetic and clinical profiles of spondylocostal dysostosis patients in Taiwan (2011) (3)
- Detection and comparison of cytomegalovirus DNA levels in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction. (2010) (3)
- Genetic risk score constructed from common genetic variants is associated with cardiovascular disease risk in type 2 diabetes mellitus (2020) (3)
- Hyperimmunoglobulinaemia D syndrome in India: report of two siblings with a novel mutation (2006) (3)
- An Increase in Phosphorylation and Truncation of Crystallin With the Progression of Cataracts☆ (2013) (3)
- Association between the TAP1 gene codon 637 polymorphism and graves’ disease (2004) (3)
- Chinese Herbal Medicine Usage Reduces Overall Mortality in HIV-Infected Patients With Osteoporosis or Fractures (2021) (3)
- Holocarboxylase synthetase deficiency: report of one case. (2006) (3)
- Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats. (2015) (3)
- Tumor Necrosis Factor-α Gene G-308A and G-238A Polymorphisms are Not Associated with Rheumatic Heart Disease in Taiwan (2006) (3)
- Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture (2014) (3)
- Effect of MPG Gene rs2858056 Polymorphism, Copy Number Variation, and Level of Serum MPG Protein on the Risk for Rheumatoid Arthritis (2015) (3)
- TAP 2 Gene Msp-I Polymorphism Might Be Associated with Calcium Oxalate Stone Disease (2005) (3)
- A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty. (2011) (3)
- JPH2 is a novel susceptibility gene on chromosome 20q associated with diabetic retinopathy in a Taiwanese population (2013) (3)
- Anti-apoptosis effects on hearts of SHSST cyclodextrin complex in a carbon tetrachloride-induced cirrhotic cardiomyopathy rat model. (2015) (2)
- Preliminary Study of Ethylene Glycol-Induced Alanine-Glyoxylate Aminotransferase 2 Expression in Rat Kidney (2009) (2)
- ITR‑284 modulates cell differentiation in human chronic myelogenous leukemia K562 cells. (2017) (2)
- Ring finger protein 39 genetic variants associate with HIV-1 plasma viral loads and its replication in cell culture (2014) (2)
- Molecular diagnosis of Gaucher disease type II. (1995) (2)
- Activation of IGF2R induces Mitochondrial-dependent Apoptosis through Gαq and Downstream Calcineurin Signaling in Myocardial Cells (2008) (2)
- Identification of novel peptides specifically binding to endometriosis by screening phage-displaying peptide libraries. (2009) (2)
- Association of variant on the promoter of cluster of differentiation 74 in graves disease and graves ophthalmopathy (2020) (2)
- Antioxidant activity and protective effects of the Angelica sinensis-hydroxypropyl-β-cyclodextrin complex on CCl4-induced hepatic failure in mice (2020) (2)
- Carrier detection of Duchenne/Becker muscular dystrophy by using fluorescent linkage analysis in Taiwan. (2000) (2)
- Timing, Dosage, and Adherence of Antiretroviral Therapy and Risk of Osteoporosis in Patients With Human Immunodeficiency Virus Infection in Taiwan: A Nested Case-Control Study (2021) (2)
- Association of the PLEKHO2 and PLEKHH1 gene polymorphisms with type 2 diabetic retinopathy in a Taiwanese population (2012) (2)
- Does Ser364Pro mutation of connexin 43 exist in Taiwanese patients with Ivemark syndrome? (2000) (2)
- Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings. (2008) (2)
- Tumor necrosis factor-alpha and interleukin-4 gene polymorphisms in Chinese patients with gout. (2007) (2)
- 2-Phenyl-4-quinolone (YT-1) induces G2/M phase arrest and an intrinsic apoptotic mechanism in human leukemia cells. (2017) (2)
- Reduced albumin in the renal cortex of ethylene glycol-treated rats (2014) (2)
- Treat Alzheimer's disease by traditional Chinese medicine? (2011) (2)
- Mutation analysis of the tumor suppressor gene PPP2R1B in human cervical cancer (2006) (2)
- Suppression of Plasminogen Activators and the MMP-2/-9 Pathway by a Zanthoxylum avicennae Extract to Inhibit the HA22T Human Hepatocellular Carcinoma Cell Migration and Invasion Effects in Vitro and in Vivo via Phosphatase 2A Activation (2013) (2)
- Erratum to: Enzyme replacement therapy for mucopolysaccharidosis VI—experience in Taiwan (2013) (2)
- Anti‐apoptotic effect of San Huang Shel Shin Tang cyclodextrin complex (SHSSTc) on CCl4‐induced hepatotoxicity in rats (2016) (2)
- Simultaneously Evaluating the Effects of One-week Fluticasone Propionate Inhalation Therapy on Lung Ventilation and Permeability in Children with Asthma (2003) (2)
- Harlequin ichthyosis: report of one case. (1998) (2)
- GPC observations of branching effects in anionic polymerization of methyl methacrylate: A preliminary study (2009) (2)
- Effects of Acrylamide-Induced Vasorelaxation and Neuromuscular Blockage: A Rodent Study (2021) (2)
- [Beta-thalassemia major complicated with Vibrio vulnificus septicemia: report of one case]. (1994) (2)
- A case of Pitt-Hopkins syndrome presented with Angelman-like syndromic phenotypes (2016) (2)
- Increased Expression of Ecto-NOX Disulfide-thiol Exchanger 1 (ENOX1) in Diabetic Mice Retina and its Involvement in Diabetic Retinopathy Development (2019) (2)
- Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses. (2011) (2)
- Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly. (2009) (2)
- Association of Tyrosyl‐DNA Phosphodiesterase 1 Polymorphism With Tourette Syndrome in Taiwanese Patients (2013) (2)
- Your height affects your health: genetic determinants and health-related outcomes in Taiwan (2022) (2)
- Functional independence of Taiwanese children with Prader–Willi syndrome (2018) (2)
- Ameliorate Effects of Li-Fu Formula on IL-6-Mediated Cardiac Hypertrophy in Hamsters Fed with a Hyper-Cholesterol Diet (2011) (2)
- High Concentration of Iopromide Induces Apoptosis and Autophagy in Human Embryonic Kidney Cells via Activating a ROS-dependent Cellular Stress Pathway (2021) (2)
- Erratum: Lumbrokinase attenuates side-stream-smoke-induced apoptosis and autophagy in young hamster hippocampus: Correlated with eNOS induction and NFκB/iNOS/COX-2 signaling suppression (Chemical Research in Toxicology (2013) 26,5 DOI: 10.1021/tx300429s (654?661)) (2013) (2)
- Agnathia in one of heterozygous twins. (1999) (2)
- Association Study of Gene Polymorphism and Bronchopulmonary Dysplasia (2005) (2)
- Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p. (2011) (2)
- A rapid, multiplexed kinase activity assay using 8-plex iTRAQ labeling, SPE, and MALDI-TOF/TOF MS. (2019) (2)
- Monosomy of chromosome 10q26 with mild psychomotor retardation: report of one case. (2002) (2)
- Effect of Chinese herbal medicines on the overall survival of patients with muscular dystrophies in Taiwan. (2021) (1)
- Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses. (2012) (1)
- Interleukin-1- b Gene, But Not the Interleukin-1 Receptor Antagonist Gene, Is Associated With Graves’ Disease (2005) (1)
- Estrogen Receptor-α and -β in Endometriosis and Normal Endometrium in Humans (2005) (1)
- Multiple pterygium syndrome: report of one case. (1999) (1)
- Inclusion complex of emodin and glycyrrhetinic acid-conjugated-β-cyclodextrin to target liver cells: synthesis, characterization, and bioactivity in vitro and in vivo (2022) (1)
- Analysis of HLA Variants and Graves’ Disease and Its Comorbidities Using a High Resolution Imputation System to Examine Electronic Medical Health Records (2022) (1)
- Chromosome 15q21-22-related polymorphisms and haplotypes are associated with susceptibility to type-2 diabetic nonproliferative retinopathy. (2012) (1)
- Lack of association between perlecan gene intron 6 BamHI polymorphism and risk of mitral valve prolapse in Taiwan Chinese. (2004) (1)
- Gene polymorphisms and bronchopulmonary dysplasia. (2006) (1)
- Erratum: Oral Lactobacillus reuteri GMN-32 treatment reduces blood glucose concentrations and promotes cardiac function in rats with streptozotocin-induced diabetes mellitus - RETRACTION( British Journal of Nutrition (2013) 1:8 DOI:10.1017/S0007114513002791) (2014) (1)
- Effect of Xanthium Strumarium on HIV-1 5′-LTR Transcriptional Activity and Viral Reactivation in Latently Infected Cells (2021) (1)
- Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population (2014) (1)
- Detection of balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses. (2010) (1)
- Antibody to Hepatitis C Virus in Multitransfused Patients with β-Thalassemia Major (1998) (1)
- Interleukin-2 receptor gene polymorphism in Chinese patients with systemic lupus erythematosus (2006) (1)
- Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1. (2007) (1)
- Contribution of Matrix Metalloproteinase-9 rs3918242 Genotypes to Childhood Leukemia Risk (2020) (1)
- Niemann-Pick disease type B with ocular involvement: report of a case. (1991) (1)
- Cannabinoid receptor type 1 antagonist inhibits progression of obesity‐associated nonalcoholic steatohepatitis in a mouse model by remodulating immune system disturbances (2020) (1)
- Typhlitis in acute childhood leukemia. (1996) (1)
- The relationship between insulin‐like growth factor‐II gene Apa I polymorphism and rheumatoid arthritis (2004) (1)
- Study of AMP-Activated Protein Kinase Agonists by Structure-Based Drug Designing (2009) (1)
- Neonatal outcome of hydrops fetalis (2002) (1)
- Different race, different face: minor anomalies in Chinese newborn infants. (2007) (1)
- Association of genetic variants in senataxin and Alzheimer's disease in a Chinese Han population in Taiwan. (2014) (1)
- Gene symbol: GCDH. Disease: Glutaricacidaemia I. (2008) (1)
- Association of genetic variations in GNB1 with response to peginterferon plus ribavirin therapy for chronic hepatitis C in a Chinese population in Taiwan (2012) (1)
- MORPHOLOGICAL AND NEUROCHEMICAL ASSESSMENT OF REGENERATED PERIPHERAL NERVES IN BRIDGING CONDUITS (2011) (1)
- A novel one‐base insertion mutation in the retinitis pigmentosa 2 gene in a large X‐linked Taiwanese family (2014) (1)
- Disease: Generalized epilepsy with febrile seizures plus (2010) (1)
- In Silico Target Analysis of Treatment for COVID-19 Using Huang-Lian-Shang-Qing-Wan, a Traditional Chinese Medicine Formula (2021) (1)
- Oral Lactobacillus reuteri GMN-32 treatment reduces blood glucose concentrations and promotes cardiac function in rats with streptozotocin-induced diabetes mellitus – RETRACTION (2013) (1)
- Prenatal diagnosis of X‐linked myotubular myopathy (2010) (1)
- Mutation analysis of human LEFTY A and LEFTY B genes in children with Ivemark syndrome. (2000) (1)
- The impact of polymorphisms in STAT6 on treatment outcome in HCV infected Taiwanese Chinese (2013) (1)
- Integrated analysis of gene modulation profile identifies pathogenic factors and pathways in the liver of diabetic mice (2019) (1)
- In Vitro Toxicological Assessment of Gadodiamide in Normal Brain SVG P12 Cells (2021) (1)
- Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice. (2019) (1)
- Reducing without Side Effects? A Novel Strategy for Designing the PPAR Agonists (2009) (1)
- Estrogen receptor a ( ESR 1 ) over-expression mediated apoptosis in Hep 3 BcellsbybindingwithSP 1 proteins (2013) (1)
- Human gene mutations. Gene symbol: EXT2. Disease: exostoses (multiple) 2. (2007) (1)
- Effect of Chinese Herbal Medicine Therapy on Risks of Overall, Diabetes-Related, and Cardiovascular Diseases-Related Mortalities in Taiwanese Patients With Hereditary Hemolytic Anemias (2022) (1)
- Genetic variants of glutamate receptor gene family in Taiwanese Kawasaki disease children with coronary artery aneurysms (2014) (1)
- Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese. (2000) (1)
- Could Traditional Chinese Medicine Used for Curing Erectile Dysfunction? (2009) (1)
- X-linked recessive myotubular myopathy proven by muscle biopsy. (1996) (1)
- Genetic variation in NOS2A is associated with a sustained virological response to peginterferon plus ribavirin therapy for chronic hepatitis C in Taiwanese Chinese (2013) (1)
- Timing and dosage of and adherence to hormone replacement therapy and fracture risk in women with menopausal syndrome in Taiwan: A nested case-control study. (2021) (1)
- Spondyloepiphyseal dysplasia congenita: report of one case. (1999) (1)
- Fabrication of SiO2@Au Core-Shell Multi-Functional Nanoparticles (MFNPs) for Imaging and Thermotherapy (2009) (1)
- MUC 2 polymorphisms are associated with endometriosis development and infertility : a case-control study (2012) (1)
- REARRANGEMENTS INVOLVING CHROMOSOMES OTHER THAN CHROMOSOME 21 (2009) (0)
- Contents Vol. 119, 2007 (2008) (0)
- Dual-Targeted Drug Design of HER2 and HSP90 by CoMFA Model and Pharmacophore Analysis (2009) (0)
- Contents Vol. 39, 2001 (2001) (0)
- Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication (2015) (0)
- Prevalence and patterns of cancer in patients with congenital disease: A national-based cohort study. (2013) (0)
- Abstract 5051: Overexpression of talin 1 (TLN1) in invasive oral squamous cell carcinoma (OSCC) (2010) (0)
- Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q. (2010) (0)
- Blocking the DNA Repair System by Traditional (2011) (0)
- Genetic and biochemical study in a patient with glutaric acidemia type I. (2004) (0)
- Haplotype of BAK1 (BCL2 antagonist killer 1) polymorphisms associated with the risk of developing Kawasaki disease in Taiwanese children (2010) (0)
- An R248C mutation of FGFR3 leading to thanatophoric dysplasia type I. (1999) (0)
- AB084. Cause of death and clinical characteristics of 34 mortality patients with mucopolysaccharidosis II in Taiwan, 1995-2012. (2015) (0)
- Are EBV Serologic and PCR Tests Correlated with Reactivation of EBV Infection during Latent Phase in Hematologic Field (1999) (0)
- Impact of shock wave lithotripsy on heart rate variability in patients with urolithiasis (2011) (0)
- Erratum: Tumor necrosis factor-a polymorphisms in age-related macular degeneration (Retina (2010) 30 (1595-1600)) (2011) (0)
- 206 DETECTION AND COMPARISON OF CYTOMEGALOVIRUS DNA LEVELS IN AMNIOTIC FLUID AND FETAL ASCITES IN A SECOND-TRIMESTER FETUS WITH MASSIVE ASCITES , HYPERECHOGENIC BOWEL , VENTRICULOMEGALY AND INTRAUTERINE GROWTH RESTRICTION (2010) (0)
- Childhood Acute lymphoblastic leukemia in Taiwan (2010) (0)
- Evaluation of plasma globotriaosylsphingosine (LysoGb3) in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4+919G A) (2013) (0)
- Relationship Between the P16 Gene Exon 3 C/G Polymorphism and Hydropyruvate Reductase (GRHPR) Gene Exon 6 G/A Polymorphism in Patients With Calcium Oxalate Stone:No Association (2002) (0)
- Letter to the Editor (2003) (0)
- Insulin-like growth factor-II gene ApaI polymorphism was not associated with systemic lupus erythematosus. (2003) (0)
- CONGENITAL ADRENAL HYPERPLASIA IN A PATIENT WITH DUCHENNE MUSCULAR DYSTROPHY (2006) (0)
- Absence of Linkage Between the Interleukin-6 Promoter Gene (-174 G/C) Polymorphism and Kawasaki Disease (2003) (0)
- Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome. (2011) (0)
- Author ' s response to reviews Title : Two polymorphisms ( rs 699947 , rs 2010963 ) in the VEGFA gene and diabetic retinopathy : An updated meta-analysis (2013) (0)
- Gene symbol: LMX1B. Disease: Nail-patella syndrome. (2008) (0)
- Corrigendum to “An Emerging Translational Model to Screen Potential Medicinal Plants for Nephrolithiasis, an Independent Risk Factor for Chronic Kidney Disease” (2015) (0)
- Reply to Ogimoto (2005) (0)
- Additional file 3: Figure S3. of Slow, progressive myopathy in neonatally treated patients with infantile-onset Pompe disease: a muscle magnetic resonance imaging study (2016) (0)
- Genetic variants of ALOXs genes in polyunsaturated fatty acid / arachidonic acid metabolism associated with type-2 diabetes development (2018) (0)
- P1-72 SODIUM-CHANNEL SCN5A GENE P1089L AND SCN1A SNP2298771 POLYMORPHISMS ARE NOT ASSOCIATED WITH DUAL AV NODAL PATHWAYS IN TAIWAN (2007) (0)
- Response: Febrile Convulsions and Genetic Susceptibility: Role of the Neuronal Nicotinic Acetylcholine Receptor α4 Subunit (2004) (0)
- training on hypertensive hearts Anti-apoptotic and pro-survival effects of exercise (2015) (0)
- Pseudo-trisomy 13 syndrome: report of one case. (1992) (0)
- Is that Possible to Design the Versatile Inhibitors for H1N1, H5N1, H5N2, and H5N7? (2009) (0)
- Original article CYP17 gene promoter allelic variant is not associated with prostate cancer (2003) (0)
- TAP1 Gene Acc I Polymorphism is Associated With Atopic Bronchial Asthma (2003) (0)
- Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of SRY gene. (1995) (0)
- COP 9 signalosome subunit 6 promotes tumorigenesis through stabilization of MDM 2 (2010) (0)
- The 1448C mutation in Chinese with type 1 and 2 Gaucher disease (1994) (0)
- Case Report Galloway-Mowat syndrome: Prenatal ultrasound and perinatal magnetic resonance imaging findings (2011) (0)
- Author Correction: NT5C2 methylation regulatory interplay between DNMT1 and insulin receptor in type 2 diabetes (2021) (0)
- Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, invitro fertilization and embryo transfer (0)
- The hypoglossia-hypodactylia syndrome: report of two cases. (1992) (0)
- Polymorphisms of the TAP2 Genes in Chinese Patients with Systemic Lupus Erythematosus in Taiwan (2008) (0)
- OMPHALOCELE IN A MALE FETUS: PRENATAL MAGNETIC RESONANCE IMAGING FINDINGS AND LITERATURE REVIEW (2009) (0)
- Retraction Retracted : The Effect of Elephantopus scaber L . on Liver Regeneration after Partial Hepatectomy Evidence-Based Complementary and Alternative Medicine (2017) (0)
- Beemer-Langer type short rib-polydactyly syndrome: report of two cases. (1994) (0)
- Association of copy number variation in Fc gamma receptor IIIb gene with risk of Graves' ophthalmopathy (2012) (0)
- Abstract O.30: Novel Biomarker for Early Diagnosis of Kawasaki Diseases (2015) (0)
- A 5.3-Mb duplication of 9p12 --> p13.1 characterized by array CGH in a female infant with developmental delay. (2010) (0)
- Genetic Association in the Open-Angle Glaucomas (2008) (0)
- Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation. (2011) (0)
- A novel mutation K167X of the XLRS1 gene (RS1) in a Taiwanese family with X-linked juvenile retinoschisis. (2000) (0)
- Subject Index Vol. 70, 2003 (2003) (0)
- Wolf-Hirschhorn (4p deletion) syndrome: report of one case. (2000) (0)
- Drug Design for XRCC4 in Silico (2009) (0)
- Drug Design for AMP-Activated Protein Kinase Agonists in Silico (2009) (0)
- Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability. (2011) (0)
- Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus. (2010) (0)
- Additional file 1: Figure S1. of Slow, progressive myopathy in neonatally treated patients with infantile-onset Pompe disease: a muscle magnetic resonance imaging study (2016) (0)
- 239 ANTI-TUMOR ACTIVITY OF HISTONE DEACETYLASE INHIBITOR FK228 (DEPSIPEPTIDE) FOR HUMAN PROSTATE CANCER CELLS (2007) (0)
- A Novel Strategy for Designing Dual-Target Inhibitors of KU86 and XRCC4 (2009) (0)
- Subject Index Vol. 75, 2005 (2005) (0)
- Investigating neurochemical techniques for assessment of nerve regenerates within polymer guides (2011) (0)
- Genetic Analysis of Acid β-Glucosidase in Patients with Multiple Myeloma from Central Taiwan: A Small-Cohort Case-Control Study (2021) (0)
- Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication (2015) (0)
- Skeletal Dysplasia Caused by FGFR3 Mutation in Taiwanese Patients (2000) (0)
- Occipital encephalocele associated with iniencephaly mimicking an unilateral nuchal tumor on prenatal ultrasound. (2008) (0)
- Association of IL12B polymorphisms with susceptibility to Graves ophthalmopathy in a Taiwan Chinese population (2012) (0)
- The Effects of One-Week Fluticasone Propionate Inhalation Therapy for Tc-99m DTPA Radioaerosol Distribution in Asthma of Children: A Preliminary Report (2003) (0)
- Lactobacillus reuteri GMN-32 treatment reduces blood glucose concentrations and promotes cardiac function in rats with streptozotocin-induced diabetes mellitus (2014) (0)
- The Anti-Hepatitis Effect by Tao-He-Cheng-Qi-Tang on Acetaminophen (APAP) Induced Rats (2011) (0)
- Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus. (2010) (0)
- Long-term follow-up results in patients with classic infantile Pompe disease receiving enzyme therapy since newborn (2013) (0)
- G syndrome: report of two cases. (1992) (0)
- Drug Design for KU86 in DNA Break Repair System (2009) (0)
- Gelsolin (GSN) induces cardiomyocyte hypertrophy and BNP expression via p38 signaling and GATA-4 transcriptional factor activation (2014) (0)
- - 1-MUC 4 gene polymorphisms associate with endometriosis development and infertility (2010) (0)
- Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus. (2010) (0)
- Subject Index Vol. 39, 2001 (2001) (0)
- Mass Spectrometry Studies of 60 kDa Proteins Extracted from Calcium Oxalate Stones (2008) (0)
- Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism. (2012) (0)
- Abstract 3091: Oncogenic roles of nuclear VCP in oral cancer development (2010) (0)
- Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus. (2010) (0)
- Tumor Necrosis Factor-α Gene Promoter Polymorphism in Chinese Patients with Systemic Lupus Erythematosus (2005) (0)
- Subject Index Vol. 67, 2001 (2001) (0)
- Erratum: Human lymphocyte antigen B‐associated transcript 2, 3, and 5 polymorphisms and haplotypes are associated with susceptibility of Kawasaki disease and coronary artery aneurysm (2011) (0)
- Contents Vol. 75, 2005 (2005) (0)
- No relationship of −627 interleukin-10 promoter polymorphism in Chinese patients with rheumatoid arthritis (2005) (0)
- Original article Glutathione S-transferase M1 gene but not insulin-like growth factor-2 gene or epidermal growth factor gene is associated with prostate cancer (2005) (0)
- Clinical Characteristics Change and the Heart Rate Variability of Subjects with Metabolic Syndrome in the Weight Loss Program (2011) (0)
- Contents Vol. 67, 2001 (2001) (0)
- A More Diverse Cervical Microbiome Associates with Better Clinical Outcomes in Patients with Endometriosis (2021) (0)
- AUTHOR COPY ONLY Estrogen receptor a (ESR1) over- expression mediated apoptosis in Hep3BcellsbybindingwithSP1proteins (2013) (0)
- Current Development of Computer-Aided Drug Design (2010) (0)
- Additional file 2: Figure S2. of Slow, progressive myopathy in neonatally treated patients with infantile-onset Pompe disease: a muscle magnetic resonance imaging study (2016) (0)
- Gene symbol: GLA. Disease: Fabry disease. (2008) (0)
- Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of an X-Y homologous region. (1996) (0)
- What is the Key Point for Designing HER2 Inhibitors? (2009) (0)
- Reduction of TLR 4 mRNA Stability and Protein Expressions through Inhibiting Cytoplasmic Translocation of HuR Transcription Factor by E 2 and / or ER α in LPS-Treated H 9 c 2 Cardiomyoblast Cells (2014) (0)
- Contents Vol. 70, 2003 (2003) (0)
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What Schools Are Affiliated With Fuu‐jen Tsai?
Fuu‐jen Tsai is affiliated with the following schools: