Fuu‐jen Tsai

Fuu‐jen Tsai's AcademicInfluence.com Rankings

Fuu‐jen Tsai

Biology

#8419

World Rank

#11490

Historical Rank

Genetics

#840

World Rank

#933

Historical Rank

biology Degrees

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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

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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:

China Medical University