Johji Inazawa
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Computer Science
Johji Inazawa's Degrees
- PhD Computer Science University of Tokyo
- Masters Computer Science University of Tokyo
- Bachelors Computer Science University of Tokyo
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(Suggest an Edit or Addition)Johji Inazawa's Published Works
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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
- Reconstitution of IKATP: An Inward Rectifier Subunit Plus the Sulfonylurea Receptor (1995) (1764)
- Causal Relationship between the Loss of RUNX3 Expression and Gastric Cancer (2002) (1064)
- Exploration of tumor-suppressive microRNAs silenced by DNA hypermethylation in oral cancer. (2008) (615)
- miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma. (2010) (590)
- Structure and chromosomal localization of the human stromal cell-derived factor 1 (SDF1) gene. (1995) (525)
- Human Fas ligand: gene structure, chromosomal location and species specificity. (1994) (466)
- Damaged epithelia regenerated by bone marrow–derived cells in the human gastrointestinal tract (2002) (393)
- Mutations in EFHC1 cause juvenile myoclonic epilepsy (2004) (332)
- Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population (2010) (293)
- Mammalian occludin in epithelial cells: its expression and subcellular distribution. (1997) (280)
- Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease (2006) (265)
- The tumor suppressive microRNA miR-218 targets the mTOR component Rictor and inhibits AKT phosphorylation in oral cancer. (2011) (247)
- PPM1D is a potential target for 17q gain in neuroblastoma. (2003) (242)
- Structural organization of the human oxytocin receptor gene. (1994) (230)
- miR-152 is a tumor suppressor microRNA that is silenced by DNA hypermethylation in endometrial cancer. (2011) (227)
- Identification of a novel gene, GASC1, within an amplicon at 9p23-24 frequently detected in esophageal cancer cell lines. (2000) (226)
- YAP is a candidate oncogene for esophageal squamous cell carcinoma. (2011) (221)
- Tumour-amplified kinase BTAK is amplified and overexpressed in gastric cancers with possible involvement in aneuploid formation (2001) (217)
- Identification of cIAP1 as a candidate target gene within an amplicon at 11q22 in esophageal squamous cell carcinomas. (2001) (214)
- Alteration in Copy Numbers of Genes as a Mechanism for Acquired Drug Resistance (2004) (212)
- Molecular cloning and chromosomal mapping of a bone marrow stromal cell surface gene, BST2, that may be involved in pre-B-cell growth. (1995) (209)
- PH Domain-Only Protein PHLDA3 Is a p53-Regulated Repressor of Akt (2009) (206)
- Reprimo, a New Candidate Mediator of the p53-mediated Cell Cycle Arrest at the G2 Phase* (2000) (202)
- Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases (2020) (191)
- Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors. (1993) (191)
- Structural Organization and Chromosomal Assignment of the Human obese Gene (*) (1995) (189)
- Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization (1999) (186)
- Genetic variants in C5 and poor response to eculizumab. (2014) (185)
- Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease. (2006) (183)
- BST-1, a surface molecule of bone marrow stromal cell lines that facilitates pre-B-cell growth. (1994) (182)
- TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomas (2002) (182)
- Molecular cloning and characterization of human caspase-activated DNase. (1998) (179)
- Structure and Expression of the Ah Receptor Repressor Gene* (2001) (177)
- Amplification and over‐expression of the AIB1 nuclear receptor co‐activator gene in primary gastric cancers (2000) (170)
- Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations (2010) (168)
- The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD). (2004) (165)
- Overexpression of SMYD2 relates to tumor cell proliferation and malignant outcome of esophageal squamous cell carcinoma. (2009) (160)
- Expression of cIAP1, a target for 11q22 amplification, correlates with resistance of cervical cancers to radiotherapy. (2002) (160)
- Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors. (1996) (151)
- PIK3CA mutation is an oncogenic aberration at advanced stages of oral squamous cell carcinoma (2006) (150)
- Association of 17q21-q24 gain in ovarian clear cell adenocarcinomas with poor prognosis and identification of PPM1D and APPBP2 as likely amplification targets. (2003) (150)
- Exosomal microRNA miR-1246 induces cell motility and invasion through the regulation of DENND2D in oral squamous cell carcinoma (2016) (146)
- The Tumor-Suppressive miR-497-195 Cluster Targets Multiple Cell-Cycle Regulators in Hepatocellular Carcinoma (2013) (143)
- Structure of the human ferrochelatase gene. Exon/intron gene organization and location of the gene to chromosome 18. (1992) (142)
- Frequent Silencing of Low Density Lipoprotein Receptor-Related Protein 1B (LRP1B) Expression by Genetic and Epigenetic Mechanisms in Esophageal Squamous Cell Carcinoma (2004) (139)
- Comparative genomic hybridization (CGH)‐arrays pave the way for identification of novel cancer‐related genes (2004) (130)
- The Clinical Significance of Aurora-A/STK15/BTAK Expression in Human Esophageal Squamous Cell Carcinoma (2005) (124)
- Transcriptional Regulation of the CLC-K1 Promoter by myc-Associated Zinc Finger Protein and Kidney-Enriched Krüppel-Like Factor, a Novel Zinc Finger Repressor (2000) (121)
- Elevated expression levels of NCOA3, TOP1, and TFAP2C in breast tumors as predictors of poor prognosis (2003) (115)
- High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridization. (1993) (114)
- A novel target gene, SKP2, within the 5p13 amplicon that is frequently detected in small cell lung cancers. (2002) (112)
- Comparative genomic hybridization of squamous cell carcinoma of the esophagus: The possible involvement of the DP1 gene in the 13q34 amplicon (1999) (111)
- Frequent silencing of the candidate tumor suppressor PCDH20 by epigenetic mechanism in non-small-cell lung cancers. (2006) (111)
- ASK1 and ASK2 differentially regulate the counteracting roles of apoptosis and inflammation in tumorigenesis (2009) (110)
- PTK2 and EIF3S3 genes may be amplification targets at 8q23‐q24 and are associated with large hepatocellular carcinomas (2003) (109)
- ANA, a novel member of Tob/BTG1 family, is expressed in the ventricular zone of the developing central nervous system (1998) (108)
- Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese (2012) (107)
- Chromosomal localization of the human and mouse hyaluronan synthase genes. (1997) (107)
- Aurora kinase B is a predictive factor for the aggressive recurrence of hepatocellular carcinoma after curative hepatectomy (2008) (106)
- Genetic Classification of Lung Adenocarcinoma Based on Array-Based Comparative Genomic Hybridization Analysis: Its Association with Clinicopathologic Features (2005) (105)
- Amplification and overexpression of SKP2 are associated with metastasis of non-small-cell lung cancers to lymph nodes. (2004) (104)
- Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome (1999) (97)
- Overexpressed NF-kappaB-inducing kinase contributes to the tumorigenesis of adult T-cell leukemia and Hodgkin Reed-Sternberg cells. (2008) (97)
- Identification of BAIAP2 (BAI-associated protein 2), a novel human homologue of hamster IRSp53, whose SH3 domain interacts with the cytoplasmic domain of BAI1 (1999) (96)
- Human arylhydrocarbon receptor repressor (AHRR) gene: genomic structure and analysis of polymorphism in endometriosis (2001) (96)
- SASPase regulates stratum corneum hydration through profilaggrin-to-filaggrin processing (2011) (96)
- Amplification and overexpression of TGIF2, a novel homeobox gene of the TALE superclass, in ovarian cancer cell lines. (2000) (96)
- SIX1 promotes epithelial–mesenchymal transition in colorectal cancer through ZEB1 activation (2012) (95)
- miR-655 Is an EMT-Suppressive MicroRNA Targeting ZEB1 and TGFBR2 (2013) (94)
- Overexpression of PDZK1 within the 1q12-q22 amplicon is likely to be associated with drug-resistance phenotype in multiple myeloma. (2004) (94)
- Identification, basic characterization and evolutionary analysis of differentially spliced mRNA isoforms of human YAP1 gene. (2012) (93)
- A novel amplification target, DUSP26, promotes anaplastic thyroid cancer cell growth by inhibiting p38 MAPK activity (2007) (92)
- Frequent silencing of a putative tumor suppressor gene melatonin receptor 1 A (MTNR1A) in oral squamous‐cell carcinoma (2008) (90)
- A novel metalloprotease/disintegrin–like gene at 17q21.3 is somatically rearranged in two primary breast cancers (1993) (90)
- Structure of the gene for human transglutaminase 1. (1992) (89)
- An alternatively spliced isoform of transcriptional repressor ATF3 and its induction by stress stimuli. (2002) (88)
- Assignment of the human Fas antigen gene (Fas) to 10q24.1. (1992) (88)
- SNO is a probable target for gene amplification at 3q26 in squamous-cell carcinomas of the esophagus. (2001) (87)
- cDNA Cloning and Chromosomal Localization of the Human Telencephalin and Its Distinctive Interaction with Lymphocyte Function-associated Antigen-1* (1997) (86)
- Expression and Gene Amplification of Actinin-4 in Invasive Ductal Carcinoma of the Pancreas (2008) (86)
- Genetically distinct and clinically relevant classification of hepatocellular carcinoma: putative therapeutic targets. (2007) (86)
- Actinin-4 gene amplification in ovarian cancer: a candidate oncogene associated with poor patient prognosis and tumor chemoresistance (2009) (84)
- Actinin-4 expression in ovarian cancer: a novel prognostic indicator independent of clinical stage and histological type (2007) (84)
- Nonrandom Chromosomal Imbalances in Esophageal Squamous Cell Carcinoma Cell Lines: Possible Involvement of the ATF3 and CENPF Genes in the 1q32 Amplicon (2000) (83)
- Reduced Levels of ATF-2 Predispose Mice to Mammary Tumors (2006) (82)
- Overexpression of SMYD2 contributes to malignant outcome in gastric cancer (2014) (82)
- miR-544a induces epithelial-mesenchymal transition through the activation of WNT signaling pathway in gastric cancer. (2015) (80)
- Chromosomal aberrations in human hepatocellular carcinomas associated with hepatitis C virus infection detected by comparative genomic hybridization (1999) (80)
- Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line (2000) (79)
- Chromosomal aberrations in colorectal cancers and liver metastases analyzed by comparative genomic hybridization (2001) (79)
- The selective continued linkage of centromeres from mitosis to interphase in the absence of mammalian separase (2006) (78)
- The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome (2011) (78)
- Genetic profile of hepatocellular carcinoma revealed by array-based comparative genomic hybridization: identification of genetic indicators to predict patient outcome. (2005) (78)
- Promoter hypermethylation contributes to frequent inactivation of a putative conditional tumor suppressor gene connective tissue growth factor in ovarian cancer. (2007) (78)
- Analysis of numerical aberrations in specific chromosomes by fluorescent in situ hybridization as a diagnostic tool in breast cancer (1996) (77)
- The human protoporphyrinogen oxidase gene (PPOX): organization and location to chromosome 1. (1995) (76)
- TERC identified as a probable target within the 3q26 amplicon that is detected frequently in non-small cell lung cancers. (2003) (75)
- Increase of bone marrow-derived secretory lineage epithelial cells during regeneration in the human intestine. (2005) (74)
- Involvement of overexpressed wild-type BRAF in the growth of malignant melanoma cell lines (2004) (74)
- cDNA sequence, gene structure, and chromosomal localization of the human ATP-sensitive potassium channel, uKATP-1, gene (KCNJ8). (1995) (74)
- SKI and MEL1 Cooperate to Inhibit Transforming Growth Factor-β Signal in Gastric Cancer Cells* (2009) (74)
- Loss of material from chromosome arm 1p during malignant progression of meningioma revealed by fluorescent in Situ hybridization (1998) (73)
- Krüppel‐like factor 12 plays a significant role in poorly differentiated gastric cancer progression (2009) (72)
- Correlation of KIT and EGFR overexpression with invasive ductal breast carcinoma of the solid‐tubular subtype, nuclear grade 3, and mesenchymal or myoepithelial differentiation (2005) (70)
- Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15 (2000) (70)
- Assignment of the human cytochrome P-450 nifedipine oxidase gene (CYP3A4) to chromosome 7 at band q22.1 by fluorescence in situ hybridization (1992) (69)
- Molecular cloning and chromosomal assignment of the human brain-type phosphodiesterase I/nucleotide pyrophosphatase gene (PDNP2). (1995) (67)
- Molecular cloning of a novel non-receptor tyrosine kinase, HYL (hematopoietic consensus tyrosine-lacking kinase). (1994) (67)
- A transcriptional variant of the LC3A gene is involved in autophagy and frequently inactivated in human cancers (2012) (67)
- Nuclear expression of cIAP-1, an apoptosis inhibiting protein, predicts lymph node metastasis and poor patient prognosis in head and neck squamous cell carcinomas. (2005) (66)
- Screening of DNA copy‐number aberrations in gastric cancer cell lines by array‐based comparative genomic hybridization (2005) (66)
- Identification of a novel gene, MASL1, within an amplicon at 8p23.1 detected in malignant fibrous histiocytomas by comparative genomic hybridization. (1999) (66)
- ADAM23, a possible tumor suppressor gene, is frequently silenced in gastric cancers by homozygous deletion or aberrant promoter hypermethylation (2005) (66)
- N-ras mutation and karyotypic evolution are closely associated with leukemic transformation in myelodysplastic syndrome. (1994) (64)
- Methylation-associated silencing of the nuclear receptor 1I2 gene in advanced-type neuroblastomas, identified by bacterial artificial chromosome array-based methylated CpG island amplification. (2005) (64)
- Molecular cloning of a human transmembrane-type protein tyrosine phosphatase and its expression in gastrointestinal cancers. (1994) (63)
- The Impact of miRNA-Based Molecular Diagnostics and Treatment of NRF2-Stabilized Tumors (2013) (63)
- Isolation and characterization of a novel gene deleted in DiGeorge syndrome. (1995) (63)
- Frequent silencing of DBC1 is by genetic or epigenetic mechanisms in non-small cell lung cancers. (2005) (63)
- Identification of a novel fusion gene in a pre‐B acute lymphoblastic leukemia with t(1;19)(q23;p13) (2004) (62)
- Frequent methylation-associated silencing of a candidate tumor-suppressor, CRABP1, in esophageal squamous-cell carcinoma (2007) (62)
- DEK oncoprotein regulates transcriptional modifiers and sustains tumor initiation activity in high-grade neuroendocrine carcinoma of the lung (2010) (61)
- Identification of ZASC1 encoding a Krüppel-like zinc finger protein as a novel target for 3q26 amplification in esophageal squamous cell carcinomas. (2003) (61)
- IQGAP1, a negative regulator of cell-cell adhesion, is upregulated by gene amplification at 15q26 in gastric cancer cell lines HSC39 and 40A (2001) (60)
- Identification of PAK4 as a putative target gene for amplification within 19q13.12‐q13.2 in oral squamous‐cell carcinoma (2009) (60)
- Genome‐wide DNA methylation profiles in liver tissue at the precancerous stage and in hepatocellular carcinoma (2009) (59)
- Differentially Regulated Genes as Putative Targets of Amplifications at 20q in Ovarian Cancers (2002) (59)
- Down‐regulation of SKP2 induces apoptosis in lung‐cancer cells (2003) (58)
- RGC32, a novel p53-inducible gene, is located on centrosomes during mitosis and results in G2/M arrest (2007) (57)
- Array‐based comparative genomic hybridization analysis of high‐grade neuroendocrine tumors of the lung (2005) (56)
- Physical Ordering of Three Polymorphic DNA Markers Spanning the Regions Containing a Tumor Suppressor Gene of Renal Cell Carcinoma by Three‐color Fluorescent in situ Hybridization (1992) (56)
- Frequent silencing of protocadherin 17, a candidate tumour suppressor for esophageal squamous cell carcinoma. (2010) (56)
- The Suppression of Aurora-A/STK15/BTAK Expression Enhances Chemosensitivity to Docetaxel in Human Esophageal Squamous Cell Carcinoma (2007) (56)
- Genetic Clustering of Clear Cell Renal Cell Carcinoma Based on Array-Comparative Genomic Hybridization: Its Association with DNA Methylation Alteration and Patient Outcome (2008) (55)
- The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomal assignment, and loss of expression in brain tumors (2001) (55)
- Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis (2010) (55)
- Early G2/M checkpoint failure as a molecular mechanism underlying etoposide-induced chromosomal aberrations. (2005) (54)
- Chromosome arm 20q gains and other genomic alterations in esophageal squamous cell carcinoma, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization. (2003) (54)
- Deletion mapping on chromosome 1p in well-differentiated gastric cancer. (1996) (54)
- Promoter analysis and chromosomal mapping of human EBAG9 gene. (2000) (53)
- ERM, a PEA3 Subfamily of Ets Transcription Factors, Can Cooperate with c-Jun (*) (1995) (53)
- Activation of B‐Myb by E2F1 in hepatocellular carcinoma (2008) (53)
- Molecular cloning of a novel apoptosis-related gene, human Nap1 (NCKAP1), and its possible relation to Alzheimer disease. (2000) (53)
- Prognostic implication of laminin-5 gamma 2 chain expression in the invasive front of colorectal cancers, disclosed by area-specific four-point tissue microarrays (2005) (53)
- Resequencing and copy number analysis of the human tyrosine kinase gene family in poorly differentiated gastric cancer. (2009) (52)
- Isolation and characterization of a novel secretory protein, stromal cell-derived factor-2 (SDF-2) using the signal sequence trap method. (1996) (52)
- Gene amplification of ESR1 in breast cancers—fact or fiction? A fluorescence in situ hybridization and multiplex ligation‐dependent probe amplification study (2012) (52)
- High resolution ordering of DNA markers by multi-color fluorescent in situ hybridization of prophase chromosomes. (1994) (50)
- A Novel Amplicon at 9p23‐24 in Squamous Cell Carcinoma of the Esophagus That Lies Proximal to GASC1 and Harbors NFIB (2001) (50)
- Correlation between genetic alteration and long‐term clinical outcome of patients with oligodendroglial tumors, with identification of a consistent region of deletion on chromosome arm 1p (2003) (50)
- A novel amplification at 17q21-23 in ovarian cancer cell lines detected by comparative genomic hybridization. (2001) (50)
- Frequent inactivation of a putative tumor suppressor, angiopoietin-like protein 2, in ovarian cancer. (2008) (50)
- Genome-wide DNA methylation profiles in both precancerous conditions and clear cell renal cell carcinomas are correlated with malignant potential and patient outcome (2008) (50)
- Tumor‐suppressive microRNA silenced by tumor‐specific DNA hypermethylation in cancer cells (2012) (49)
- Epigenetic silencing of prostaglandin E receptor 2 (PTGER2) is associated with progression of neuroblastomas (2007) (49)
- Involvement of cyclin D3 in liver metastasis of colorectal cancer, revealed by genome-wide copy-number analysis (2005) (49)
- Cloning of cDNAs encoding the human BAG1 protein and localization of the human BAG1 gene to chromosome 9p12. (1996) (49)
- Clonal origin of Philadelphia chromosome negative cells with trisomy 8 appearing during the course of alpha-interferon therapy for Ph positive chronic myelocytic leukemia. (1995) (48)
- Molecular cloning of a human RP105 homologue and chromosomal localization of the mouse and human RP105 genes (Ly64 and LY64). (1996) (48)
- CD44 is a potential target of amplification within the 11p13 amplicon detected in gastric cancer cell lines (2000) (48)
- Autophagy is required for cell survival under L-asparaginase-induced metabolic stress in acute lymphoblastic leukemia cells (2017) (48)
- miR-634 Activates the Mitochondrial Apoptosis Pathway and Enhances Chemotherapy-Induced Cytotoxicity. (2015) (48)
- Potential of tumor-suppressive miR-596 targeting LGALS3BP as a therapeutic agent in oral cancer. (2013) (48)
- Association of over-expressed TFDP1 with progression of hepatocellular carcinomas (2003) (47)
- The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation. (2002) (46)
- Unfavorable prognostic factors associated with high frequency of microsatellite instability and comparative genomic hybridization analysis in endometrial cancer. (2003) (46)
- Integrated genomic and functional analyses reveal glyoxalase I as a novel metabolic oncogene in human gastric cancer (2014) (46)
- 22q13 microduplication in two patients with common clinical manifestations: A recognizable syndrome? (2007) (46)
- Identification of SMURF1 as a possible target for 7q21.3‐22.1 amplification detected in a pancreatic cancer cell line by in‐house array‐based comparative genomic hybridization (2008) (46)
- Amplification on double‐minute chromosomes and partial‐tandem duplication of the MILL gene in leukemic cells of a patient with acute myelogenous leukemia (1998) (46)
- The unbalanced 1;7 translocation in de novo myelodysplastic syndrome and its clinical implication (1990) (46)
- Cloning and chromosomal mapping of human glucuronyltransferase involved in biosynthesis of the HNK-1 carbohydrate epitope. (2000) (45)
- Assignment of the human granulocyte colony-stimulating factor receptor gene (CSF3R) to chromosome 1 at region p35-p34.3. (1991) (45)
- Genome‐wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage (2010) (45)
- MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas (2002) (45)
- Genetic or epigenetic silencing of low density lipoprotein receptor‐related protein 1B expression in oral squamous cell carcinoma (2006) (45)
- Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system (2016) (45)
- Different drug sensitivity in two neuroblastoma cell lines established from the same patient before and after chemotherapy (1991) (44)
- miR-509-5p and miR-1243 increase the sensitivity to gemcitabine by inhibiting epithelial-mesenchymal transition in pancreatic cancer (2017) (44)
- Lysosomal-Associated Protein Multispanning Transmembrane 5 Gene (LAPTM5) Is Associated with Spontaneous Regression of Neuroblastomas (2009) (44)
- PRTFDC1, a possible tumor-suppressor gene, is frequently silenced in oral squamous-cell carcinomas by aberrant promoter hypermethylation (2007) (44)
- Novel targets for the 18p11.3 amplification frequently observed in esophageal squamous cell carcinomas. (2002) (44)
- Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma (2016) (43)
- Significant impact of miRNA–target gene networks on genetics of human complex traits (2016) (43)
- Cloning, expression and chromosomal localization of a novel gene for protein tyrosine phosphatase (PTP-U2) induced by various differentiation-inducing agents. (1995) (43)
- Assignment of cardiac homeobox gene CSX to human chromosome 5q34. (1995) (43)
- POU2AF1, an amplification target at 11q23, promotes growth of multiple myeloma cells by directly regulating expression of a B-cell maturation factor, TNFRSF17 (2008) (42)
- Grb10/GrbIR as an in vivo substrate of Tec tyrosine kinase (1998) (42)
- Genomic structure and mapping of human orphan receptor LXR alpha: upregulation of LXRa mRNA during monocyte to macrophage differentiation. (2000) (42)
- miR-432 Induces NRF2 Stabilization by Directly Targeting KEAP1 (2017) (42)
- High Expression of p62 Protein Is Associated with Poor Prognosis and Aggressive Phenotypes in Endometrial Cancer. (2015) (41)
- High Expression of SQSTM1/p62 Protein Is Associated with Poor Prognosis in Epithelial Ovarian Cancer (2014) (41)
- The CASK gene harbored in a deletion detected by array‐CGH as a potential candidate for a gene causative of X‐linked dominant mental retardation (2008) (41)
- Association of KLK5 overexpression with invasiveness of urinary bladder carcinoma cells (2007) (41)
- Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH) (2017) (40)
- GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12 (2018) (40)
- Overexpressed Skp2 within 5p amplification detected by array‐based comparative genomic hybridization is associated with poor prognosis of glioblastomas (2005) (39)
- The Japanese Society of Pathology Guidelines on the handling of pathological tissue samples for genomic research: Standard operating procedures based on empirical analyses (2018) (39)
- Alpha‐smooth‐muscle actin and desmin expressions in human neuroblastoma cell lines (1991) (39)
- An expression profile of genes in human retina and isolation of a complementary DNA for a novel rod photoreceptor protein. (1997) (39)
- Frequent deletions of material from chromosome arm 1p in oligodendroglial tumors revealed by double‐target fluorescence in situ hybridization and microsatellite analysis (1995) (38)
- GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines (2003) (38)
- Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH) (2011) (37)
- Human arylhydrocarbon receptor: functional expression and chromosomal assignment to 7p21. (1994) (37)
- Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation (2000) (37)
- 12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population (2019) (37)
- Surgical contribution to recurrence-free survival in patients with macrovascular-invasion-negative hepatocellular carcinoma. (2009) (36)
- Expression of catalase and myeloperoxidase genes in hydrogen peroxide-resistant HL-60 cells. (1991) (36)
- Identification of target genes within an amplicon at 14q12‐q13 in esophageal squamous cell carcinoma (2001) (36)
- Genome-Wide Association Study of Breast Cancer in the Japanese Population (2013) (35)
- Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy (2019) (35)
- Isolation, characterization and structural organization of the gene and pseudogene for the dihydrolipoamide succinyltransferase component of the human 2-oxoglutarate dehydrogenase complex. (1994) (35)
- The human homologue of the murine Llglh gene (LLGL) maps within the Smith-Magenis syndrome region in 17p11.2. (1996) (35)
- The Whole Nucleotide Sequence and Chromosomal Localization of the Gene for Human Metabotropic Glutamate Receptor Subtype 6 (1997) (35)
- Analysis of sentinel node involvement in gastric cancer. (2007) (34)
- ACTN4 gene amplification and actinin‐4 protein overexpression drive tumour development and histological progression in a high‐grade subset of ovarian clear‐cell adenocarcinomas (2012) (34)
- Neuroradiologic Features of CASK Mutations (2010) (34)
- Abstract 2080: miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma (2010) (34)
- Clinicopathologic analysis of breast carcinoma with chromosomal aneusomy detected by fluorescence in situ hybridization (2001) (34)
- Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1. (1995) (34)
- Clinicopathological significance of WT1 expression in ovarian cancer: a possible accelerator of tumor progression in serous adenocarcinoma (2007) (34)
- Clinical and radiological features of Japanese patients with a severe phenotype due to CASK mutations (2012) (34)
- Non-incidental coamplification of Myc and ERBB2, and Myc and EGFR, in gastric adenocarcinomas (2007) (34)
- Cloning and characterization of a novel Rab-family gene, Rab36, within the region at 22q11.2 that is homozygously deleted in malignant rhabdoid tumors. (1999) (33)
- PTPN13, a fas-associated protein tyrosine phosphatase, is located on the long arm of chromosome 4 at band q21.3. (1996) (33)
- Assignment of the human renal dipeptidase gene (DPEP1) to band q24 of chromosome 16. (1992) (33)
- Pax-5 Is Essential for κ Sterile Transcription during Igκ Chain Gene Rearrangement1 (2004) (33)
- Identification and characterization of human PKNOX2, a novel homeobox-containing gene. (2001) (33)
- Partial tandem duplication of GRIA3 in a male with mental retardation (2007) (33)
- Heterozygous deletion at 14q22.1–q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly (2008) (32)
- DNA amplification and expression of FADD in oral squamous cell carcinoma. (2009) (32)
- NF-κB Inducing Kinase, a Central Signaling Component of the Non-Canonical Pathway of NF-κB, Contributes to Ovarian Cancer Progression (2014) (32)
- Molecular Cytogenetic Analysis of 17 Renal Cancer Cell Lines: Increased Copy Number at 5q31‐33 in Cell Lines from Nonpapillary Carcinomas (2000) (32)
- Genomic loss and epigenetic silencing of very-low-density lipoprotein receptor involved in gastric carcinogenesis (2006) (32)
- Cancer-associated miRNAs and their therapeutic potential (2021) (32)
- Identification of CpG islands hypermethylated in human lung cancer by the arbitrarily primed-PCR method (1998) (31)
- Increased gene dosage of myelin protein zero causes Charcot‐Marie‐Tooth disease (2012) (31)
- The hypusine cascade promotes cancer progression and metastasis through the regulation of RhoA in squamous cell carcinoma (2016) (31)
- A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progression. (2003) (31)
- Genome‐wide association study identifies gastric cancer susceptibility loci at 12q24.11‐12 and 20q11.21 (2018) (30)
- Microsatellite instability is an early genetic event in myelodysplastic syndrome. (1995) (30)
- Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array‐based comparative genomic hybridization (2005) (30)
- Detailed deletion mapping in squamous cell carcinomas of the esophagus narrows a region containing a putative tumor suppressor gene to about 200 kilobases on distal chromosome 9q. (1996) (29)
- High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: the precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs. (1995) (29)
- Dermokine as a novel biomarker for early-stage colorectal cancer (2010) (28)
- Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion of SNF5/INI1 in a newly established cell line derived from extrarenal rhabdoid tumor (2004) (28)
- Assignment of the human mitochondrial NADP(+)-specific isocitrate dehydrogenase (IDH2) gene to 15q26.1 by in situ hybridization. (1996) (28)
- Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation (2010) (28)
- Fibroblast growth factor signals regulate transforming growth factor‐β‐induced endothelial‐to‐myofibroblast transition of tumor endothelial cells via Elk1 (2019) (28)
- Overexpression of NF-κB inducing kinase underlies constitutive NF-κB activation in lung cancer cells. (2010) (28)
- γ-Glutamylcyclotransferase as a novel immunohistochemical biomarker for the malignancy of esophageal squamous tumors. (2014) (28)
- HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome (2011) (28)
- Molecular cloning and mapping of a human cDNA (SC5DL) encoding a protein homologous to fungal sterol-C5-desaturase. (1996) (27)
- miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein (2018) (27)
- Detection of numerical and structural alterations and fusion of chromosomes 16 and 1 in low-grade papillary breast carcinoma by fluorescence in situ hybridization. (1997) (27)
- Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene (1999) (26)
- Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan (2003) (26)
- Skp2 overexpression is a p27Kip1‐independent predictor of poor prognosis in patients with biliary tract cancers (2004) (26)
- Molecular alterations in AKT and its protein activation in human lung carcinomas. (2012) (25)
- Genomic structure and chromosomal localization of the gene encoding translin, a recombination hotspot binding protein. (1997) (25)
- Analysis of histological therapeutic effect, apoptosis rate and p53 status after combined treatment with radiation, hyperthermia and 5-fluorouracil suppositories for advanced rectal cancers. (1998) (25)
- Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines (1999) (25)
- Human dihydrolipoamide succinyltransferase: cDNA cloning and localization on chromosome 14q24.2-q24.3. (1993) (25)
- Expression of cIAP-1 correlates with nodal metastasis in squamous cell carcinoma of the tongue. (2008) (25)
- Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies (2011) (24)
- Identification of amplified DNA sequences on double minute chromosomes in a leukemic cell line KY821 by means of spectral karyotyping and comparative genomic hybridization (1998) (24)
- Characterization of an embryonal rhabdomyosarcoma cell line showing amplification and over‐expression of the N‐myc oncogene (1990) (24)
- Cell culture in esophageal squamous cell carcinoma and the association with molecular markers. (2003) (24)
- Assignment of the human mitochondrial NAD+ -specific isocitrate dehydrogenase alpha subunit (IDH3A) gene to 15q25.1-->q25.2by in situ hybridization. (1996) (23)
- Induction of mcl1/EAT, Bcl-2 related gene, by retinoic acid or heat shock in the human embryonal carcinoma cells, NCR-G3. (1996) (23)
- A novel human RasGAP‐like gene that maps within the prostate cancer susceptibility locus at chromosome 1q25 (1998) (22)
- Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1). (1996) (22)
- Assignment of the human myeloperoxidase gene (MPO) to bands q21.3----q23 of chromosome 17. (1989) (22)
- Human ryudocan core protein: molecular cloning and characterization of the cDNA, and chromosomal localization of the gene. (1993) (22)
- Human Gene for β-Microseminoprotein: Its Promoter Structure and Chromosomal Localization (1995) (21)
- Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis (2007) (21)
- Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia (2007) (21)
- Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma (2017) (20)
- Isolation, characterization and mapping of the mouse and human RB1CC1 genes. (2002) (20)
- Detection and isolation of a novel human gene located on Xp11.2-p11.4 that escapes X-inactivation using a two-dimensional DNA mapping method. (1998) (20)
- Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese (2018) (20)
- Chromosomal localization and cDNA sequence of human BTEB, a GC box binding protein (1993) (20)
- Ovarian cancer therapeutic potential of glutamine depletion based on GS expression (2018) (20)
- Homozygous deletion in a neuroblastoma cell line defined by a high‐density STS map spanning human chromosome band 1p36 (2001) (20)
- Fluorescence in situ hybridization analysis of chromosomal localization of three human cytochrome P450 2C genes (CYP2C8, 2C9, and 2C10) at 10q24.1 (1994) (20)
- Genomic copy‐number alterations of MYC and FHIT genes are associated with survival in esophageal squamous‐cell carcinoma (2012) (20)
- Structural analysis of the gene encoding RP58, a sequence-specific transrepressor associated with heterochromatin. (2000) (20)
- Molecular cloning and genomic analysis of mouse glucuronyltransferase involved in biosynthesis of the HNK-1 epitope. (2002) (20)
- Integrative array-based approach identifies MZB1 as a frequently methylated putative tumor suppressor in hepatocellular carcinoma. (2012) (20)
- Isolation and mapping of a human gene (RPD3L1) that is homologous to RPD3, a transcription factor in Saccharomyces cerevisiae. (1996) (19)
- Assignment of the human ST2 gene to chromosome 2 at q11.2 (1996) (19)
- miR-1293, a Candidate for miRNA-Based Cancer Therapeutics, Simultaneously Targets BRD4 and the DNA Repair Pathway. (2020) (19)
- Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation (2011) (19)
- Chromosome 9q33q34 microdeletion with early infantile epileptic encephalopathy, severe dystonia, abnormal eye movements, and nephroureteral malformations. (2014) (19)
- Familial nasal NK/T‐cell lymphoma and pesticide use (2001) (19)
- Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study (2016) (18)
- Gene-expression phenotypes for vascular invasiveness of hepatocellular carcinomas. (2010) (18)
- Down-regulation of LAPTM5 in human cancer cells (2016) (18)
- Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion (2012) (18)
- Genomic alterations in primary gastric cancers analyzed by comparative genomic hybridization and clinicopathological factors. (2000) (18)
- ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array‐based comparative genomic hybridization (2008) (18)
- The brain finger protein gene (ZNF179), a member of the RING finger family, maps within the Smith-Magenis syndrome region at 17p11.2. (1997) (18)
- Assignment of the human calpastatin gene (CAST) to chromosome 5 at region q14----q22. (1990) (18)
- Clinical and molecular cytogenetic characterization of two patients with non‐mutational aberrations of the FMR2 gene (2007) (17)
- Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11–p12: LRRC1, GCLC, KIAA0057 and CLIC5 (2002) (17)
- HECT-type Ubiquitin Ligase ITCH Targets Lysosomal-associated Protein Multispanning Transmembrane 5 (LAPTM5) and Prevents LAPTM5-mediated Cell Death* (2011) (17)
- A novel gene in the chromosomal region for juvenile myoclonic epilepsy on 6p12 encodes a brain-specific lysosomal membrane protein. (2001) (17)
- Genetic analysis of multifocal superficial urothelial cancers by array-based comparative genomic hybridisation (2007) (17)
- Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation. (2000) (17)
- Isolation and chromosomal localization of the human cone cGMP phosphodiesterase gamma cDNA (PDE6H). (1996) (17)
- Association of 17 q 21-q 24 Gain in Ovarian Clear Cell Adenocarcinomas with Poor Prognosis and Identification of PPM 1 D and APPBP 2 as Likely Amplification Targets 1 (2003) (16)
- Detection of an i(17q) chromosome by fluorescent in situ hybridization with a chromosome 17 alpha satellite DNA probe. (1992) (16)
- Expression and chromosomal assignment of PTPH1 gene encoding a cytosolic protein tyrosine phosphatase homologous to cytoskeletal‐associated proteins (1993) (16)
- Increase in GFAP‐positive astrocytes in histone demethylase GASC1/KDM4C/JMJD2C hypomorphic mutant mice (2016) (16)
- Chromosomal localization of the protein tyrosine phosphatase G1 gene and characterization of the aberrant transcripts in human colon cancer cells (1994) (15)
- Establishment and characterization of a cisplatin-resistant human neuroblastoma cell line. (1999) (15)
- Philadelphia chromosome-negative cells with trisomy 8 after busulfan and interferon treatment of Ph1-positive chronic myelogenous leukemia. (1996) (15)
- PIK 3 CA mutation is an oncogenic aberration at advanced stages of oral squamous cell carcinoma (2006) (15)
- Germline mutation of the RET proto-oncogene in children with total intestinal aganglionosis. (1997) (15)
- Genome-Wide DNA Methylation Profiles in Renal Tumors of Various Histological Subtypes and Non-Tumorous Renal Tissues (2011) (15)
- BCL2L2 is a probable target for novel 14q11.2 amplification detected in a non‐small cell lung cancer cell line (2007) (15)
- Potential in a single cancer cell to produce heterogeneous morphology, radiosensitivity and gene expression. (2005) (15)
- Establishment of a cell line from a malignant rhabdoid tumor of the liver lacking the function of two tumor suppressor genes, hSNF5/INI1 and p16. (2005) (15)
- Detection of numerical alterations of chromosomes 3, 7, 17 and X in low-grade intracystic papillary tumors of the breast by multi-color fluorescencein situ hybridization (1997) (15)
- cDNA cloning, genomic structure and chromosomal mapping of the mouse glucuronyltransferase-S involved in the biosynthesis of the HNK-1 carbohydrate epitope. (2002) (14)
- Detection of chromosomal aneusomy by fluorescence in situ hybridization in fine‐needle aspirates from breast tumors (2000) (14)
- Frequent association of alternative splicing of NER, a nuclear hormone receptor gene in cancer tissues (1997) (14)
- Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy (2006) (14)
- A complete Not I restriction map covering the entire long arm of human chromosome 11 (1997) (14)
- Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin Syndrome (2015) (14)
- The incidence of hypoplasia of the corpus callosum in patients with dup (X)(q28) involving MECP2 is associated with the location of distal breakpoints (2012) (14)
- Diverse responses to retinoid in morphological differentiation, tumorigenesis and n‐myc expression in human neuroblastoma sublines (1989) (14)
- Significance of GSTP1 for predicting the prognosis and chemotherapeutic efficacy in esophageal squamous cell carcinoma. (2013) (14)
- An 8-cM interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers. (2001) (14)
- Precise localization of the human gene encoding cell adhesion kinase β (CAKβ/PYK2) to chromosome 8 at p21.1 by fluorescence in situ hybridization (1996) (14)
- Isolation and mapping of a human gene (DIFF6) homologous to yeast CDC3, CDC10, CDC11, and CDC12, and mouse Diff6. (1996) (13)
- Improving the Efficacy of EGFR Inhibitors by Topical Treatment of Cutaneous Squamous Cell Carcinoma with miR-634 Ointment (2020) (13)
- Chromosome mapping of human (ZNF147) and mouse genes for estrogen-responsive finger protein (efp), a member of the RING finger family. (1995) (13)
- Receptor tyrosine kinase amplification is predictive of distant metastasis in patients with oral squamous cell carcinoma (2017) (13)
- Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1. (1996) (13)
- Diverse involvement of isoforms and gene aberrations of Akt in human lung carcinomas (2015) (13)
- Rejoining between 9q+ and Philadelphia chromosomes results in normal-looking chromosomes 9 and 22 in Ph1-negative chronic myelocytic leukemia (1989) (13)
- Pax-5 is essential for kappa sterile transcription during Ig kappa chain gene rearrangement. (2004) (13)
- Cytogenetic studies in 32 patients with myelodysplastic syndrome: insights to specific chromosomal abnormalities and prognosis. (1987) (13)
- Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation (2021) (13)
- Identical deletion at 14q13.3 including PAX9 and NKX2-1 in siblings from mosaicism of unaffected parent (2015) (12)
- Breakpoint junction of interstitial homozygous deletion at chromosome 2q33 in a small cell lung carcinoma. (1996) (12)
- Overexpressed NF- (cid:1) B–inducing kinase contributes to the tumorigenesis of adult T-cell leukemia and Hodgkin Reed-Sternberg cells (2008) (12)
- Aberrations of chromosomes 1 and 17 in six human osteosarcoma cell lines using double-target fluorescence in situ hybridization. (1998) (12)
- Stabilization of phenotypic plasticity through mesenchymal-specific DNA hypermethylation in cancer cells (2012) (11)
- Subcloning and characterization of highly metastatic cells derived from human esophageal squamous cell carcinoma KYSE150 cells by in vivo selection (2017) (11)
- Radiation sensitivities of 31 human oesophageal squamous cell carcinoma cell lines (2005) (11)
- Identification of an Efs isoform that lacks the SH3 domain and chromosomal mapping of human Efs (1997) (11)
- Isolation and mapping of a human gene (RABL) encoding a small GTP-binding protein homologous to the Ras-related RAB gene. (1996) (11)
- Genomic structure and chromosomal mapping of the human Site-1 protease (S1P) gene (2000) (10)
- Assignment of the human antizyme gene (OAZ) to chromosome 19p13.3 by fluorescence in situ hybridization. (1996) (10)
- Clinical efficacy of haematopoietic stem cell transplantation for adult adrenoleukodystrophy (2020) (10)
- Molecular cloning of the breakpoint of t(11;22)(q23;q11) chromosome translocation in an adult acute myelomonocytic leukaemia (1996) (10)
- Copy number alterations in urothelial carcinomas: their clinicopathological significance and correlation with DNA methylation alterations (2010) (10)
- Precise ordering of 26 cosmid markers on chromosome region 3p23-->p21.3 by two-color FISH on human prophase chromosomes and stretched DNAs. (1995) (10)
- Identification and characterization of transforming growth factor beta‐induced in circulating tumor cell subline from pancreatic cancer cell line (2018) (10)
- A Simple G-Banding Technique Adaptable for Fluorescent in situ Hybridization (FISH) and Physical Ordering of Human Renin (REN) and Catepsin E (CTSE) Genes by Multi-Color FISH. (1993) (10)
- Relationship between chromosomal aberrations by fluorescence in situ hybridization and DNA ploidy by cytofluorometry in osteosarcoma. (1999) (9)
- Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses (1994) (9)
- Absence in Ph-negative, M-BCR rearrangement-positive chronic myelogenous leukemia of linkage between 5' ABL and 3' M-BCR sequences in Philadelphia translocation. (1992) (9)
- Array comparative genomic hybridization analysis discloses chromosome copy number alterations as indicators of patient outcome in lymph node-negative breast cancer (2019) (9)
- Precise localization of the human gene encoding cell adhesion kinase beta (CAK beta/PYK2) to chromosome 8 at p21.1 by fluorescence in situ hybridization. (1996) (9)
- Chromosomal mapping of the human smooth muscle actin gene (enteric type, ACTA3) to 2p13.1 and molecular nature of the hindIII polymorphism. (1995) (9)
- Genomic structure and chromosomal localization of the gene encoding TRAX, a Translin-associated factor X (2000) (9)
- The oncogenic role of GASC1 in chemically induced mouse skin cancer (2015) (9)
- SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements (2016) (9)
- FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenes. (1996) (9)
- Cloning and characterization of an interstitial deletion at chromosome 11p15 in a sporadic breast cancer. (1992) (9)
- Diagnosis and Prognostication of Ductal Adenocarcinomas of the Pancreas Based on Genome-Wide DNA Methylation Profiling by Bacterial Artificial Chromosome Array-Based Methylated CpG Island Amplification (2010) (8)
- Bipolar affective disorder associated with β-thalassemia minor (1995) (8)
- Suppression of MET Signaling Mediated by Pitavastatin and Capmatinib Inhibits Oral and Esophageal Cancer Cell Growth (2020) (8)
- Infrequent activation of mitogen-activated protein kinase in human colon cancers. (1999) (8)
- Significance of Akt activation and AKT gene increases in soft tissue tumors. (2014) (8)
- The human insulin receptor substrate-1 gene (IRS1) is localized on 2q36. (1994) (8)
- Genomic organization, sequence and chromosomal localization of the mouse Tbr2 gene and a comparative study with Tbr1. (2000) (8)
- The Suppression of Aurora-A / STK 15 / BTAK Expression Enhances Chemosensitivity to Docetaxel in Human Esophageal Squamous Cell Carcinoma (2007) (8)
- miR-766-5p Targets Super-Enhancers by Downregulating CBP and BRD4 (2021) (8)
- Publisher Correction: miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein (2018) (7)
- Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle (2001) (7)
- Identification of the homozygously deleted region at chromosome 1p36.2 in human neuroblastoma. (2000) (7)
- Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population (2019) (7)
- Distribution of breakpoint within the breakpoint cluster region (bcr) in chronic myelogenous leukemia with a complex philadelphia chromosome translocation (1989) (7)
- Cytogenetic analysis of spontaneously discharged products of conception by array-based comparative genomic hybridization (2016) (7)
- Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia‐de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array‐based comparative genomic hybridization (2007) (7)
- Regional assignment of nonspecific cross-reacting antigen (NCA) of the CEA gene family to chromosome 19 at band q13.2. (1989) (7)
- Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel (2019) (7)
- Large scale genome-wide association study in a Japanese population identified 45 novel susceptibility loci for 22 diseases (2019) (7)
- Chromosomal loci of 50 human keratinocyte cDNAs assigned by fluorescence in situ hybridization. (1995) (7)
- Chromosomal translocation, t(1;11)(q12;p15), in an extragonadal immature teratoma. (1997) (6)
- Simultaneous existence of double minute chromosomes and a homogeneously staining region in a retinoblastoma cell line (Y79) and amplification of N-myc at HSR. (1989) (6)
- Germline mutations of the RET proto-oncogene in pedigree with MEN type 2A: DNA analysis and its implications for pediatric surgery. (1996) (6)
- Ploidy analysis in paraffin-embedded malignant fibrous histiocytoma by DNA cytofluorometry and flourescence in situ hybridization. (1997) (6)
- Multiplex PCR/liquid chromatography assay for screening of subtelomeric rearrangements. (2007) (6)
- Proceedings of the schistosome genome project. (1997) (6)
- Mild prominence of the Sylvian fissure in a Bainbridge‐Ropers syndrome patient with a novel frameshift variant in ASXL3 (2017) (6)
- Reexamination of chromosomal loci of human muscle actin genes by fluorescence in situ hybridization (1995) (5)
- Novel targets for the 18 p 11 . 3 amplification frequently observed in esophageal squamous cell carcinomas (2001) (5)
- Microsatellite instability is an early genetic event in myelodysplastic syndrome [letter] (1995) (5)
- A Rare Genetic Polymorphism In C5 Confers Poor Response To The Anti-C5 Monoclonal Antibody Eculizumab In 11 Japanese Patients With PNH (2012) (5)
- Synergistic suppression of the clonogenicity of U937 leukemic cells by combinations of recombinant human interleukin 4 and granulocyte colony-stimulating factor. (1992) (5)
- Isolation of region-specific cosmids by hybridization with microdissection clones from human chromosome 10q11.1-q21.1. (1993) (5)
- DNA analysis using long-term preserved fixed cytogenetic preparations (1988) (5)
- Bipolar affective disorder associated with beta-thalassemia minor. (1995) (5)
- The use of diamox in the sequential methotrexate-5-fluorouracil therapy of advanced gastrointestinal cancer. (1988) (5)
- Esophageal squamous cell carcinoma developed 11 years after allogeneic bone marrow transplantation for acute lymphatic leukemia. (2013) (5)
- Myelomonocytic crisis with t(5;17) and a p53 mutation in a patient with chronic myelogenous leukemia (1994) (5)
- Assignment of the human protein tyrosine phosphatase, receptor-type, zeta (PTPRZ) gene to chromosome band 7q31.3. (1995) (5)
- Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes (2008) (5)
- p53 gene mutation is not directly related to tumoricidal effects of preoperative radiochemohyperthermia therapy for rectal cancers (1996) (5)
- Multiple Primary Cancers with Microsatellite Instability: Report of a Case (1996) (4)
- Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta (1999) (4)
- Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia (2009) (4)
- An unspliced cDNA for human dihydrolipoamide succinyltransferase: characterization and mapping of the gene to chromosome 14q24.2-q24.3. (1993) (4)
- Human gene for beta-microseminoprotein: its promoter structure and chromosomal localization. (1995) (4)
- Isolation and characterisation of lymphatic endothelial cells from lung tissues affected by lymphangioleiomyomatosis (2021) (4)
- A case of incomplete DiGeorge syndrome associated with partial monosomy 22q11.1 due to maternal 14;22 translocation (1989) (4)
- The human caspase-activated DNase gene (hCAD): genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locus (1999) (4)
- Successful Imatinib Treatment of Cardiac Involvement of FIP1L1-PDGFRA-Positive Chronic Eosinophilic Leukemia Followed by Severe Hepatotoxicity (2007) (4)
- Autophagy Inhibition Sensitizes Acute Lymphoblastic Leukemia Cells to L-Asparaginase (2015) (3)
- Identification of PDHX as a metabolic target for esophageal squamous cell carcinoma (2021) (3)
- Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2 (1993) (3)
- Lack of involvement of the G-CSF gene by chromosomal translocation t(15;17) in acute promyelocytic leukemia. (1990) (3)
- Multistep Carcinogenesis of Esophageal Carcinoma (1997) (3)
- Molecular Cloning , Characterization , and Chromosomal Localization of a Novel Protein-Tyrosine Phosphatase , HPTPq (2002) (3)
- Advances in Brief Frequent Silencing of Low Density Lipoprotein Receptor-Related Protein 1 B ( LRP 1 B ) Expression by Genetic and Epigenetic Mechanisms in Esophageal Squamous Cell Carcinoma (2004) (3)
- Integrative genome‐wide analyses reveal the transcriptional aberrations in Japanese esophageal squamous cell carcinoma (2021) (3)
- A missense variant in NUF2, a component of the kinetochore NDC80 complex, causes impaired chromosome segregation and aneuploidy associated with microcephaly and short stature (2021) (3)
- Long arm deletion of chromosome 7 unrelated to original karyotype in recurrent t(8;21) acute myeloblastic leukemia. (1990) (3)
- dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia (2007) (3)
- Concurrent targeting of MAP3K3 and BRD4 by miR-3140-3p overcomes acquired resistance to BET inhibitors in neuroblastoma cells (2021) (3)
- Regional chromosomal assignment of carcinoembryonic antigen gene (CEA) to chromosome 19 at band q13.2. (1991) (2)
- Genomic structure and chromosomal mapping of the human Site-1 protease (2000) (2)
- Identi fi cation , basic characterization and evolutionary analysis of differentially spliced mRNA isoforms of human YAP 1 gene (2012) (2)
- An improved rapid procedure for fluorescence in situ hybridization that is applicable to intraoperative cancer cytodiagnosis. (2000) (2)
- Missing Y chromosome in Ph1-negative chronic myeloid leukemia with bcr rearrangement. Evidence for a bcr-abl recombination on chromosome 22 by in situ hybridization. (1991) (2)
- Clinical Utility of Germline Genetic Testing in Japanese Men Undergoing Prostate Biopsy (2022) (2)
- Karyotypic evolution in acute myelomonocytic leukemia with pericentric inversion of chromosome 16. (1987) (2)
- [Human neuroblastoma cell lines having smooth muscle cell markers]. (1991) (2)
- Genomic landscape of a mouse model of diffuse-type gastric adenocarcinoma (2021) (2)
- Clinical and cytogenetic features in six patients with chronic myelogenous leukemia and a complex Philadelphia translocation. (1989) (2)
- Expression of cIAP 1 , a Target for 11 q 22 Amplification , Correlates with Resistance of Cervical Cancers to Radiotherapy 1 (2002) (2)
- [Clinical evaluation of a combination treatment with cefmenoxime and cefsulodin of severe infections in leukemia and related disorders]. (1988) (2)
- Chromosomal Assignment of the Gene for Protein Tyrosine Phosphatase HPTPδ (1993) (2)
- Abstract 2532: High expression of MiR-432-3p is associated with the chemoresistance by NRF2 stabilization via directly targeting KEAP1 (2017) (1)
- Augmentation of lenvatinib efficacy by topical treatment of miR-634 ointment in anaplastic thyroid cancer (2021) (1)
- [Detection of minimal residual clone after sex-mismatched bone marrow transplantation by fluorescent in situ hybridization]. (1993) (1)
- Potential for reversing miR-634-mediated cytoprotective processes to improve efficacy of chemotherapy against oral squamous cell carcinoma (2022) (1)
- Bone marrow-derived cells regenerate damaged epithelia in the human gastrointestinal tract (2003) (1)
- Abstracts of the 12th European Colloquium on Cytogenetics of Domestic Animals (1996) (1)
- [Genetic and epigenetic alteration in cancer]. (2006) (1)
- [Detection of numerical aberrations in chromosomes by fluorescence in situ hybridization in fine needle aspirates in the preoperative diagnosis of cancer]. (1999) (1)
- Cancers Small-Cell Lung − by Epigenetic Mechanism in Non PCDH 20 Frequent Silencing of the Candidate Tumor Suppressor (2006) (1)
- BCL 2 L 2 is a probable target for novel 14 q 11 . 2 amplification detected in a non-small cell lung cancer cell line (2007) (1)
- [A case of invasive renal pelvic cancer: usefulness of auxiliary diagnosis using fluorescence in situ hybridization]. (1997) (1)
- 144 GENOME-WIDE ASSOCIATION STUDY IDENTIFIES MULTIPLE NEW SUSCEPTIBILITY LOCI FOR PROSTATE CANCER IN JAPANESE POPULATION (2011) (1)
- Induction of mdl/EAT, Bd-2 Related Gene, byRetinoicAcidor HeatShock in the Human Embryonal Carcinoma Cells, NCR-G3 (1996) (1)
- predictor of poor prognosis in patients with biliary tract cancers (2004) (1)
- [Chromosome abnormalities in patients with myelodysplastic syndrome and its prognostic implication]. (1986) (1)
- Chromosomes and Clinical Features in 6 Cases of Gliomas (1991) (1)
- FISH as a tool for genome mapping and positional cloning. (1995) (0)
- [T-cell acute lymphoblastic leukemia associated with leukemic pericarditis, presenting t (5; 12) chromosome abnormality]. (1985) (0)
- Abstract 4191: HECT-type ubiquitin ligase ITCH targets lysosomal-associated protein multispanning transmembrane 5 (LAPTM5) and prevents LAPTM5-mediated cell death (2012) (0)
- Abstract 1992: Exploring target genes of eukaryotic initiation factor 5A in cancer using RNA sequence analysis (2016) (0)
- [DNA mismatch genes in colorectal cancer]. (2011) (0)
- Expanding the BBMRI-ERIC Directory into a Global Catalogue of COVID-19-Ready Collections: A Joint Initiative of BBMRI-ERIC and ISBER (2020) (0)
- Subject Index, Vol. 78, 1997 (1997) (0)
- A method for detection of an oral squamous and means for its suppression (2009) (0)
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- cDNA cloning and chromosomal localization of the human ciliary neurotrophic factor gene (1995) (0)
- [Improved quality of life in a patient with Borrmann type 4 gastric cancer treated with combination chemotherapy]. (1987) (0)
- Laboratory of DNA Information Analysis Laboratory of Sequence Analysis Laboratory of Genome Database (2018) (0)
- Abstract 3880: Exploring the role of up-regulated genes in highly metastatic oral cancer subline using spontaneous metastatic mouse model. (2013) (0)
- Abstract 3071: Frequent silencing ofprotocadherin 17, a candidate tumour suppressor for esophageal squamous-cell carcinoma (2010) (0)
- [Cancer genomics in post-sequence era]. (2005) (0)
- 434 Four loci at 11q12, 10q26, 3p11.2, and 2p11 are associated with prostate cancer susceptibility in the Japanese population (2012) (0)
- Integrative cancer genomics in the era of precision cancer medicine (2021) (0)
- Abstract 2093: Functional screening of tumor-suppressive microRNAs silenced by DNA hypermethylation in oral squamous cell carcinoma (2010) (0)
- Exploring Epithelial-Mesenchymal Transition: Suppressive miRNAs Using Combination of Cell-Based Reporter System and miRNA Library (2017) (0)
- [Cytogenetic evidence of the coexistence of CFU-GM-derived colonies with abnormal and normal karyotypes in a patient with myelodysplastic syndrome]. (1987) (0)
- Multi-color FISH : Application to the Simultaneous Detection of Chromosome Aberrations in Neuro-epithelial Tumor Cell Lines (1995) (0)
- Abstract 4991: Functional significance of potential oncogeneYAPand its isoforms in esophageal squamouse cell carcinoma (ESCC) (2010) (0)
- ASSOCIATION OF KALLIKREIN 5-OVEREXPRESSION WITH INVASIVENESS OF URINARY BLADDER CARCINOMA CELLS (2008) (0)
- Supplementary Material for: Genome-Wide DNA Methylation Profiles in Renal Tumors of Various Histological Subtypes and Non-Tumorous Renal Tissues (2017) (0)
- MECP2 Duplication Syndrome in Male Patients with Severe Mental Retardation and Intractable Epilepsy (2010) (0)
- [Chromosome abnormality 20q- in primary acquired sideroblastic anemia]. (1988) (0)
- [Blepharophimosis, epicanthus inversus, and ptosis syndrome(BPES)]. (2000) (0)
- Abstract 5200: MicroRNA-634 induces caspase-dependent apoptosis by targeting anti-apopotic and mitochondria-related genes in human cancer cells (2014) (0)
- Abstract 1989: Gene expression signature of the non-cancerous liver tissue associated with the early recurrence of hepatocellular carcinoma (2010) (0)
- Isolation of novel genes within the amplified regions in tumors detected by comparative genomic hybridization (CGH) (1999) (0)
- Assignment of the Human Mitochondrial NAD+-Specific Isocitrate Dehydrogenase α Subunit (IDH3A) Gene to 15q25.1 → q25.2 byin SituHybridization: Volume32,Number 2 (1996), pages 295–296: (1996) (0)
- [Application of high resolution FISH to genome analysis and cancer genetics]. (1996) (0)
- MicroRNA-based diagnosis and therapy in NRF2-stabilized tumor (2015) (0)
- Radiation sensitivity of 51 human cancer cell lines (2003) (0)
- Publisher Correction: miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein (2018) (0)
- [Relation of karyotypic findings to chemotherapy response in patients with preleukemia]. (1989) (0)
- [Development and application of bacterial artificial chromosome (BAC)-based CGH-array]. (2005) (0)
- P2‐2: Mesenchymal stem cells cultured in serum‐free medium suppress murine bleomycin‐induced pulmonary fibrosis by enhancing regulatory T cell induction (2021) (0)
- Abstract LB-385:miR-3140suppresses tumor cell growth by targetingBRD4via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein (2018) (0)
- Subject Index, Vol. 74, 1996 (1996) (0)
- Abstract 2586: Therapeutic potential of the topical treatment ofmiR-634ointment for cutaneous squamous cell carcinoma (2019) (0)
- Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH) (2011) (0)
- Analysis of genomic imbalances in squamous cell carcinoma of the esophagus (1999) (0)
- Identification of the breakpoint of inv(X) with severe mental, neural and muscle disease : (2000) (0)
- Identification of novel cancer-related genes through genomic and epigenomic analyses of gastrointestinal cancer (2010) (0)
- Abstract 325: ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array-based comparative genomic hybridization (2010) (0)
- Abstract 3869: Exploration of mechanisms for chromothripsis by irradiation (2015) (0)
- Abstract 2415: Phenotypic stabilization of mesenchymal-like cancer cells through mesenchymal-specific DNA hypermethylation (2012) (0)
- [Clinical evaluation of a combination therapy with aztreonam and clindamycin for severe infections in leukemia and related disorders]. (1989) (0)
- [Translocation (8;14)(q24;q32) in ALL(L3) with bladder invasion]. (1987) (0)
- CARCINOEMBRYONIC ANTIGEN (CEA) FAMILY GENES ARE LOCATED ON HUMAN CHROMOSOME 19 AT BAND q13.2 (1990) (0)
- Gasc1 may affect skin carcinogenesis by regulating expression level of estrogen related gene (2013) (0)
- Alterations of the p53 gene in Philadelphia chromosome-positive leukemia including chronic myelogenous leukemia and acute leukemia. (1992) (0)
- miR-509-5p and miR-1243 increase the sensitivity to gemcitabine by inhibiting epithelial-mesenchymal transition in pancreatic cancer (2017) (0)
- Abstract 163: Identification and characterization of TGFBI in circulating tumor cell subline from pancreatic cancer cell line (2019) (0)
- [Chromosome abnormalities in neuroblastoma]. (1989) (0)
- Radiation Sensitive Cells Dedifferentiated from a Cultured Human Esophageal Cancer Cell Line (2002) (0)
- Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases (2020) (0)
- Imaging flow cytometry-based multiplex FISH for three IGH translocations in multiple myeloma. (2023) (0)
- Abstract 4111: A transcriptional variant of the LC3A gene is involved in autophagy and frequently inactivated in human cancers (2012) (0)
- Contents, Vol. 78, 1997 (1997) (0)
- Significance of GSTP 1 for predicting the prognosis and chemotherapeutic efficacy in esophageal squamous cell carcinoma (0)
- Abstract 2278: The hypusine cascade promotes cancer progression and metastasis through the regulation of RhoA in squamous cell carcinoma (2015) (0)
- Abstract 4020: Exploring target gene(s) within chromosome 19-amplification detected in a subclone from metastatic tumors in mouse transplantable OSCC (2014) (0)
- Abstract 318: Hierarchical clustering analysis of array CGH data identifies clinicopathologically distinct groups of lymph-node-negative invasive breast cancer (2011) (0)
- Abstract 2497: Differential requirement of amino acids on cell survival of ovarian cancer cells (2017) (0)
- The oncogenic role of GASC1 in chemically induced mouse skin cancer (2015) (0)
- Abstract 1368: Genome-wide screening of DNA methylation markers to predict the presence of lymph node metastasis in esophageal squamous cell carcinoma (2014) (0)
- Array comparative genomic hybridization analysis discloses chromosome copy number alterations as indicators of patient outcome in lymph node-negative breast cancer (2019) (0)
- Clinical impact of hemizygous deletion detection and panel-size in comprehensive genomic profiling. (2020) (0)
- New Editors, Features and Procedures (1989) (0)
- Diagnostic clinical application of two-color fluorescence in situ hybridization that detects chromosome 1 and 17 alterations to direct touch smear and liquid-based thin-layer cytologic preparations of endometrial cancers (2004) (0)
- Amendment history : Erratum ( August 2006 ) Early G 2 / M checkpoint failure as a molecular mechanism underlying etoposide-induced chromosomal aberrations (2018) (0)
- Abstract 1685: Inactivation of a transcriptional variant of MAP1LC3A gene in human cancers. (2013) (0)
- Abstract 347: Gene expression signature of the gross morphology and the specific role of EpCAM in hepatocellular carcinoma (2011) (0)
- Abstract 1846: Potential of tumor-suppressive miR-596 targeting LGALS3BP as a therapeutic agent in oral cancer. (2013) (0)
- Genetic diagnosis of cancer (1998) (0)
- IDENTIFICATION OF NINE NEW SUSCEPTIBILITY LOCI FOR PROSTATE CANCER IN THE JAPANESE POPULATION: MP70‐09 (2018) (0)
- Optimization of PGD for recurrent t(11;22) carrier (2019) (0)
- [Present status of gene diagnosis in cancer]. (1992) (0)
- HECT-typeUbiquitinLigaseITCHTargetsLysosomal-associated Protein Multispanning Transmembrane 5 (LAPTM5) and (2011) (0)
- Massive computational identification of somatic variants in exonic splicing enhancers using The Cancer Genome Atlas (2019) (0)
- Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese (2018) (0)
- Reproducibility, performance, and clinical utility of a genetic risk prediction model for prostate cancer in Japanese patients. (2012) (0)
- Abstract 4932: Exploration of EMT-related microRNAs using function-based screening with expression analysis of E-cadherin in Panc1 line (2012) (0)
- Cell Death and Survival The Impact of miRNA-Based Molecular Diagnostics and Treatment of NRF 2-Stabilized Tumors (2014) (0)
- CLINICAL REPORT Neuroradiologic Features of CASK Mutations (2010) (0)
- miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein (2018) (0)
- [Applications of FISH to chromosome analysis in hematological malignancies]. (1992) (0)
- [Mapping of human chromosome 6,8, and 17]. (1993) (0)
- Genomic organization and fine-mapping of the human leucine zipper-bearing kinase (LZK) gene. (2002) (0)
- [i(17q) appearing in acute phase in Ph1-negative, BCR-negative CML]. (1992) (0)
- Abstract 4842: Lysosomal-associated protein multispanning transmembrane 5 gene (LAPTM5) is associated with spontaneous regression of neuroblastomas (2010) (0)
- Molecular Cytogenetic Characterization of the Critical Deletion at 17p11.2 in Japanese Patients with Smith-Magenis Syndrome (SMS) (2003) (0)
- Addendum to the report of the fourth international workshop on human chromosome 12 mapping 1997 (1997) (0)
- Abstract 3302: Autophagy is required for cell survival under L-asparaginase-induced metabolic stress in acute lymphoblastic leukemia cells (2017) (0)
- Exploration of mechanisms for chromothripsis by irradiation. (2015) (0)
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What Schools Are Affiliated With Johji Inazawa?
Johji Inazawa is affiliated with the following schools: