Johji Inazawa

Q: What Schools Are Affiliated With Johji Inazawa

Johji Inazawa is affiliated with the following schools: Kyoto Prefectural University of Medicine, University of Tokyo, Institute of Science Tokyo, Osaka University, Kyoto University

Johji Inazawa's AcademicInfluence.com Rankings

Johji Inazawa

Computer Science

#6929

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#7297

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Machine Learning

#2406

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#2436

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Artificial Intelligence

#2691

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#2732

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Database

#4003

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#4162

Historical Rank

computer-science Degrees

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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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Johji Inazawa'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

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)
[Exploration of novel molecular targets for cancer therapy based on genomic aberrations]. (2005) (0)
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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