Inazawa Johge | Department Of Hygiene Kyoto Prefectural University Of Medicine

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著作論文

Overexpressed Skp2 within 5p amplification detected by array-based comparative genomic hybridization is associated with poor prognosis of glioblastomas
Array-based comparative genomic hybridization analysis of high-grade neuroendocrine tumors of the lung
Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines
IQGAP1, a negative regulator of cell-cell adhesion, is upregulated by gene amplification at 15q26 in gastric cancer cell lines HSC39 and 40A
Genome-wide array-based comparative genomic hybridization analysis of pancreatic adenocarcinoma : Identification of genetic indicators that predict patient outcome
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
Increased Apoptosis Rate by Hyperthermochemoradiotherapy for Advanced Rectal Cancers
Philadelphia chromosome-negative cells with trisomy 8 after busulfan and interferon treatment of Ph^1-positive chronic myelogenous leukemia
Genomic Structure and Mapping of Human Orphan Receptor LXR Alpha : Upregulation of LXRa mRNA During Monocyte to Macrophage Differentiation
ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array-based comparative genomic hybridization
Multiple Primary Cancers with Microsatellite Instability: Report of a Case
Frequent silencing of a putative tumor suppressor gene melatonin receptor 1 A (MTNR1A) in oral squamous-cell carcinoma
PIK3CA mutation is an oncogenic aberration at advanced stages of oral squamous cell carcinoma
Skp2 overexpression is a p27^-independent predictor of poor prognosis in patients with biliary tract cancers
Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene
Differentially Regulated Genes as Putative Targets of Amplifications at 20q in Ovarian Cancers
Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
Genomic structure and chromosomal mapping of the human Site-1 protease (S1P) gene
Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1 ; 19)(q23 ; p13)
Activation of B-Myb by E2F1 in hepatocellular carcinoma
Association of over-expressed TFDP1 with progression of hepatocellular carcinomas
Multi-color FISH : Application to the Simultaneous Detection of Chromosome Aberrations in Neuro-epithelial Tumor Cell Lines
The c-Jun NH_2-terminal kinase3 (JNK3) gene : genomic structure, chromosomal assignment, and loss of expression in brain tumors
Molecular Cytogenetic Analysis of 17 Renal Cancer Cell Lines: Increased Copy Number at 5q31-33 in Cell Lines from Nonpapillary Carcinomas
Genetic or epigenetic silencing of low density lipoprotein receptor-related protein 1B expression in oral squamous cell carcinoma
CARCINOEMBRYONIC ANTIGEN (CEA) FAMILY GENES ARE LOCATED ON HUMAN CHROMOSOME 19 AT BAND q13.2 (In situ Hybridization III. : Application for Medical Investigation)
Human arylhydrocarbon receptor repressor (AHRR) gene : genomic structure and analysis of polymorphism in endometriosis
Identification of amplified DNA sequences on double minute chromosomes in a leukemic cell line KY821 by means of spectral karyotyping and comparative genomic hubridzation
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
Identification of PAK4 as a putative target gene for amplification within 19q13.12-q13.2 in oral squamous-cell carcinoma
Genome-wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage
GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines
REEXAMINATION OF CHROMOSOMAL LOCI OF HUMAN MUSCLE ACTIN GENES BY FLUORESCENCE IN SITU HYBRIDIZATION
Human Gene for β-Microseminoprotein: Its Promoter Structure and Chromosomal Localization^1
Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation

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