Inazawa Johji | Department Of Molecular Cytogenetics Medical Research Institute And School Of Biomedical Science Tok

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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
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
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
Oxidation Resistance of Cr-N-O Thin Films Prepared by Pulsed Laser Deposition
ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array-based comparative genomic hybridization
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
Differentially Regulated Genes as Putative Targets of Amplifications at 20q in Ovarian Cancers
Oxidation Resistance of Cr-N-O Thin Films Prepared by Pulsed Laser Deposition
Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1 ; 19)(q23 ; p13)
MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas
Nonrandom Chromosomal Imbalances in Esophageal Squamous Cell Carcinoma Cell Lines : Possible Involvement of the ATF3 and CENPF Genes in the 1q32 Amplicon
Successful Imatinib Treatment of Cardiac Involvement of FIP1L1-PDGFRA-Positive Chronic Eosinophilic Leukemia Followed by Severe Hepatotoxicity
Activation of B-Myb by E2F1 in hepatocellular carcinoma
Association of over-expressed TFDP1 with progression of hepatocellular carcinomas
The c-Jun NH_2-terminal kinase3 (JNK3) gene : genomic structure, chromosomal assignment, and loss of expression in brain tumors
A Novel Amplicon at 9p23-24 in Squamous Cell Carcinoma of the Esophagus That Lies Proximal to GASC1 and Harbors NFIB
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
Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes
Human arylhydrocarbon receptor repressor (AHRR) gene : genomic structure and analysis of polymorphism in endometriosis
The human caspase-activated DNase gene (hCAD) : genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locus
Identification of PAK4 as a putative target gene for amplification within 19q13.12-q13.2 in oral squamous-cell carcinoma
Identification of the breakpoint of inv(X) with severe mental, neural and muscle disease
Genome-wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage
Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes
GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines
Dermokine as a novel biomarker for early-stage colorectal cancer
Identification of charcoal in Quaternary sediments and estimation of the charred temperature by reflectance measurements and H / C ratio analysis and observation through reflectance and scanning electron microscopy
Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation
Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia

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