Imoto Issei | 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
Array-based comparative genomic hybridization analysis of high-grade neuroendocrine tumors of the lung
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
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
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
A Novel Amplicon at 9p23-24 in Squamous Cell Carcinoma of the Esophagus That Lies Proximal to GASC1 and Harbors NFIB
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
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
Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis

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