Imoto Issei | Department Of Molecular Cytogenetics Medical Research Institute And Graduate School Of Biomedical Sc

スポンサーリンク

概要

関連著者

もっと見る

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
Genome-wide array-based comparative genomic hybridization analysis of pancreatic adenocarcinoma : Identification of genetic indicators that predict patient outcome
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
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
Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line
Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
The c-Jun NH_2-terminal kinase3 (JNK3) gene : genomic structure, chromosomal assignment, and loss of expression in brain tumors
Human arylhydrocarbon receptor repressor (AHRR) gene : genomic structure and analysis of polymorphism in endometriosis
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
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
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
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia

もっと見る

スポンサーリンク