Nakamura Yusuke | Human genome center

スポンサーリンク

概要

関連著者

もっと見る

著作論文

PJ-438 Identification of Proteins that Bind Galectin-2, Encoded by a Gene Associated with Myocardial Infarction Using Tandem Affinity Purification Method(Acute myocardial infarction, basic-4 (IHD) PJ74,Poster Session (Japanese),The 70th Anniversary Annual
Association of a single-nucleotide polymorphism in the immunoglobulin μ-binding protein 2 gene with immunoglobulin A nephropathy
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients
Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy
SNP projects in Japan
PJ-363 Functional Impacts of Selectin Haplotypes on Leukocyte-endothelial Interaction(Molecular Biology, Vascular 2 (H) : PJ61)(Poster Session (Japanese))
FISH MAPPING OF A TRANSLOCATION BREAKPOINT AT 6q21 (OR q22) IN A PATIENT WITH HETEROTAXIA
Allelic Losses of Loci at 3p25.1,8p22,13q12,17p13.3,and 22q13 Correlate with Postoperative Recurrence in Breast Cancer
Identification of Rad51 alteration in patients with bilateral breast cancer
Genetic dissection of the complex pathological manifestations of collagen disease in MRL/lpr mice
TWO DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D8S1442 AND D8S1443 LOCI
Cancer Genomics and Molecular Diagnosis : The Nineteenth International Symposium of Sapporo Cancer Seminar
Correlation of Allelic Losses and Clinicopathological Factors in 504 Primary Breast Cancers
Association of Allelic Losses at 3p25.1, 13q12, or 17p13.3 with Poor Prognosis in Breast Cancers with Lymph Node Metastasis
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
Bcl-X_L Antisense Sensitizes Human Colon Cancer Cell Line to 5-Fluorouracil
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases
Adenovirus-mediated p53AIP1 gene transfer as a new strategy for treatment of p53-resistant tumors
Nijmegen breakage syndrome : Sequence analysis of an 800-kb genomic region on chromosome 8q21.
Genetic diagnosis of cancer
Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome
Identification of ALDH4 as a p53-inducible gene and its protective role in cellular stresses
hCDC4b, a regulator of cyclin E, as a direct transcriptional target of p53

もっと見る

スポンサーリンク