Nagai H | Department Of Molecular Biology Institute Of Gerontology Nippon Medical School

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概要

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著作論文

Overrepresentation of the EBAG9 Gene at 8q23 Associated with Early-Stage Breast Cancers
Down-regulation of members of glycolipid-enriched membrane raft gene family, MAL and BENE, in cervical squamous cell cancers
Characterization of liver-cirrhosis nodules by analysis of gene-expression profiles and patterns of allelic loss
Monotherapy with Paclitaxel as Third-Line Chemotherapy against Anthracycline-Pretreated and Docetaxel-Refractory Metastatic Breast Cancer
Genetic mapping of allelic loss on chromosome 6q within heterogeneous prostate carcinoma
Identification of a 1-Mb Common Region at 16q24.1-24.2 Deleted in Hepatocellular Carcinoma
Identification of a 1-cM Region of Common Deletion on 4q35 Associated With Progression of Hepatocellular Carcinoma
PTEN/MMAC1 Mutations in Hepatocellular Carcinomas: Somatic Inactivation of Both Alleles in Tumors
Expression profiling to predict postoperative prognosis for estrogen receptor-negative breast cancers by analysis of 25,344 genes on a cDNA microarray
Up-regulation of transcriptional factor E2F1 in papillary and anaplastic thyroid cancers
Amplification, up-regulation and over-expression of C3G (CRK SH3 domain-binding guanine nucleotide-releasing factor) in non-small cell lung cancers
Upregulation and Overexpression of Human X-box Binding Protein 1 (hXBP-1) Gene in Primary Breast Cancers
Amplification, up-regulation and over-expression of DVL-1, the human counterpart of the Drosophila disheveled gene, in primary breast cancers
Association of common missense changes in ELAC2 (HPC2) with prostate cancer in a Japanese case-control series
DNA alterations during multi-step development of human hepatocellular carcinomas revealed by laser capture microdissection
Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line
FRS-090 Identification of a Novel Disease Gene for Hypertrophic Cardiomyopathy(FRS19,Genetic Abnormalities in Cardiac Hypertrophy and Cardiomyopathy (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Soc
Hypermethylation associated with inactivation of the SOCS-1 gene, a JAK/STAT inhibitor, in human hepatoblastomas
Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
Down-regulation in Multiple Human Cancers of a Novel Gene, DMHC, from 17q25.1 That Encodes an Integral Membrane Protein
Three Aberrant Splicing Variants of the HMGIC Gene Transcribed in Uterine Leiomyomas
Head-to-head juxtaposition of Fas-associated phosphatase-1 (FAP-1) and c-Jun NH2-terminal kinase 3 (JNK3) genes : genomic structure and seven polymorphisms of the FAP-1 gene
Genomic structure and eight novel exonic polymorphisms of the human N-cadherin gene
The c-Jun NH_2-terminal kinase3 (JNK3) gene : genomic structure, chromosomal assignment, and loss of expression in brain tumors
Gene fusion involving HMGIC is a frequent aberration in uterine leiomyomas
Localization of a Target Region of Allelic Loss to a 1-cM Interval on Chromosome 16p.13.13 in Hepatocellular Carcinoma
USEFULNESS OF THE 44 & 48-LEAD SYSTEM OF BODY SURFACE POTENTIAL MAPS IN PATIENTS WITH ACUTE MYOCARDIAL INFARCTION : ECG, VCG, Mapping : 53 Annual Scientific Meeting, Japanese Circulation Society

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