From cancer genomics to thoracic oncology : discovery of new biomarkers and therapeutic targets for lung and esophageal carcinoma
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概要
- 論文の詳細を見る
- 2008-02-10
著者
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Daigo Yataro
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
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Nakamura Yusuke
Laboratory For Genotyping Riken Snp Research Center C/o Riken Yokohama Institute
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Daigo Yataro
Laboratory Of Genome Technology Human Genome Center Institute Of Medical Science The University Of Tokyo
関連論文
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- New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
- A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
- Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
- High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population
- A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction
- Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction
- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
- Japanese single nucleotide polymorphism database for 267 possible drug-related genes
- A high-throughput SNP typing system for genome-wide association studies
- PJ-152 A functional SNP in the Proteasome Subunit Alpha Type 6 Gene confers Risk of Myocardial Infarction in Japanese Population(Acute myocardial infarction, basic-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-212 Identification of a Novel non-coding RNA, MIAT, that Confers Risk of Myocardial Infarction(Genetics/Genetically engineered models/Gene therapy-2(H/M), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-340 Large-Scale Genetic Association Study of 30 Inflammation-Related Genes for Myocardial Infarction Using Tag SNPs from HapMap Data(Genetics/Genetically engineered models/Gene therapy-1 (M) OJ57,Oral Presentation (Japanese),The 70th Anniversary Annual
- Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene
- Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21
- Genome-wide association study to identify genes related to myocardial infarction
- A high-throughput SNP typing system for genome-wide association studies in patients with myocardial infarction
- High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2
- Isolation and mapping of a novel human kidney- and liver-specific gene homologous to the bacterial acetyltransferases
- Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin
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- Identification of C2orf18, termed ANT2BP (ANT2-binding protein), as one of the key molecules involved in pancreatic carcinogenesis
- Over-expression of cysteine proteinase inhibitor cystatin 6 promotes pancreatic cancer growth
- INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
- Variations in the FTO gene are associated with severe obesity in the Japanese
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- Critical roles of T-LAK cell-originated protein kinase in cytokinesis
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- Infrequent Mutation of the H-Cadherin Gene on Chromosome 16q24 in Human Breast Cancers
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- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- A Gln/Arg polymorphism at codon 349 of the hBUBR1 gene
- Identification of p53-46F as a super p53 with an enhanced ability to induce p53-dependent apoptosis
- Radioimmunotherapy of solid tumors targeting a cell-surface protein, FZD10 : therapeutic efficacy largely depends on radiosensitivity
- Mapping of a New Target Region of Allelic Loss to a 6-cM Interval at 21q21 in Primary Breast Cancers
- Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10
- Association of the RIP2 Gene with Childhood Atopic Asthma
- Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma
- Genomic organization and mapping of the human activin receptor type IIB (hActR-IIB) gene
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- An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway
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- Detection of novel cancer-testis antigen-specific T-cell responses in TIL, regional lymph nodes, and PBL in patients with esophageal squamous cell carcinoma
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- Isolation and characterization of a novel serine threonine kinase gene on chromosome 3p22-21.3
- Vaccination with multiple peptides derived from novel cancer-testis antigens can induced specific T-cell responses and clinical responses in advanced esophageal cancer
- Validation of the histone methyltransferase EZH2 as a therapeutic target for various types of human cancer and as a prognostic marker
- Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
- A novel tumor-associated antigen, cell division cycle 45-like can induce cytotoxic T-lymphocytes reactive to tumor cells
- From cancer genomics to thoracic oncology : discovery of new biomarkers and therapeutic targets for lung and esophageal carcinoma