A high-throughput SNP typing system for genome-wide association studies
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2001-08-01
著者
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Ozaki Kouichi
Laboratory for Cardiovascular Diseases, Center for Genomic Medicine, RIKEN
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Tanaka Toshihiro
Laboratory for Cardiovascular Diseases, Center for Genomic Medicine, RIKEN
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Nakamura Yusuke
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, University of T
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OHNISHI Yozo
Laboratory for SNP Analysis, RIKEN Center for Genomic Medicine
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Akiba Takashi
Department Of Medicine Kidney Center Tokyo Women's Medical University
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Takei Takashi
東京女子医科大学 腎臓病総合医療センター
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Ohnishi Yozo
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
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Ohnishi Yozo
Department Of Internal Medicine School Of Medicine Keio University
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Ohnishi Yozo
Inst. Of Physical And Chemical Res. (riken) Tokyo Jpn
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Ohnishi Yozo
Laboratory For Cardiovascular Diseases Snp Research Center The Institute Of Physical And Chemical Re
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Ozaki K
Laboratory For Cardiovascular Diseases Center For Genomic Medicine Riken
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YAMADA Ryo
Laboratory for Rheumatic Diseases, SNP Research Center, The Institute of Physical and Chemical Resea
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Ohnishi Yozo
Laboratory For Snp Analysis Riken Center For Genomic Medicine
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SUZUKI Hideyuki
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University
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Nagane Yutaka
Department Of Urology Sanai Hospital
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Ohno Yoichi
Department Of Internal Medicine School Of Medicine Keio University
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Ozaki Kouichi
Laboratory For Cardiovascular Diseases Research Group For Disease-causing Mechanisms Snp Research Ce
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Tanaka Torao
Department Of Medicine Division Of Gastroenterology Social Insurance Chuo General Hospital
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OKAZAKI Kuniyasu
Kunitomi Surgical Clinic of Okayama
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Tanaka Toshihiro
Laboratory For Cardiovascular Diseases Center For Genomic Medicine Riken
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Higuchi Shoko
Laboratory For Genotyping Snp Research Center Institute Of Physical And Chemical Research Yokohama I
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Nakamura Yusuke
Department Of Public Health Jichi Medical School
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Yamada Ryo
Laboratory For Rheumatic Diseases Snp Research Center The Institute Of Physical And Chemical Researc
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Tada Takashi
Riken Tokyo Jpn
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Nakamura Yusuke
Laboratory For Molecular Medicine Human Genome Center The Institute Of Medical Science University Of
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Yamada Ryo
Laboratory For Rheumatic Diseases Center For Genomic Medicine The Institute Of Physical And Chemical
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Nakamura Yusuke
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science University Of Toky
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Okazaki Kuniyasu
Otsuka Gen Research Institute Otsuka Pharmaceutical Co. Ltd
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Ozaki Kouichi
Laboratory Of Molecular Medicine Institute Of Medical Science University Of Tokyo
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Nakamura Yusuke
Laboratory For Genotyping Riken Snp Research Center C/o Riken Yokohama Institute
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Tsuruo Takashi
Laboratory Of Biomedical Research Institute Of Molecular And Cellular Biosciences University Of Toky
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Ozaki Kouichi
Laboratory For Cardiovascular Diseases Center For Genomic Medicine Riken
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Ohnishi Yozo
Laboratory For Cardiovascular Disease Center For Genomic Medicine
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Ozaki Kouichi
Laboratory For Cardiovascular Disease Center For Genomic Medicine
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Tanaka Toshihiro
Laboratory For Cardiovascular Disease Snp Research Center The Institute Of Physical And Chemical Research (riken)
関連論文
- OE-294 A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd A
- FRS-004 Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction(FRS1,New Molecules for Cardiovascular Regulation (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Socie
- OE-071 A Genom-Wide Association Study of SNPs in the risk of Atherosclerosis Obliterans(Heart failure, clinical(01)(M),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
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- A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction
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- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
- Japanese single nucleotide polymorphism database for 267 possible drug-related genes
- OE-294 A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd A
- FRS-004 Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction(FRS1,New Molecules for Cardiovascular Regulation (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Socie
- 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
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- A high-throughput SNP typing system for genome-wide association studies
- OE-294 A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd A
- FRS-004 Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction(FRS1,New Molecules for Cardiovascular Regulation (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Socie
- 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)
- 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
- 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
- SNP projects in Japan
- 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
- EphA4 receptor, overexpressed in pancreatic ductal adenocarcinoma, promotes cancer cell growth
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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
- OE-294 A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd A
- INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
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- 1P-044 DNAメチル化維持を仲介するSRAドメインのヘミメチル化DNA認識について熱力学的解析(蛋白質・構造機能相関(1),第46回日本生物物理学会年会)
- Prediction of Sensitivity to STI571 among Chronic Myeloid Leukemia Patients by Genome-wide cDNA Microarray Analysis
- Microarray Analysis of Gene-expression Profiles in Diffuse Large B-cell Lymphoma : Identification of Genes Related to Disease Progression
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- Distinct pattern of gene expression in pyothorax-associated lymphoma (PAL), a lymphoma developing in long-standing inflammation
- Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1, showing homology to a metastasis-associated gene, MTA1
- Correlation of Allelic Loss with Poor Postoperative Survival in Breast Cancer
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- Detailed Deletion Mapping of Chromosome Arm 3p in Breast Cancers : A 2-cM Region on 3p 14.3-21.1 and a 5-cM Region on 3p 24.3-25.1 Commonly Deleted in Tumors
- Correlation of Allelic Losses and Clinicopathological Factors in Primary Breast Cancers
- Mapping of a Breast Cancer Tumor Suppressor Gene Locus to a 4-cM Interval on Chromosome 18q21
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- Multiplex Mutation Screening of the BRCA1 Gene in 1000 Japanese Breast Cancers
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- Gene-based SNP discovery as part of the Japanese Millennium Genome Project : identification of 190 562 genetic variations in the human genome
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- Association of genetic polymorphisms in SLCO1B3 and ABCC2 with docetaxel-induced leukopenia
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- 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
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- Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population
- Two Distinct Commonly Deleted Regions on Chromosome 13q Suggest Involvement of BRCA2 and Retinoblastoma Genes in Sporadic Breast Carcinomas
- An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway
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- Analysis of APCL, a Brain-specific Adenomatous Polyposis Coli Homologue, for Mutations and Expression in Brain Tumors
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- Stanniocalcin 2 overexpression in castration-resistant prostate cancer and aggressive prostate cancer
- PJ-207 Multiple Congenital and Acquired Predisposing Factors Aggravates Secondary Long QT Syndrome(Arrhythmia,diagnosis/Pathophysiology/EPS(13)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
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