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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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2002-11-01
著者
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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
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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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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Nagane Yutaka
Department Of Urology Sanai Hospital
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Tsunoda Tatsuhiko
Research Center For Animal Life Science Shiga University Of Medical Science
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Nakamura Y
東京大学医科学研究所ヒトゲノム解析センター ゲノムシークエンス解析分野
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Ohno Yoichi
Department Of Internal Medicine School Of Medicine Keio University
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Tanaka T
Laboratory For Cardiovascular Diseases Center For Genomic Medicine Riken
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Tanaka Torao
Department Of Medicine Division Of Gastroenterology Social Insurance Chuo General Hospital
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HAGA Hisanori
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, University of T
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Tanaka Toshihiro
Laboratory For Cardiovascular Diseases Center For Genomic Medicine Riken
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Teranishi Tetsuya
Division Of Diabetes Metabolism And Endocrinology Department Of Internal Medicine Kobe University Gr
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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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Haga Hisanori
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science University Of Toky
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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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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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Ohnishi Yozo
Laboratory For Cardiovascular Disease Center For Genomic Medicine
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KUMASAKA Natsuhiko
Laboratory for Medical Informatics, Center for Genomic Medicine, The Institute of Physical and Chemical Research (RIKEN)
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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
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- New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
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- 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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- 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
- 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
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- Genome-wide association study to identify genes related to myocardial infarction
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- SNP projects in Japan
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- Isolation and mapping of a novel human kidney- and liver-specific gene homologous to the bacterial acetyltransferases
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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
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- 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
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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
- Identification of candidate predictive markers of anticancer drug sensitivity using a panel of human cancer cell lines
- Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genes
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- Identification of p53-46F as a super p53 with an enhanced ability to induce p53-dependent apoptosis
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- Mapping of a New Target Region of Allelic Loss to a 6-cM Interval at 21q21 in Primary Breast Cancers
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- Association of the RIP2 Gene with Childhood Atopic Asthma
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- Genomic organization and mapping of the human activin receptor type IIB (hActR-IIB) gene
- 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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- 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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