Tanaka Toshihiro | Laboratory For Cardiovascular Diseases Center For Genomic Medicine Riken

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著作論文

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
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
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
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
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
Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels
Genetic variations in five genes involved in the excitement of cardiomyocytes
Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome
High-density SNP map of human ITR, a gene associated with vascular remodeling
Gene-based SNP discovery as part of the Japanese Millennium Genome Project : identification of 190 562 genetic variations in the human genome
Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population
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)
Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population
Inflammation as a risk factor for myocardial infarction
Identification by differential display of eight known genes induced during in vivo intimal hyperplasia
Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene
Functional Variations in Two Genes Encoding Functionally Associated Proteins Confer Risk of Myocardial Infarction(Clinical Approach to Personalized Medicine in Cardiovascular disease, The 69th Annual Scientific Meeting of the Japanese Circulation Society)
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

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