Tanaka T | 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
OE-009 Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
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 the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in 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
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
The characteristics of relapse in adult-onset minimal-change nephrotic syndrome
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
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
SNP projects in Japan
A case of Mikulicz's disease complicated with severe interstitial nephritis associated with IgG4
Arterial Stiffness in Patients with Non-Diabetic Chronic Kidney Disease (CKD)
Low-Dose Losartan Therapy Reduces Proteinuria in Normotensive Patients with Immunoglobulin A Nephropathy
Clinical assessment of low-dose steroid therapy for patients with IgA nephropathy : a prospective study in a single center
PJ-224 Primal role of intracellular zinc in PKC-dependent monocyte signalling and adhesive interaction(Atherosclerosis, basic(06)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
Identification of missense mutation (G365R) of the Butyrylcholinesterase (BChE) gene in a Japanese patient with familial cholinesterasemia
Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus
Lack of Association of LRP5 and LRP6 Polymorphisms with Type 2 Diabetes Mellitus in the Japanese Population
Association Study of the Effect of WFS1 Polymorphisms on Risk of Type 2 Diabetes in Japanese Population
Association of Serum MCP-1 Concentration and MCP-1 Polymorphism with Insulin Resistance in Japanese Individuals with Obese type 2 Diabetes
A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
Membrane Localization of Protein-Tyrosine Phosphatase 1B is Essential for its Activation of Sterol Regulatory Element-Binding Protein-1 Gene Expression and Consequent Hypertriglyceridaemia
Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels
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
Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease
Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10
LARGE MUCOSA-ASSOCIATED LYMPHOID TISSUE LYMPHOMA SIMULATING MULTIPLE POLYPOID LESIONS AT THE CECUM AND RECTUM
NODULE-AGGREGATING LESION OF THE ILEUM : REPORT OF A CASE AND A REVIEW OF THE LITERATURE
Activation of an estrogen/estrogen receptor signaling by BIG3 through its inhibitory effect on nuclear transport of PHB2/REA in breast cancer
Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility
Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes
Making a haplotype catalog with estimated frequencies based on SNP homozygotes
pHCR : a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis

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