Aritoshi Iida | Laboratory For Pharmacogenetics Snp Research Center The Institute Of Physical And Chemical Research

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著作論文

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
A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction
Japanese single nucleotide polymorphism database for 267 possible drug-related genes
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
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)
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
SNP projects in Japan
Allelic Loss at 1p34,13q12,17p13.3,and 17q21.1 Correlates With Poor Postoperative Prognosis in Breast Cancer
Correlation of Allelic Losses and Clinicopathological Factors in Primary Breast Cancers
Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
High-density SNP map of human ITR, a gene associated with vascular remodeling
Two Target Regions of Allelic Loss on Chromosome 9 in Urinary-bladder Cancer
Mapping of a New Target Region of Allelic Loss to a 6-cM Interval at 21q21 in Primary Breast Cancers
Identification of 20 novel SNPs in the guanine nucleotide binding protein alpha 12 gene locus
Catalog of 300 SNPs in 23 genes encoding G-protein coupled receptors
Catalog of 178 variations in the Japanese population among eight human genes encoding G protein-coupled receptors (GPCRs)
Catalog of 680 variations among eight cytochrome P450 (CYP) genes, nine esterase genes, and two other genes in the Japanese population
Catalog of 668 SNPs detected among 31 genes encoding potential drug targets on the cell surface
Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population
Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes : UGT2A1, UGT2B15, and UGT8
906 variations among 27 genes encoding cytochrome P450 (CYP) enzymes and aldehyde dehydrogenases (ALDHs) in the Japanese population
Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters : ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8
Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR)
Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families
Three Aberrant Splicing Variants of the HMGIC Gene Transcribed in Uterine Leiomyomas
Frequent Allelic Loss at 7p14-15 Associated with Aggressive Histologic Types of Breast Cancer
Mapping of a New Target Region of Allelic Loss to a 2-cM Interval at 22q 13.1 in Primary Breast Cancer
Seventy genetic variations in human microsomal and soluble epoxide hydrolase genes (EPHX1 and EPHX2) in the Japanese population
Identification of sequence polymorphisms in CALM2 and analysis of association with hip osteoarthritis in a Japanese population

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