Identification of 45 novel SNPs in the 83-kb region containing peptidylarginine deiminase types 1 and 3 loci on chromosomal band 1p36. 13
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2004-07-01
著者
-
Nakamura Yusuke
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, University of T
-
IIDA Aritoshi
Laboratory for Genotyping, SNP Research Center, The Institute of Physical and Chemical Research (RIK
-
Iida Aritoshi
Laboratory For Pharmacogenetics Research Group Of Personalized Medicine Riken Snp Research Center C/
-
Nakamura Y
Laboratory For Pharmacogenetics Research Group Of Personalized Medicine Riken Snp Research Center C/
-
Iida Aritoshi
Laboratory For Bone And Joint Diseases Center For Genomic Medicine Riken
-
Nakamura Yusuke
Laboratory For Genotyping Riken Snp Research Center C/o Riken Yokohama Institute
関連論文
- 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
- 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
- High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the 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
- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
- Japanese single nucleotide polymorphism database for 267 possible drug-related genes
- 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
- 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
- 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
- Novel tumor marker REG4 detected in serum of patients with resectable pancreatic cancer and feasibility for antibody therapy targeting REG4
- High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis
- 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
- INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
- Variations in the FTO gene are associated with severe obesity in the Japanese
- 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
- Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines
- Isolation of a Novel Gene Showing Reduced Expression in Metastatic Colorectal Carcinoma Cell Lines and Carcinomas
- 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
- Frequent Allelic Loss at 6q26-27 in Breast Carcinomas of the Solid-tubular Histologic Type
- 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
- Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer
- Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP)
- A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
- Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
- Critical roles of T-LAK cell-originated protein kinase in cytokinesis
- Involvement of kinesin family member 2C/mitotic centromere-associated kinesin overexpression in mammary carcinogenesis
- Enhanced SMYD3 expression is essential for the growth of breast cancer cells
- Multiplex Mutation Screening of the BRCA1 Gene in 1000 Japanese Breast Cancers
- Infrequent Mutation of the H-Cadherin Gene on Chromosome 16q24 in Human Breast Cancers
- Non-transmissible Sendai virus encoding granulocyte macrophage colony-stimulating factor is a novel and potent vector system for producing autologous tumor vaccines
- Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
- 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
- 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
- Impact of CYP2D6^*10 on recurrence-free survival in breast cancer patients receiving adjuvant tamoxifen therapy
- Association of genetic polymorphisms in SLCO1B3 and ABCC2 with docetaxel-induced leukopenia
- Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease
- No Evidence of Mutation in the Human PTC Gene, Responsible for Nevoid Basal Cell Carcinoma Syndrome, in Human Primary Squamous Cell Carcinomas of the Esophagus and Lung
- Complete cDNA sequence and genomic organization of a human pancreas-specific gene homologous to Caenorhabditis elegans sel-1
- Molecular cloning, expression, and mapping of a novel human cDNA, GRP17, highly homologous to human gadd45 and murine MyD118
- Isolation and characterization of a human cDNA encoding a protein homologous to the 7.2-kDa protein (subunit X) of bovine ubiquinol-cytochrome C reductase
- Loci on murine chromosomes 7 and 13 that modify the phenotype of the NOA mouse, an animal model of atopic dermatitis
- Allelic Loss at 1p34-36 Predicts Poor Prognosis in Node-negative Breast Cancer
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- 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
- Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10
- Association of the RIP2 Gene with Childhood Atopic Asthma
- Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma
- 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
- Nonrandom Chromosomal Imbalances in Esophageal Squamous Cell Carcinoma Cell Lines : Possible Involvement of the ATF3 and CENPF Genes in the 1q32 Amplicon
- Isolation and Characterization of Human NBL4, a Gene Involved in the β-Catenin/Tcf Signaling Pathway
- Analysis of APCL, a Brain-specific Adenomatous Polyposis Coli Homologue, for Mutations and Expression in Brain Tumors
- High-resolution SNP map in the 55-kb region containing the selectin gene family on chromosome 1q24-q25
- Stanniocalcin 2 overexpression in castration-resistant prostate cancer and aggressive prostate cancer
- Oncogenic role of NALP7 in testicular seminomas
- Novel 5α-steroid reductase (SRD5A3, type-3) is overexpressed in hormone-refractory prostate cancer
- Identification of brain-specific splicing variants of the hDLG1 gene and altered splicing in neuroblastoma cell lines
- Fibroblast growth factor receptor 1 oncogene partner as a novel prognostic biomarker and therapeutic target for lung cancer
- Characterization of SEZ6L2 cell-surface protein as a novel prognostic marker for lung cancer
- 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)
- Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locus
- Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population