Genome-wide association database developed in the Japanese Integrated Database Project

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概要

• 論文の詳細を見る
• Nature Publishing Groupの論文
• 2009-09-01

著者

• Inoue Ituro

  Department Of Human Genetics University Of Utah

• Tsuji Shoji

  Department Of Neurology Brain Research Institute Niigata University

• Koike Asako

  Hitachi Ltd Central Research Laboratory

• Nishida Nao

  Department Of Human Genetics Graduate School Of Medicine University Of Tokyo

• Nishida Nao

  Department Of Human Genetics Graduate School Of Medicine The University Of Tokyo

• Tokunaga K

  Department Of Human Genetics Graduate School Of Medicine University Of Tokyo

• Tokunaga Katsushi

  Department Of Cardiology Nagoya University Graduate School Of Medicine

• Koike Asako

  Central Research Laboratory Hitachi Ltd

• TSUJI Shoji

  Department of Neurology, Graduate School of Medicine, University of Tokyo

関連論文

• A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
• Combining effects of polymorphism of tumor necrosis factor α5'-flanking region and HLA-DRB1 on radiological progression in patients with rheumatoid arthritis
• Epidemiology of X-linked adrenoleukodystrophy in Japan
• Targeting Id1 and Id3 inhibits peritoneal metastasis of gastric cancer
• Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects
• TDP-43 M337V Mutation in Familial Amyotrophic Lateral Sclerosis in Japan
• Polymorphisms of HLA Genes in Western Javanese (Indonesia) and Their Association to Tuberculosis
• Appropriate data cleaning methods for genome-wide association study
• Identification of Hypertension-Susceptibility Genes and Pathways by a Systemic Multiple Candidate Gene Approach : The Millennium Genome Project for Hypertension
• Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium
• Autosomal recessive juvenile parkinsonism
• Interaction of expanded polyglutamine stretches with nuclear transcription factors leads to aberrant transcriptional regulation in polyglutamine diseases
• Polyglutamine disease : Recent advances in the neuropathology of dentatorubral-pallidoluysian atrophy
• Genotype-phenotype correlation in CAG-repeat diseases
• Power of association test for detecting minor histocompatibility gene causing graft-versus-host disease following bone barrow transplantation
• Quantitative Evaluation of the Pyramidal Tract Segmented by Diffusion Tensor Tractography : Feasibility Study in Patients with Amyotrophic Lateral Sclerosis
• Haplotypes of BRCA1 Mutation Alleles in Japanese Ovarian and Breast-Ovarian Cancer Families: A Novel Method for Detecting BRCA1 Associated Ovarian Cancer
• HLA-DRB1 alleles encoding the shared epitope associated with rheumatoid arthritis confer additional susceptibility to seronegative spondyloarthropathies in HLA-B27-positive Japanese individuals
• Machado-Joseph disease gene products carrying different carboxyl termini
• Contribution of Sp1 to initiation of transcription of angiotensinogen
• Molecular cloning and functional analysis of a factor that binds to the proximal promoter of human angiotensinogen
• Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population
• Association study of the dysbindin (DTNBP1) gene in schizophrenia from the Japanese population
• Establishment of a method of anonymization of DNA samples in genetic research
• Molecular genetic analyses of human NKG2C (KLRC2) gene deletion
• Effect of Genetic Polymorphism of OATP-C (SLCO1B1) on Lipid-Lowering Response to HMG-CoA Reductase Inhibitors
• FTO polymorphisms in oceanic populations
• Polymorphisms in the ABO blood group gene in three populations in the New Georgia group of the Solomon Islands
• HLA-DRB1 polymorphism on Ha'ano island of the Kingdom of Tonga
• De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
• Spermatogenic ability is different among males in different Y chromosome lineage
• Y chromosome compound haplotypes with the microsatellite markers DXYS265, DXYS266, and DXYS241
• Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage
• MERRF/MELAS overlap syndrome associated with 3243 tRNA^mutation of mitochondrial DNA
• FGFR2 is associated with hair thickness in Asian populations
• Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene
• A novel apolipoprotein E5 variant with a 24-bp insertion causing hyperlipidemia
• Underediting of GluR2 mRNA, a neuronal death inducing molecular change in sporadic ALS, does not occur in motor neurons in ALS1 or SBMA
• HLA-DRB1 polymorphism on Ha’ano island of the Kingdom of Tonga
• A Case of a Japanese Patient with Cleidocranial Dysplasia Possessing a Mutation of CBFA1 Gene
• Functional Polymorphism of the Myeloperoxidase Gene in Hypertensive Nephrosclerosis Dialysis Patients
• Haplotype analysis of NAD(P)H oxidase p22 phox polymorphisms in end-stage renal disease
• A 52-year-old man with hypohidrosis
• Cerebellar Ataxia and Peripheral Neuropathy due to Chronic Bromvalerylurea Poisoning
• Transmission disequilibrium test and haplotype analysis of the NOTCH4 gene in Japanese patients with schizophrenia
• Researches on Neurological Diseases in the New Millennium
• Two phenotypes and anticipation observed in Japanese cases with early onset torsion dystonia(DYT1) : pathophysiological consideration
• Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)
• UNSTABLE EXPANSION OF TRIPLET REPEATS AS A NEW DISEASE MECHANISM FOR NEURODEGENERATIVE DISEASES
• Gene expression profiling of advanced-stage serous ovarian cancers distinguishes novel subclasses and implicates ZEB2 in tumor progression and prognosis
• Comparative study of the haplotype structure and linkage disequilibrium of chromosome 1p36.2 region in the Korean and Japanese populations
• Formation of a Ligand-based Mixed-valence Cluster Triggered by Dehydration Condensation of Semiquinonates with o-Phenylenediamines
• λ-Interferons and the single nucleotide polymorphisms : A milestone to tailor-made therapy for chronic hepatitis C
• HLA-DRB1 Polymorphism of Balopa Islanders in Papua New Guinea
• Haplotype analyses with the human leucocyte antigen and tumour necrosis factor-alpha genes in narcolepsy families
• Possible association of human leucocyte antigen DR1 with delayed sleep phase syndrome
• Linkage disequilibrium structure of the 5q31-33 region in a Thai population
• Strong linkage disequilibrium of a HbE variant with the (AT)_9(T)_5 repeat in the BP1 binding site upstream of the β-globin gene in the Thai population
• Fcγ receptor IIA and IIIB polymorphisms are associated with susceptibility to cerebral malaria
• Sequence Analysis of Fibroblast Growth Factor Receptor 2 (FGFR2) in Japanese Patients with Craniosynostosis
• Polymorphisms of promoter and coding regions of the arylamine N-acetyltransferase 2 (NAT2) gene in the Indonesian population : proposal for a new nomenclature
• HLA and Human Mate Choice: Tests on Japanese Couples
• Study of aspartate at residue 9 of HLA-C molecules in Japanese patients with psoriasis vulgaris
• Polymorphisms of HLA-A and -B Genes in the Kyrgyz Populations
• Selecting a contingency table in a population-based association study : allele frequency or positivity?
• ITPA gene variant protects against anemia induced by pegylated interferon-α and ribavirin therapy for Japanese patients with chronic hepatitis C
• Role of B cell inhibitory receptor polymorphisms in systemic lupus erythematosus : a negative times a negative makes a positive
• Thermal Expantion of the Intermetallic Compound MgNi_2
• Power of genome-wide linkage disequilibrium testing by using microsatellite markers
• The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers
• Population Genetic Study in Hainan Island, China (I)--Distribution of Blood Genetic Markers
• A genome-wide CNV association study on panic disorder in a Japanese population
• Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease
• Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms
• Genetics of Moyamoya disease
• Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population
• Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis
• Culture-negative Brain Abscess with Streptococcus intermedius Infection with Diagnosis Established by Direct Nucleotide Sequence Analysis of the 16S Ribosomal RNA Gene
• Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population
• Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association
• Replication of a genome-wide association study of panic disorder in a Japanese population
• Genome-wide association study of panic disorder in the Japanese population
• FGFR2 is associated with hair thickness in Asian populations
• Serum albumin level accurately reflects antioxidant potentials in idiopathic nephrotic syndrome
• Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer
• Genome-wide association database developed in the Japanese Integrated Database Project
• Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1^*1501-DQB1^*0602 haplotype
• DRD4 VNTR polymorphism in Oceanic populations
• Production of Nitric Oxide Is Lower in Shiga Toxin-Stimulated Neutrophils of Infants Compared to Those of Children or Adults
• Successful Treatment of an Unresectable Inflammatory Myofibroblastic Tumor of the Frontal Bone Using a Cyclooxygenase-2 Inhibitor and Methotrexate
• Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages
• The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations
• Elective Cesarean Section at 37 Weeks Is Associated with the Higher Risk of Neonatal Complications

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