Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism.
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Is the gene encoding Chibby implicated as a tumour suppressor in colorectal cancer ?A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese populationThe Ser96Ala variant in histidine-rich calcium-binding protein is associated with life-threatening ventricular arrhythmias in idiopathic dilated cardiomyopathyMolecular analysis of a mutated FSH receptor detected in a patient with spontaneous ovarian hyperstimulation syndromeJapanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studiesMutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndromeAn aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritisMutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in IndiaGenome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore ChineseA single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes.DNA sequence variations of the entire anti-Mullerian hormone (AMH) gene promoter and AMH protein expression in patients with the Mayer-Rokitanski-Kuster-Hauser syndrome.Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences.Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin.Large scale genotyping study for asthma in the Japanese population.Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.Association between the SERPING1 gene and age-related macular degeneration and polypoidal choroidal vasculopathy in JapaneseChange of positive selection pressure on HIV-1 envelope gene inferred by early and recent samples.Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese.Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populationsRenin gene polymorphisms in bangladeshi hypertensive populationReplication study for the association between four Loci identified by a genome-wide association study on European American subjects with type 1 diabetes and susceptibility to diabetic nephropathy in Japanese subjects with type 2 diabetes.Differential expression of immunophilins FKBP51 and FKBP52 in the frontal cortex of HIV-infected patients with major depressive disorder.Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing.Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.Fluorescent nucleoside analogue displays enhanced emission upon pairing with guanine.CYP4F2 genetic variant alters required warfarin doseGenotyping of human platelet antigens 1 to 6 and 15 by high-resolution amplicon melting and conventional hybridization probes.A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C.Assessing genetic susceptibility to diabetic nephropathy.Japanese single nucleotide polymorphism database for 267 possible drug-related genes.Functional single nucleotide polymorphism-based association studies.iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing.Two functional coding single nucleotide polymorphisms in STK15 (Aurora-A) coordinately increase esophageal cancer risk.Insulin-like growth factor 1 is not associated with high myopia in a large Japanese cohort.Preventive advice given by patients with type 2 diabetes to their offspring.Angiotensin II type 1 receptor polymorphisms and susceptibility to hypertension: a HuGE review.Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.The discovery of human genetic variations and their use as disease markers: past, present and future.
P2860
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P2860
Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Gene-based SNP discovery as pa ...... ingle-nucleotide polymorphism.
@en
type
label
Gene-based SNP discovery as pa ...... ingle-nucleotide polymorphism.
@en
prefLabel
Gene-based SNP discovery as pa ...... ingle-nucleotide polymorphism.
@en
P2093
P356
P1476
Gene-based SNP discovery as pa ...... ingle-nucleotide polymorphism.
@en
P2093
Hisanori Haga
Ryo Yamada
Yozo Ohnishi
Yusuke Nakamura
P2888
P304
P356
10.1007/S100380200092
P577
2002-01-01T00:00:00Z