Disparity between association and linkage analysis for HNF1A G319S in type 2 diabetes in Canadian Oji-Cree
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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2000-05-01
著者
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Hegele Robert
ブラジル
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Harris Stewart
Thames Valley Family Practice Research Centre University Of Western Ontario
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HEGELE Robert
Blackburn Cardiovascular Genetics Laboratory, John P. Robarts Research Institute
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Hegele R
Robarts Res. Inst. Ontario Can
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HANLEY Anthony
Samuel Lunenfeld Research Institute and Department of Medicine, University of Toronto
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ZINMAN Bernard
Samuel Lunenfeld Research Institute and Department of Medicine, University of Toronto
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ANDERSON Carol
Blackburn Cardiovascular Genetics Laboratory, John P. Roberts Research Institute
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Anderson Carol
Blackburn Cardiovascular Genetics Laboratory John P. Roberts Research Institute
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Zinman Bernard
Samuel Lunenfeld Research Institute And Department Of Medicine University Of Toronto
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Hanley Anthony
Samuel Lunenfeld Research Institute And Department Of Medicine University Of Toronto
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Hegele Robert
Blackburn Cardiovascular Genetics Laboratory John P. Robarts Research Institute
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Hanley Anthhony
Samuel Lunenfeld Research Institute and Department of Medicine, University of Toronto
関連論文
- Human aryl hydrocarbon receptor nuclear translocator gene (ARNT) D/N511 polymorphism
- Disparity between association and linkage analysis for HNF1A G319S in type 2 diabetes in Canadian Oji-Cree
- The ADD1 G460W polymorphism is not associated with variation in blood pressure in Canadian Oji-Cree
- Genome-wide scanning for type 2 diabetes susceptibility in Canadian Oji-Cree, using 190 microsatellite markers
- -6A Promoter variant of angiotensinogen and blood pressure variation in Canadian Oji-Cree
- ABCC6 gene polymorphism associated with variation in plasma lipoproteins
- Polymorphisms in the gene encoding phosphatidylserine-specific phospholipase A1 (PSPLA1)
- Identification of polymorphisms in the human SHP1 gene
- Functional promoter polymorphism in SREBP cleavage-activating protein (SCAP)
- DNA polymorphism and mutations in CPN1, including the genomic basis of carboxypeptidase N deficiency
- Identification of single-nucleotide polymorphisms in the human LPIN1 gene
- DNA polymorphisms in ITPA including basis of inosine triphosphatase deficiency
- Single nucleotide polymorphisms of the very low density lipoprotein receptor (VLDLR) gene
- Single nucleotide polymorphisms of the resistin (RSTN) gene
- Single nucleotide polymorphisms of RXRA encoding retinoid X receptor alpha
- DNA polymorphisms of lipase related genes
- Human C-reactive protein (CRP) 1059G/C polymorphism
- Human hepatocyte nuclear factor-1β (HNF1B) 1968A/G polymorphism
- Human cathepsin S gene (CTSS) promoter -25G/A polymorphism
- Polymorphisms in PNLIP, encoding pancreatic lipase, and associations with metabolic traits
- LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)
- Single nucleotide polymorphisms of the fukutin gene
- Single-nucleotide polymorphisms of the nuclear lamina proteome