Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. - sprookjes - yvandenbroek - TriplyDB

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

http://www.wikidata.org/entity/Q33905197

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Genes, diet and type 2 diabetes mellitus: a review Is genetic testing useful to predict type 2 diabetes?A variant in CDKAL1 influences insulin response and risk of type 2 diabetes Exercise training, genetics and type 2 diabetes-related phenotypes.Effects of interacting networks of cardiovascular risk genes on the risk of type 2 diabetes mellitus (the CODAM study).No association between a candidate TCF7L2 variant and risk of breast or ovarian cancer.Principal component and linkage analysis of cardiovascular risk traits in the Norfolk isolate.Finding disease genes: a fast and flexible approach for analyzing high-throughput data.Investigating parent of origin effects in studies of type 2 diabetes and obesity Subsets of Finns with high HDL to total cholesterol ratio show evidence for linkage to type 2 diabetes on chromosome 6q.Genetics of gestational diabetes mellitus and type 2 diabetes.Genomic imprinting in diabetes.Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait.Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activation.The search for genetic risk factors of type 2 diabetes mellitus.High-resolution quantitative trait locus analysis reveals multiple diabetes susceptibility loci mapped to intervals<800 kb in the species-conserved Niddm1i of the GK rat.Genetics of type 2 diabetes-pitfalls and possibilities.Transcriptomic identification of ADH1B as a novel candidate gene for obesity and insulin resistance in human adipose tissue in Mexican Americans from the Veterans Administration Genetic Epidemiology Study (VAGES)Contribution of the TCF7L2 rs7903146 (C/T) gene polymorphism to the susceptibility to type 2 diabetes mellitus in Cameroon.TCF7L2: the biggest story in diabetes genetics since HLA?Genetic Testing and Type 2 Diabetes Risk Awareness.Parent-of-Origin Effects of the APOB Gene on Adiposity in Young Adults.The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology.Effect of SNPs in protein kinase C zeta gene on gene expression in the reporter gene detection system Complex trait mapping in isolated populations: Are specific statistical methods required?Impaired glucagon-like peptide-1-induced insulin secretion in carriers of transcription factor 7-like 2 (TCF7L2) gene polymorphisms.The role of the Wnt signaling pathway in incretin hormone production and function.The involvement of the wnt signaling pathway and TCF7L2 in diabetes mellitus: The current understanding, dispute, and perspective Identification of shared genetic susceptibility locus for coronary artery disease, type 2 diabetes and obesity: a meta-analysis of genome-wide studies.Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans.Overweight condition and waist circumference and a candidate gene within the 12q24 locus.Programming of DNA methylation in type 2 diabetes.Centenarians as super-controls to assess the biological relevance of genetic risk factors for common age-related diseases: a proof of principle on type 2 diabetes.Replication study of candidate genes associated with type 2 diabetes based on genome-wide screening Ordered stratification to reduce heterogeneity in linkage to diabetes-related quantitative traits.Genetic architecture of type 2 diabetes: recent progress and clinical implications Genetic variant in the IGF2BP2 gene may interact with fetal malnutrition to affect glucose metabolism.Human QTL linkage mapping Tissue-specific alternative splicing of TCF7L2.A genomics study of type 2 diabetes mellitus in U.S. Air Force personnel.

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P2860

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

http://www.wikidata.org/entity/Q33905197

description

2003 nî lūn-bûn

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2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի հուլիսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

@ast

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

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type

label

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

@ast

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

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prefLabel

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

@ast

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

@en

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American Journal of Human Genetics

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Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

@en

P2093

Anna Sigurlin Einarsdottir

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Augustine Kong

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Brian K Rhees

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Eyrun Edda Hjorleifsdottir

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Gudbjorg Th Orlygsdottir

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Gudrun Thora Bjornsdottir

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Gunnar Sigurdsson

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Inga Reynisdottir

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Jarema P Kochan

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Jeffrey R Gulcher

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

Reduction in the Incidence of Type 2 Diabetes with Lifestyle Intervention or Metformin

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom

Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association.

A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance

Localization of a susceptibility gene for common forms of stroke to 5q12

Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group

Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)

Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study

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323-335

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10.1086/377139

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2

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73

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Vilmundur Gudnason

Gudmar Thorleifsson

Rafn Benediktsson

Skarphedinn Halldorsson

Kári Stefánsson

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2003-07-08T00:00:00Z

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10669404

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12851856

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type-2 diabetes

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1180371

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