Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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Maturity onset diabetes of the young in India - a distinctive mutation pattern identified through targeted next-generation sequencing.Susceptibility background for type 2 diabetes in eleven Mexican Indigenous populations: HNF4A gene analysis.

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Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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name

Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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type

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Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

@en

P1476

Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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Barry I Freedman

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Donald W Bowden

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Maggie C Y Ng

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

Nicholette D Palmer

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Pamela J Hicks

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P2860

Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene

The maturity-onset diabetes of the young (MODY1) transcription factor HNF4alpha regulates expression of genes required for glucose transport and metabolism

A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young

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

Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

Hepatocyte nuclear factor 4alpha (nuclear receptor 2A1) is essential for maintenance of hepatic gene expression and lipid homeostasis

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.

Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1.

Identification of human plasma kallikrein gene polymorphisms and evaluation of their role in end-stage renal disease.

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scholarly article

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10.4172/2155-6156.1000145

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Jacklyn Nikole Hellwege

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2011-10-01T00:00:00Z

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233890085

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23227446

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3515062

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Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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P2860

P2860

Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

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P1433

P1476

P2093

P2860

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P5875

P698

P932