Role of the single nucleotide polymorphism rs7903146 of TCF7L2 in inducing nonsense-mediated decay.

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A HuGE Review and Meta-Analyses of Genetic Associations in New Onset Diabetes after Kidney Transplantation Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicities

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Q26770675-4B9C4A2A-984A-4158-96EC-0917D2E43039 Q36239934-3B1DDB23-9157-44AD-B9C2-D6D14FDE82BF

P2860

Role of the single nucleotide polymorphism rs7903146 of TCF7L2 in inducing nonsense-mediated decay.

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2014 nî lūn-bûn

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Role of the single nucleotide ...... ucing nonsense-mediated decay.

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Role of the single nucleotide ...... ucing nonsense-mediated decay.

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Role of the single nucleotide ...... ucing nonsense-mediated decay.

@en

P1476

Role of the single nucleotide ...... ucing nonsense-mediated decay.

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Marta Pradas-Juni

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Nathalie Nicod

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Ramon Gomis

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P2860

The human T-cell transcription factor-4 gene: structure, extensive characterization of alternative splicings, and mutational analysis in colorectal cancer cell lines

Alternative splicing of Tcf7l2 transcripts generates protein variants with differential promoter-binding and transcriptional activation properties at Wnt/beta-catenin targets

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

TCF7L2 variation predicts hyperglycemia incidence in a French general population: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study.

Genotype and tissue-specific effects on alternative splicing of the transcription factor 7-like 2 gene in humans

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program

Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.

TCF7L2 variants are associated with increased proinsulin/insulin ratios but not obesity traits in the Framingham Heart Study.

TCF7L2 polymorphisms modulate proinsulin levels and beta-cell function in a British Europid population.

Functional analysis of TCF7L2 genetic variants associated with type 2 diabetes.

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2193-1801-3-41

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scholarly article

case report

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10.1186/2193-1801-3-41

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2014-01-22T00:00:00Z

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260109382

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1006634273

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24498581

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single-nucleotide polymorphism

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3909145

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Role of the single nucleotide polymorphism rs7903146 of TCF7L2 in inducing nonsense-mediated decay.

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P2860

P2860

Role of the single nucleotide polymorphism rs7903146 of TCF7L2 in inducing nonsense-mediated decay.

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P5875

P6179

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P5875

P6179

P698

P921

P932