Pages that link to "Q37793987"
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The following pages link to Molecular function of TCF7L2: Consequences of TCF7L2 splicing for molecular function and risk for type 2 diabetes (Q37793987):
Displaying 26 items.
- Genetic and epigenetic control of metabolic health (Q27026287) (← links)
- Moving on from GWAS: functional studies on the G6PC2 gene implicated in the regulation of fasting blood glucose (Q33699177) (← links)
- KCNJ11, ABCC8 and TCF7L2 polymorphisms and the response to sulfonylurea treatment in patients with type 2 diabetes: a bioinformatics assessment. (Q33771570) (← links)
- TCF7L2 is a master regulator of insulin production and processing (Q34555421) (← links)
- The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis (Q34989092) (← links)
- Transcription Factor 7-Like 2 (TCF7L2) rs7903146 Polymorphism as a Risk Factor for Gestational Diabetes Mellitus: A Meta-Analysis (Q35983720) (← links)
- Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico (Q36031559) (← links)
- Cell type-specific binding patterns reveal that TCF7L2 can be tethered to the genome by association with GATA3. (Q36378040) (← links)
- Disease, Models, Variants and Altered Pathways-Journeying RGD Through the Magnifying Glass (Q36427543) (← links)
- Cloning and sequence analysis of SLC25A13 transcripts in human amniocytes (Q36508164) (← links)
- Diabetes and obesity-related genes and the risk of neural tube defects in the national birth defects prevention study (Q36606588) (← links)
- TCF7L2 and glucose metabolism: time to look beyond the pancreas (Q36635405) (← links)
- Pancreatic beta-cell function and type 2 diabetes risk: quantify the causal effect using a Mendelian randomization approach based on meta-analyses (Q36714258) (← links)
- Analysis of protein isoforms: can we do it better? (Q37240124) (← links)
- Genetic susceptibility to type 2 diabetes and obesity: follow-up of findings from genome-wide association studies. (Q37639793) (← links)
- From mice to humans (Q38045180) (← links)
- The use of proteases complementary to trypsin to probe isoforms and modifications. (Q38668408) (← links)
- Expression and Splice Variant Analysis of Human TCF4 Transcription Factor in Esophageal Cancer (Q38900424) (← links)
- Survival of pancreatic beta cells is partly controlled by a TCF7L2-p53-p53INP1-dependent pathway (Q39464436) (← links)
- Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts (Q41343079) (← links)
- Tcf7l2 plays pleiotropic roles in the control of glucose homeostasis, pancreas morphology, vascularization and regeneration (Q41548418) (← links)
- Involvement of PUF60 in Transcriptional and Post-transcriptional Regulation of Hepatitis B Virus Pregenomic RNA Expression (Q41921247) (← links)
- Pancreatic alpha cell-selective deletion of Tcf7l2 impairs glucagon secretion and counter-regulatory responses to hypoglycaemia in mice. (Q42281469) (← links)
- The rs7903146 Variant in the TCF7L2 Gene Increases the Risk of Prediabetes/Type 2 Diabetes in Obese Adolescents by Impairing β-Cell Function and Hepatic Insulin Sensitivity (Q48021869) (← links)
- Carriers of the TCF7L2 rs7903146, rs12255372 Risk Alleles in the South Tamil Nadu T2DM Patients Present with Early Incidence and Insulin Dependence (Q91711166) (← links)
- TCF7L2 regulates pancreatic β-cell function through PI3K/AKT signal pathway (Q91939475) (← links)