Webbläsaren som du använder stöds inte av denna webbplats. Alla versioner av Internet Explorer stöds inte längre, av oss eller Microsoft (läs mer här: * https://www.microsoft.com/en-us/microsoft-365/windows/end-of-ie-support).

Var god och använd en modern webbläsare för att ta del av denna webbplats, som t.ex. nyaste versioner av Edge, Chrome, Firefox eller Safari osv.

GCKR : How genetic variation across the allelic spectrum influences protein function and metabolic traits in humans

Författare

Summary, in English

Genome-wide association studies (GWAS) have generated considerable interest in glucokinase regulatory protein (GKRP; gene name GCKR) which is an inhibitor of hepatic glucokinase (GCK), an enzyme that plays a critical role in glucose update and disposal in liver. From the initial discovery of GCKR variants associated with triglyceride and glucose levels through the identification of pleiotropic associations with a wide variety of metabolic phenotypes, we have learned a great deal about the importance of GKRP as a critical node in hepatic metabolism. GKRP remains one of the few well-studied GWAS loci where attempts have been made to understand the functional as well as the phenotypic impact of genetic variants across the allelic spectrum. Given the interest in developing liver-specific glucokinase activators and small molecules which disrupt the GKRP:GCK interaction for the treatment of type 2 diabetes, these genetic insights provide a wealth of information regarding efficacy and potential adverse on-target effects in humans.

Publiceringsår

2016-01-01

Språk

Engelska

Sidor

317-336

Publikation/Tidskrift/Serie

The Genetics of Type 2 Diabetes and Related Traits: Biology, Physiology and Translation

Dokumenttyp

Del av eller Kapitel i bok

Förlag

Springer International Publishing

Ämne

  • Medical Genetics

Status

Published

Forskningsgrupp

  • Diabetes - Cardiovascular Disease

ISBN/ISSN/Övrigt

  • ISBN: 9783319015743
  • ISBN: 9783319015736