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Human biliverdin reductase-based peptides activate and inhibit glucose uptake through direct interaction with the kinase domain of insulin receptor

Insulin binding changes conformation of the insulin receptor kinase (IRK) domain and initiates glucose uptake through the insulin, IGF-1, phosphatidyl inositol 3-kinase (PI3K), and MAPK pathways; human biliverdin reductase (hBVR) is an IRK substrate and pathway effector. This is the first report on...

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Detalhes bibliográficos
Main Authors: Gibbs, Peter E. M., Lerner-Marmarosh, Nicole, Poulin, Amelia, Farah, Elie, Maines, Mahin D.
Formato: Artigo
Idioma:Inglês
Publicado em: Federation of American Societies for Experimental Biology 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4021440/
https://ncbi.nlm.nih.gov/pubmed/24568842
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.13-247015
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