Alterations in Lipid Signaling Underlie Lipodystrophy Secondary to AGPAT2 Mutations

Congenital generalized lipodystrophy (CGL), secondary to AGPAT2 mutation is characterized by the absence of adipocytes and development of severe insulin resistance. In the current study, we investigated the adipogenic defect associated with AGPAT2 mutations. Adipogenesis was studied in muscle-derive...

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Detaylı Bibliyografya
Asıl Yazarlar: Subauste, Angela R., Das, Arun K., Li, Xiangquan, Elliot, Brandon, Evans, Charles, El Azzouny, Mahmoud, Treutelaar, Mary, Oral, Elif, Leff, Todd, Burant, Charles F.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Diabetes Association 2012
Konular:
Pathophysiology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3478532/
https://ncbi.nlm.nih.gov/pubmed/22872237
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2337/db12-0004
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