The Human Lipodystrophy Gene BSCL2/Seipin May Be Essential for Normal Adipocyte Differentiation

OBJECTIVE—Berardinelli-Seip congenital lipodystrophy type 2 (BSCL2) is a recessive disorder featuring near complete absence of adipose tissue. Remarkably, although the causative gene, BSCL2, has been known for several years, its molecular function and its role in adipose tissue development have not...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Payne, Victoria A., Grimsey, Neil, Tuthill, Antoinette, Virtue, Sam, Gray, Sarah L., Nora, Edoardo Dalla, Semple, Robert K., O'Rahilly, Stephen, Rochford, Justin J.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Diabetes Association 2008
Pynciau:
Metabolism
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2494687/
https://ncbi.nlm.nih.gov/pubmed/18458148
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2337/db08-0184
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