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The Human Lipodystrophy Gene Product Berardinelli-Seip Congenital Lipodystrophy 2/Seipin Plays a Key Role in Adipocyte Differentiation

Mutations in the Berardinelli-Seip congenital lipodystrophy 2 gene (BSCL2) are the underlying defect in patients with congenital generalized lipodystrophy type 2. BSCL2 encodes a protein called seipin, whose function is largely unknown. In this study, we investigated the role of Bscl2 in the regulat...

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Detalhes bibliográficos
Main Authors: Chen, Weiqin, Yechoor, Vijay K., Chang, Benny Hung-Junn, Li, Ming V., March, Keith L., Chan, Lawrence
Formato: Artigo
Idioma:Inglês
Publicado em: The Endocrine Society 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2754678/
https://ncbi.nlm.nih.gov/pubmed/19574402
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/en.2009-0236
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