Central Nervous System Imprinting of the G Protein G(s)α and Its Role in Metabolic Regulation

Albright hereditary osteodystrophy is a monogenic obesity disorder due to heterozygous mutations of G(s)α, the G protein which mediates receptor-stimulated cAMP generation, in which obesity only develops when the mutation is on the maternal allele. Likewise, mice with maternal (but not paternal) ger...

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Main Authors: Chen, Min, Wang, Jie, Dickerson, Kathryn E., Kelleher, James, Xie, Tao, Gupta, Divakar, Lai, Edwin W., Pacak, Karel, Gavrilova, Oksana, Weinstein, Lee S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2698878/
https://ncbi.nlm.nih.gov/pubmed/19490909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cmet.2009.05.004
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