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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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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | 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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