Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.

Patients who have pseudohypoparathyroidism type I associated with Albright hereditary osteodystrophy commonly have a genetic deficiency of the alpha subunit of the G protein that stimulates adenylyl cyclase (alpha Gs) (ATP pyrophosphate-lyase, EC 4.6.1.1). To discover the molecular mechanism that ca...

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Publicado en:	Proc Natl Acad Sci U S A
Principais autores:	Levine, M A, Ahn, T G, Klupt, S F, Kaufman, K D, Smallwood, P M, Bourne, H R, Sullivan, K A, Van Dop, C
Formato:	Artigo
Idioma:	Inglês
Publicado:	National Academy of Sciences 1988
Assuntos:	Research Article
Acceso en liña:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC279602/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2829196/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.2.617
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