Molecular Basis and Clinical Manifestation of McCune-Albright Syndrome.
- 1 January 2000
- journal article
- Published by Japanese Society for Pediatric Endocrinology in Clinical Pediatric Endocrinology
- Vol. 9 (1) , 1-5
- https://doi.org/10.1297/cpe.9.1
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- A Novel GNAS1 Mutation, R201G, in McCune–Albright SyndromeJournal of Bone and Mineral Research, 1999
- Structural elements of Gα subunits that interact with Gβγ, receptors, and effectorsCell, 1993
- Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome.Proceedings of the National Academy of Sciences, 1992
- Activating Mutations of the Stimulatory G Protein in the McCune–Albright SyndromeNew England Journal of Medicine, 1991
- Mapping of the gene encoding the α subunit of the stimulatory G protein of adenylyl cyclase (GNAS1) to 20q13.2 → q13.3 in human by in situ hybridizationGenomics, 1991
- Clinical Characteristics of Acromegalic Patients whose Pituitary Tumors Contain Mutant GsProteinJournal of Clinical Endocrinology & Metabolism, 1990
- GTPase inhibiting mutations activate the α chain of Gs and stimulate adenylyl cyclase in human pituitary tumoursNature, 1989
- Altered Gs and adenylate cyclase activity in human GH-secreting pituitary adenomasNature, 1987
- OSTEODYSTROPHIA FIBROSAAmerican Journal of Diseases of Children, 1937
- Syndrome Characterized by Osteitis Fibrosa Disseminata, Areas of Pigmentation and Endocrine Dysfunction, with Precocious Puberty in FemalesNew England Journal of Medicine, 1937