The Role of Genomic Imprinting of Gsα in the Pathogenesis of Albright Hereditary Osteodystrophy
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference40 articles.
1. Albright hereditary osteodystrophy, pseudohypoparathyroidism and Gs deficiency;Weinstein,1998
2. Pseudohypoparathyroidism: defective excretion of 3′,5′-AMP in response to parathyroid hormone;Chase;J. Clin. Invest.,1969
3. Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds;Levine;J. Clin. Endocrinol. Metab.,1986
4. Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism;Levine;Biochem. Biophys. Res. Commun.,1980
5. Defect of receptor-cyclase coupling protein in pseudohypoparathyroidism;Farfel;New Engl. J. Med.,1980
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