Editorial: The stimulatory g protein α-subunit gene: Mutations and imprinting lead to complex phenotypes

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 10, 2001, Pages 4622-4626

  Weinstein, Lee S ^a  

^a NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE NUCLEOTIDE BINDING PROTEIN; HETEROTRIMERIC GUANINE NUCLEOTIDE BINDING PROTEIN; STIMULATORY GUANINE NUCLEOTIDE BINDING PROTEIN;

ALBRIGHT SYNDROME; EDITORIAL; GENE MUTATION; GENOME IMPRINTING; HUMAN; HYPOPHYSIS ADENOMA; PHENOTYPE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; CALCINOSIS; GENETICS; LIMB MALFORMATION; MUTATION; NOTE; PSEUDOHYPOPARATHYROIDISM;

CALCINOSIS; GTP-BINDING PROTEIN ALPHA SUBUNITS, GS; HETEROTRIMERIC GTP-BINDING PROTEINS; HUMANS; LIMB DEFORMITIES, CONGENITAL; MUTATION; PHENOTYPE; PSEUDOHYPOPARATHYROIDISM;

EID: 0034752247     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.86.10.4622     Document Type: Editorial

References (27)

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4. Identification of a mutation in the gene encoding the α subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome
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6. Progressive osseous heteroplasia
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12. Activity of the stimulatory guanine nudeotide-binding protein is reduced in erythrocytes from patients with pseudobypoparathyroidism and pseudopseudobypoparathyroidism: Biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds
13. The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins
14. Parental origin of transcription from the human GNAS1 gene
15. sα gene
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18. The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3
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27. Imprinting of mouse Kvlqt1 is developmentally regulated