Literature DB >> 8299203

G protein mutations in human disease.

L S Weinstein1, A Shenker.   

Abstract

The heterotrimeric G proteins couple cell-surface receptors for extracellular signals to intracellular effectors that generate second messengers. Abnormal G protein signalling, resulting from posttranslational modifications by bacterial toxins, altered gene expression, or gene mutations, may lead to diverse biological consequences. Mutations within G protein alpha subunit genes that lead to either constitutive activation or loss of function have been identified. Such G protein mutations play a role in the pathogenesis of several human diseases, including sporadic endocrine tumors, McCune-Albright syndrome, and Albright hereditary osteodystrophy.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8299203     DOI: 10.1016/0009-9120(93)90109-j

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  8 in total

1.  Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.

Authors:  L C Wilson; M E Oude Luttikhuis; P T Clayton; W D Fraser; R C Trembath
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

2.  A 4-base pair deletion mutation of Gs alpha gene in a Japanese patient with pseudohypoparathyroidism.

Authors:  M Yokoyama; K Takeda; K Iyota; T Okabayashi; K Hashimoto
Journal:  J Endocrinol Invest       Date:  1996-04       Impact factor: 4.256

3.  Diverse somatic mutation patterns and pathway alterations in human cancers.

Authors:  Zhengyan Kan; Bijay S Jaiswal; Jeremy Stinson; Vasantharajan Janakiraman; Deepali Bhatt; Howard M Stern; Peng Yue; Peter M Haverty; Richard Bourgon; Jianbiao Zheng; Martin Moorhead; Subhra Chaudhuri; Lynn P Tomsho; Brock A Peters; Kanan Pujara; Shaun Cordes; David P Davis; Victoria E H Carlton; Wenlin Yuan; Li Li; Weiru Wang; Charles Eigenbrot; Joshua S Kaminker; David A Eberhard; Paul Waring; Stephan C Schuster; Zora Modrusan; Zemin Zhang; David Stokoe; Frederic J de Sauvage; Malek Faham; Somasekar Seshagiri
Journal:  Nature       Date:  2010-07-28       Impact factor: 49.962

4.  A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease.

Authors:  W J Pavan; R A Liddell; A Wright; G Thibaudeau; P G Matteson; K M McHugh; L D Siracusa
Journal:  Mamm Genome       Date:  1995-01       Impact factor: 2.957

5.  Deficient type I protein kinase A isozyme activity in systemic lupus erythematosus T lymphocytes.

Authors:  G M Kammer; I U Khan; C J Malemud
Journal:  J Clin Invest       Date:  1994-07       Impact factor: 14.808

6.  Pseudohypoparathyroidism type Ia: two new heterozygous frameshift mutations in exons 5 and 10 of the Gs alpha gene.

Authors:  H Shapira; M Mouallem; M S Shapiro; Y Weisman; Z Farfel
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

7.  Pseudohypoparathyroidism type 1a and insulin resistance in a child.

Authors:  Benjamin U Nwosu; Mary M Lee
Journal:  Nat Rev Endocrinol       Date:  2009-06       Impact factor: 43.330

8.  Gs G protein-coupled receptor signaling in osteoblasts elicits age-dependent effects on bone formation.

Authors:  Edward C Hsiao; Benjamin M Boudignon; Bernard P Halloran; Robert A Nissenson; Bruce R Conklin
Journal:  J Bone Miner Res       Date:  2010-03       Impact factor: 6.741

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.