Literature DB >> 11285295

Imprints of disease at GNAS1.

M Lalande1.   

Abstract

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Year:  2001        PMID： 11285295      PMCID： PMC199585          DOI： 10.1172/JCI12645

Source DB:  PubMed          Journal:  J Clin Invest        ISSN： 0021-9738            Impact factor:   14.808


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  13 in total

Review 1.  Genomic imprinting, uniparental disomy and foetal growth.

Authors:  M A Preece; G E Moore
Journal:  Trends Endocrinol Metab       Date:  2000-09       Impact factor: 12.015

Review 2.  Imprinting: focusing on the center.

Authors:  I Ben-Porath; H Cedar
Journal:  Curr Opin Genet Dev       Date:  2000-10       Impact factor: 5.578

3.  Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy.

Authors:  J L Patten; D R Johns; D Valle; C Eil; P A Gruppuso; G Steele; P M Smallwood; M A Levine
Journal:  N Engl J Med       Date:  1990-05-17       Impact factor: 91.245

4.  Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins.

Authors:  B E Hayward; V Moran; L Strain; D T Bonthron
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

5.  A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2.

Authors:  J Peters; S F Wroe; C A Wells; H J Miller; D Bodle; C V Beechey; C M Williamson; G Kelsey
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

Review 6.  Imprinting in Albright's hereditary osteodystrophy.

Authors:  S J Davies; H E Hughes
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

7.  Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly.

Authors:  B E Hayward; A Barlier; M Korbonits; A B Grossman; P Jacquet; A Enjalbert; D T Bonthron
Journal:  J Clin Invest       Date:  2001-03       Impact factor: 14.808

8.  Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.

Authors:  L S Weinstein; P V Gejman; E Friedman; T Kadowaki; R M Collins; E S Gershon; A M Spiegel
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

9.  The Role of Genomic Imprinting of Galpha in the Pathogenesis of Albright Hereditary Osteodystrophy.

Authors: 
Journal:  Trends Endocrinol Metab       Date:  1999-04       Impact factor: 12.015

10.  A GNAS1 imprinting defect in pseudohypoparathyroidism type IB.

Authors:  J Liu; D Litman; M J Rosenberg; S Yu; L G Biesecker; L S Weinstein
Journal:  J Clin Invest       Date:  2000-11       Impact factor: 14.808
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  6 in total

1.  Possible genomic imprinting of three human obesity-related genetic loci.

Authors:  Chuanhui Dong; Wei-Dong Li; Frank Geller; Lei Lei; Ding Li; Olga Y Gorlova; Johannes Hebebrand; Christopher I Amos; Robert D Nicholls; R Arlen Price
Journal:  Am J Hum Genet       Date:  2005-01-12       Impact factor: 11.025

2.  Increasing alternative promoter repertories is positively associated with differential expression and disease susceptibility.

Authors:  Song Liu
Journal:  PLoS One       Date:  2010-03-01       Impact factor: 3.240

3.  A novel polymorphism at the GNAS1 gene associated with low circulating calcium levels.

Authors:  Laura Masi; Francesca Del Monte; Alessia Gozzini; Maria Laura De Feo; Riccardo Gionata Gheri; Annasilvia Neri; Alberto Falchetti; Antonietta Amedei; Rosario Imbriaco; Carmelo Mavilia; Annalisa Tanini; Maria Luisa Brandi
Journal:  Clin Cases Miner Bone Metab       Date:  2007-05

Review 4.  Epigenetics and obesity.

Authors:  Reinhard Stöger
Journal:  Pharmacogenomics       Date:  2008-12       Impact factor: 2.533

5.  Identification of a novel mutation in a pseudohypoparathyroidism family.

Authors:  Zhi-Min Miao; Can Wang; Bin-Bin Wang; Dong-Mei Meng; Dong-Mei Su; Zhi Cheng; Qiao-Lian Wen; Lin Han; Qing Yu; Xu Ma; Chang-Gui Li
Journal:  Int J Endocrinol       Date:  2011-07-21       Impact factor: 3.257

6.  Pseudohypoparathyroidism presenting with ventricular arrhythmia: a case report.

Authors:  Sedat Işıkay; İlyas Akdemir; Kutluhan Yılmaz
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-03
  6 in total

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