Publication:
The GNAS Complex Locus and Human Diseases Associated with Loss-of-Function Mutations or Epimutations within This Imprinted Gene

dc.contributor.authorDEMİRCİOĞLU, SERAP
dc.contributor.authorsTuran, Serap; Bastepe, Murat
dc.date.accessioned2022-03-10T11:40:08Z
dc.date.accessioned2026-01-11T11:14:33Z
dc.date.available2022-03-10T11:40:08Z
dc.date.issued2013
dc.description.abstractGNAS is a complex imprinted locus leading to several different gene products that show exclusive monoallelic expression. GNAS also encodes the a-subunit of the stimulatory G protein (Gs alpha), a ubiquitously expressed signaling protein that is essential for the actions of many hormones and other endogenous molecules. Gsa is expressed biallelically in most tissues but its expression is silenced from the paternal allele in a small number of tissues. The tissue-specific paternal silencing of Gsa results in different parent-of-origin-specific phenotypes in patients who carry inactivating GNAS mutations. In this paper, we review the GNAS complex locus and discuss how disruption of Gsa expression and the expression of other GNAS products shape the phenotypes of human disorders caused by mutations in this gene. (C) 2013 S. Karger AG, Basel
dc.identifier.doi10.1159/000355384
dc.identifier.eissn1663-2826
dc.identifier.issn1663-2818
dc.identifier.pubmed24107509
dc.identifier.urihttps://hdl.handle.net/11424/219966
dc.identifier.wosWOS:000326934800002
dc.language.isoeng
dc.publisherKARGER
dc.relation.ispartofHORMONE RESEARCH IN PAEDIATRICS
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGNAS
dc.subjectPseudohypoparathyroidism
dc.subjectalpha-Subunit of the stimulatory G protein
dc.subjectPSEUDOHYPOPARATHYROIDISM-TYPE-IB
dc.subjectXL-ALPHA-S
dc.subjectALBRIGHT HEREDITARY OSTEODYSTROPHY
dc.subjectPROGRESSIVE OSSEOUS HETEROPLASIA
dc.subjectG-PROTEIN
dc.subjectGS-ALPHA
dc.subjectAUTOSOMAL-DOMINANT
dc.subjectHORMONE RESISTANCE
dc.subjectCONTROL REGION
dc.subjectPARATHYROID-HORMONE
dc.titleThe GNAS Complex Locus and Human Diseases Associated with Loss-of-Function Mutations or Epimutations within This Imprinted Gene
dc.typereview
dspace.entity.typePublication
oaire.citation.endPage241
oaire.citation.issue4
oaire.citation.startPage229
oaire.citation.titleHORMONE RESEARCH IN PAEDIATRICS
oaire.citation.volume80

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