Isolation and characterization of the human Gs alpha gene
about
Violating the splicing rules: TG dinucleotides function as alternative 3' splice sites in U2-dependent intronsA human homologue of the yeast GST1 gene codes for a GTP-binding protein and is expressed in a proliferation-dependent manner in mammalian cellsA novel mutation in the switch 3 region of Gsalpha in a patient with Albright hereditary osteodystrophy impairs GDP binding and receptor activationMolecular cloning and sequence analysis of cDNA and genomic DNA for the human cone transducin alpha subunitSequence analysis of cDNA and genomic DNA for a putative pertussis toxin-insensitive guanine nucleotide-binding regulatory protein alpha subunitAlbright's hereditary osteodystrophyMaintenance of cellular levels of G-proteins: different efficiencies of alpha s and alpha o synthesis in GH3 cellsStructure of the human gene and two rat cDNAs encoding the alpha chain of GTP-binding regulatory protein Go: two different mRNAs are generated by alternative splicingDifferent forms of Go alpha mRNA arise by alternative splicing of transcripts from a single gene on human chromosome 16A reappraisal of non-consensus mRNA splice sitesAn analysis of vertebrate mRNA sequences: intimations of translational controlExpression profiling of cardiac genes in human hypertrophic cardiomyopathy: insight into the pathogenesis of phenotypesOscillating evolution of a mammalian locus with overlapping reading frames: an XLalphas/ALEX relay.Differential expression of novel Gs alpha signal transduction protein cDNA speciesMazabraud syndrome in two patients: clinical overlap with McCune-Albright syndromeTwo overlapping reading frames in a single exon encode interacting proteins--a novel way of gene usageXLalphas, the extra-long form of the alpha-subunit of the Gs G protein, is significantly longer than suspected, and so is its companion AlexTransgenic overexpression of the extra-large Gsα variant XLαs enhances Gsα-mediated responses in the mouse renal proximal tubule in vivoTransgenerational Effects of Di-(2-Ethylhexyl) Phthalate (DEHP) on Stress Hormones and Behavior.Sequence and genomic organization of the human G-protein Golfalpha gene (GNAL) on chromosome 18p11, a susceptibility region for bipolar disorder and schizophrenia.Proteolytic activation and function of the cytokine Spätzle in the innate immune response of a lepidopteran insect, Manduca sexta.Molecular cloning and characterization of GPA1, a G protein alpha subunit gene from Arabidopsis thalianaBidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteinsImprinting in Albright's hereditary osteodystrophyParental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.Parental origin of transcription from the human GNAS1 gene.Intragenic GNAS deletion involving exon A/B in pseudohypoparathyroidism type 1A resulting in an apparent loss of exon A/B methylation: potential for misdiagnosis of pseudohypoparathyroidism type 1BMolecular cloning and sequence determination of four different cDNA species coding for alpha-subunits of G proteins from Xenopus laevis oocytes.Alternative splicing of the latency-related transcript of bovine herpesvirus 1 yields RNAs containing unique open reading framesDNA sequence polymorphisms within the bovine guanine nucleotide-binding protein Gs subunit alpha (Gsα)-encoding (GNAS) genomic imprinting domain are associated with performance traitsMutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresisVariable imprinting of the heterotrimeric G protein G(s) alpha-subunit within different segments of the nephron.Analysis of GNAS1 and overlapping transcripts identifies the parental origin of mutations in patients with sporadic Albright hereditary osteodystrophy and reveals a model system in which to observe the effects of splicing mutations on translated andIdentification of a methylation imprint mark within the mouse Gnas locus.The role of GNAS and other imprinted genes in the development of obesity.Detection of functional overlapping genes: simulation and case studies.Developmental differences in the expression of the cholera toxin sensitive subunit (Gs alpha) of adenylate cyclase in the rat small intestine.A GNAS1 imprinting defect in pseudohypoparathyroidism type IBPotent constitutive cyclic AMP-generating activity of XLαs implicates this imprinted GNAS product in the pathogenesis of McCune-Albright syndrome and fibrous dysplasia of bone.Pseudohypoparathyroidism: one gene, several syndromes.
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Isolation and characterization of the human Gs alpha gene
description
1988 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1988
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im April 1988 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1988/04/01)
@sk
vědecký článek publikovaný v roce 1988
@cs
wetenschappelijk artikel (gepubliceerd op 1988/04/01)
@nl
наукова стаття, опублікована у квітні 1988
@uk
name
Isolation and characterization of the human Gs alpha gene
@ast
Isolation and characterization of the human Gs alpha gene
@en
Isolation and characterization of the human Gs alpha gene
@nl
type
label
Isolation and characterization of the human Gs alpha gene
@ast
Isolation and characterization of the human Gs alpha gene
@en
Isolation and characterization of the human Gs alpha gene
@nl
prefLabel
Isolation and characterization of the human Gs alpha gene
@ast
Isolation and characterization of the human Gs alpha gene
@en
Isolation and characterization of the human Gs alpha gene
@nl
P2093
P2860
P356
P1476
Isolation and characterization of the human Gs alpha gene
@en
P2093
P2860
P304
P356
10.1073/PNAS.85.7.2081
P407
P577
1988-04-01T00:00:00Z