Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9519
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dc.contributor.authorHogarth, P Marken
dc.contributor.authorHulett, M Den
dc.contributor.authorOsman, Nen
dc.date.accessioned2015-05-15T22:38:33Z
dc.date.available2015-05-15T22:38:33Z
dc.date.issued1992-05-16en
dc.identifier.citationImmunologic Research; 11(3-4): 217-25en
dc.identifier.govdoc1287117en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9519en
dc.description.abstractMolecular studies of murine Fc gamma R have revealed much exciting new information about the structure and regulation of Fc gamma RI and Fc gamma RII genes and of the Fc gamma RI protein. The Fc gamma RI gene is composed of six exons, whereas the Fc gamma RII gene is composed of ten. The extracellular domains are encoded by individual exons in both genes (three in Fc gamma RI and two in Fc gamma RII); however, the Fc gamma RII gene shows greatest complexity in the region encoding the cytoplasmic tail and membrane spanning region, which is encoded by four exons compared to only one in the Fc gamma RI gene. Expression of Fc gamma RII is controlled by elements within the first 641 bases upstream of the transcription initiation site. The function of the domains of Fc gamma RI has been defined with the surprising finding that in the absence of the third domain the first two extracellular domains function as a broadly specific low affinity Fc gamma RII-like receptor.en
dc.language.isoenen
dc.subject.otherAmino Acid Sequenceen
dc.subject.otherAnimalsen
dc.subject.otherBase Sequenceen
dc.subject.otherBiological Evolutionen
dc.subject.otherDNA.geneticsen
dc.subject.otherExonsen
dc.subject.otherGene Expression Regulationen
dc.subject.otherMiceen
dc.subject.otherMolecular Sequence Dataen
dc.subject.otherPolymerase Chain Reactionen
dc.subject.otherReceptors, IgG.genetics.physiologyen
dc.subject.otherRecombinant Proteins.geneticsen
dc.subject.otherSequence Homology, Amino Aciden
dc.titleFc gamma receptors: gene structure and receptor function.en
dc.typeJournal Articleen
dc.identifier.journaltitleImmunologic researchen
dc.identifier.affiliationAustin Research Institute, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages217-25en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/1287117en
dc.type.austinJournal Articleen
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
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