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http://purl.uniprot.org/citations/1694015http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1694015http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1694015http://www.w3.org/2000/01/rdf-schema#comment"A novel cDNA clone (20.5) which is differentially expressed between two closely related T-lymphoma cell clones was isolated by subtraction-enriched differential screening. SL12.4 cells, from which the cDNA was isolated, have characteristics of thymocytes at an intermediate stage in development. A sister cell clone derived from the same tumor, SL12.3, does not express this mRNA, has a distinct phenotype, and expresses fewer genes required for mature T-cell function. The cDNA sequence predicts a highly hydrophobic protein (approximately 49.5 kilodaltons) which contains seven putative membrane spanning domains. The gene was expressed on concanavalin A-activated T lymphocytes and was designated Tea (T-cell early activation gene). The Tea gene mapped to chromosome 8 and appeared to be conserved among mammalian and avian species. The Tea gene is distinct from, but bears extensive amino acid and DNA sequence similarity with, the murine ecotropic retroviral receptor which is encoded by the Rec-1 gene. Neither gene product displayed significant homology with other known transmembrane-spanning proteins. Thus, the Tea and Rec-1 genes establish a new family encoding multiple membrane-spanning proteins."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.org/dc/terms/identifier"doi:10.1128/mcb.10.7.3663-3674.1990"xsd:string
http://purl.uniprot.org/citations/1694015http://purl.org/dc/terms/identifier"doi:10.1128/mcb.10.7.3663-3674.1990"xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Kozak C.A."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Kozak C.A."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Wilkinson M.F."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Wilkinson M.F."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Finley K."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Finley K."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Kakuda D."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Kakuda D."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Macleod C.L."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/author"Macleod C.L."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/date"1990"xsd:gYear
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/date"1990"xsd:gYear
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/name"Mol. Cell. Biol."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/name"Mol. Cell. Biol."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/pages"3663-3674"xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/pages"3663-3674"xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/title"Activated T cells express a novel gene on chromosome 8 that is closely related to the murine ecotropic retroviral receptor."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/title"Activated T cells express a novel gene on chromosome 8 that is closely related to the murine ecotropic retroviral receptor."xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/1694015http://purl.uniprot.org/core/volume"10"xsd:string