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http://purl.uniprot.org/citations/10101682http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10101682http://www.w3.org/2000/01/rdf-schema#comment"Nineteen mAb directed against murine fusion regulatory protein-1 (mFRP-1)/4F2/CD98 were isolated and their biological properties were analysed. Intriguingly, mFRP-1 was found to be an alloantigen, namely, FRP-1.1 (DBA/2 and CBA mice type) and FRP-1.2 (BALB/c, C57BL/6 and C3H/He mice type). The nucleotide sequences of FRP-1.1 and FRP-1.2 were determined, demonstrating that amino acid change at 129 (P<-->R) is related to the alloantigenicity. mFRP-1 is expressed on thymocytes, on spleen cells, on peripheral lymphocytes and on blood monocytes, suggesting that the physiological role in vivo of murine FRP-1 is different from that of human FRP-1. The biological activities of antimFRP-1 mAbs showed by the present study are: (i) enhancement of Newcastle disease virus-induced cell fusion; (ii) suppression of HIVgp160-mediated cell fusion; and (iii) induction of aggregation and multinucleated giant cells of monocytes/macrophages."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.org/dc/terms/identifier"doi:10.1046/j.1440-1711.1999.00792.x"xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Ito Y."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Tajima M."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Kawano M."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Komada H."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Kozuka Y."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Tsumura H."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Tsurudome M."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Nishio M."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Kusagawa S."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Shimura K."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Yoshimura S."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/author"Kusaura T."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/date"1999"xsd:gYear
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/name"Immunol Cell Biol"xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/pages"19-27"xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/title"Isolation and characterization of monoclonal antibodies directed against murine FRP-1/CD98/4F2 heavy chain: murine FRP-1 is an alloantigen and amino acid change at 129 (P<-->R) is related to the alloantigenicity."xsd:string
http://purl.uniprot.org/citations/10101682http://purl.uniprot.org/core/volume"77"xsd:string
http://purl.uniprot.org/citations/10101682http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10101682
http://purl.uniprot.org/citations/10101682http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10101682
http://purl.uniprot.org/uniprot/#_A0A0U1RP32-mappedCitation-10101682http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10101682
http://purl.uniprot.org/uniprot/#_A0A0U1RP98-mappedCitation-10101682http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10101682
http://purl.uniprot.org/uniprot/#_A0A0U1RPG5-mappedCitation-10101682http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10101682