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http://purl.uniprot.org/citations/17610414http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17610414http://www.w3.org/2000/01/rdf-schema#comment"Human B7-H3, a novel member of B7 family, has two isoforms (2IgB7-H3 and 4IgB7-H3). As costimulatory functions of both isoforms are not clarified, there has been much discussion on their expression patterns, T-cell responses, etc. This study generated two specific mouse anti-human 2IgB7-H3 monoclonal antibodies (mAbs) (7D7 and 10F1), whose specificities are quite different from those of the available B7-H3 mAb (21D4) by competition assay. The use of antibodies indicated that B7-H3 was found to have different expression patterns on monocyte-derived dendritic cells, that is the isoform 2IgB7-H3 is tended to express on immature dendritic cells (iDCs), whereas 4IgB7-H3 could be detected in the whole process of maturation of dendritic cells. The isoform 4IgB7-H3 was shown in the immunohistochemistry assay to be more widely expressed than 2IgB7-H3 in human benign and malignant hepatic tissues. Furthermore, flow cytometry and reverse transcription-polymerase chain reaction indicated that 4IgB7-H3 rather than 2IgB7-H3 was the major isoform on many human tumor cell lines. In addition, both 2IgB7-H3- and 4IgB7-H3-transfected cells could promote T-cell proliferation, which could be blocked by 7D7 mAb. These two novel antibodies may shed light on the function of the two B7-H3 isoforms."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.org/dc/terms/identifier"doi:10.1111/j.1399-0039.2007.00853.x"xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Ge Y."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Chen Y.J."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Xu L."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Zhou Y.H."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Wang Q."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Xie F."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Zhang X.G."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Wang X.F."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Zhang G.B."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/author"Ma Z.Y."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/name"Tissue Antigens"xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/pages"96-104"xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/title"4IgB7-H3 is the major isoform expressed on immunocytes as well as malignant cells."xsd:string
http://purl.uniprot.org/citations/17610414http://purl.uniprot.org/core/volume"70"xsd:string
http://purl.uniprot.org/citations/17610414http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17610414
http://purl.uniprot.org/citations/17610414http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/17610414
http://purl.uniprot.org/uniprot/#_A6MDC5-mappedCitation-17610414http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17610414
http://purl.uniprot.org/uniprot/#_Q8VE98-mappedCitation-17610414http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17610414
http://purl.uniprot.org/uniprot/A6MDC5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17610414
http://purl.uniprot.org/uniprot/Q8VE98http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17610414