RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/16432184http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16432184http://www.w3.org/2000/01/rdf-schema#comment"Genetically primed adult C57BL mice were deleted of exon 5 of the gene encoding the transcription factor PU.1 by IFN activation of Cre recombinase. After a 13-week delay, conditionally deleted (PU.1(-/-)) mice began dying of myeloid leukemia, and 95% of the mice surviving from early postinduction death developed transplantable myeloid leukemia whose cells were deleted of PU.1 and uniformly Gr-1 positive. The leukemic cells formed autonomous colonies in semisolid culture with varying clonal efficiency, but colony formation was enhanced by IL-3 and sometimes by granulocyte-macrophage colony-stimulating factor. Nine of 13 tumors analyzed had developed a capacity for autocrine IL-3 or granulocyte-macrophage colony-stimulating factor production, and there was evidence of rearrangement of the IL-3 gene. Acquisition of autocrine growth-factor production and autonomous growth appeared to be major events in the transformation of conditionally deleted PU.1(-/-) cells to fully developed myeloid leukemic populations."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.org/dc/terms/identifier"doi:10.1073/pnas.0510616103"xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/author"Wu L."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/author"Metcalf D."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/author"Mifsud S."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/author"Di Rago L."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/author"Nutt S."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/author"Dakic A."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/date"2006"xsd:gYear
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/name"Proc Natl Acad Sci U S A"xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/pages"1486-1491"xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/title"Inactivation of PU.1 in adult mice leads to the development of myeloid leukemia."xsd:string
http://purl.uniprot.org/citations/16432184http://purl.uniprot.org/core/volume"103"xsd:string
http://purl.uniprot.org/citations/16432184http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16432184
http://purl.uniprot.org/citations/16432184http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16432184
http://purl.uniprot.org/uniprot/#_E9QAI9-mappedCitation-16432184http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16432184
http://purl.uniprot.org/uniprot/#_E9Q6W1-mappedCitation-16432184http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16432184
http://purl.uniprot.org/uniprot/#_P17433-mappedCitation-16432184http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16432184
http://purl.uniprot.org/uniprot/#_Q3U5L4-mappedCitation-16432184http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16432184
http://purl.uniprot.org/uniprot/P17433http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/16432184
http://purl.uniprot.org/uniprot/Q3U5L4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/16432184
http://purl.uniprot.org/uniprot/E9QAI9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/16432184
http://purl.uniprot.org/uniprot/E9Q6W1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/16432184