pubmed-article:1717255 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1717255 | lifeskim:mentions | umls-concept:C0080090 | lld:lifeskim |
pubmed-article:1717255 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
pubmed-article:1717255 | lifeskim:mentions | umls-concept:C1332792 | lld:lifeskim |
pubmed-article:1717255 | lifeskim:mentions | umls-concept:C1514562 | lld:lifeskim |
pubmed-article:1717255 | lifeskim:mentions | umls-concept:C1883221 | lld:lifeskim |
pubmed-article:1717255 | lifeskim:mentions | umls-concept:C1883204 | lld:lifeskim |
pubmed-article:1717255 | lifeskim:mentions | umls-concept:C1880389 | lld:lifeskim |
pubmed-article:1717255 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:1717255 | pubmed:dateCreated | 1991-10-25 | lld:pubmed |
pubmed-article:1717255 | pubmed:abstractText | The granulocyte colony-stimulating factor (G-CSF) receptor has a composite structure consisting of an immunoglobulin(Ig)-like domain, a cytokine receptor-homologous (CRH) domain and three fibronectin type III (FNIII) domains in the extracellular region. Introduction of G-CSF receptor cDNA into IL-3-dependent murine myeloid cell line FDC-P1 and pro-B cell line BAF-B03, which normally do not respond to G-CSF, enabled them to proliferate in response to G-CSF. On the other hand, expression of the G-CSF receptor cDNA in the IL-2-dependent T cell line CTLL-2 did not enable it to grow in response to G-CSF, although G-CSF could transiently stimulate DNA synthesis. Mutational analyses of the G-CSF receptor in FDC-P1 cells indicated that the N-terminal half of the CRH domain was essential for the recognition of G-CSF, but the Ig-like, FNIII and cytoplasmic domains were not. The CRH domain and a portion of the cytoplasmic domain of about 100 amino acids in length were indispensable for transduction of the G-CSF-triggered growth signal. | lld:pubmed |
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pubmed-article:1717255 | pubmed:language | eng | lld:pubmed |
pubmed-article:1717255 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1717255 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:1717255 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1717255 | pubmed:month | Oct | lld:pubmed |
pubmed-article:1717255 | pubmed:issn | 0261-4189 | lld:pubmed |
pubmed-article:1717255 | pubmed:author | pubmed-author:PakC YCY | lld:pubmed |
pubmed-article:1717255 | pubmed:author | pubmed-author:NagataSS | lld:pubmed |
pubmed-article:1717255 | pubmed:author | pubmed-author:SetoYY | lld:pubmed |
pubmed-article:1717255 | pubmed:author | pubmed-author:FukunagaRR | lld:pubmed |
pubmed-article:1717255 | pubmed:author | pubmed-author:Ishizaka-Iked... | lld:pubmed |
pubmed-article:1717255 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1717255 | pubmed:volume | 10 | lld:pubmed |
pubmed-article:1717255 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1717255 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1717255 | pubmed:pagination | 2855-65 | lld:pubmed |
pubmed-article:1717255 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:1717255 | pubmed:year | 1991 | lld:pubmed |
pubmed-article:1717255 | pubmed:articleTitle | Functional domains of the granulocyte colony-stimulating factor receptor. | lld:pubmed |
pubmed-article:1717255 | pubmed:affiliation | Osaka Bioscience Institute, Japan. | lld:pubmed |
pubmed-article:1717255 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1717255 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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