pubmed-article:8677747 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8677747 | lifeskim:mentions | umls-concept:C0143630 | lld:lifeskim |
pubmed-article:8677747 | lifeskim:mentions | umls-concept:C1334291 | lld:lifeskim |
pubmed-article:8677747 | lifeskim:mentions | umls-concept:C1704632 | lld:lifeskim |
pubmed-article:8677747 | lifeskim:mentions | umls-concept:C0871261 | lld:lifeskim |
pubmed-article:8677747 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:8677747 | lifeskim:mentions | umls-concept:C2911692 | lld:lifeskim |
pubmed-article:8677747 | lifeskim:mentions | umls-concept:C1706817 | lld:lifeskim |
pubmed-article:8677747 | pubmed:issue | 3-4 | lld:pubmed |
pubmed-article:8677747 | pubmed:dateCreated | 1996-8-14 | lld:pubmed |
pubmed-article:8677747 | pubmed:abstractText | Stem cell factor (SCF) interacts with the receptor tyrosine kinase c-Kit and has potent effects on hematopoiesis. We have examined the role of JAK2 in the SCF signal transduction pathway. JAK2 and c-Kit were constitutively associated, and treatment with SCF resulted in rapid and transient tyrosine phosphorylation of JAK2. Incubation of cells with JAK2 antisense oligonucleotides resulted in significant decreases in SCF-induced proliferation. These data suggest that JAK2 plays a role in SCF-induced proliferation. | lld:pubmed |
pubmed-article:8677747 | pubmed:language | eng | lld:pubmed |
pubmed-article:8677747 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8677747 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:8677747 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:8677747 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8677747 | pubmed:issn | 0001-5792 | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:LongoD LDL | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:RuscettiF WFW | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:KellerJ RJR | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:MoyWW | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:FerrisD KDK | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:LinnekinDD | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:WeilerS RSR | lld:pubmed |
pubmed-article:8677747 | pubmed:author | pubmed-author:DeBerryC SCS | lld:pubmed |
pubmed-article:8677747 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8677747 | pubmed:volume | 95 | lld:pubmed |
pubmed-article:8677747 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8677747 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8677747 | pubmed:pagination | 224-8 | lld:pubmed |
pubmed-article:8677747 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:8677747 | pubmed:year | 1996 | lld:pubmed |
pubmed-article:8677747 | pubmed:articleTitle | JAK2 is constitutively associated with c-Kit and is phosphorylated in response to stem cell factor. | lld:pubmed |
pubmed-article:8677747 | pubmed:affiliation | Laboratory of Leukocyte Biology, National Cancer Institute - Frederick Cancer Research and Development Center, Md 21702 (USA). | lld:pubmed |
pubmed-article:8677747 | pubmed:publicationType | Journal Article | lld:pubmed |
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