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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1986-3-26
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pubmed:abstractText |
Abelson murine leukemia virus (A-MuLV) and Harvey murine sarcoma virus (Ha-MSV) are retroviruses carrying unrelated onc genes. However, both of these viruses are capable of stimulating the growth and differentiation of erythroid precursor cells; the target cells for both appear at the same time during fetal development and follow a similar pattern throughout ontogeny. In addition, the colonies induced by each virus are morphologically similar and synthesize the adult form of hemoglobin. However, A-MuLV-infected cells are Epo-independent, whereas Ha-MSV-infected cells are Epo-dependent. Superinfection of Ha-MSV-infected cells with A-MuLV overrides their Epo-dependency. Thus, the consequences of the infection are determined by the interaction of the different onc gene products with identical or similar erythroid cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0092-8674
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
31
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pubmed:volume |
44
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
337-44
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3002634-Abelson murine leukemia virus,
pubmed-meshheading:3002634-Animals,
pubmed-meshheading:3002634-Cell Differentiation,
pubmed-meshheading:3002634-Cell Division,
pubmed-meshheading:3002634-Erythrocytes,
pubmed-meshheading:3002634-Erythropoiesis,
pubmed-meshheading:3002634-Erythropoietin,
pubmed-meshheading:3002634-Harvey murine sarcoma virus,
pubmed-meshheading:3002634-Hemoglobins,
pubmed-meshheading:3002634-Leukemia Virus, Murine,
pubmed-meshheading:3002634-Lymphocytes,
pubmed-meshheading:3002634-Mice,
pubmed-meshheading:3002634-Sarcoma Viruses, Murine,
pubmed-meshheading:3002634-Tissue Distribution
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pubmed:year |
1986
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pubmed:articleTitle |
Abelson virus drives the differentiation of Harvey virus-infected erythroid cells.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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