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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1988-3-11
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pubmed:abstractText |
We describe here the transduction of murine hematopoietic progenitor cells with the dominant selectable neomycin drug-resistance (Neo) gene using a recombinant adeno-associated virus (AAV) vector. Successful transformation of progenitor cells to drug resistance was determined to be approximately 1.5% by colony formation in the presence of geneticin sulfate (G-418). The value of AAV as an alternative to the retrovirus vector systems is discussed.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0042-6822
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
162
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
483-6
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2829430-Bone Marrow,
pubmed-meshheading:2829430-Bone Marrow Cells,
pubmed-meshheading:2829430-Cells, Cultured,
pubmed-meshheading:2829430-Dependovirus,
pubmed-meshheading:2829430-Genetic Vectors,
pubmed-meshheading:2829430-Hematopoietic Stem Cells,
pubmed-meshheading:2829430-Humans,
pubmed-meshheading:2829430-Transformation, Genetic
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pubmed:year |
1988
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pubmed:articleTitle |
Gene transfer into hematopoietic progenitor cells mediated by an adeno-associated virus vector.
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pubmed:affiliation |
Department of Pathology, University of Florida, Gainesville 32610.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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