Source:http://linkedlifedata.com/resource/pubmed/id/12516048
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2003-1-7
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pubmed:abstractText |
As an alternative method to the conventional therapies for Hunter's syndrome, which is a lethal lysosomal storage disorder, we have developed gene delivery vehicles using a series of retroviral vectors. The objective of this study was to develop a safe and efficient retroviral vector and to optimize conditions for efficient transduction of human bone marrow CD34+ stem cells using our vector.
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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
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pubmed:month |
Jan
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pubmed:issn |
1099-498X
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2002 John Wiley & Sons, Ltd.
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pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
18-29
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:12516048-Bone Marrow Cells,
pubmed-meshheading:12516048-Cell Line,
pubmed-meshheading:12516048-Gene Therapy,
pubmed-meshheading:12516048-Genes, MDR,
pubmed-meshheading:12516048-Genetic Vectors,
pubmed-meshheading:12516048-Humans,
pubmed-meshheading:12516048-Iduronate Sulfatase,
pubmed-meshheading:12516048-Mucopolysaccharidosis II,
pubmed-meshheading:12516048-Retroviridae,
pubmed-meshheading:12516048-Stem Cells,
pubmed-meshheading:12516048-Transduction, Genetic
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pubmed:year |
2003
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pubmed:articleTitle |
Construction of a high efficiency retroviral vector for gene therapy of Hunter's syndrome.
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pubmed:affiliation |
Institute of Molecular Biology and Genetics, Seoul National University, Kwan-Ak-Gu, Seoul 151-742, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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