| pubmed-article:9924027 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0019682 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0019699 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0085243 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0085112 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0301944 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0882849 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0751781 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C1160185 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0086597 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0443252 | lld:lifeskim |
| pubmed-article:9924027 | lifeskim:mentions | umls-concept:C0442335 | lld:lifeskim |
| pubmed-article:9924027 | pubmed:issue | 5402 | lld:pubmed |
| pubmed-article:9924027 | pubmed:dateCreated | 1999-2-11 | lld:pubmed |
| pubmed-article:9924027 | pubmed:abstractText | Efficient gene transfer into human hematopoietic stem cells (HSCs) is an important goal in the study of the hematopoietic system as well as for gene therapy of hematopoietic disorders. A lentiviral vector based on the human immunodeficiency virus (HIV) was able to transduce human CD34+ cells capable of stable, long-term reconstitution of nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. High-efficiency transduction occurred in the absence of cytokine stimulation and resulted in transgene expression in multiple lineages of human hematopoietic cells for up to 22 weeks after transplantation. | lld:pubmed |
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| pubmed-article:9924027 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9924027 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9924027 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9924027 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9924027 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:9924027 | pubmed:issn | 0036-8075 | lld:pubmed |
| pubmed-article:9924027 | pubmed:author | pubmed-author:MosierD EDE | lld:pubmed |
| pubmed-article:9924027 | pubmed:author | pubmed-author:VermaI MIM | lld:pubmed |
| pubmed-article:9924027 | pubmed:author | pubmed-author:SmithK AKA | lld:pubmed |
| pubmed-article:9924027 | pubmed:author | pubmed-author:MiyoshiHH | lld:pubmed |
| pubmed-article:9924027 | pubmed:author | pubmed-author:TorbettB EBE | lld:pubmed |
| pubmed-article:9924027 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9924027 | pubmed:day | 29 | lld:pubmed |
| pubmed-article:9924027 | pubmed:volume | 283 | lld:pubmed |
| pubmed-article:9924027 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9924027 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9924027 | pubmed:pagination | 682-6 | lld:pubmed |
| pubmed-article:9924027 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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| pubmed-article:9924027 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:9924027 | pubmed:articleTitle | Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors. | lld:pubmed |
| pubmed-article:9924027 | pubmed:affiliation | Laboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA 92037, USA. | lld:pubmed |
| pubmed-article:9924027 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9924027 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9924027 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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