Transcriptional Targeting of Lentiviral Vectors by Long Terminal Repeat Enhancer Replacement
Gene therapy of many genetic diseases requires permanent gene transfer into self-renewing stem cells and restriction of transgene expression to specific progenies. Human immunodeficiency virus (HIV)-derived lentiviral vectors are very effective in transducing rare, nondividing stem cell populations...
Sábháilte in:
| Foilsithe in: | J Virol |
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| Príomhchruthaitheoirí: | , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
American Society for Microbiology (ASM)
2002
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| Ábhair: | |
| Rochtain ar líne: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC136069/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11907239/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/JVI.76.8.3996-4007.2002 |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
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