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Modified branched peptides with a histidine-rich tail enhance in vitro gene transfection
Successful gene therapy depends on the development of efficient, non-toxic gene delivery systems. To accomplish this objective, our laboratory has focused on solid-phase synthesized peptide carriers, in which the amino acid sequence can be varied precisely to augment intracellular DNA transport. We...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2005
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC549579/ https://www.ncbi.nlm.nih.gov/pubmed/15731333 http://dx.doi.org/10.1093/nar/gni040 |