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Improved gene delivery to human saphenous vein cells and tissue using a peptide-modified adenoviral vector
The establishment of efficient gene delivery to target human tissue is a major obstacle for transition of gene therapy from the pre-clinical phases to the clinic. The poor long-term patency rates for coronary artery bypass grafting (CABG) is a major clinical problem that lacks an effective and prove...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2004
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC524365/ https://www.ncbi.nlm.nih.gov/pubmed/15473900 http://dx.doi.org/10.1186/1479-0556-2-14 |