Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.

Gene transfer vectors based on adeno-associated virus (AAV) are emerging as highly promising for use in human gene therapy by virtue of their characteristics of wide host range, high transduction efficiencies, and lack of cytopathogenicity. To better define the biology of AAV-mediated gene transfer,...

Cijeli opis

Bibliografski detalji

Izdano u:	J Virol
Glavni autori:	Podsakoff, G, Wong, K K, Chatterjee, S
Format:	Artigo
Jezik:	Inglês
Izdano:	American Society for Microbiology (ASM) 1994
Teme:	Research Article
Online pristup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC236967/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8057446/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.68.9.5656-5666.1994
Oznake:	Dodaj oznaku Bez oznaka, Budi prvi tko označuje ovaj zapis!