Author:
McLean Jesse R.,Smith Gaynor A.,Rocha Emily M.,Hayes Melissa A.,Beagan Jonathan A.,Hallett Penelope J.,Isacson Ole
Reference37 articles.
1. Therapeutic in vivo gene transfer for genetic disease using AAV: progress and challenges;Mingozzi;Nat. Rev. Genet.,2011
2. Analysis of AAV serotypes 1–9 mediated gene expression and tropism in mice after systemic injection;Zincarelli;Mol. Ther.,2008
3. Analysis of transduction efficiency, tropism and axonal transport of AAV serotypes 1, 2, 5, 6, 8 and 9 in the mouse brain;Aschauer;PLoS ONE,2013
4. Recombinant AAV viral vectors pseudotyped with viral capsids from serotypes 1, 2, and 5 display differential efficiency and cell tropism after delivery to different regions of the central nervous system;Burger;Mol. Ther.,2004
5. Adeno-associated virus (AAV) vectors in the CNS;McCown;Curr. Gene Ther.,2011
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