miRNA-mediated post-transcriptional silencing of transgenes leads to increased adeno-associated viral vector yield and targeting specificity
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
https://www.nature.com/articles/gt201750.pdf
Reference50 articles.
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3. Heldermon CD, Qin EY, Ohlemiller KK, Herzog ED, Brown JR, Vogler C et al. Disease correction by combined neonatal intracranial AAV and systemic lentiviral gene therapy in Sanfilippo Syndrome type B mice. Gene Ther 2013; 20: 913–921.
4. Lehrke M, Lebherz C . AAV-mediated gene therapy for atherosclerosis. Curr Atheroscler Rep 2014; 16: 434.
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