Engineering Liver-detargeted AAV9 Vectors for Cardiac and Musculoskeletal Gene Transfer-Reference-Cited by-同舟云学术

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Engineering Liver-detargeted AAV9 Vectors for Cardiac and Musculoskeletal Gene Transfer

Published:2011-06 Issue:6 Volume:19 Page:1070-1078
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Pulicherla Nagesh,Shen Shen,Yadav Swati,Debbink Kari,Govindasamy Lakshmanan,Agbandje-McKenna Mavis,Asokan Aravind

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference46 articles.

1. Two decades of clinical gene therapy–success is finally mounting;Herzog;Discov Med,2010

2. AAV's anatomy: roadmap for optimizing vectors for translational success;Mitchell;Curr Gene Ther,2010

3. Analysis of AAV serotypes 1-9 mediated gene expression and tropism in mice after systemic injection;Zincarelli;Mol Ther,2008

4. Robust systemic transduction with AAV9 vectors in mice: efficient global cardiac gene transfer superior to that of AAV8;Inagaki;Mol Ther,2006

5. Recombinant adeno-associated virus serotype 9 leads to preferential cardiac transduction in vivo;Pacak;Circ Res,2006

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5. Gene therapy for the leukodystrophies: From preclinical animal studies to clinical trials;Neurotherapeutics;2024-07

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