Ocular gene therapy: introduction to the special issue
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.nature.com/articles/gt2011189.pdf
Reference9 articles.
1. Vandenberghe LH, Auricchio A . Novel adeno-associated viral vectors for retinal gene therapy. Gene Therapy 2012; 19: 162–168.
2. Balaggan KS, Ali RR . Ocular gene delivery using lentiviral vectors. Gene Therapy 2012; 19: 145–153.
3. Dalkara D, Byrne LC, Lee T, Hoffmann NV, Schaffer DV, Flannery JG . Enhanced gene delivery to the neonatal retina through systemic administration of Tyrosine-mutated AAV9. Gene Therapy 2012; 19: 176–181.
4. Balaggan KS, Duran Y, Georgiadis A, Thaung C, Barker SE, Buch PK et al. Absence of ocular malignant transformation after sub-retinal delivery of rAAV2/2 or integrating lentiviral vectors in p53-deficient mice. Gene Therapy 2012; 19: 182–188.
5. Smith AJ, Bainbridge JWB, Ali RR . Gene supplementation therapy for recessive forms of inherited retinal dystrophies. Gene Therapy 2012; 19: 154–161.
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