Photoreceptor-targeted gene delivery using intravitreally administered AAV vectors in dogs-Reference-Cited by-同舟云学术

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Photoreceptor-targeted gene delivery using intravitreally administered AAV vectors in dogs

Published:2015-10-15 Issue:2 Volume:23 Page:223-230
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Boyd R F,Sledge D G,Boye S L,Boye S E,Hauswirth W W,Komáromy A M,Petersen-Jones S M,Bartoe J T

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/gt201596.pdf

Reference45 articles.

1. Nonnenmacher M, Weber T . Intracellular transport of recombinant adeno-associated virus vectors. Gene Ther 2012; 19: 649–658.

2. Asokan A, Schaffer DV, Samulski RJ . The AAV vector toolkit: poised at the clinical crossroads. Mol Ther 2012; 20: 699–708.

3. Dalkara D, Sahel JA . Gene therapy for inherited retinal degenerations. C R Biol 2014; 337: 185–192.

4. Jacobson SG, Cideciyan AV, Ratnakaram R, Heon E, Schwartz SB, Roman AJ et al. Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years. Arch Ophthalmol 2012; 130: 9–24.

5. Nork TM, Murphy CJ, Kim CB, Ver Hoeve JN, Rasmussen CA, Miller PE et al. Functional and anatomic consequences of subretinal dosing in the cynomolgus macaque. Arch Ophthalmol 2012; 130: 65–75.

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