Gene delivery to the eye using adeno-associated viral vectors
- 9 October 2002
- journal article
- review article
- Published by Elsevier BV in Methods
- Vol. 28 (2), 267-275
- https://doi.org/10.1016/s1046-2023(02)00232-3
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Long-Term Protection of Retinal Structure but Not Function Using RAAV.CNTF in Animal Models of Retinitis PigmentosaMolecular Therapy, 2001
- Reporter expression persists 1 year after adeno-associated virus-mediated gene transfer to the optic nerve.American Journal of Ophthalmology, 1999
- Persistent transgene product in retina, optic nerve and brain after intraocular injection of rAAVVision Research, 1999
- Adeno‐associated virus‐mediated gene transfer into human retinal pigment epithelium cellsAustralian and New Zealand Journal of Ophthalmology, 1998
- Prolonged delivery of brain-derived neurotrophic factor by adenovirus-infected Müller cells temporarily rescues injured retinal ganglion cellsProceedings of the National Academy of Sciences of the United States of America, 1998
- Adeno-Associated Virus Gene Transfer to Mouse RetinaHuman Gene Therapy, 1998
- Rescue of photoreceptor function by AAV-mediated gene transfer in a mouse model of inherited retinal degenerationGene Therapy, 1997
- Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virusProceedings of the National Academy of Sciences of the United States of America, 1997
- Evaluation of recombinant adeno-associated virus as a gene transfer vector for the retinaCurrent Eye Research, 1997
- Gene transfer into the mouse retina mediated by an adeno-associated viral vectorHuman Molecular Genetics, 1996