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Nathalie Provost

French Institute of Health and Medical Research

32

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Evaluation of AAV-based optogene transfer for the treatment of canine models of inherited retinal dystrophies

2016 Investigative Ophthalmology & Visual Science
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AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs.

2016 Molecular Therapy
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Successful Gene Therapy in the RPGRIP1-deficient Dog: a Large Model of Cone-Rod Dystrophy

2014 Molecular Therapy
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AAV-mediated gene therapy restores retinal function and vision in the RPGRIP1-deficient dog

2012 Investigative Ophthalmology & Visual Science
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Regulation of Retinal Function but Nonrescue of Vision in RPE65-deficient Dogs Treated With Doxycycline-regulatable AAV Vectors

2010 Molecular Therapy
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Regulation of Retinal Function but Non Rescue of Vision in Rpe65-Deficient Dogs Treated With Doxycycline-Regulatable Aav Vectors

2010 Investigative Ophthalmology & Visual Science
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Detection of Intact rAAV Particles up to 6 Years After Successful Gene Transfer in the Retina of Dogs and Primates

2009 Molecular Therapy
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The RPGRIP1-deficient dog, a promising canine model for gene therapy

2009 Molecular Vision
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Characterization of the Retinal Degeneration Affecting the Miniature Longhaired Dachshunds Carrying a Mutation in the Rpgrip Gene

2008 Investigative Ophthalmology & Visual Science
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Subretinal Delivery of Recombinant AAV Serotype 8 Vector in Dogs Results in Gene Transfer to Neurons in the Brain

2008 Molecular Therapy
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