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Fabienne Rolling

French Institute of Health and Medical Research
University of Nantes

68

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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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Vitreous body: A barrier for AAV-mediated gene transfer to inner retinal neurons of macaque

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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AAV-mediated efficient gene transfer in retinal ganglion cells of dogs and non-human primates

2015 Investigative Ophthalmology & Visual Science
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Transgene regulation using the tetracycline-inducible TetR-KRAB system after AAV-mediated gene transfer in rodents and nonhuman primates.

2014 PLOS ONE
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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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Changes in S and L/M cone opsin expression in the RPE65 dog model following AAV mediated gene addition therapy

2013 Investigative Ophthalmology & Visual Science
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Gene therapy in Leber congenital amaurosis due to rpe mutations: results of the first six patients included in a clinical trial

2013 Investigative Ophthalmology & Visual Science
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Efficacy and safety of gene therapy with AAV4 in childhood blindness due to rpe65 mutations

2012 Acta Ophthalmologica
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Adeno-Associated Virus Mediated Gene Therapy for Retinal Degenerative Diseases

2012 Methods of Molecular Biology
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