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Human Gene Therapy Methods|May 28, 2016
Vitrectomy Before Intravitreal Injection of AAV2/2 Vector Promotes Efficient Transduction of Retinal Ganglion Cells in Dogs and Nonhuman PrimatesKizito-Tshitoko Tshilenge, Baptiste Ameline, Michel Weber, et al.
Bulletin Et Memoires De L'Academie Royale De Medecine De Belgique|May 17, 2007
Gene therapeutic prospects in early onset of severe retinal dystrophy: restoration of vision in RPE65 Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epitheliumF Rolling, Guylène Le Meur, Knut Stieger, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 5, 2013
Successful gene therapy in the RPGRIP1-deficient dog: a large model of cone-rod dystrophyElsa Lhériteau, Lolita Petit, Michel Weber, et al.
Molecular Therapy. Methods & Clinical Development|February 8, 2024
Mannose-coupled AAV2: A second-generation AAV vector for increased retinal gene therapy efficiencyMathieu Mével, Virginie Pichard, Mohammed Bouzelha, et al.
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