Cécile Fortuny
Cécile Fortuny
Geverifieerd e-mailadres voor berkeley.edu
Geciteerd door
Geciteerd door
Retinoschisin gene therapy in photoreceptors, Müller glia or all retinal cells in the Rs1h−/− mouse
LC Byrne, BE Öztürk, T Lee, C Fortuny, M Visel, D Dalkara, DV Schaffer, ...
Gene therapy 21 (6), 585-592, 2014
In vivo–directed evolution of adeno-associated virus in the primate retina
LC Byrne, TP Day, M Visel, JA Strazzeri, C Fortuny, D Dalkara, ...
JCI insight 5 (10), 2020
Visual stimulation switches the polarity of excitatory input to starburst amacrine cells
AL Vlasits, R Bos, RD Morrie, C Fortuny, JG Flannery, MB Feller, ...
Neuron 83 (5), 1172-1184, 2014
Neuron-glia signaling in developing retina mediated by neurotransmitter spillover
JM Rosa, R Bos, GS Sack, C Fortuny, A Agarwal, DE Bergles, ...
Elife 4, e09590, 2015
Mutation-independent gene therapies for rod-cone dystrophies
C Fortuny, JG Flannery
Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 75-81, 2018
In vivo directed evolution of AAV in the primate retina
LC Byrne, TP Day, M Visel, C Fortuny, D Dalkara, WH Merigan, ...
bioRxiv, 847459, 2019
AAV-mediated combination therapy of neurotrophic and anti-apoptotic factors in a mouse model of inherited retinal degeneration
C Fortuny, L Byrne, D Dalkara, T Lee, BE Ozturk
Investigative Ophthalmology & Visual Science 54 (15), 2746-2746, 2013
Aav vectors for gene editing
M Mohr, K Baney, A Sidore, C Fortuny, A Maroof, A Wright, BT Staahl, ...
US Patent App. 18/266,076, 2024
Optimization of AAV Gene Delivery Vector Achieves Selective, Safe and Strong Muller Glia Targeting in Healthy and Diseased Rodent Retina
C Fortuny, CK Baker, JG Flannery
MOLECULAR THERAPY 28 (4), 484-485, 2020
AAV-mediated Targeting of Müller Glia in Healthy and Diseased Retina
C Fortuny, C Baker, JG Flannery
Investigative Ophthalmology & Visual Science 60 (9), 2907-2907, 2019
Development of Novel Adeno-Associated Virus-Mediated Gene Therapies for the Treatment of Inherited Retinal Degeneration
C Fortuny
UC Berkeley, 2019
Optimization of AAV-mediated Gene Delivery for Targeting Mitochondria in the Outer Retina and Müller glia.
EA Zin, C Fortuny, NP Sabetfakhri, RJ Choi, C Dunlap, J Flannery
Investigative Ophthalmology & Visual Science 58 (8), 4090-4090, 2017
Optimization of Mitochondrial AAV-Mediated Gene Delivery for Outer Retina and Glia
C Fortuny, E Zin, C Dunlap, N Sabetfakhri, R Choi, JG Flannery
MOLECULAR THERAPY 25 (5), 249-250, 2017
Evaluation of CRB1 gene delivery in the rd8 mouse
TP Day, C Fortuny, Y Oh, D Schaffer, JG Flannery
Investigative Ophthalmology & Visual Science 57 (12), 1183-1183, 2016
Expanding the Potential of AAV Vectors for the Treatment of Intractable Inherited Retinal Degenerations
T Day, N Commins, C Fortuny, T Lee, J Flannery, D Schaffer
Retinoschisin Gene Therapy in Photoreceptors, Muller Glia, or All Retinal Cells in the Mouse Model of X-Linked Retinoschisis
LC Byrne, BE Ozturk, T Lee, C Fortuny, M Visel, D Dalkara, DV Schaffer, ...
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–16