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Alun R Barnard

Showing results (21-30 of 68) with videos related to

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Translational Vision Science & Technology|July 15, 2017
Impact of Vital Dyes on Cell Viability and Transduction Efficiency of AAV Vectors Used in Retinal Gene Therapy Surgery: An In Vitro and In Vivo AnalysisAnna P Salvetti, Maria I Patrício, Alun R Barnard, et al.
Investigative Ophthalmology & Visual Science|May 7, 2010
Retinal pigment epithelium defects accelerate photoreceptor degeneration in cell type-specific knockout mouse models of choroideremiaTanya Tolmachova, Silene T Wavre-Shapton, Alun R Barnard, et al.
International Journal of Molecular Sciences|August 27, 2020
Analysis of Early Cone Dysfunction in an In Vivo Model of Rod-Cone DystrophyMark M Hassall, Michelle E McClements, Alun R Barnard, et al.
Plos One|February 15, 2013
Non-image-forming light driven functions are preserved in a mouse model of autosomal dominant optic atrophyGeorgia Perganta, Alun R Barnard, Christiana Katti, et al.
Molecular Therapy. Methods & Clinical Development|January 1, 2020
Inclusion of PF68 Surfactant Improves Stability of rAAV Titer when Passed through a Surgical Device Used in Retinal Gene TherapyMaria I Patrício, Christopher I Cox, Clare Blue, et al.
Human Gene Therapy|November 2, 2018
An AAV Dual Vector Strategy Ameliorates the Stargardt Phenotype in Adult <i>Abca4<sup>-/-</sup></i> MiceMichelle E McClements, Alun R Barnard, Mandeep S Singh, et al.
Gene Therapy|March 22, 2021
Functional expression of complement factor I following AAV-mediated gene delivery in the retina of mice and human cellsAnna K Dreismann, Michelle E McClements, Alun R Barnard, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 7, 2020
Repair of Retinal Degeneration following Ex Vivo Minicircle DNA Gene Therapy and Transplantation of Corrected Photoreceptor ProgenitorsAlona O Barnea-Cramer, Mandeep Singh, Dominik Fischer, et al.
Experimental Eye Research|August 2, 2011
Specific deficits in visual electrophysiology in a mouse model of dominant optic atrophyAlun R Barnard, Peter Charbel Issa, Georgia Perganta, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 22, 2015
CNTF Gene Therapy Confers Lifelong Neuroprotection in a Mouse Model of Human Retinitis PigmentosaDaniel M Lipinski, Alun R Barnard, Mandeep S Singh, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Translational Vision Science & Technology|July 15, 2017
Impact of Vital Dyes on Cell Viability and Transduction Efficiency of AAV Vectors Used in Retinal Gene Therapy Surgery: An In Vitro and In Vivo AnalysisAnna P Salvetti, Maria I Patrício, Alun R Barnard, et al.
Investigative Ophthalmology & Visual Science|May 7, 2010
Retinal pigment epithelium defects accelerate photoreceptor degeneration in cell type-specific knockout mouse models of choroideremiaTanya Tolmachova, Silene T Wavre-Shapton, Alun R Barnard, et al.
International Journal of Molecular Sciences|August 27, 2020
Analysis of Early Cone Dysfunction in an In Vivo Model of Rod-Cone DystrophyMark M Hassall, Michelle E McClements, Alun R Barnard, et al.
Plos One|February 15, 2013
Non-image-forming light driven functions are preserved in a mouse model of autosomal dominant optic atrophyGeorgia Perganta, Alun R Barnard, Christiana Katti, et al.
Molecular Therapy. Methods & Clinical Development|January 1, 2020
Inclusion of PF68 Surfactant Improves Stability of rAAV Titer when Passed through a Surgical Device Used in Retinal Gene TherapyMaria I Patrício, Christopher I Cox, Clare Blue, et al.
Human Gene Therapy|November 2, 2018
An AAV Dual Vector Strategy Ameliorates the Stargardt Phenotype in Adult <i>Abca4<sup>-/-</sup></i> MiceMichelle E McClements, Alun R Barnard, Mandeep S Singh, et al.
Gene Therapy|March 22, 2021
Functional expression of complement factor I following AAV-mediated gene delivery in the retina of mice and human cellsAnna K Dreismann, Michelle E McClements, Alun R Barnard, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 7, 2020
Repair of Retinal Degeneration following Ex Vivo Minicircle DNA Gene Therapy and Transplantation of Corrected Photoreceptor ProgenitorsAlona O Barnea-Cramer, Mandeep Singh, Dominik Fischer, et al.
Experimental Eye Research|August 2, 2011
Specific deficits in visual electrophysiology in a mouse model of dominant optic atrophyAlun R Barnard, Peter Charbel Issa, Georgia Perganta, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 22, 2015
CNTF Gene Therapy Confers Lifelong Neuroprotection in a Mouse Model of Human Retinitis PigmentosaDaniel M Lipinski, Alun R Barnard, Mandeep S Singh, et al.
Pageof 7