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Michelle E McClements

Showing results (41-50 of 65) with videos related to

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Translational Vision Science & Technology|April 4, 2022
Tropism of AAV Vectors in Photoreceptor-Like Cells of Human iPSC-Derived Retinal OrganoidsMichelle E McClements, Hannah Steward, William Atkin, et al.
The CRISPR Journal|August 25, 2020
Promoter Orientation within an AAV-CRISPR Vector Affects Cas9 Expression and Gene Editing EfficiencyLewis E Fry, Caroline F Peddle, Marta Stevanovic, et al.
Nature Communications|August 17, 2021
Mirtron-mediated RNA knockdown/replacement therapy for the treatment of dominant retinitis pigmentosaHarry O Orlans, Michelle E McClements, 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.
Molecular Diagnosis & Therapy|July 2, 2024
Gene Therapies in Clinical Development to Treat Retinal DisordersMichelle E McClements, Maram E A Abdalla Elsayed, Lauren Major, 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.
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.
Molecular Therapy. Methods & Clinical Development|September 6, 2021
Characterizing the cellular immune response to subretinal AAV gene therapy in the murine retinaLaurel C Chandler, Michelle E McClements, Imran H Yusuf, 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.
Investigative Ophthalmology & Visual Science|December 29, 2018
A Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3Mark M Hassall, Alun R Barnard, Harry O Orlans, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Translational Vision Science & Technology|April 4, 2022
Tropism of AAV Vectors in Photoreceptor-Like Cells of Human iPSC-Derived Retinal OrganoidsMichelle E McClements, Hannah Steward, William Atkin, et al.
The CRISPR Journal|August 25, 2020
Promoter Orientation within an AAV-CRISPR Vector Affects Cas9 Expression and Gene Editing EfficiencyLewis E Fry, Caroline F Peddle, Marta Stevanovic, et al.
Nature Communications|August 17, 2021
Mirtron-mediated RNA knockdown/replacement therapy for the treatment of dominant retinitis pigmentosaHarry O Orlans, Michelle E McClements, 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.
Molecular Diagnosis & Therapy|July 2, 2024
Gene Therapies in Clinical Development to Treat Retinal DisordersMichelle E McClements, Maram E A Abdalla Elsayed, Lauren Major, 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.
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.
Molecular Therapy. Methods & Clinical Development|September 6, 2021
Characterizing the cellular immune response to subretinal AAV gene therapy in the murine retinaLaurel C Chandler, Michelle E McClements, Imran H Yusuf, 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.
Investigative Ophthalmology & Visual Science|December 29, 2018
A Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3Mark M Hassall, Alun R Barnard, Harry O Orlans, et al.
Pageof 7