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Meike Visel

Showing results (1-10 of 25) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|November 15, 2012
Adeno-associated viral vectors for gene therapy of inherited retinal degenerationsJohn G Flannery, Meike Visel
Molecular Vision|April 26, 2008
In vitro analysis of promoter activity in Müller cellsScott F Geller, Phillip S Ge, Meike Visel, et al.
Molecular Vision|June 15, 2007
Functional promoter testing using a modified lentiviral transfer vectorScott F Geller, Phillip S Ge, Meike Visel, et al.
Biomed Research International|April 25, 2022
AAV Induced Expression of Human Rod and Cone Opsin in Bipolar Cells of a Mouse Model of Retinal DegenerationMichelle E McClements, Federica Staurenghi, Meike Visel, et al.
Nature Communications|August 7, 2021
Cell specific photoswitchable agonist for reversible control of endogenous dopamine receptorsPrashant Donthamsetti, Nils Winter, Adam Hoagland, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 1, 2017
Optogenetic Retinal Gene Therapy with the Light Gated GPCR Vertebrate RhodopsinBenjamin M Gaub, Michael H Berry, Meike Visel, et al.
Molecular Therapy. Methods & Clinical Development|September 6, 2021
Outcomes of progranulin gene therapy in the retina are dependent on time and route of deliveryEmilia A Zin, Daisy Han, Jennifer Tran, et al.
Human Gene Therapy|December 22, 2009
Changes in adeno-associated virus-mediated gene delivery in retinal degenerationKathleen D Kolstad, Deniz Dalkara, Karen Guerin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 13, 2009
Inner limiting membrane barriers to AAV-mediated retinal transduction from the vitreousDeniz Dalkara, Kathleen D Kolstad, Natalia Caporale, et al.
Science Translational Medicine|June 14, 2013
In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreousDeniz Dalkara, Leah C Byrne, Ryan R Klimczak, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|November 15, 2012
Adeno-associated viral vectors for gene therapy of inherited retinal degenerationsJohn G Flannery, Meike Visel
Molecular Vision|April 26, 2008
In vitro analysis of promoter activity in Müller cellsScott F Geller, Phillip S Ge, Meike Visel, et al.
Molecular Vision|June 15, 2007
Functional promoter testing using a modified lentiviral transfer vectorScott F Geller, Phillip S Ge, Meike Visel, et al.
Biomed Research International|April 25, 2022
AAV Induced Expression of Human Rod and Cone Opsin in Bipolar Cells of a Mouse Model of Retinal DegenerationMichelle E McClements, Federica Staurenghi, Meike Visel, et al.
Nature Communications|August 7, 2021
Cell specific photoswitchable agonist for reversible control of endogenous dopamine receptorsPrashant Donthamsetti, Nils Winter, Adam Hoagland, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 1, 2017
Optogenetic Retinal Gene Therapy with the Light Gated GPCR Vertebrate RhodopsinBenjamin M Gaub, Michael H Berry, Meike Visel, et al.
Molecular Therapy. Methods & Clinical Development|September 6, 2021
Outcomes of progranulin gene therapy in the retina are dependent on time and route of deliveryEmilia A Zin, Daisy Han, Jennifer Tran, et al.
Human Gene Therapy|December 22, 2009
Changes in adeno-associated virus-mediated gene delivery in retinal degenerationKathleen D Kolstad, Deniz Dalkara, Karen Guerin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 13, 2009
Inner limiting membrane barriers to AAV-mediated retinal transduction from the vitreousDeniz Dalkara, Kathleen D Kolstad, Natalia Caporale, et al.
Science Translational Medicine|June 14, 2013
In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreousDeniz Dalkara, Leah C Byrne, Ryan R Klimczak, et al.
Pageof 3