Search research articles
Contact Us
Filters
Showing results (1-10 of 25) with videos related to
Page
of 3
Sort By:
Methods in Molecular Biology (Clifton, N.J.)
|
November 15, 2012
Adeno-associated viral vectors for gene therapy of inherited retinal degenerations
John G Flannery, Meike Visel
Molecular Vision
|
April 26, 2008
In vitro analysis of promoter activity in Müller cells
Scott F Geller, Phillip S Ge, Meike Visel, et al.
Molecular Vision
|
June 15, 2007
Functional promoter testing using a modified lentiviral transfer vector
Scott 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 Degeneration
Michelle E McClements, Federica Staurenghi, Meike Visel, et al.
Nature Communications
|
August 7, 2021
Cell specific photoswitchable agonist for reversible control of endogenous dopamine receptors
Prashant 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 Rhodopsin
Benjamin 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 delivery
Emilia A Zin, Daisy Han, Jennifer Tran, et al.
Human Gene Therapy
|
December 22, 2009
Changes in adeno-associated virus-mediated gene delivery in retinal degeneration
Kathleen 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 vitreous
Deniz 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 vitreous
Deniz Dalkara, Leah C Byrne, Ryan R Klimczak, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Methods in Molecular Biology (Clifton, N.J.)
|
November 15, 2012
Adeno-associated viral vectors for gene therapy of inherited retinal degenerations
John G Flannery, Meike Visel
Molecular Vision
|
April 26, 2008
In vitro analysis of promoter activity in Müller cells
Scott F Geller, Phillip S Ge, Meike Visel, et al.
Molecular Vision
|
June 15, 2007
Functional promoter testing using a modified lentiviral transfer vector
Scott 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 Degeneration
Michelle E McClements, Federica Staurenghi, Meike Visel, et al.
Nature Communications
|
August 7, 2021
Cell specific photoswitchable agonist for reversible control of endogenous dopamine receptors
Prashant 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 Rhodopsin
Benjamin 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 delivery
Emilia A Zin, Daisy Han, Jennifer Tran, et al.
Human Gene Therapy
|
December 22, 2009
Changes in adeno-associated virus-mediated gene delivery in retinal degeneration
Kathleen 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 vitreous
Deniz 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 vitreous
Deniz Dalkara, Leah C Byrne, Ryan R Klimczak, et al.
Page
of 3