Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E Boye

Showing results (141-150 of 190) with videos related to

Pageof 19
Sort By:
Molecular Vision|October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosisAlejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Translational Vision Science & Technology|December 17, 2024
Inherited Retinal Degenerations and Non-Neovascular Age-Related Macular Degeneration: Progress and Unmet NeedsJacque L Duncan, Angela Bowman, Amy Laster, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical regionL Heidet, L Cohen-Solal, E Boye, et al.
Molecular Therapy. Nucleic Acids|September 18, 2017
Rationally Engineered AAV Capsids Improve Transduction and Volumetric Spread in the CNSNicholas M Kanaan, Rhyomi C Sellnow, Sanford L Boye, et al.
American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 1, 1997
Diffuse leiomyomatosis associated with X-linked Alport syndrome: extracellular matrix study using immunohistochemistry and in situ hybridizationL Heidet, Y Cai, Y Sado, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 24, 2012
Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber's hereditary optic neuropathy in a mouse modelHong Yu, Rajeshwari D Koilkonda, Tsung-Han Chou, et al.
Human Gene Therapy|November 26, 2015
Cone-Specific Promoters for Gene Therapy of Achromatopsia and Other Retinal DiseasesGuo-Jie Ye, Ewa Budzynski, Peter Sonnentag, et al.
Frontiers in Neuroscience|December 20, 2016
Novel Methodology for Creating Macaque Retinas with Sortable Photoreceptors and Ganglion CellsShreyasi Choudhury, Christianne E Strang, John J Alexander, et al.
Communications Biology|September 14, 2024
TUBB4B is essential for the cytoskeletal architecture of cochlear supporting cells and motile cilia developmentUrikhan Sanzhaeva, Helen Boyd-Pratt, Philip T R Bender, et al.
Pageof 19

Showing results (141-150 of 190) with videos related to

Sort By:
Pageof 19
Molecular Vision|October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosisAlejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Translational Vision Science & Technology|December 17, 2024
Inherited Retinal Degenerations and Non-Neovascular Age-Related Macular Degeneration: Progress and Unmet NeedsJacque L Duncan, Angela Bowman, Amy Laster, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical regionL Heidet, L Cohen-Solal, E Boye, et al.
Molecular Therapy. Nucleic Acids|September 18, 2017
Rationally Engineered AAV Capsids Improve Transduction and Volumetric Spread in the CNSNicholas M Kanaan, Rhyomi C Sellnow, Sanford L Boye, et al.
American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 1, 1997
Diffuse leiomyomatosis associated with X-linked Alport syndrome: extracellular matrix study using immunohistochemistry and in situ hybridizationL Heidet, Y Cai, Y Sado, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 24, 2012
Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber's hereditary optic neuropathy in a mouse modelHong Yu, Rajeshwari D Koilkonda, Tsung-Han Chou, et al.
Human Gene Therapy|November 26, 2015
Cone-Specific Promoters for Gene Therapy of Achromatopsia and Other Retinal DiseasesGuo-Jie Ye, Ewa Budzynski, Peter Sonnentag, et al.
Frontiers in Neuroscience|December 20, 2016
Novel Methodology for Creating Macaque Retinas with Sortable Photoreceptors and Ganglion CellsShreyasi Choudhury, Christianne E Strang, John J Alexander, et al.
Communications Biology|September 14, 2024
TUBB4B is essential for the cytoskeletal architecture of cochlear supporting cells and motile cilia developmentUrikhan Sanzhaeva, Helen Boyd-Pratt, Philip T R Bender, et al.
Pageof 19