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Edwin M Stone

Showing results (351-360 of 384) with videos related to

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Cell Transplantation|June 27, 2022
Biocompatibility of Human Induced Pluripotent Stem Cell-Derived Retinal Progenitor Cell Grafts in Immunocompromised RatsIan C Han, Laura R Bohrer, Katherine N Gibson-Corley, et al.
Acta Biomaterialia|May 6, 2019
Two-photon polymerized poly(caprolactone) retinal cell delivery scaffolds and their systemic and retinal biocompatibilityJessica R Thompson, Kristan S Worthington, Brian J Green, et al.
Ophthalmology. Retina|November 2, 2023
Vitreoretinal Procedures in Patients with Inherited Retinal DiseaseBeau J Fenner, Farzad Jamshidi, Rupak Bhuyan, et al.
Gene Therapy|September 14, 2021
Development and biological characterization of a clinical gene transfer vector for the treatment of MAK-associated retinitis pigmentosaBudd A Tucker, Erin R Burnight, Cathryn M Cranston, et al.
The CRISPR Journal|December 18, 2023
CRISPRi-Mediated Treatment of Dominant Rhodopsin-Associated Retinitis PigmentosaErin R Burnight, Luke A Wiley, Nathaniel K Mullin, et al.
Ophthalmology. Retina|August 20, 2021
Intrafamilial Variability of Ocular Manifestations of von Hippel-Lindau DiseaseRandy Christopher Bowen, H Culver Boldt, Robert F Mullins, et al.
American Journal of Human Genetics|April 20, 2010
Discovery and functional analysis of a retinitis pigmentosa gene, C2ORF71Darryl Y Nishimura, Lisa M Baye, Rahat Perveen, et al.
Human Mutation|January 13, 2015
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomalyRalph J Hazlewood, Benjamin R Roos, Frances Solivan-Timpe, et al.
Journal of Bioinformatics and Computational Biology|January 4, 2008
Transcript annotation prioritization and screening system (TrAPSS) for mutation screeningBrian M O'Leary, Steven G Davis, Michael F Smith, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathyTomas S Aleman, Nagasamy Soumittra, Artur V Cideciyan, et al.
Pageof 39

Showing results (351-360 of 384) with videos related to

Sort By:
Pageof 39
Cell Transplantation|June 27, 2022
Biocompatibility of Human Induced Pluripotent Stem Cell-Derived Retinal Progenitor Cell Grafts in Immunocompromised RatsIan C Han, Laura R Bohrer, Katherine N Gibson-Corley, et al.
Acta Biomaterialia|May 6, 2019
Two-photon polymerized poly(caprolactone) retinal cell delivery scaffolds and their systemic and retinal biocompatibilityJessica R Thompson, Kristan S Worthington, Brian J Green, et al.
Ophthalmology. Retina|November 2, 2023
Vitreoretinal Procedures in Patients with Inherited Retinal DiseaseBeau J Fenner, Farzad Jamshidi, Rupak Bhuyan, et al.
Gene Therapy|September 14, 2021
Development and biological characterization of a clinical gene transfer vector for the treatment of MAK-associated retinitis pigmentosaBudd A Tucker, Erin R Burnight, Cathryn M Cranston, et al.
The CRISPR Journal|December 18, 2023
CRISPRi-Mediated Treatment of Dominant Rhodopsin-Associated Retinitis PigmentosaErin R Burnight, Luke A Wiley, Nathaniel K Mullin, et al.
Ophthalmology. Retina|August 20, 2021
Intrafamilial Variability of Ocular Manifestations of von Hippel-Lindau DiseaseRandy Christopher Bowen, H Culver Boldt, Robert F Mullins, et al.
American Journal of Human Genetics|April 20, 2010
Discovery and functional analysis of a retinitis pigmentosa gene, C2ORF71Darryl Y Nishimura, Lisa M Baye, Rahat Perveen, et al.
Human Mutation|January 13, 2015
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomalyRalph J Hazlewood, Benjamin R Roos, Frances Solivan-Timpe, et al.
Journal of Bioinformatics and Computational Biology|January 4, 2008
Transcript annotation prioritization and screening system (TrAPSS) for mutation screeningBrian M O'Leary, Steven G Davis, Michael F Smith, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathyTomas S Aleman, Nagasamy Soumittra, Artur V Cideciyan, et al.
Pageof 39