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Luke A Wiley

Showing results (41-50 of 53) with videos related to

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Human Gene Therapy|November 22, 2017
Assessment of Adeno-Associated Virus Serotype Tropism in Human Retinal ExplantsLuke A Wiley, Erin R Burnight, Emily E Kaalberg, et al.
Progress in Retinal and Eye Research|March 27, 2018
CRISPR-Cas9 genome engineering: Treating inherited retinal degenerationErin R Burnight, Joseph C Giacalone, Jessica A Cooke, et al.
Human Gene Therapy|September 19, 2020
Retinal Tropism and Transduction of Adeno-Associated Virus Varies by Serotype and Route of Delivery (Intravitreal, Subretinal, or Suprachoroidal) in RatsIan C Han, Justine L Cheng, Erin R Burnight, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 21, 2014
Endothelial cell FGF signaling is required for injury response but not for vascular homeostasisSunday S Oladipupo, Craig Smith, Andrea Santeford, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Modeling MEK inhibitor-Associated Retinopathy <i>in vitro</i> using human induced pluripotent stem cell-derived retinal pigment epithelial cellsLola P Lozano, Madeleine Jennisch, Renato Jensen, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
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.
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.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Human Gene Therapy|November 22, 2017
Assessment of Adeno-Associated Virus Serotype Tropism in Human Retinal ExplantsLuke A Wiley, Erin R Burnight, Emily E Kaalberg, et al.
Progress in Retinal and Eye Research|March 27, 2018
CRISPR-Cas9 genome engineering: Treating inherited retinal degenerationErin R Burnight, Joseph C Giacalone, Jessica A Cooke, et al.
Human Gene Therapy|September 19, 2020
Retinal Tropism and Transduction of Adeno-Associated Virus Varies by Serotype and Route of Delivery (Intravitreal, Subretinal, or Suprachoroidal) in RatsIan C Han, Justine L Cheng, Erin R Burnight, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 21, 2014
Endothelial cell FGF signaling is required for injury response but not for vascular homeostasisSunday S Oladipupo, Craig Smith, Andrea Santeford, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Modeling MEK inhibitor-Associated Retinopathy <i>in vitro</i> using human induced pluripotent stem cell-derived retinal pigment epithelial cellsLola P Lozano, Madeleine Jennisch, Renato Jensen, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
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.
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.
Pageof 6