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Human Gene Therapy
|
May 6, 2005
Gene transfer to respiratory epithelia with lentivirus pseudotyped with Jaagsiekte sheep retrovirus envelope glycoprotein
Patrick L Sinn, Andrea K Penisten, Erin R Burnight, et al.
Progress in Retinal and Eye Research
|
November 1, 2020
Patient derived stem cells for discovery and validation of novel pathogenic variants in inherited retinal disease
Nathaniel K Mullin, Andrew P Voigt, Jessica A Cooke, et al.
Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics
|
October 1, 2021
Chimeric Helper-Dependent Adenoviruses Transduce Retinal Ganglion Cells and Müller Cells in Human Retinal Explants
Ian C Han, Erin R Burnight, Emily E Kaalberg, et al.
Human Molecular Genetics
|
May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profiles
Andrew P Voigt, Nathaniel K Mullin, S Scott Whitmore, et al.
Genes
|
April 10, 2019
Correction of NR2E3 Associated Enhanced S-cone Syndrome Patient-specific iPSCs using CRISPR-Cas9
Laura R Bohrer, Luke A Wiley, Erin R Burnight, et al.
Human Gene Therapy
|
August 29, 2019
Helper-Dependent Adenovirus Transduces the Human and Rat Retina but Elicits an Inflammatory Reaction When Delivered Subretinally in Rats
Ian C Han, Erin R Burnight, Mallory J Ulferts, et al.
Human Gene Therapy
|
July 13, 2016
Using Patient-Specific Induced Pluripotent Stem Cells and Wild-Type Mice to Develop a Gene Augmentation-Based Strategy to Treat CLN3-Associated Retinal Degeneration
Luke A Wiley, Erin R Burnight, Arlene V Drack, et al.
Human Molecular Genetics
|
November 6, 2023
Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical data
Erin R Burnight, Beau J Fenner, Ian C Han, et al.
Scientific Reports
|
July 30, 2016
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness
Luke A Wiley, Erin R Burnight, Adam P DeLuca, et al.
Human Gene Therapy
|
May 21, 2019
Development of a Molecularly Stable Gene Therapy Vector for the Treatment of <i>RPGR</i>-Associated X-Linked Retinitis Pigmentosa
Joseph C Giacalone, Jeaneen L Andorf, Qihong Zhang, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Human Gene Therapy
|
May 6, 2005
Gene transfer to respiratory epithelia with lentivirus pseudotyped with Jaagsiekte sheep retrovirus envelope glycoprotein
Patrick L Sinn, Andrea K Penisten, Erin R Burnight, et al.
Progress in Retinal and Eye Research
|
November 1, 2020
Patient derived stem cells for discovery and validation of novel pathogenic variants in inherited retinal disease
Nathaniel K Mullin, Andrew P Voigt, Jessica A Cooke, et al.
Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics
|
October 1, 2021
Chimeric Helper-Dependent Adenoviruses Transduce Retinal Ganglion Cells and Müller Cells in Human Retinal Explants
Ian C Han, Erin R Burnight, Emily E Kaalberg, et al.
Human Molecular Genetics
|
May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profiles
Andrew P Voigt, Nathaniel K Mullin, S Scott Whitmore, et al.
Genes
|
April 10, 2019
Correction of NR2E3 Associated Enhanced S-cone Syndrome Patient-specific iPSCs using CRISPR-Cas9
Laura R Bohrer, Luke A Wiley, Erin R Burnight, et al.
Human Gene Therapy
|
August 29, 2019
Helper-Dependent Adenovirus Transduces the Human and Rat Retina but Elicits an Inflammatory Reaction When Delivered Subretinally in Rats
Ian C Han, Erin R Burnight, Mallory J Ulferts, et al.
Human Gene Therapy
|
July 13, 2016
Using Patient-Specific Induced Pluripotent Stem Cells and Wild-Type Mice to Develop a Gene Augmentation-Based Strategy to Treat CLN3-Associated Retinal Degeneration
Luke A Wiley, Erin R Burnight, Arlene V Drack, et al.
Human Molecular Genetics
|
November 6, 2023
Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical data
Erin R Burnight, Beau J Fenner, Ian C Han, et al.
Scientific Reports
|
July 30, 2016
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness
Luke A Wiley, Erin R Burnight, Adam P DeLuca, et al.
Human Gene Therapy
|
May 21, 2019
Development of a Molecularly Stable Gene Therapy Vector for the Treatment of <i>RPGR</i>-Associated X-Linked Retinitis Pigmentosa
Joseph C Giacalone, Jeaneen L Andorf, Qihong Zhang, et al.
Page
of 3