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Human Molecular Genetics
|
August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease
Terry A Braun, Robert F Mullins, Alex H Wagner, et al.
Stem Cells Translational Medicine
|
May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell Replacement
Jessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
American Journal of Human Genetics
|
July 25, 2020
Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant Maculopathy
Divya Sinha, Benjamin Steyer, Pawan K Shahi, et al.
Human Molecular Genetics
|
October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis
Adam P DeLuca, S Scott Whitmore, Jenna Barnes, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 17, 2017
Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration
Erin R Burnight, Manav Gupta, Luke A Wiley, et al.
Ophthalmology
|
October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13
Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
Nature
|
July 18, 2014
ABCB5 is a limbal stem cell gene required for corneal development and repair
Bruce R Ksander, Paraskevi E Kolovou, Brian J Wilson, et al.
Ophthalmology
|
February 3, 2024
A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal Disease
Beau J Fenner, S Scott Whitmore, Adam P DeLuca, et al.
Page
of 15
Search research articles
Search
Showing results (141-150 of 148) with videos related to
Sort By:
Page
of 15
You have reached the last page of results.
This site can display upto 148 results.
Human Molecular Genetics
|
August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease
Terry A Braun, Robert F Mullins, Alex H Wagner, et al.
Stem Cells Translational Medicine
|
May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell Replacement
Jessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
American Journal of Human Genetics
|
July 25, 2020
Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant Maculopathy
Divya Sinha, Benjamin Steyer, Pawan K Shahi, et al.
Human Molecular Genetics
|
October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis
Adam P DeLuca, S Scott Whitmore, Jenna Barnes, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 17, 2017
Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration
Erin R Burnight, Manav Gupta, Luke A Wiley, et al.
Ophthalmology
|
October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13
Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
Nature
|
July 18, 2014
ABCB5 is a limbal stem cell gene required for corneal development and repair
Bruce R Ksander, Paraskevi E Kolovou, Brian J Wilson, et al.
Ophthalmology
|
February 3, 2024
A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal Disease
Beau J Fenner, S Scott Whitmore, Adam P DeLuca, et al.
Page
of 15