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Budd A Tucker

Showing results (141-150 of 148) with videos related to

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Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry 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 ReplacementJessica 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 MaculopathyDivya Sinha, Benjamin Steyer, Pawan K Shahi, et al.
Human Molecular Genetics|October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosisAdam 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 DegenerationErin 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 PRDM13Kent 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 repairBruce 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 DiseaseBeau J Fenner, S Scott Whitmore, Adam P DeLuca, et al.
Pageof 15

Showing results (141-150 of 148) with videos related to

Sort By:
Pageof 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 diseaseTerry 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 ReplacementJessica 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 MaculopathyDivya Sinha, Benjamin Steyer, Pawan K Shahi, et al.
Human Molecular Genetics|October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosisAdam 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 DegenerationErin 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 PRDM13Kent 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 repairBruce 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 DiseaseBeau J Fenner, S Scott Whitmore, Adam P DeLuca, et al.
Pageof 15