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Edwin M Stone

Showing results (361-370 of 384) with videos related to

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Plos One|March 29, 2013
A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel LociTodd E Scheetz, John H Fingert, Kai Wang, et al.
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.
Investigative Ophthalmology & Visual Science|July 16, 2011
Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse modelTomas S Aleman, Artur V Cideciyan, Geoffrey K Aguirre, et al.
JAMA Ophthalmology|March 1, 2019
Myocilin Mutations in Patients With Normal-Tension GlaucomaWallace L M Alward, Carly van der Heide, Cheryl L Khanna, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Annie P Chiang, John S Beck, Hsan-Jan Yen, 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.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2007
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesityRoger E Davis, Ruth E Swiderski, Kamal Rahmouni, et al.
Visual Neuroscience|December 8, 2005
Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouseLawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
Pageof 39

Showing results (361-370 of 384) with videos related to

Sort By:
Pageof 39
Plos One|March 29, 2013
A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel LociTodd E Scheetz, John H Fingert, Kai Wang, et al.
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.
Investigative Ophthalmology & Visual Science|July 16, 2011
Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse modelTomas S Aleman, Artur V Cideciyan, Geoffrey K Aguirre, et al.
JAMA Ophthalmology|March 1, 2019
Myocilin Mutations in Patients With Normal-Tension GlaucomaWallace L M Alward, Carly van der Heide, Cheryl L Khanna, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Annie P Chiang, John S Beck, Hsan-Jan Yen, 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.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2007
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesityRoger E Davis, Ruth E Swiderski, Kamal Rahmouni, et al.
Visual Neuroscience|December 8, 2005
Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouseLawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
Pageof 39