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Edwin M Stone

Showing results (221-230 of 384) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 10, 2011
Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosaBudd A Tucker, Todd E Scheetz, Robert F Mullins, et al.
Plos Genetics|October 12, 2012
Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degenerationVinit B Mahajan, Jessica M Skeie, Alexander G Bassuk, et al.
SLAS Technology|July 16, 2023
Automated human induced pluripotent stem cell colony segmentation for use in cell culture automation applicationsKimerly A Powell, Laura R Bohrer, Nicholas E Stone, et al.
Ocular Immunology and Inflammation|April 21, 2023
Retinal Sublayer Analysis in Autoimmune Retinopathy and Identification of New Optical Coherence Tomography PhenotypesChristopher R Fortenbach, S Scott Whitmore, Matthew J Thurtell, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retinaArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
The Journal of Clinical Investigation|April 23, 2024
NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal developmentNathaniel K Mullin, Laura R Bohrer, Andrew P Voigt, et al.
American Journal of Ophthalmology|March 5, 2003
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 geneRobert A Honkanen, Darryl Y Nishimura, Ruth E Swiderski, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2019
Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degenerationAndrew P Voigt, Kelly Mulfaul, Nathaniel K Mullin, et al.
BMJ Open Ophthalmology|January 7, 2022
Correlation of features on OCT with visual acuity and Gass lesion type in Best vitelliform macular dystrophyRazek G Coussa, Christopher R Fortenbach, D Brice Critser, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Pageof 39

Showing results (221-230 of 384) with videos related to

Sort By:
Pageof 39
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2011
Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosaBudd A Tucker, Todd E Scheetz, Robert F Mullins, et al.
Plos Genetics|October 12, 2012
Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degenerationVinit B Mahajan, Jessica M Skeie, Alexander G Bassuk, et al.
SLAS Technology|July 16, 2023
Automated human induced pluripotent stem cell colony segmentation for use in cell culture automation applicationsKimerly A Powell, Laura R Bohrer, Nicholas E Stone, et al.
Ocular Immunology and Inflammation|April 21, 2023
Retinal Sublayer Analysis in Autoimmune Retinopathy and Identification of New Optical Coherence Tomography PhenotypesChristopher R Fortenbach, S Scott Whitmore, Matthew J Thurtell, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retinaArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
The Journal of Clinical Investigation|April 23, 2024
NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal developmentNathaniel K Mullin, Laura R Bohrer, Andrew P Voigt, et al.
American Journal of Ophthalmology|March 5, 2003
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 geneRobert A Honkanen, Darryl Y Nishimura, Ruth E Swiderski, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2019
Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degenerationAndrew P Voigt, Kelly Mulfaul, Nathaniel K Mullin, et al.
BMJ Open Ophthalmology|January 7, 2022
Correlation of features on OCT with visual acuity and Gass lesion type in Best vitelliform macular dystrophyRazek G Coussa, Christopher R Fortenbach, D Brice Critser, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Pageof 39