Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Anand Swaroop

Showing results (221-230 of 338) with videos related to

Pageof 34
Sort By:
Scientific Reports|March 28, 2020
Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1Dunja Lukovic, Ana Artero Castro, Koray Dogan Kaya, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Plos Genetics|December 28, 2020
Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degenerationPassley Hargrove-Grimes, Anupam K Mondal, Jessica Gumerson, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
Epigenetics|June 13, 2015
Differential DNA methylation identified in the blood and retina of AMD patientsVerity F Oliver, Andrew E Jaffe, Jin Song, et al.
The Journal of Biological Chemistry|September 7, 2002
Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation functionXuejiao Wang, Siqun Xu, Carlo Rivolta, et al.
JAMA Ophthalmology|May 18, 2013
Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutationsSarwar Zahid, Naheed Khan, Kari Branham, et al.
Plos One|May 12, 2015
Clinical and genetic factors associated with progression of geographic atrophy lesions in age-related macular degenerationFelix Grassmann, Monika Fleckenstein, Emily Y Chew, et al.
Investigative Ophthalmology & Visual Science|April 27, 2016
Treatment Paradigms for Retinal and Macular Diseases Using 3-D Retina Cultures Derived From Human Reporter Pluripotent Stem Cell LinesRossukon Kaewkhaw, Manju Swaroop, Kohei Homma, et al.
Plos Genetics|April 19, 2012
Transcriptional regulation of rod photoreceptor homeostasis revealed by in vivo NRL targetome analysisHong Hao, Douglas S Kim, Bernward Klocke, et al.
Pageof 34

Showing results (221-230 of 338) with videos related to

Sort By:
Pageof 34
Scientific Reports|March 28, 2020
Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1Dunja Lukovic, Ana Artero Castro, Koray Dogan Kaya, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Plos Genetics|December 28, 2020
Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degenerationPassley Hargrove-Grimes, Anupam K Mondal, Jessica Gumerson, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
Epigenetics|June 13, 2015
Differential DNA methylation identified in the blood and retina of AMD patientsVerity F Oliver, Andrew E Jaffe, Jin Song, et al.
The Journal of Biological Chemistry|September 7, 2002
Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation functionXuejiao Wang, Siqun Xu, Carlo Rivolta, et al.
JAMA Ophthalmology|May 18, 2013
Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutationsSarwar Zahid, Naheed Khan, Kari Branham, et al.
Plos One|May 12, 2015
Clinical and genetic factors associated with progression of geographic atrophy lesions in age-related macular degenerationFelix Grassmann, Monika Fleckenstein, Emily Y Chew, et al.
Investigative Ophthalmology & Visual Science|April 27, 2016
Treatment Paradigms for Retinal and Macular Diseases Using 3-D Retina Cultures Derived From Human Reporter Pluripotent Stem Cell LinesRossukon Kaewkhaw, Manju Swaroop, Kohei Homma, et al.
Plos Genetics|April 19, 2012
Transcriptional regulation of rod photoreceptor homeostasis revealed by in vivo NRL targetome analysisHong Hao, Douglas S Kim, Bernward Klocke, et al.
Pageof 34