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

Edwin M Stone

Showing results (131-140 of 384) with videos related to

Pageof 39
Sort By:
HGG Advances|October 2, 2024
Exonic splice variant discovery using in vitro models of inherited retinal diseaseNathaniel K Mullin, Laura R Bohrer, Kristin R Anfinson, et al.
Acta Biomaterialia|March 30, 2017
Two-photon polymerization for production of human iPSC-derived retinal cell graftsKristan S Worthington, Luke A Wiley, Emily E Kaalberg, et al.
Human Mutation|May 4, 2006
Genome-wide identification of pseudogenes capable of disease-causing gene conversionJared M Bischof, Annie P Chiang, Todd E Scheetz, et al.
Current Protocols in Stem Cell Biology|March 8, 2018
CRISPR-Cas9-Based Genome Editing of Human Induced Pluripotent Stem CellsJoseph C Giacalone, Tasneem P Sharma, Erin R Burnight, et al.
Ophthalmology|November 4, 2018
The ARMS2 A69S Polymorphism Is Associated with Delayed Rod-Mediated Dark Adaptation in Eyes at Risk for Incident Age-Related Macular DegenerationRobert F Mullins, Gerald McGwin, Karen Searcey, et al.
American Journal of Ophthalmology|November 27, 2007
LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United StatesJohn H Fingert, Wallace L M Alward, Young H Kwon, et al.
Stem Cells Translational Medicine|December 20, 2015
Concise Review: Patient-Specific Stem Cells to Interrogate Inherited Eye DiseaseJoseph C Giacalone, Luke A Wiley, Erin R Burnight, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision|April 13, 2007
Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerationsArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Human Molecular Genetics|August 15, 2013
BBS mutations modify phenotypic expression of CEP290-related ciliopathiesYan Zhang, Seongjin Seo, Sajag Bhattarai, et al.
Investigative Ophthalmology & Visual Science|February 27, 2014
Photoreceptor cells with profound structural deficits can support useful vision in miceStewart Thompson, Frederick R Blodi, Swan Lee, et al.
Pageof 39

Showing results (131-140 of 384) with videos related to

Sort By:
Pageof 39
HGG Advances|October 2, 2024
Exonic splice variant discovery using in vitro models of inherited retinal diseaseNathaniel K Mullin, Laura R Bohrer, Kristin R Anfinson, et al.
Acta Biomaterialia|March 30, 2017
Two-photon polymerization for production of human iPSC-derived retinal cell graftsKristan S Worthington, Luke A Wiley, Emily E Kaalberg, et al.
Human Mutation|May 4, 2006
Genome-wide identification of pseudogenes capable of disease-causing gene conversionJared M Bischof, Annie P Chiang, Todd E Scheetz, et al.
Current Protocols in Stem Cell Biology|March 8, 2018
CRISPR-Cas9-Based Genome Editing of Human Induced Pluripotent Stem CellsJoseph C Giacalone, Tasneem P Sharma, Erin R Burnight, et al.
Ophthalmology|November 4, 2018
The ARMS2 A69S Polymorphism Is Associated with Delayed Rod-Mediated Dark Adaptation in Eyes at Risk for Incident Age-Related Macular DegenerationRobert F Mullins, Gerald McGwin, Karen Searcey, et al.
American Journal of Ophthalmology|November 27, 2007
LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United StatesJohn H Fingert, Wallace L M Alward, Young H Kwon, et al.
Stem Cells Translational Medicine|December 20, 2015
Concise Review: Patient-Specific Stem Cells to Interrogate Inherited Eye DiseaseJoseph C Giacalone, Luke A Wiley, Erin R Burnight, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision|April 13, 2007
Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerationsArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Human Molecular Genetics|August 15, 2013
BBS mutations modify phenotypic expression of CEP290-related ciliopathiesYan Zhang, Seongjin Seo, Sajag Bhattarai, et al.
Investigative Ophthalmology & Visual Science|February 27, 2014
Photoreceptor cells with profound structural deficits can support useful vision in miceStewart Thompson, Frederick R Blodi, Swan Lee, et al.
Pageof 39