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

Catherine Cukras

Showing results (51-60 of 58) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 58 results.
Translational Vision Science & Technology|December 30, 2021
Conversion of Central Subfield Thickness Measurements of Diabetic Macular Edema Across Cirrus and Spectralis Optical Coherence Tomography InstrumentsJennifer K Sun, Kristin Josic, Michele Melia, et al.
Ophthalmology Science|March 18, 2026
Simultaneous Segmentation of Geographic Atrophy in Longitudinally Acquired Fundus Autofluorescence ImagesSouvick Mukherjee, Emily Chew, Tiarnán D L Keenan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 11, 2018
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal DeliveryCatherine Cukras, Henry E Wiley, Brett G Jeffrey, et al.
Communications Biology|December 10, 2021
AMPK modulation ameliorates dominant disease phenotypes of CTRP5 variant in retinal degenerationKiyoharu J Miyagishima, Ruchi Sharma, Malika Nimmagadda, et al.
American Journal of Human Genetics|November 28, 2016
Mutations in REEP6 Cause Autosomal-Recessive Retinitis PigmentosaGavin Arno, Smriti A Agrawal, Aiden Eblimit, et al.
Medrxiv : the Preprint Server for Health Sciences|October 14, 2024
Genetic Risk of Reticular Pseudodrusen in Age-Related Macular Degeneration: <i>HTRA1</i> /lncRNA <i>BX842242.1</i> dominates, with no evidence for Complement Cascade involvementSamaneh Farashi, Carla J Abbott, Brendan Re Ansell, et al.
Nature Communications|December 8, 2025
HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvementSamaneh Farashi, Carla J Abbott, Brendan R E Ansell, et al.
NPJ Genomic Medicine|April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypesRyan E Schmidt, Amy E Pohodich, David Birch, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Translational Vision Science & Technology|December 30, 2021
Conversion of Central Subfield Thickness Measurements of Diabetic Macular Edema Across Cirrus and Spectralis Optical Coherence Tomography InstrumentsJennifer K Sun, Kristin Josic, Michele Melia, et al.
Ophthalmology Science|March 18, 2026
Simultaneous Segmentation of Geographic Atrophy in Longitudinally Acquired Fundus Autofluorescence ImagesSouvick Mukherjee, Emily Chew, Tiarnán D L Keenan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 11, 2018
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal DeliveryCatherine Cukras, Henry E Wiley, Brett G Jeffrey, et al.
Communications Biology|December 10, 2021
AMPK modulation ameliorates dominant disease phenotypes of CTRP5 variant in retinal degenerationKiyoharu J Miyagishima, Ruchi Sharma, Malika Nimmagadda, et al.
American Journal of Human Genetics|November 28, 2016
Mutations in REEP6 Cause Autosomal-Recessive Retinitis PigmentosaGavin Arno, Smriti A Agrawal, Aiden Eblimit, et al.
Medrxiv : the Preprint Server for Health Sciences|October 14, 2024
Genetic Risk of Reticular Pseudodrusen in Age-Related Macular Degeneration: <i>HTRA1</i> /lncRNA <i>BX842242.1</i> dominates, with no evidence for Complement Cascade involvementSamaneh Farashi, Carla J Abbott, Brendan Re Ansell, et al.
Nature Communications|December 8, 2025
HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvementSamaneh Farashi, Carla J Abbott, Brendan R E Ansell, et al.
NPJ Genomic Medicine|April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypesRyan E Schmidt, Amy E Pohodich, David Birch, et al.
Pageof 6