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

Dror Sharon

Showing results (81-90 of 150) with videos related to

Pageof 15
Sort By:
Journal of Medical Genetics|May 22, 2016
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing dataSamer Khateb, Mor Hanany, Ayat Khalaileh, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 20, 2015
Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 AchromatopsiaEyal Banin, Elisha Gootwine, Alexey Obolensky, et al.
International Journal of Molecular Sciences|September 10, 2021
Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy EfficacyMartial Mbefo, Adeline Berger, Karine Schouwey, et al.
Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
JAMA Ophthalmology|December 27, 2014
Association between missense mutations in the BBS2 gene and nonsyndromic retinitis pigmentosaElia Shevach, Manir Ali, Liliana Mizrahi-Meissonnier, et al.
Retina (Philadelphia, Pa.)|January 29, 2021
SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular DiagnosisClaudia Yahalom, Oded Volovelsky, Michal Macarov, et al.
EMBO Molecular Medicine|March 20, 2024
Fine-tuning FAM161A gene augmentation therapy to restore retinal functionYvan Arsenijevic, Ning Chang, Olivier Mercey, et al.
Ophthalmology|December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical AspectsAdva Kimchi, Samer Khateb, Rong Wen, et al.
Molecular Vision|March 2, 2019
A novel intronic mutation of <i>PDE6B</i> is a major cause of autosomal recessive retinitis pigmentosa among Caucasus JewsYasmin Tatour, Jonathan Tamaiev, Shamaly Shamaly, et al.
Scientific Reports|September 17, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutationsAvigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, et al.
Pageof 15

Showing results (81-90 of 150) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|May 22, 2016
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing dataSamer Khateb, Mor Hanany, Ayat Khalaileh, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 20, 2015
Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 AchromatopsiaEyal Banin, Elisha Gootwine, Alexey Obolensky, et al.
International Journal of Molecular Sciences|September 10, 2021
Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy EfficacyMartial Mbefo, Adeline Berger, Karine Schouwey, et al.
Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
JAMA Ophthalmology|December 27, 2014
Association between missense mutations in the BBS2 gene and nonsyndromic retinitis pigmentosaElia Shevach, Manir Ali, Liliana Mizrahi-Meissonnier, et al.
Retina (Philadelphia, Pa.)|January 29, 2021
SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular DiagnosisClaudia Yahalom, Oded Volovelsky, Michal Macarov, et al.
EMBO Molecular Medicine|March 20, 2024
Fine-tuning FAM161A gene augmentation therapy to restore retinal functionYvan Arsenijevic, Ning Chang, Olivier Mercey, et al.
Ophthalmology|December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical AspectsAdva Kimchi, Samer Khateb, Rong Wen, et al.
Molecular Vision|March 2, 2019
A novel intronic mutation of <i>PDE6B</i> is a major cause of autosomal recessive retinitis pigmentosa among Caucasus JewsYasmin Tatour, Jonathan Tamaiev, Shamaly Shamaly, et al.
Scientific Reports|September 17, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutationsAvigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, et al.
Pageof 15