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

Samer Khateb

Showing results (21-30 of 70) with videos related to

Pageof 7
Sort By:
Nucleic Acids Research|July 11, 2003
The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)nPnina Weisman-Shomer, Esther Cohen, Inbal Hershco, et al.
Plos One|December 20, 2012
Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing lossSamer Khateb, Lina Zelinger, Tamar Ben-Yosef, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 8, 2026
Evaluating the Efficacy of a Novel Triangle Suture Technique in Scleral-Fixation of Intraocular LensOr Shmueli, Nir Erdinest, Salome Goldmann, et al.
Investigative Ophthalmology & Visual Science|January 14, 2026
Altered High-Density Lipoprotein Expression Pattern in the Aqueous Humor From Eyes With Age-Related Macular DegenerationAdi Kramer, Batya Rinsky, Sarah Elbaz-Hayoun, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|May 5, 2026
Exploring the role of low-dose atropine in myopia management in children with inherited retinal diseasesRotem Azmon, Asaf Kreindler, Ben Ezra Kahtan, et al.
Journal of Medical Genetics|May 1, 2014
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndromeSamer Khateb, Lina Zelinger, Liliana Mizrahi-Meissonnier, et al.
Molecular Vision|June 2, 2020
A unique <i>PRDM13</i>-associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique <i>CFH</i> variantPrasanthi Namburi, Samer Khateb, Segev Meyer, et al.
Genes|November 27, 2024
A Leaky Deep Intronic Splice Variant in <i>CLRN1</i> Is Associated with Non-Syndromic Retinitis PigmentosaMaria Abu Elasal, Samer Khateb, Daan M Panneman, et al.
Acta Ophthalmologica|March 30, 2019
The combination of whole-exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophiesAlaa Abu Diab, Ala'a AlTalbishi, Boris Rosin, et al.
Scientific Reports|August 21, 2019
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli PopulationsAlaa AlTalbishi, Lina Zelinger, Christina Zeitz, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Nucleic Acids Research|July 11, 2003
The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)nPnina Weisman-Shomer, Esther Cohen, Inbal Hershco, et al.
Plos One|December 20, 2012
Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing lossSamer Khateb, Lina Zelinger, Tamar Ben-Yosef, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 8, 2026
Evaluating the Efficacy of a Novel Triangle Suture Technique in Scleral-Fixation of Intraocular LensOr Shmueli, Nir Erdinest, Salome Goldmann, et al.
Investigative Ophthalmology & Visual Science|January 14, 2026
Altered High-Density Lipoprotein Expression Pattern in the Aqueous Humor From Eyes With Age-Related Macular DegenerationAdi Kramer, Batya Rinsky, Sarah Elbaz-Hayoun, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|May 5, 2026
Exploring the role of low-dose atropine in myopia management in children with inherited retinal diseasesRotem Azmon, Asaf Kreindler, Ben Ezra Kahtan, et al.
Journal of Medical Genetics|May 1, 2014
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndromeSamer Khateb, Lina Zelinger, Liliana Mizrahi-Meissonnier, et al.
Molecular Vision|June 2, 2020
A unique <i>PRDM13</i>-associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique <i>CFH</i> variantPrasanthi Namburi, Samer Khateb, Segev Meyer, et al.
Genes|November 27, 2024
A Leaky Deep Intronic Splice Variant in <i>CLRN1</i> Is Associated with Non-Syndromic Retinitis PigmentosaMaria Abu Elasal, Samer Khateb, Daan M Panneman, et al.
Acta Ophthalmologica|March 30, 2019
The combination of whole-exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophiesAlaa Abu Diab, Ala'a AlTalbishi, Boris Rosin, et al.
Scientific Reports|August 21, 2019
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli PopulationsAlaa AlTalbishi, Lina Zelinger, Christina Zeitz, et al.
Pageof 7