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Samer Khateb

Showing results (11-20 of 70) with videos related to

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BMC Ophthalmology|February 16, 2024
Disease quiescence in endophthalmitis patients treated with anti-VEGF injections for retinal pathologiesBrice Nguedia Vofo, Majd Saada, Antonio Rivera, et al.
The Journal of Biological Chemistry|June 1, 2005
Homodimeric MyoD preferentially binds tetraplex structures of regulatory sequences of muscle-specific genesShulamit Etzioni, Anat Yafe, Samer Khateb, et al.
Nucleic Acids Research|August 25, 2007
The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNASamer Khateb, Pnina Weisman-Shomer, Inbal Hershco-Shani, et al.
International Journal of Molecular Sciences|April 12, 2022
Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Termination Codon in <i>FAM161A</i>Avigail Beryozkin, Ananya Samanta, Prakadeeswari Gopalakrishnan, et al.
Retina (Philadelphia, Pa.)|October 23, 2024
ROLE OF VISUAL EVOKED POTENTIAL AND OCULAR TRAUMA SCORE AS PREDICTORS OF VISUAL RECOVERY IN EYE GLOBE INJURIESBrice N Vofo, Ayala Katzir, Mohammad Homiedat, et al.
European Journal of Ophthalmology|November 1, 2022
Prevalence and associated factors of cystoid macular edema in children with early onset inherited retinal dystrophiesRavid Ben-Avi, Antonio Rivera, Karen Hendler, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 1, 2018
Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular diseaseClaudia Yahalom, Anat Blumenfeld, Karen Hendler, et al.
Genes|July 27, 2024
Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal GenesMaria Abu Elasal, Samira Mousa, Manar Salameh, et al.
Ophthalmology. Retina|April 30, 2026
Tetracyclines and Risk of Proliferative Vitreoretinopathy Following Rhegmatogenous Retinal DetachmentItay Nitzan, Yossi Eshel, Tehila Shlomov, et al.
Genes|May 25, 2024
Simultaneous Detection of Common Founder Mutations Using a Cost-Effective Deep Sequencing PanelSapir Shalom, Mor Hanany, Avital Eilat, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
BMC Ophthalmology|February 16, 2024
Disease quiescence in endophthalmitis patients treated with anti-VEGF injections for retinal pathologiesBrice Nguedia Vofo, Majd Saada, Antonio Rivera, et al.
The Journal of Biological Chemistry|June 1, 2005
Homodimeric MyoD preferentially binds tetraplex structures of regulatory sequences of muscle-specific genesShulamit Etzioni, Anat Yafe, Samer Khateb, et al.
Nucleic Acids Research|August 25, 2007
The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNASamer Khateb, Pnina Weisman-Shomer, Inbal Hershco-Shani, et al.
International Journal of Molecular Sciences|April 12, 2022
Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Termination Codon in <i>FAM161A</i>Avigail Beryozkin, Ananya Samanta, Prakadeeswari Gopalakrishnan, et al.
Retina (Philadelphia, Pa.)|October 23, 2024
ROLE OF VISUAL EVOKED POTENTIAL AND OCULAR TRAUMA SCORE AS PREDICTORS OF VISUAL RECOVERY IN EYE GLOBE INJURIESBrice N Vofo, Ayala Katzir, Mohammad Homiedat, et al.
European Journal of Ophthalmology|November 1, 2022
Prevalence and associated factors of cystoid macular edema in children with early onset inherited retinal dystrophiesRavid Ben-Avi, Antonio Rivera, Karen Hendler, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 1, 2018
Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular diseaseClaudia Yahalom, Anat Blumenfeld, Karen Hendler, et al.
Genes|July 27, 2024
Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal GenesMaria Abu Elasal, Samira Mousa, Manar Salameh, et al.
Ophthalmology. Retina|April 30, 2026
Tetracyclines and Risk of Proliferative Vitreoretinopathy Following Rhegmatogenous Retinal DetachmentItay Nitzan, Yossi Eshel, Tehila Shlomov, et al.
Genes|May 25, 2024
Simultaneous Detection of Common Founder Mutations Using a Cost-Effective Deep Sequencing PanelSapir Shalom, Mor Hanany, Avital Eilat, et al.
Pageof 7