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Showing results (251-260 of 293) with videos related to

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Investigative Ophthalmology & Visual Science|August 1, 2006
Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variantsArijit Mukhopadhyay, Konstantinos Nikopoulos, Alessandra Maugeri, et al.
Acta Ophthalmologica|February 2, 2021
Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophiesMays Talib, Mary J van Schooneveld, Jan Wijnholds, et al.
Retina (Philadelphia, Pa.)|March 13, 2018
CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up StudyMays Talib, Mary J van Schooneveld, Alberta A Thiadens, et al.
Investigative Ophthalmology & Visual Science|March 27, 2019
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease SpectrumSanne K Verbakel, Ramon A C van Huet, Anneke I den Hollander, et al.
Acta Ophthalmologica|September 26, 2023
Quality of life in patients with CRB1-associated retinal dystrophies: A longitudinal studyJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Stem Cell Reports|August 4, 2023
CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoidsThilo M Buck, Peter M J Quinn, Lucie P Pellissier, et al.
Clinical & Experimental Ophthalmology|July 11, 2026
CRB1-Associated Inherited Retinal Dystrophies: Prospective Natural History Study With 4 Years of Follow-UpJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Ophthalmic Research|July 30, 2024
Genetic Testing of Patients with Inherited Retinal Diseases in the European Countries: An International Survey by the European Vision InstituteGiacomo Calzetti, Kerstin Schwarzwälder, Giorgia Ottonelli, et al.
Stem Cell Reports|April 9, 2019
Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5Peter M Quinn, Thilo M Buck, Aat A Mulder, et al.
JAMA Ophthalmology|October 22, 2016
Association of Axial Length With Risk of Uncorrectable Visual Impairment for Europeans With MyopiaJ Willem L Tideman, Margaretha C C Snabel, Milly S Tedja, et al.
Pageof 30

Showing results (251-260 of 293) with videos related to

Sort By:
Pageof 30
Investigative Ophthalmology & Visual Science|August 1, 2006
Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variantsArijit Mukhopadhyay, Konstantinos Nikopoulos, Alessandra Maugeri, et al.
Acta Ophthalmologica|February 2, 2021
Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophiesMays Talib, Mary J van Schooneveld, Jan Wijnholds, et al.
Retina (Philadelphia, Pa.)|March 13, 2018
CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up StudyMays Talib, Mary J van Schooneveld, Alberta A Thiadens, et al.
Investigative Ophthalmology & Visual Science|March 27, 2019
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease SpectrumSanne K Verbakel, Ramon A C van Huet, Anneke I den Hollander, et al.
Acta Ophthalmologica|September 26, 2023
Quality of life in patients with CRB1-associated retinal dystrophies: A longitudinal studyJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Stem Cell Reports|August 4, 2023
CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoidsThilo M Buck, Peter M J Quinn, Lucie P Pellissier, et al.
Clinical & Experimental Ophthalmology|July 11, 2026
CRB1-Associated Inherited Retinal Dystrophies: Prospective Natural History Study With 4 Years of Follow-UpJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Ophthalmic Research|July 30, 2024
Genetic Testing of Patients with Inherited Retinal Diseases in the European Countries: An International Survey by the European Vision InstituteGiacomo Calzetti, Kerstin Schwarzwälder, Giorgia Ottonelli, et al.
Stem Cell Reports|April 9, 2019
Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5Peter M Quinn, Thilo M Buck, Aat A Mulder, et al.
JAMA Ophthalmology|October 22, 2016
Association of Axial Length With Risk of Uncorrectable Visual Impairment for Europeans With MyopiaJ Willem L Tideman, Margaretha C C Snabel, Milly S Tedja, et al.
Pageof 30