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Showing results (931-940 of 1,250) with videos related to

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American Journal of Human Genetics|September 3, 2024
Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosaAna Belén Iglesias-Romero, Karolina Kaminska, Mathieu Quinodoz, et al.
Investigative Ophthalmology & Visual Science|November 12, 2024
The Electroretinogram I-Wave, a Component Originating in the Retinal OFF-Pathway, Associates With a Myopia Genetic Risk PolymorphismZihe Xu, Jit Kai Tan, Krishnika Vetrivel, et al.
Acta Ophthalmologica|January 1, 2019
Unilateral pigmentary retinopathy: a retrospective case seriesMarie-Hélène Errera, Anthony G Robson, Tracey Wong, et al.
Journal of Neurointerventional Surgery|January 10, 2016
Prevalence of dural venous sinus stenosis and hypoplasia in a generalized populationChristopher R Durst, David A Ornan, Michael A Reardon, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, et al.
Investigative Ophthalmology & Visual Science|April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher SyndromeJuan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 12, 2025
PolyPath: Adapting a Large Multimodal Model for Multislide Pathology Report GenerationFaruk Ahmed, Lin Yang, Tiam Jaroensri, et al.
Ophthalmology|April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular PhenotypeArundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Bioorganic & Medicinal Chemistry Letters|March 20, 2003
1H-Pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinasesRaj N Misra, David B Rawlins, Hai-yun Xiao, et al.
Ophthalmic Genetics|October 7, 2025
A novel missense <i>TUBB4B</i> variant outside of the canonical hotspot is associated with cone-rod dystrophy and sensorineural hearing lossLauren Y Cao, Anna Duemler, Emily H Jung, et al.
Pageof 125

Showing results (931-940 of 1,250) with videos related to

Sort By:
Pageof 125
American Journal of Human Genetics|September 3, 2024
Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosaAna Belén Iglesias-Romero, Karolina Kaminska, Mathieu Quinodoz, et al.
Investigative Ophthalmology & Visual Science|November 12, 2024
The Electroretinogram I-Wave, a Component Originating in the Retinal OFF-Pathway, Associates With a Myopia Genetic Risk PolymorphismZihe Xu, Jit Kai Tan, Krishnika Vetrivel, et al.
Acta Ophthalmologica|January 1, 2019
Unilateral pigmentary retinopathy: a retrospective case seriesMarie-Hélène Errera, Anthony G Robson, Tracey Wong, et al.
Journal of Neurointerventional Surgery|January 10, 2016
Prevalence of dural venous sinus stenosis and hypoplasia in a generalized populationChristopher R Durst, David A Ornan, Michael A Reardon, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, et al.
Investigative Ophthalmology & Visual Science|April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher SyndromeJuan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 12, 2025
PolyPath: Adapting a Large Multimodal Model for Multislide Pathology Report GenerationFaruk Ahmed, Lin Yang, Tiam Jaroensri, et al.
Ophthalmology|April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular PhenotypeArundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Bioorganic & Medicinal Chemistry Letters|March 20, 2003
1H-Pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinasesRaj N Misra, David B Rawlins, Hai-yun Xiao, et al.
Ophthalmic Genetics|October 7, 2025
A novel missense <i>TUBB4B</i> variant outside of the canonical hotspot is associated with cone-rod dystrophy and sensorineural hearing lossLauren Y Cao, Anna Duemler, Emily H Jung, et al.
Pageof 125