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Ian M MacDonald

Showing results (81-90 of 130) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|March 3, 2007
Choroideremia carriers maintain a normal electro-oculogram (EOG)Ryan J Yau, Christina A Sereda, Kerry E McTaggart, et al.
Retinal Cases & Brief Reports|November 13, 2014
De novo mutation in a choroideremia carrierSimge Bozbeyoglu, Gerald A Fishman, Edwin M Stone, et al.
Ophthalmic Genetics|August 4, 2011
Phenotype and genotype of patients with autosomal recessive bestrophinopathyIan M MacDonald, H V Gudiseva, Adda Villanueva, et al.
Investigative Ophthalmology & Visual Science|March 20, 2012
Dietary docosahexaenoic acid supplementation prevents age-related functional losses and A2E accumulation in the retinaBlake Dornstauder, Miyoung Suh, Sharee Kuny, et al.
Cells|October 3, 2020
Progressive Photoreceptor Dysfunction and Age-Related Macular Degeneration-Like Features in <i>rp1l1</i> Mutant ZebrafishNicole C L Noel, Nathan J Nadolski, Jennifer C Hocking, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|March 1, 2003
Autosomal dominant macular dystrophy in a large Canadian familyLarry A Donoso, Gregory Hageman, Arcilee Frost, et al.
American Journal of Medical Genetics. Part A|February 19, 2026
Identification of Two Novel Mutations in the CHM Gene Causing ChoroideremiaFarshad Niri, Alina Radziwon, Rachel Mah, et al.
Experimental Eye Research|February 5, 2026
PIKfyve is an essential component of the endolysosomal pathway within photoreceptors and the retinal pigment epitheliumKaren Attia, Ifrah Anjum, Susanne Lingrell, et al.
Translational Vision Science & Technology|July 28, 2020
Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal DegenerationsIan M MacDonald, Christopher Moen, Jacque L Duncan, et al.
Human Mutation|August 31, 2002
Mutational analysis of patients with the diagnosis of choroideremiaKerry E McTaggart, Mai Tran, Dean Y Mah, et al.
Pageof 13

Showing results (81-90 of 130) with videos related to

Sort By:
Pageof 13
Documenta Ophthalmologica. Advances in Ophthalmology|March 3, 2007
Choroideremia carriers maintain a normal electro-oculogram (EOG)Ryan J Yau, Christina A Sereda, Kerry E McTaggart, et al.
Retinal Cases & Brief Reports|November 13, 2014
De novo mutation in a choroideremia carrierSimge Bozbeyoglu, Gerald A Fishman, Edwin M Stone, et al.
Ophthalmic Genetics|August 4, 2011
Phenotype and genotype of patients with autosomal recessive bestrophinopathyIan M MacDonald, H V Gudiseva, Adda Villanueva, et al.
Investigative Ophthalmology & Visual Science|March 20, 2012
Dietary docosahexaenoic acid supplementation prevents age-related functional losses and A2E accumulation in the retinaBlake Dornstauder, Miyoung Suh, Sharee Kuny, et al.
Cells|October 3, 2020
Progressive Photoreceptor Dysfunction and Age-Related Macular Degeneration-Like Features in <i>rp1l1</i> Mutant ZebrafishNicole C L Noel, Nathan J Nadolski, Jennifer C Hocking, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|March 1, 2003
Autosomal dominant macular dystrophy in a large Canadian familyLarry A Donoso, Gregory Hageman, Arcilee Frost, et al.
American Journal of Medical Genetics. Part A|February 19, 2026
Identification of Two Novel Mutations in the CHM Gene Causing ChoroideremiaFarshad Niri, Alina Radziwon, Rachel Mah, et al.
Experimental Eye Research|February 5, 2026
PIKfyve is an essential component of the endolysosomal pathway within photoreceptors and the retinal pigment epitheliumKaren Attia, Ifrah Anjum, Susanne Lingrell, et al.
Translational Vision Science & Technology|July 28, 2020
Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal DegenerationsIan M MacDonald, Christopher Moen, Jacque L Duncan, et al.
Human Mutation|August 31, 2002
Mutational analysis of patients with the diagnosis of choroideremiaKerry E McTaggart, Mai Tran, Dean Y Mah, et al.
Pageof 13