Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Molecular Neurobiology|June 19, 2018
Cell Death Pathways in Mutant Rhodopsin Rat Models Identifies Genotype-Specific Targets Controlling Retinal DegenerationIshaq A Viringipurampeer, Cheryl Y Gregory-Evans, Andrew L Metcalfe, et al.
Molecular Vision|July 9, 2016
An ex vivo gene therapy approach in X-linked retinoschisisAbu E Bashar, Andrew L Metcalfe, Ishaq A Viringipurampeer, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|August 6, 2011
Non-invasive anterior segment and posterior segment optical coherence tomography and phenotypic characterization of aniridiaKevin Gregory-Evans, Richard Cheong-Leen, Sheena M George, et al.
Tissue Engineering. Part C, Methods|February 1, 2013
Differentiation of human embryonic stem cells using size-controlled embryoid bodies and negative cell selection in the production of photoreceptor precursor cellsAnat Yanai, Christopher R J Laver, Aaron W Joe, et al.
Journal of Glaucoma|March 20, 2025
Incidence and Association of Angle-Closure Glaucoma in Retinitis Pigmentosa: A Meta-AnalysisBrendan K Tao, Madeleine Wong, Maheshver Shunmugam, et al.
Human Molecular Genetics|February 24, 2012
Pax2 regulates a fadd-dependent molecular switch that drives tissue fusion during eye developmentIshaq A Viringipurampeer, Todd Ferreira, Shannon DeMaria, et al.
Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale|June 18, 2024
IGF-1 Mediated Neuroprotective Effects of Olfactory-Derived Mesenchymal Stem Cells on Auditory Hair CellsMarc J W Lammers, Emily Young, Anat Yanai, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 9, 2017
Correlation of novel PAX6 gene abnormalities in aniridia and clinical presentationNaif S Sannan, Cheryl Y Gregory-Evans, Christopher J Lyons, et al.
Human Molecular Genetics|March 25, 2016
NLRP3 inflammasome activation drives bystander cone photoreceptor cell death in a P23H rhodopsin model of retinal degenerationIshaq A Viringipurampeer, Andrew L Metcalfe, Abu E Bashar, et al.
Orphanet Journal of Rare Diseases|August 21, 2025
Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics servicesTasha Wainstein, Cyrus Boelman, Connie Ens, et al.
Pageof 7