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Mariya Moosajee

Showing results (31-40 of 176) with videos related to

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JAMA Ophthalmology|November 13, 2018
Retinal Angiography Findings in Male Infant With Incontinentia Pigmenti and Sickle Cell TraitMariya Moosajee, M Adam Ali, Sui Chien Wong
Genes|March 6, 2021
Acceptability of Telegenetics for Families with Genetic Eye DiseasesSuzannah Bell, Urvi Karamchandani, Kirsten Malcolmson, et al.
Stem Cell Reports|May 31, 2024
Disruption of common ocular developmental pathways in patient-derived optic vesicle models of microphthalmiaJonathan Eintracht, Nicholas Owen, Philippa Harding, et al.
International Journal of Molecular Sciences|June 24, 2022
The Natural History of <i>CNGB1</i>-Related Retinopathy: A Longitudinal Phenotypic AnalysisDaniel J Jackson, Adam M Dubis, Mariya Moosajee
Eye (London, England)|October 29, 2023
Longitudinal structure-function analysis of molecularly-confirmed CYP4V2 Bietti Crystalline DystrophyRiccardo Cheloni, Neil Clough, Daniel Jackson, et al.
Antioxidants (Basel, Switzerland)|September 28, 2023
Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for ChoroideremiaHajrah Sarkar, Manuela Lahne, Neelima Nair, et al.
Eye (London, England)|June 6, 2019
Cellular imaging of inherited retinal diseases using adaptive opticsJasdeep S Gill, Mariya Moosajee, Adam M Dubis
European Journal of Human Genetics : EJHG|May 18, 2018
CUGC for congenital primary aphakiaHajrah Sarkar, William Moore, Bart P Leroy, et al.
Journal of Medical Internet Research|January 25, 2021
Correction: A Newly Developed Web-Based Resource on Genetic Eye Disorders for Users With Visual Impairment (Gene.Vision): Usability StudyJian Lee Yeong, Peter Thomas, James Buller, et al.
Ebiomedicine|August 8, 2021
Translational readthrough of ciliopathy genes BBS2 and ALMS1 restores protein, ciliogenesis and function in patient fibroblastsJonathan Eintracht, Elizabeth Forsythe, Helen May-Simera, et al.
Pageof 18

Showing results (31-40 of 176) with videos related to

Sort By:
Pageof 18
JAMA Ophthalmology|November 13, 2018
Retinal Angiography Findings in Male Infant With Incontinentia Pigmenti and Sickle Cell TraitMariya Moosajee, M Adam Ali, Sui Chien Wong
Genes|March 6, 2021
Acceptability of Telegenetics for Families with Genetic Eye DiseasesSuzannah Bell, Urvi Karamchandani, Kirsten Malcolmson, et al.
Stem Cell Reports|May 31, 2024
Disruption of common ocular developmental pathways in patient-derived optic vesicle models of microphthalmiaJonathan Eintracht, Nicholas Owen, Philippa Harding, et al.
International Journal of Molecular Sciences|June 24, 2022
The Natural History of <i>CNGB1</i>-Related Retinopathy: A Longitudinal Phenotypic AnalysisDaniel J Jackson, Adam M Dubis, Mariya Moosajee
Eye (London, England)|October 29, 2023
Longitudinal structure-function analysis of molecularly-confirmed CYP4V2 Bietti Crystalline DystrophyRiccardo Cheloni, Neil Clough, Daniel Jackson, et al.
Antioxidants (Basel, Switzerland)|September 28, 2023
Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for ChoroideremiaHajrah Sarkar, Manuela Lahne, Neelima Nair, et al.
Eye (London, England)|June 6, 2019
Cellular imaging of inherited retinal diseases using adaptive opticsJasdeep S Gill, Mariya Moosajee, Adam M Dubis
European Journal of Human Genetics : EJHG|May 18, 2018
CUGC for congenital primary aphakiaHajrah Sarkar, William Moore, Bart P Leroy, et al.
Journal of Medical Internet Research|January 25, 2021
Correction: A Newly Developed Web-Based Resource on Genetic Eye Disorders for Users With Visual Impairment (Gene.Vision): Usability StudyJian Lee Yeong, Peter Thomas, James Buller, et al.
Ebiomedicine|August 8, 2021
Translational readthrough of ciliopathy genes BBS2 and ALMS1 restores protein, ciliogenesis and function in patient fibroblastsJonathan Eintracht, Elizabeth Forsythe, Helen May-Simera, et al.
Pageof 18