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Mariya Moosajee

Showing results (91-100 of 176) with videos related to

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Investigative Ophthalmology & Visual Science|October 28, 2003
Transcriptional regulation and expression of the dominant drusen gene FBLN3 (EFEMP1) in mammalian retinaJames Blackburn, Emma E Tarttelin, Cheryl Y Gregory-Evans, et al.
Cells|November 26, 2022
Changes in Mitochondrial Size and Morphology in the RPE and Photoreceptors of the Developing and Ageing ZebrafishThomas Burgoyne, Maria Toms, Chris Way, et al.
Zebrafish|January 5, 2017
Spectral Domain Optical Coherence Tomography: An In Vivo Imaging Protocol for Assessing Retinal Morphology in Adult ZebrafishMaria Toms, Dhani Tracey-White, Dhakshi Muhundhakumar, et al.
Molecular Therapy. Nucleic Acids|July 24, 2023
Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugsDulce Lima Cunha, Hajrah Sarkar, Jonathan Eintracht, et al.
Stem Cell Research|May 19, 2023
Establishment and characterization of an iPSC line (UCLi023-A) derived from a Late-Onset Retinal Degeneration patient carrying a founder mutation in C1QTNF5Ana Alonso-Carriazo Fernández, Phoebe Ashley-Norman, Zaynab Butt, et al.
Stem Cell Research|December 29, 2020
Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditionsCécile Méjécase, Philippa Harding, Hajrah Sarkar, et al.
Stem Cell Research|February 1, 2021
Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6Philippa Harding, Dulce Lima Cunha, Cécile Méjécase, et al.
Human Molecular Genetics|September 24, 2008
Translational bypass of nonsense mutations in zebrafish rep1, pax2.1 and lamb1 highlights a viable therapeutic option for untreatable genetic eye diseaseMariya Moosajee, Kevin Gregory-Evans, Charles D Ellis, et al.
Stem Cell Research|January 18, 2025
Generation of a human iPSC line (UCLi025-A) from a patient with PHARC syndrome harbouring biallelic variants in ABHD12Sara Romero-Vázquez, Katy Linkens, Lyes Toualbi, et al.
Stem Cell Research|July 3, 2021
Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variantsHajrah Sarkar, Cécile Méjécase, Philippa Harding, et al.
Pageof 18

Showing results (91-100 of 176) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|October 28, 2003
Transcriptional regulation and expression of the dominant drusen gene FBLN3 (EFEMP1) in mammalian retinaJames Blackburn, Emma E Tarttelin, Cheryl Y Gregory-Evans, et al.
Cells|November 26, 2022
Changes in Mitochondrial Size and Morphology in the RPE and Photoreceptors of the Developing and Ageing ZebrafishThomas Burgoyne, Maria Toms, Chris Way, et al.
Zebrafish|January 5, 2017
Spectral Domain Optical Coherence Tomography: An In Vivo Imaging Protocol for Assessing Retinal Morphology in Adult ZebrafishMaria Toms, Dhani Tracey-White, Dhakshi Muhundhakumar, et al.
Molecular Therapy. Nucleic Acids|July 24, 2023
Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugsDulce Lima Cunha, Hajrah Sarkar, Jonathan Eintracht, et al.
Stem Cell Research|May 19, 2023
Establishment and characterization of an iPSC line (UCLi023-A) derived from a Late-Onset Retinal Degeneration patient carrying a founder mutation in C1QTNF5Ana Alonso-Carriazo Fernández, Phoebe Ashley-Norman, Zaynab Butt, et al.
Stem Cell Research|December 29, 2020
Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditionsCécile Méjécase, Philippa Harding, Hajrah Sarkar, et al.
Stem Cell Research|February 1, 2021
Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6Philippa Harding, Dulce Lima Cunha, Cécile Méjécase, et al.
Human Molecular Genetics|September 24, 2008
Translational bypass of nonsense mutations in zebrafish rep1, pax2.1 and lamb1 highlights a viable therapeutic option for untreatable genetic eye diseaseMariya Moosajee, Kevin Gregory-Evans, Charles D Ellis, et al.
Stem Cell Research|January 18, 2025
Generation of a human iPSC line (UCLi025-A) from a patient with PHARC syndrome harbouring biallelic variants in ABHD12Sara Romero-Vázquez, Katy Linkens, Lyes Toualbi, et al.
Stem Cell Research|July 3, 2021
Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variantsHajrah Sarkar, Cécile Méjécase, Philippa Harding, et al.
Pageof 18