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Frontiers in Cellular Neuroscience|September 25, 2020
The Use of Induced Pluripotent Stem Cells as a Model for Developmental Eye DisordersJonathan Eintracht, Maria Toms, Mariya Moosajee
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.
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.
F1000Research|July 11, 2022
Efficient embryoid-based method to improve generation of optic vesicles from human induced pluripotent stem cellsJonathan Eintracht, Philippa Harding, Dulce Lima Cunha, et al.
Genes|December 22, 2019
The Spectrum of PAX6 Mutations and Genotype-Phenotype Correlations in the EyeDulce Lima Cunha, Gavin Arno, Marta Corton, 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.
European Journal of Human Genetics : EJHG|October 7, 2020
PAX6 missense variants in two families with isolated foveal hypoplasia and nystagmus: evidence of paternal postzygotic mosaicismDulce Lima Cunha, Nicholas Owen, Vijay Tailor, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Anophthalmia including next-generation sequencing-based approachesPhilippa Harding, Brian P Brooks, David FitzPatrick, 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.
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