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Survey of Ophthalmology
|
October 17, 2024
Meta-analysis of treatment outcomes for patients with m.11778G>A MT-ND4 Leber hereditary optic neuropathy
Nancy J Newman, Valérie Biousse, Patrick Yu-Wai-Man, et al.
Scientific Reports
|
September 28, 2017
Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation
Valeria Chichagova, Dean Hallam, Joseph Collin, et al.
Brain : a Journal of Neurology
|
June 16, 2009
Gene-environment interactions in Leber hereditary optic neuropathy
Matthew Anthony Kirkman, Patrick Yu-Wai-Man, Alex Korsten, et al.
Cancer Informatics
|
August 11, 2021
Pan-Cancer Survival Classification With Clinicopathological and Targeted Gene Expression Features
Daniel Zhao, Daniel Y Kim, Peter Chen, et al.
International Journal of Molecular Sciences
|
July 12, 2025
CRISPRa-Mediated Increase of OPA1 Expression in Dominant Optic Atrophy
Giada Becchi, Michael Whitehead, Joshua P Harvey, et al.
EMBO Molecular Medicine
|
May 20, 2021
High-throughput screening identifies suppressors of mitochondrial fragmentation in OPA1 fibroblasts
Emma Cretin, Priscilla Lopes, Elodie Vimont, et al.
Orphanet Journal of Rare Diseases
|
October 24, 2014
Leber's hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients
Konstantin Dimitriadis, Miriam Leonhardt, Patrick Yu-Wai-Man, et al.
Human Molecular Genetics
|
June 2, 2022
Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells
Paul E Sladen, Katarina Jovanovic, Rosellina Guarascio, et al.
Molecular Vision
|
January 5, 2011
Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy
Gavin Hudson, Patrick Yu-Wai-Man, Phillip G Griffiths, et al.
Ophthalmology
|
November 2, 2010
Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies
Patrick Yu-Wai-Man, Suma P Shankar, Valérie Biousse, et al.
Page
of 19
Search research articles
Search
Showing results (81-90 of 183) with videos related to
Sort By:
Page
of 19
Survey of Ophthalmology
|
October 17, 2024
Meta-analysis of treatment outcomes for patients with m.11778G>A MT-ND4 Leber hereditary optic neuropathy
Nancy J Newman, Valérie Biousse, Patrick Yu-Wai-Man, et al.
Scientific Reports
|
September 28, 2017
Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation
Valeria Chichagova, Dean Hallam, Joseph Collin, et al.
Brain : a Journal of Neurology
|
June 16, 2009
Gene-environment interactions in Leber hereditary optic neuropathy
Matthew Anthony Kirkman, Patrick Yu-Wai-Man, Alex Korsten, et al.
Cancer Informatics
|
August 11, 2021
Pan-Cancer Survival Classification With Clinicopathological and Targeted Gene Expression Features
Daniel Zhao, Daniel Y Kim, Peter Chen, et al.
International Journal of Molecular Sciences
|
July 12, 2025
CRISPRa-Mediated Increase of OPA1 Expression in Dominant Optic Atrophy
Giada Becchi, Michael Whitehead, Joshua P Harvey, et al.
EMBO Molecular Medicine
|
May 20, 2021
High-throughput screening identifies suppressors of mitochondrial fragmentation in OPA1 fibroblasts
Emma Cretin, Priscilla Lopes, Elodie Vimont, et al.
Orphanet Journal of Rare Diseases
|
October 24, 2014
Leber's hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients
Konstantin Dimitriadis, Miriam Leonhardt, Patrick Yu-Wai-Man, et al.
Human Molecular Genetics
|
June 2, 2022
Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells
Paul E Sladen, Katarina Jovanovic, Rosellina Guarascio, et al.
Molecular Vision
|
January 5, 2011
Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy
Gavin Hudson, Patrick Yu-Wai-Man, Phillip G Griffiths, et al.
Ophthalmology
|
November 2, 2010
Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies
Patrick Yu-Wai-Man, Suma P Shankar, Valérie Biousse, et al.
Page
of 19