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Opa1 Deficiency Promotes Development of Retinal Vascular Lesions in Diabetic Retinopathy

International journal of molecular sciences, 2021-05, Vol.22 (11), p.5928

2021

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Symmetric arrangement of mitochondria:plasma membrane contacts between adjacent photoreceptor cells regulated by Opa1

Proceedings of the National Academy of Sciences - PNAS, 2020-07, Vol.117 (27), p.15684-15693

2020

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Photostimulation of mitochondria as a treatment for retinal neurodegeneration

Mitochondrion, 2017-09, Vol.36, p.85-95

2017

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Mitochondria and vision – a life in mitochondria always on the move

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

Votruba, Marcela

2024

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What OPA1 models teach us about potential therapy

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

Votruba, Marcela

2024

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Red Light Irradiation In Vivo Upregulates DJ-1 in the Retinal Ganglion Cell Layer and Protects against Axotomy-Related Dendritic Pruning

International journal of molecular sciences, 2021-08, Vol.22 (16), p.8380

2021

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A Perspective on Accelerated Aging Caused by the Genetic Deficiency of the Metabolic Protein, OPA1

Frontiers in neurology, 2021-04, Vol.12, p.641259-641259

2021

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Potential Therapeutic Benefit of NAD + Supplementation for Glaucoma and Age-Related Macular Degeneration

Nutrients, 2020-09, Vol.12 (9), p.2871

2020

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Retinal involvement in mitochondrial disease

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

Votruba, Marcela

2022

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COVID‐19 vaccination and vision loss in three older male individuals homoplasmic for m.14484T>C mutation in the ND6 gene

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275)

Votruba, Marcela

2022

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COVID‐19 vaccination and vision loss in three older male individuals homoplasmic for m.14484 T > C mutation in the ND6 gene

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

Votruba, Marcela

2022

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Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function

Human molecular genetics, 2007-06, Vol.16 (11), p.1307-1318

2007

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OPA1 Mutation and Late‐Onset Cardiomyopathy: Mitochondrial Dysfunction and mtDNA Instability

Journal of the American Heart Association, 2012-10, Vol.1 (5), p.e003012-n/a

2012

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Oral nicotinamide provides robust, dose-dependent structural and metabolic neuroprotection of retinal ganglion cells in experimental glaucoma

Acta neuropathologica communications, 2024-08, Vol.12 (1), p.137-17

2024

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Genetic landscape of inherited retinal dystrophies in a Welsh Tertiary Referral Centre

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

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OPA1 , encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

Nature genetics, 2000-10, Vol.26 (2), p.211-215

2000

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Can the retina be used to diagnose and plot the progression of Alzheimer's disease?

Acta ophthalmologica (Oxford, England), 2017-12, Vol.95 (8), p.768-777

2017

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Non-image-forming light driven functions are preserved in a mouse model of autosomal dominant optic atrophy

PloS one, 2013-02, Vol.8 (2), p.e56350

2013

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High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy

BioMed research international, 2013-01, Vol.2013 (2013), p.1-12

2013

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A novel NR2E3 gene mutation in autosomal recessive retinitis pigmentosa with cystic maculopathy

Acta ophthalmologica (Oxford, England), 2018-06, Vol.96 (4), p.e535-e536

2018

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NAM as a neuroprotective therapeutic intervention for mitochondrial optic neuropathies

Biochimica et biophysica acta. Bioenergetics, 2024-09, Vol.1865, p.149143, Article 149143

2024

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SDOCT Thickness Measurements of Various Retinal Layers in Patients with Autosomal Dominant Optic Atrophy due to OPA1 Mutations

BioMed research international, 2013-01, Vol.2013 (2013), p.1-5

2013

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A novel NR 2E3 gene mutation in autosomal recessive retinitis pigmentosa with cystic maculopathy

Acta ophthalmologica (Oxford, England), 2018-06, Vol.96 (4)

2018

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Opa1 Deficiency Leads to Diminished Mitochondrial Bioenergetics With Compensatory Increased Mitochondrial Motility

Investigative ophthalmology & visual science, 2020-06, Vol.61 (6), p.42-42

2020

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A neurodegenerative perspective on mitochondrial optic neuropathies

Acta Neuropathologica, 2016-12, Vol.132 (6), p.789-806

2016

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Opa1 Deficiency Promotes Development of Retinal Vascular Lesions in Diabetic Retinopathy

Symmetric arrangement of mitochondria:plasma membrane contacts between adjacent photoreceptor cells regulated by Opa1

Photostimulation of mitochondria as a treatment for retinal neurodegeneration

Mitochondria and vision – a life in mitochondria always on the move

What OPA1 models teach us about potential therapy

Red Light Irradiation In Vivo Upregulates DJ-1 in the Retinal Ganglion Cell Layer and Protects against Axotomy-Related Dendritic Pruning

A Perspective on Accelerated Aging Caused by the Genetic Deficiency of the Metabolic Protein, OPA1

Potential Therapeutic Benefit of NAD + Supplementation for Glaucoma and Age-Related Macular Degeneration

Retinal involvement in mitochondrial disease

COVID‐19 vaccination and vision loss in three older male individuals homoplasmic for m.14484T>C mutation in the ND6 gene

COVID‐19 vaccination and vision loss in three older male individuals homoplasmic for m.14484 T > C mutation in the ND6 gene

Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function

OPA1 Mutation and Late‐Onset Cardiomyopathy: Mitochondrial Dysfunction and mtDNA Instability

Oral nicotinamide provides robust, dose-dependent structural and metabolic neuroprotection of retinal ganglion cells in experimental glaucoma

Genetic landscape of inherited retinal dystrophies in a Welsh Tertiary Referral Centre

OPA1 , encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

Can the retina be used to diagnose and plot the progression of Alzheimer's disease?

Non-image-forming light driven functions are preserved in a mouse model of autosomal dominant optic atrophy

High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy

A novel NR2E3 gene mutation in autosomal recessive retinitis pigmentosa with cystic maculopathy

NAM as a neuroprotective therapeutic intervention for mitochondrial optic neuropathies

SDOCT Thickness Measurements of Various Retinal Layers in Patients with Autosomal Dominant Optic Atrophy due to OPA1 Mutations

A novel NR 2E3 gene mutation in autosomal recessive retinitis pigmentosa with cystic maculopathy

Opa1 Deficiency Leads to Diminished Mitochondrial Bioenergetics With Compensatory Increased Mitochondrial Motility

A neurodegenerative perspective on mitochondrial optic neuropathies

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