Mitochondrial Oxidative Phosphorylation Compensation May Preserve Vision in Patients with OPA1-Linked Autosomal Dominant Optic Atrophy
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Title
Mitochondrial Oxidative Phosphorylation Compensation May Preserve Vision in Patients with OPA1-Linked Autosomal Dominant Optic Atrophy
Authors
Keywords
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Journal
PLoS One
Volume 6, Issue 6, Pages e21347
Publisher
Public Library of Science (PLoS)
Online
2011-06-23
DOI
10.1371/journal.pone.0021347
References
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Related references
Note: Only part of the references are listed.- Multi-system neurological disease is common in patients with OPA1 mutations
- (2010) P. Yu-Wai-Man et al. BRAIN
- Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy
- (2010) Nico Fuhrmann et al. Molecular Neurodegeneration
- The optic nerve head in acquired optic neuropathies
- (2010) Evelyn C. O'Neill et al. Nature Reviews Neurology
- The Prevalence and Natural History of Dominant Optic Atrophy Due to OPA1 Mutations
- (2010) Patrick Yu-Wai-Man et al. OPHTHALMOLOGY
- OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background
- (2009) Denis Pierron et al. BMC Medical Genetics
- Germline genomic variants associated with childhood acute lymphoblastic leukemia
- (2009) Lisa R Treviño et al. NATURE GENETICS
- Heterozygous Mutation of Opa1 in Drosophila Shortens Lifespan Mediated through Increased Reactive Oxygen Species Production
- (2009) Sha Tang et al. PLoS One
- Heterozygous Mutation of Drosophila Opa1 Causes the Development of Multiple Organ Abnormalities in an Age-Dependent and Organ-Specific Manner
- (2009) Parvin Shahrestani et al. PLoS One
- Hereditary optic neuropathies share a common mitochondrial coupling defect
- (2008) Arnaud Chevrollier et al. ANNALS OF NEUROLOGY
- Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy
- (2008) Vladimir I Mayorov et al. BMC BIOCHEMISTRY
- The natural history of OPA1-related autosomal dominant optic atrophy
- (2008) A C Cohn et al. BRITISH JOURNAL OF OPHTHALMOLOGY
- A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function
- (2008) Marco Spinazzi et al. HUMAN MOLECULAR GENETICS
- Inherited mitochondrial optic neuropathies
- (2008) P Yu-Wai-Man et al. JOURNAL OF MEDICAL GENETICS
- The Molecular Mechanisms of OPA1-Mediated Optic Atrophy in Drosophila Model and Prospects for Antioxidant Treatment
- (2008) Will Yarosh et al. PLoS Genetics
- The C. elegans Opa1 Homologue EAT-3 Is Essential for Resistance to Free Radicals
- (2008) Takayuki Kanazawa et al. PLoS Genetics
- OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
- (2007) P. Amati-Bonneau et al. BRAIN
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