Found: 23
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Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41531-021-00182-x
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- Publication type:
- Article
Mitochondrial dysfunction within the synapses of substantia nigra neurons in Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2018, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41531-018-0044-6
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- Publication type:
- Article
Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis.
- Published in:
- Nucleic Acids Research, 2016, v. 44, n. 11, p. 5313, doi. 10.1093/nar/gkw382
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- Publication type:
- Article
The ageing mitochondrial genome.
- Published in:
- Nucleic Acids Research, 2007, v. 35, n. 22, p. 7399, doi. 10.1093/nar/gkm635
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- Publication type:
- Article
Mitochondrial DNA and disease.
- Published in:
- Journal of Pathology, 2012, v. 226, n. 2, p. 274, doi. 10.1002/path.3028
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- Publication type:
- Article
What causes mitochondrial DNA deletions in human cells?
- Published in:
- Nature Genetics, 2008, v. 40, n. 3, p. 275, doi. 10.1038/ng.f.94
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- Publication type:
- Article
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 515, doi. 10.1038/ng1769
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- Publication type:
- Article
Mitochondrial DNA Mutations in Disease, Aging, and Neurodegeneration.
- Published in:
- Annals of the New York Academy of Sciences, 2008, v. 1147, p. 21, doi. 10.1196/annals.1427.016
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- Publication type:
- Article
Mitochondrial DNA Mutations and Aging.
- Published in:
- Annals of the New York Academy of Sciences, 2007, v. 1100, p. 227, doi. 10.1196/annals.1395.024
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- Publication type:
- Article
No excess of mitochondrial DNA deletions within muscle in progressive multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2013, v. 19, n. 14, p. 1858, doi. 10.1177/1352458513490547
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- Publication type:
- Article
Age related mitochondrial degenerative disorders in humans.
- Published in:
- Biotechnology Journal, 2008, v. 3, n. 6, p. 750, doi. 10.1002/biot.200800066
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- Publication type:
- Article
Microangiopathy in the cerebellum of patients with mitochondrial DNA disease.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 6, p. 1736, doi. 10.1093/brain/aws110
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- Publication type:
- Article
Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 1, p. 62, doi. 10.1093/brain/awr326
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- Publication type:
- Article
Parkinson's disease neurons exhibit alterations in mitochondrial quality control proteins.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00564-3
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- Publication type:
- Article
Subcellular origin of mitochondrial DNA deletions in human skeletal muscle.
- Published in:
- 2018
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- Publication type:
- journal article
Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis.
- Published in:
- Annals of Neurology, 2011, v. 69, n. 3, p. 481, doi. 10.1002/ana.22109
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- Publication type:
- Article
Mitochondrial Mutations: Newly Discovered Players in Neuronal Degeneration.
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- Neuroscientist, 2011, v. 17, n. 6, p. 645, doi. 10.1177/1073858411385469
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- Publication type:
- Article
Mitochondrial Dysfunction in Parkinson's Disease—Cause or Consequence?
- Published in:
- Biology (2079-7737), 2019, v. 8, n. 2, p. 38, doi. 10.3390/biology8020038
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- Publication type:
- Article
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's Disease.
- Published in:
- Movement Disorders, 2022, v. 37, n. 2, p. 302, doi. 10.1002/mds.28849
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- Publication type:
- Article
Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls.
- Published in:
- 2020
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- Publication type:
- Letter
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level.
- Published in:
- Nucleic Acids Research, 2019, v. 47, n. 14, p. 7430, doi. 10.1093/nar/gkz472
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- Publication type:
- Article
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3043, doi. 10.1093/hmg/ddq209
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- Publication type:
- Article
The low abundance of clonally expanded mitochondrial DNA point mutations in aged substantia nigra neurons.
- Published in:
- Aging Cell, 2009, v. 8, n. 4, p. 496, doi. 10.1111/j.1474-9726.2009.00492.x
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- Publication type:
- Article