Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
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Title
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
Authors
Keywords
-
Journal
Scientific Reports
Volume 8, Issue 1, Pages -
Publisher
Springer Nature
Online
2018-07-30
DOI
10.1038/s41598-018-30143-z
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Related references
Note: Only part of the references are listed.- MtDNA-maintenance defects: syndromes and genes
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- Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations
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- Selective removal of deletion-bearing mitochondrial DNA in heteroplasmic Drosophila
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- Syndromic parkinsonism and dementia associated withOPA1missense mutations
- (2015) Valerio Carelli et al. ANNALS OF NEUROLOGY
- Mitochondrial Dynamics Is a Distinguishing Feature of Skeletal Muscle Fiber Types and Regulates Organellar Compartmentalization
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- Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations
- (2015) Valerio Carelli et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- Context-Dependent Role of Mitochondrial Fusion-Fission in Clonal Expansion of mtDNA Mutations
- (2015) Zhi Yang Tam et al. PLoS Computational Biology
- Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle
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- Mitochondrial DNA: Impacting Central and Peripheral Nervous Systems
- (2014) Valerio Carelli et al. NEURON
- Mitochondrial Biogenesis Drives a Vicious Cycle of Metabolic Insufficiency and Mitochondrial DNA Deletion Mutation Accumulation in Aged Rat Skeletal Muscle Fibers
- (2013) Allen Herbst et al. PLoS One
- OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophy
- (2012) K. S. Sitarz et al. NEUROLOGY
- Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies
- (2012) L. Iommarini et al. NEUROLOGY
- Single deletions in mitochondrial DNA – Molecular mechanisms and disease phenotypes in clinical practice
- (2012) R.D.S. Pitceathly et al. NEUROMUSCULAR DISORDERS
- Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations
- (2010) Hsiuchen Chen et al. CELL
- OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules
- (2010) Patrick Yu-Wai-Man et al. HUMAN MOLECULAR GENETICS
- OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
- (2007) P. Amati-Bonneau et al. BRAIN
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