Found: 5
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Effects on mitochondrial transcription of manipulating mTERF protein levels in cultured human HEK293 cells.
- Published in:
- BMC Molecular Biology, 2010, v. 11, p. 72, doi. 10.1186/1471-2199-11-72
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- Publication type:
- Article
Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome.
- Published in:
- Brain: A Journal of Neurology, 2008, v. 131, n. 11, p. 2841, doi. 10.1093/brain/awn236
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- Publication type:
- Article
Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 23, p. 3822, doi. 10.1093/hmg/ddn280
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- Publication type:
- Article
Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 10, p. 1406, doi. 10.1093/hmg/ddn028
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- Publication type:
- Article
Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 6, p. 897, doi. 10.1093/hmg/ddl007
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- Publication type:
- Article