Found: 10
Select item for more details and to access through your institution.
Triplex real-time PCR-an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cells.
- Published in:
- Scientific Reports, 2015, p. 9906, doi. 10.1038/srep09906
- By:
- Publication type:
- Article
Therapeutic potential of somatic cell nuclear transfer for degenerative disease caused by mitochondrial DNA mutations.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep03844
- By:
- Publication type:
- Article
Pathogenic mitochondrial mt-tRNA<sup>Ala</sup> variants are uniquely associated with isolated myopathy.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1735, doi. 10.1038/ejhg.2015.73
- By:
- Publication type:
- Article
Clonal Expansion of Early to Mid-Life Mitochondrial DNA Point Mutations Drives Mitochondrial Dysfunction during Human Ageing.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004620
- By:
- Publication type:
- Article
Accurate Measurement of Mitochondrial DNA Deletion Level and Copy Number Differences in Human Skeletal Muscle.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0114462
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- Article
Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 1, p. 183, doi. 10.1093/brain/awq320
- By:
- Publication type:
- Article
The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families.
- Published in:
- Brain: A Journal of Neurology, 2010, v. 133, n. 10, p. 2952, doi. 10.1093/brain/awq232
- By:
- Publication type:
- Article
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.
- Published in:
- Brain: A Journal of Neurology, 2009, v. 132, n. 11, p. 3165, doi. 10.1093/brain/awp221
- By:
- Publication type:
- Article
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expression.
- Published in:
- Clinical Science, 2015, v. 128, n. 12, p. 895, doi. 10.1042/CS20140705
- By:
- Publication type:
- Article