A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis-Reference-Cited by-同舟云学术

A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis

Published:2015-10-15 Issue:1 Volume:5 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Rocha Mariana C.,Grady John P.,Grünewald Anne,Vincent Amy,Dobson Philip F.,Taylor Robert W.,Turnbull Doug M.,Rygiel Karolina A.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep15037.pdf

Reference61 articles.

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2. Greaves, L. C., Reeve, A. K., Taylor, R. W. & Turnbull, D. M. Mitochondrial DNA and disease. J Pathol 226, 274–286 (2012).

3. Campbell, G. R. et al. Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis. Ann Neurol 69, 481–492 (2011).

4. Oldfors, A., Larsson, N.-G., Lindberg, C. & Holme, E. Mitochondrial DNA deletions in inclusion body myositis. Brain 116, 325–336 (1993).

5. Reeve, A. K. et al. Nature of mitochondrial DNA deletions in substantia nigra neurons. Am J Hum Genet 82, 228–235 (2008).

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