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Annals of Neurology|October 29, 2002
Rescue of a mitochondrial deficiency causing Leber Hereditary Optic NeuropathyJohn Guy, Xiaoping Qi, Francesco Pallotti, et al.
The Journal of Biological Chemistry|June 25, 1989
A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissuesR Rizzuto, H Nakase, B Darras, et al.
Muscle & Nerve|October 15, 1998
Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reactionM Sciacco, P Gasparo-Rippa, T H Vu, et al.
EMBO Reports|November 14, 2015
ApoE4 upregulates the activity of mitochondria-associated ER membranesMarc D Tambini, Marta Pera, Ellen Kanter, et al.
Archives of Neurology|July 12, 2012
Congenital megaconial myopathy due to a novel defect in the choline kinase Beta genePurificacion Gutiérrez Ríos, Arun A Kalra, Jon D Wilson, et al.
Nucleic Acids Research|September 11, 1981
Transcription of the beta-like globin genes and pseudogenes of the goat in a cell-free systemD S Luse, J R Haynes, D VanLeeuwen, et al.
The Journal of Clinical Investigation|October 28, 2010
Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in miceNatalia Papeta, Zongyu Zheng, Eric A Schon, et al.
Neurology|February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approachH J Tritschler, E Bonilla, A Lombes, et al.
Gene|October 1, 1992
Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidaseE Arnaudo, M Hirano, R S Seelan, et al.
Human Molecular Genetics|October 20, 2009
Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2Hua Yang, Sonja Brosel, Rebeca Acin-Perez, et al.
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