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Mitochondrion|October 11, 2011
Parkinson's disease-like neuromuscular defects occur in prenyl diphosphate synthase subunit 2 (Pdss2) mutant miceCarly G K Ziegler, Min Peng, Marni J Falk, et al.
Mitochondrion|October 12, 2011
Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathiesJuan J Arredondo, M Esther Gallardo, Pablo García-Pavía, et al.
Mitochondrion|December 14, 2011
Influence of erythrocyte oxygenation and intravascular ATP on resting and exercising skeletal muscle blood flow in humans with mitochondrial myopathyTina D Jeppesen, John Vissing, José González-Alonso
Mitochondrion|July 30, 2011
Mitochondrial calcium homeostasis as potential target for mitochondrial medicineCarlotta Giorgi, Chiara Agnoletto, Angela Bononi, et al.
Mitochondrion|August 23, 2011
A novel mitotropic oligolysine nanocarrier: Targeted delivery of covalently bound D-Luciferin to cell mitochondriaTheodossis A Theodossiou, Zili Sideratou, Dimitris Tsiourvas, et al.
Mitochondrion|June 28, 2011
New mitochondrial tRNA HIS mutation in a family with lactic acidosis and stroke-like episodes (MELAS)Maria Antonietta Calvaruso, Michel A Willemsen, Richard J Rodenburg, et al.
Mitochondrion|June 14, 2011
Increased availability of endogenous and dietary oleic acid contributes to the upregulation of cardiac fatty acid oxidationPawel Dobrzyn, Aleksandra Pyrkowska, Magdalena Jazurek, et al.
Mitochondrion|March 17, 2011
Mitochondrial changes associated with demyelination: consequences for axonal integrityGraham R Campbell, Don J Mahad
Mitochondrion|July 16, 2011
Pharmacological targeting of mitochondrial complex I deficiency: the cellular level and beyondPeggy Roestenberg, Ganesh R Manjeri, Federica Valsecchi, et al.
Mitochondrion|July 12, 2011
The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutationYaping Qian, Xiangtian Zhou, Min Liang, et al.
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