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Mitochondrion|June 16, 2010
Illness-induced exacerbation of Leigh syndrome in a patient with the MTATP6 mutation, m. 9185 T>CRussell P Saneto, Keshav K SinghMitochondrion|May 22, 2010
A quantitative assay for mitochondrial fusion using Renilla luciferase complementationHuiyan Huang, Seok-Yong Choi, Michael A FrohmanMitochondrion|August 6, 2010
Mitochondrial dysfunction in CD4+ lymphocytes from stavudine-treated HIV patientsLloyd Einsiedel, Catherine L Cherry, Freya L Sheeran, et al.Mitochondrion|May 4, 2010
Phosphorylation pattern of the NDUFS4 subunit of complex I of the mammalian respiratory chainDomenico De Rasmo, Giuseppe Palmisano, Salvatore Scacco, et al.Mitochondrion|March 3, 2009
Dysfunction of mitochondria Ca2+ uptake in cystic fibrosis airway epithelial cellsFabrice Antigny, Nathalie Girardin, Dorothée Raveau, et al.Mitochondrion|March 24, 2009
Mitochondrial disorder with OPA1 mutation lacking optic atrophyMargherita Milone, Brian R Younge, Jing Wang, et al.Mitochondrion|May 23, 2009
Two novel cosegregating mutations in tRNAMet and COX III, in a patient with exercise intolerance and autoimmune polyendocrinopathyB Bortot, E Barbi, S Biffi, et al.Mitochondrion|May 23, 2009
Novel insights into phenotype and mitochondrial proteome of yeast mutants lacking proteins Sco1p or Sco2pTania Gamberi, Francesca Magherini, Marina Borro, et al.Mitochondrion|June 9, 2009
De novo mutation in POLG leads to haplotype insufficiency and Alpers syndromeSherine S L Chan, Robert K Naviaux, Alice A Basinger, et al.Pageof 198