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Mitochondrion|August 22, 2017
Two new cases of mitochondrial myopathy with exercise intolerance, hyperlactatemia and cardiomyopathy, caused by recessive SLC25A4 mutationsAnouk Tosserams, Constantinos Papadopoulos, Claude Jardel, et al.Mitochondrion|March 13, 2016
Multiple splicing pathways of group II trans-splicing introns in wheat mitochondriaKaren Massel, Jordan R Silke, Linda BonenMitochondrion|November 10, 2020
Mitochondrial genetic effect on atrial fibrillation: A case-control studyElena Roselló-Díez, Leif Hove-Madsen, Virginia Pérez-Grijalba, et al.Mitochondrion|November 21, 2020
Mitochondrial neuropathy and neurogenic features in mitochondrial myopathyJian-Qiang Lu, Mark A TarnopolskyMitochondrion|November 22, 2020
Mitochondrial dysfunction in schizophrenia: With a focus on postmortem studiesRosalinda C RobertsMitochondrion|January 19, 2023
Advancing mitochondria as a therapeutic agentAndrés Caicedo, Keshav K SinghMitochondrion|January 7, 2021
Characterization of the interactome of c-Src within the mitochondrial matrix by proximity-dependent biotin identificationHala Guedouari, Yasmine Ould Amer, Nicolas Pichaud, et al.Mitochondrion|January 7, 2021
Meta-analysis of gene expression patterns in Down syndrome highlights significant alterations in mitochondrial and bioenergetic pathwaysLaszlo Pecze, Csaba SzaboMitochondrion|January 7, 2021
Mitochondrial protein phosphorylation in yeast revisitedJan Frankovsky, Veronika Vozáriková, Jozef Nosek, et al.Mitochondrion|January 7, 2021
Mitogenomics of the endemic Ethiopian rats: looking for footprints of adaptive evolution in sky islandsVeronika Bartáková, Anna Bryjová, Violaine Nicolas, et al.Pageof 198