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Keywords: mitochondrial diseases
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Biochem J (2021) 478 (6): 1179–1197.
Published: 19 March 2021
...-mediated end joining mitochondrial diseases nonhomologous end joining Mitochondria, the ‘powerhouse of the cell’, possess their own genome (mtDNA). Due to its role in oxidative phosphorylation, the mitochondrial genome gets exposed to reactive oxygen species (ROS) frequently and is more prone...
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Biochem J (2003) 370 (3): 751–762.
Published: 15 March 2003
...Rodrigue ROSSIGNOL; Benjamin FAUSTIN; Christophe ROCHER; Monique MALGAT; Jean-Pierre MAZAT; Thierry LETELLIER The study of mitochondrial diseases has revealed dramatic variability in the phenotypic presentation of mitochondrial genetic defects. To attempt to understand this variability, different...
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Biochem J (1999) 342 (3): 551–554.
Published: 05 September 1999
... these findings in relation to the involvement of complex I in mitochondrial diseases. 1 To whom correspondence should be addressed, at Instituto de Biologia Molecular e Celular ( asvideir@icbas.up.pt ). 11 2 1999 7 5 1999 6 7 1999 The Biochemical Society, London © 1999 1999...
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