Davidson, M

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

King, M. P., Koga, Y., Davidson, M., & Schon, E. A. (1992) · Molecular and Cellular Biology

Mitochondrial Function and PathologyRNA and protein synthesis mechanisms

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A functionally dominant mitochondrial DNA mutation

Sacconi, S., Salviati, L., Nishigaki, Y., Walker, W. F., Hernandez-Rosa, E., Trevisson, E., Delplace, S., Desnuelle, C., Shanske, S., Hirano, M., et al. (2008) · Human Molecular Genetics

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

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Sex differences in exercise-induced physiological myocardial hypertrophy are modulated by oestrogen receptor beta

Dworatzek, E., Mahmoodzadeh, S., Schubert, C., Westphal, C., Leber, J., Kusch, A., Kararigas, G., Fliegner, D., Moulin, M., Ventura-Clapier, R., et al. (2014) · Cardiovascular Research

Cardiovascular Effects of ExerciseEstrogen and related hormone effects

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A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?

Swalwell, H., Blakely, E. L., Sutton, R., Tonska, K., Elstner, M., He, L., Taivassalo, T., Burns, D. K., Turnbull, D. M., Haller, R. G., et al. (2008) · European Journal of Human Genetics

Mitochondrial Function and PathologyGenomics and Rare Diseases

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