Mercy M. Davidson

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

Lefkothea C. Papadopoulou, Carolyn M. Sue, Mercy M. Davidson et al. · Nature Genetics · 1999 · 571 citations

Life Sciences, Genetics, Molecular Genetics +10

Evidence of ROS generation by mitochondria in cells with impaired electron transport chain and mitochondrial DNA damage

Hiroko P. Indo, Mercy M. Davidson, Hsiu‐Chuan Yen et al. · Mitochondrion · 2006 · 524 citations

Life Sciences, Biochemistry, Cell Biology +16

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

Michael P. King, Yasutoshi Koga, Mercy M. Davidson et al. · Molecular and Cellular Biology · 1992 · 421 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

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.

Michael P. King, Yasutoshi Koga, Mercy M. Davidson et al. · Molecular and Cellular Biology · 1992 · 350 citations

Life Sciences, Genetics, Molecular Biology +17

SIRT3-mediated inhibition of FOS through histone H3 deacetylation prevents cardiac fibrosis and inflammation

Xavier Palomer, M. Silvia Román-Azcona, Javier Pizarro‐Delgado et al. · Signal Transduction and Targeted Therapy · 2020 · 199 citations · Full text

Veterinary Medicine, Cardiology, Molecular Biology +17