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Seminars in Cell & Developmental Biology|December 12, 2001
Pathogenesis of primary defects in mitochondrial ATP synthesisE A Schon, S Santra, F Pallotti, et al.
Annals of Neurology|September 25, 2004
Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cellsSumana Santra, Robert W Gilkerson, Mercy Davidson, et al.
Trends in Molecular Medicine|June 18, 2010
Therapeutic prospects for mitochondrial diseaseEric A Schon, Salvatore DiMauro, Michio Hirano, et al.
Nucleic Acids Research|February 11, 1993
Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELASY Koga, M Davidson, E A Schon, et al.
Molecular Biology of the Cell|September 16, 2003
New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reportersCarl D Gajewski, Lichuan Yang, Eric A Schon, et al.
Molecular and Cellular Biology|February 1, 1992
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 episodesM P King, Y Koga, M Davidson, et al.
International Reviews of Immunology|January 1, 1990
Dendritic cells in the respiratory tractP G Holt, M A Schon-Hegrad, P G McMenamin
Muscle & Nerve. Supplement|January 1, 1995
Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA(Leu(UUR)) geneY Koga, M Davidson, E A Schon, et al.
Genome Biology|June 29, 2022
Bookend: precise transcript reconstruction with end-guided assemblyMichael A Schon, Stefan Lutzmayer, Falko Hofmann, et al.
Biochemical and Biophysical Research Communications|March 15, 1988
Transthyretin is synthesized in the mammalian eyeR L Martone, J Herbert, A Dwork, et al.
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