Michael P. King

Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by Complementation

Michael P. King, Giuseppe Attardi · Science · 1989 · 1.6K citations

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

Mitochondrial Myopathy, Strokelike Episodes, Mitochondrial Biogenesis +15

[27] Isolation of human cell lines lacking mitochondrial DNA

Michael P. King, Giuseppe Attardi · Methods in enzymology on CD-ROM/Methods in enzymology · 1996 · 354 citations

Dna, Mitochondrial Function, Genetics +7

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 · 349 citations

Mitochondrial Myopathy, Strokelike Episodes, Mitophagy +14

Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA

Michael P. King, Giuseppe Attardi · Cell · 1988 · 283 citations

Mitophagy, Dna, Genetics +16