Attardi, Giuseppe

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation termination

Enriquez, J. A., Chomyn, A., & Attardi, G. (1995) · Nature Genetics

Mitochondrial Function and PathologyRNA and protein synthesis mechanisms

Cited by 285

Low Reserve of Cytochrome c Oxidase Capacity in Vivo in the Respiratory Chain of a Variety of Human Cell Types

Villani, G., Greco, M., Papa, S., & Attardi, G. (1998) · Journal of Biological Chemistry

Mitochondrial Function and PathologyCancer and biochemical research

Cited by 225

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes

Chomyn, A., Enriquez, J. A., Micol, V., Fernandez-Silva, P., & Attardi, G. (2000) · Journal of Biological Chemistry

RNA and protein synthesis mechanismsMitochondrial Function and Pathology

Cited by 197

Hypersensitivity to oxygen and shortened lifespan in a Drosophila mitochondrial complex II mutant

Walker, D. W., Hájek, P., Muffat, J., Knoepfle, D., Cornelison, S., Attardi, G., & Benzer, S. (2006) · Proceedings of the National Academy of Sciences

Mitochondrial Function and PathologyGenetics, Aging, and Longevity in Model Organisms

Cited by 105

Search for differences in post-transcriptional modification patterns of mitochondrial DNA-encoded wild-type and mutant human tRNALys and tRNALeu(UUR)

Helm, M., Florentz, C., Chomyn, A., & Attardi, G. (1999) · Nucleic Acids Research

RNA modifications and cancerRNA and protein synthesis mechanisms

Cited by 99