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Selected Publications for Giuseppe Attardi
- Michikawa, Y., Mazzucchelli, F., Bresolin, N., Scarlato, G. and Attardi, G. 1999. Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication. Science 286, 774-779.
- Bai, Y., Shakeley, R. M. and Attardi, G. 2000. Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria. Mol. Cell Biol. 20, 805-815.
- Enriquez, J. A., Cabezas-Herrera, J., Bayona-Bafaluy, P. and Attardi, G. 2000. Very rare complementation between mitochondria carrying different mtDNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells. J. Biol. Chem. 275, 11207-11215.
- Chomyn, A., Enriquez, J. A., Micol, V., Fernandez-Silva, P. and Attardi, G. 2000. 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. J. Biol. Chem. 275, 19198-19209.
- Guan, M.-X., Fischel-Ghodsian, N. and Attardi, G. 2000. A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity. Hum. Mol. Genet. 9, 1787-1793.
- Villani, G. and Attardi, G. 2001. In vivo control of respiration by cytochrome c oxidase in human cells. Free Rad. Biol. Med., 29, 202-210.
- Hájek, P., Villani, G. and Attardi, G. 2000. Rate limiting step preceding cytochrome c release in cells primed for Fas-mediated apoptosis is revealed by cell sorting and respiration analysis. J. Biol. Chem. 276, 606-615.
- Puranam, R. S. and Attardi, G. 2001. The RNase P associated with HeLa cell mitochondria contains an RNA component identical in sequence to that of the nuclear RNaseP. Mol. Cell. Biol., 21, 548-556.
- Guan, M.-X., Fischel-Ghodsian, N. and Attardi, G. 2001. Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation. Human Mol. Genet. 10, 573-580.
- Wang, Y., Michikawa, Y., Mallidis, C., Bai, Y., Woodhouse, L., Yarasheski, K.E., Miller, C.A., Askanas, V., Engel, W.K., Bhasin, S., and Attardi, G. 2001. Muscles-specific mutations accumulte with aging in critical human mtDNA control sites for replication. Proc. Natl. Acad. Sci. USA, 98, 4022-4027.
