Authors:
Gensler, S
Weber, K
Schmitt, WE
Perez-Martos, A
Enriquez, JA
Montoya, J
Wiesner, RJ
Citation: S. Gensler et al., Mechanism of mammalian mitochondrial DNA replication: import of mitochondrial transcription factor A into isolated mitochondria stimulates 7S DNA synthesis, NUCL ACID R, 29(17), 2001, pp. 3657-3663
Authors:
Ruiz-Pesini, E
Alvarez, E
Enriquez, JA
Lopez-Perez, MJ
Citation: E. Ruiz-pesini et al., Association between seminal plasma carnitine and sperm mitochondrial enzymatic activities, INT J ANDR, 24(6), 2001, pp. 335-340
Authors:
Chomyn, A
Enriquez, JA
Micol, V
Fernandez-Silva, P
Attardi, G
Citation: A. Chomyn et al., The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNA(Leu(UUR)) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes, J BIOL CHEM, 275(25), 2000, pp. 19198-19209
Authors:
Enriquez, JA
Cabezas-Herrera, J
Bayona-Bafaluy, MP
Attardi, G
Citation: Ja. Enriquez et al., Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells, J BIOL CHEM, 275(15), 2000, pp. 11207-11215
Authors:
Tiranti, V
Hoertnagel, K
Carrozzo, R
Galimberti, C
Munaro, M
Granatiero, M
Zelante, L
Gasparini, P
Marzella, R
Rocchi, M
Bayona-Bafaluy, MP
Enriquez, JA
Uziel, G
Bertini, E
Dionisi-Vici, C
Franco, B
Meitinger, T
Zeviani, M
Citation: V. Tiranti et al., Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency, AM J HU GEN, 63(6), 1998, pp. 1609-1621