FERRERO FORTUNATI, Iliana

FERRERO FORTUNATI, Iliana  

Dipartimento di Genetica, Biologia dei Microrganismi, Antropologia, Evoluzione (attivo dal 01/01/2003 al 25/07/2012)  

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A Klaac null mutant of Kluyveromyces lactis is complemented by a single copy of the Saccharomyces cerevisiae AAC1 gene 1-gen-1999 Viola, Anna Maria; Lodi, Tiziana; FERRERO FORTUNATI, Iliana
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy. Neuromuscul Disorders. 1-gen-2008 Galassi, G; Lamantea, E; Invernizzi, F; Tavani, F; Pisano, I; FERRERO FORTUNATI, Iliana; Palmieri, L; Zeviani, M.
Allelism of IMP1 and GAL2 genes of Saccharomyces cerevisiae 1-gen-1992 Donnini, Claudia; Lodi, Tiziana; FERRERO FORTUNATI, Iliana; Algeri, A. A.; Puglisi, Pier Paolo
Antimycin- and hydroxamate-insensitive respiration in yeast 1-gen-1985 Lodi, Tiziana; Viola, Am; Rossi, Carlo; FERRERO FORTUNATI, Iliana
Carbon catabolite repression in Kluyveromyces lactis: isolation and characterization of the KlDLD gene encoding the mitochondrial enzyme D-lactate ferricytochrome c oxidoreductase. 1-gen-1994 Lodi, Tiziana; Oconnor, D; Goffrini, Paola; FERRERO FORTUNATI, Iliana
Catabolite repression by galactose in overexpressed GAL4 strains of Saccharomyces cerevisiae 1-gen-1991 Lodi, Tiziana; Donnini, Claudia; FERRERO FORTUNATI, Iliana
Clinical and molecular features of mitochondrial DNA depletion syndromes. 1-gen-2008 Spinazzola, A; Invernizzi, F; Carrara, F; Lamantea, E; Donati, A; Dirocco, M; Giordano, I; MEZNARIC PETRUSA, M; Baruffini, E; FERRERO FORTUNATI, Iliana; Zeviani, M.
Clinical and molecular features of mitochondrial DNA depletion syndromes. 1-gen-2009 Spinazzola, A; Invernizzi, F; Carrara, F; Lamantea, E; Donati, A; Dirocco, M; Giordano, I; MEZNARIC PETRUSA, M; Baruffini, Enrico; FERRERO FORTUNATI, Iliana; Zeviani, M.
Cloning and characterization of the lactate-specific inducible gene KlCYB2, encoding the cytochrome b2 of Kluyveromyces lactis 1-gen-2000 Alberti, A.; Goffrini, Paola; FERRERO FORTUNATI, Iliana; Lodi, Tiziana
Comet assay application in environmental monitoring: DNA damage in human leukocytes and plant cells in comparison with bacterial and yeast cells. 1-gen-1999 Poli, Paola; Buschini, Annamaria; Restivo, Francesco Maria; A., Ficarelli; F., Cassoni; FERRERO FORTUNATI, Iliana; Rossi, Carlo
Comet assay application in environmental monitoring: DNA damage in human leukocytes and plant cells in comparison with bacterial and yeast tests 1-gen-1999 Poli, Paola; Buschini, Annamaria; Restivo, Francesco Maria; A., Ficarelli; F., Cassoni; FERRERO FORTUNATI, Iliana; Rossi, Carlo
COMMON POLG GENETIC VARIANTS INCREASE THERISK OF SODIUM VALPROATE INDUCED LIVER INJURYAND FAILURE 1-gen-2009 C. P., Day; J. D., Stewart; R., Horvath; R. J., Fontana; P. B., Watkins; S., Bulst; Baruffini, Enrico; FERRERO FORTUNATI, Iliana; P. F., Chinnery
Complementazione del mutante nullo in Klaac del lievito Kluyveromyces lactis con il gene AAC3 di Saaccharomyces cerevisiae 1-gen-2002 Fontanesi, F; DE FILIPPI, S; FERRERO FORTUNATI, Iliana; Viola, Am
Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy 1-gen-2005 Palmieri, L; Alberio, S.; Pisano, I; Lodi, Tiziana; MEZNARIC PETRUSA, M; Zidar, J; Santoro, A; Scarcia, P; Fontanesi, F; Lamantea, E; FERRERO FORTUNATI, Iliana; Zeviani, M.
Construction and validation of a yeast model system for studying in vivo the susceptibility to stavudine of DNA polymerase gamma allelic variants 1-gen-2009 Baruffini, Enrico; FERRERO FORTUNATI, Iliana; Lodi, Tiziana
Construction and validation of a yeast model system for studying in vivo the susceptibility to stavudine of Polg allelic variants 1-gen-2009 Baruffini, Enrico; FERRERO FORTUNATI, Iliana; Lodi, Tiziana
Construction of a yeast model system for studying in vivo susceptibility to stavudine of Polg allelic variants 1-gen-2010 Baruffini, Enrico; FERRERO FORTUNATI, Iliana; Lodi, Tiziana
Costruzione di un mutante imp2 termosensibile di Saccharomyces cerevisiae 1-gen-2001 Alberti, A; FERRERO FORTUNATI, Iliana; Donnini, Claudia
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 1-gen-2018 Garone, C; D'Souza, Ar; Dallabona, C; Lodi, T; Rebelo-Guiomar, P; Rorbach, J; Donati, A; Procopio, E; Montomoli, M; Guerrini, R; Zeviani, M; Calvo, S; Mootha, V; Dimauro, S; Ferrero, I; Minczuk, M
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 1-gen-2017 Garone, C; D'Souza, Ar; Dallabona, C; Lodi, T; Rebelo-Guiomar, P; Rorbach, J; Donati, Ma; Procopio, E; Montomoli, M; Guerrini, R; Zeviani, M; Calvo, Se; Mootha, Vk; Dimauro, S; Ferrero, I; Minczuk, M.