Giordano, L; Deceglie, S; D'Adamo, P; Valentino, M L; La Morgia, C; Fracasso, F; Roberti, M; Cappellari, M; Petrosillo, G; Ciaravolo, S; Parente, D; Giordano, C; Maresca, A; Iommarini, L; Del Dotto, V; Ghelli, A M; Salomao, S R; Berezovsky, A; Belfort, R; Sadun, A A; Carelli, V; Loguercio Polosa, P; Cantatore, P, Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways, «CELL DEATH & DISEASE», 2015, 6, Article number: e2021, pp. 1 - 10 [articolo]Open Access
Torraco, Alessandra; Peralta, Susana; Iommarini, Luisa; Diaz, Francisca, Mitochondrial diseases part I: Mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factors, «MITOCHONDRION», 2015, 21, pp. 76 - 91 [articolo]
Iommarini, Luisa; Peralta, Susana; Torraco, Alessandra; Diaz, Francisca, Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function, «MITOCHONDRION», 2015, 22, pp. 96 - 118 [articolo]
Peralta, Susana; Torraco, Alessandra; Iommarini, Luisa; Diaz, Francisca, Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficiencies, «MITOCHONDRION», 2015, 23, pp. 71 - 80 [articolo]
Carelli, V.; Musumeci, O.; Caporali, L.; Zanna, C.; La Morgia, C.; Del Dotto, V.; Porcelli, A.M.; Rugolo, M.; Valentino, M.L.; Iommarini, L.; Maresca, A.; Barboni, P.; Carbonelli, M.; Trombetta, C.; Valente, E.M.; Patergnani, S.; Giorgi, C.; Pinton, P.; Rizzo, G.; Tonon, C.; Lodi, R.; Avoni, P.; Liguori, R.; Baruzzi, A.; Toscano, A.; Zeviani, M., Syndromic parkinsonism and dementia associated with OPA1 missense mutations, «ANNALS OF NEUROLOGY», 2015, 78, pp. 21 - 38 [articolo]Open Access
Pisano, Annalinda; Preziuso, Carmela; Iommarini, Luisa; Perli, Elena; Grazioli, Paola; Campese, Antonio F; Maresca, Alessandra; Montopoli, Monica; Masuelli, Laura; Sadun, Alfredo A; D'Amati, Giulia; Carelli, Valerio; Ghelli, Anna; Giordano, Carla, Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy, «HUMAN MOLECULAR GENETICS», 2015, 24, pp. 6921 - 6931 [articolo]
Vatrinet R;Iommarini L;Kurelac I;De Luise M;Gasparre G;Porcelli AM, Targeting respiratory complex I to prevent the Warburg effect., «THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY», 2015, 63, pp. 41 - 45 [articolo]
Carossa V;Ghelli A;Tropeano CV;Valentino ML;Iommarini L;Maresca A;Caporali L;Morgia CL;Liguori R;Barboni P;Carbonelli M;Rizzo G;Tonon C;Lodi R;Martinuzzi A;Nardo VD;Rugolo M;Ferretti L;Gandini F;Pala M;Achilli A;Olivieri A;Torroni A;Carelli V, A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance., «HUMAN MUTATION», 2014, 35, pp. 954 - 958 [articolo]
Clara Musicco;Antonella Cormio;Maria Antonietta Calvaruso;Luisa Iommarini;Giuseppe Gasparre;Anna Maria Porcelli;Anna Maria Timperio;Lello Zolla;Maria Nicola Gadaleta, Analysis of Mitochondrial Proteome of Cybrid Cells Harbouring a Truncative Mitochondrial DNA Mutation in Respiratory Complex I, «MOLECULAR BIOSYSTEMS», 2014, 10, pp. 1313 - 1319 [articolo]
L. Iommarini;I. Kurelac;M. Capristo;M. A. Calvaruso;V. Giorgio;C. Bergamini;A. Ghelli;P. Nanni;C. De Giovanni;V. Carelli;R. Fato;P. L. Lollini;M. Rugolo;G. Gasparre;A. M. Porcelli, Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment, «HUMAN MOLECULAR GENETICS», 2014, 23, pp. 1453 - 1466 [articolo]
Giordano C;Iommarini L;Giordano L;Maresca A;Pisano A;Valentino ML;Caporali L;Liguori R;Deceglie S;Roberti M;Fanelli F;Fracasso F;Ross-Cisneros FN;D'Adamo P;Hudson G;Pyle A;Yu-Wai-Man P;Chinnery PF;Zeviani M;Salomao SR;Berezovsky A;Belfort R Jr;Ventura DF;Moraes M;Moraes Filho M;Barboni P;Sadun F;De Negri A;Sadun AA;Tancredi A;Mancini M;d'Amati G;Loguercio Polosa P;Cantatore P;Carelli V, Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy., «BRAIN», 2014, 137, pp. 335 - 353 [articolo]
Iommarini L.; Calvaruso M.A.; Kurelac I.; Gasparre G.; Porcelli A.M., Complex I impairment in mitochondrial diseases and cancer: parallel roads leading to different outcomes., «THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY», 2013, 45(1), pp. 47 - 63 [articolo]
Caporali L;Ghelli AM;Iommarini L;Maresca A;Valentino ML;La Morgia C;Liguori R;Zanna C;Barboni P;De Nardo V;Martinuzzi A;Rizzo G;Tonon C;Lodi R;Calvaruso MA;Cappelletti M;Porcelli AM;Achilli A;Pala M;Torroni A;Carelli V, Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions., «BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE», 2013, 1832, pp. 445 - 452 [articolo]
Bartoletti-Stella A;Mariani E;Kurelac I;Maresca A;Caratozzolo MF;Iommarini L;Carelli V;Eusebi LH;Guido A;Cenacchi G;Fuccio L;Rugolo M;Tullo A;Porcelli AM;Gasparre G, Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α., «CELL DEATH & DISEASE», 2013, 4, Article number: e663, pp. 1 - 11 [articolo]Open Access
Mancini C;Roncaglia P;Brussino A;Stevanin G;Lo Buono N;Krmac H;Maltecca F;Gazzano E;Bartoletti Stella A;Calvaruso MA;Iommarini L;Cagnoli C;Forlani S;Le Ber I;Durr A;Brice A;Ghigo D;Casari G;Porcelli AM;Funaro A;Gasparre G;Gustincich S;Brusco A, Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways., «BMC MEDICAL GENOMICS», 2013, 6, pp. 22 - 32 [articolo]Open Access
