Sfoglia per Autore
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function
2011 Gasparre G; Kurelac I; Capristo M; Iommarini L; Ghelli A; Ceccarelli C; Nicoletti G; Nanni P; De Giovanni C; Scotlandi K; Betts CM; Carelli V; Lollini PL; Romeo G; Rugolo M; Porcelli AM
Mitochondrial complex I and cell death: a semi-automatic shogun model
2011 Gonzalez-Halphen D; Ghelli A; Iommarini L; Carelli V; Degli Esposti M
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.
2011 Carelli V.; Schimpf S.; Fuhrmann N.; Valentino M.L.; Zanna C.; Iommarini L.; Papke M.; Schaich S.; Tippmann S.; Baumann B.; Barboni P.; Longanesi L.; Rugolo M.; Ghelli A.; Alavi M.V.; Youle R.J.; Bucchi L.; Carroccia R.; Giannoccaro M.P.; Tonon C.; Lodi R.; Cenacchi G.; Montagna P.; Liguori R.; Wissinger B.
Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance
2012 Leonardo Caporali;Carla Giordano;Luisa Iommarini;Alessandra Maresca;Pio D'adamo;Solange R. Salomao;Rubens Belfort;Alfredo Sadun;Valerio Carelli
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy.
2012 Achilli A.; Iommarini L.; Olivieri A.; Pala M.; Hooshiar Kashani B.; Reynier P.; La Morgia C.; Valentino M.L.; Liguori R.; Pizza F.; Barboni P.; Sadun F.; De Negri A.M.; Zeviani M.; Dollfus H.; Moulignier A.; Ducos G.; Orssaud C.; Bonneau D.; Procaccio V.; Leo-Kottler B.; Fauser S.; Wissinger B.; Amati-Bonneau P.; Torroni A.; Carelli V.
Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies
2012 Iommarini L.; Maresca A.; Caporali L.; Valentino M.L.; Liguori R.; Giordano C.; Carelli V.
Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder
2012 Ghelli A.; Tropeano C.V.; Calvaruso M.A.; Marchesini A.; Iommarini L.; Porcelli A.M.; Zanna C.; Gasparre G.; Kurelac I.; De Nardo V.; Martinuzzi A.; Vissing J.; Selamoglu N.; Daldal F.; Rugolo M.
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α.
2013 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
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells
2013 Calabrese C.; Iommarini L.; Kurelac I.; Calvaruso M.A.; Capristo M.; Lollini P.L.; Nanni P.; Bergamini C.; Nicoletti G.; De Giovanni C.; Ghelli A.; Giorgio V.; Caratozzolo M.F.; Marzano F.; Manzari C.; Betts C.M.; Carelli V.; Ceccarelli C.; Attimonelli M.; Romeo G.; Fato R.; Rugolo M.; Tullo A.; Gasparre G.; Porcelli A.M.
Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways.
2013 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
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes
2013 Ghelli A.; Tropeano C.V.; Calvaruso M.A.; Marchesini A.; Iommarini L.; Porcelli A.M.; Zanna C.; De Nardo V.; Martinuzzi A.; Wibrand F.; Vissing J.; Kurelac I.; Gasparre G.; Selamoglu N.; Daldal F.; Rugolo M.
Complex I impairment in mitochondrial diseases and cancer: parallel roads leading to different outcomes.
2013 Iommarini L.; Calvaruso M.A.; Kurelac I.; Gasparre G.; Porcelli A.M.
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions.
2013 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
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment
2014 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
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance.
2014 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
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.
2014 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
Analysis of Mitochondrial Proteome of Cybrid Cells Harbouring a Truncative Mitochondrial DNA Mutation in Respiratory Complex I
2014 Clara Musicco;Antonella Cormio;Maria Antonietta Calvaruso;Luisa Iommarini;Giuseppe Gasparre;Anna Maria Porcelli;Anna Maria Timperio;Lello Zolla;Maria Nicola Gadaleta
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways
2015 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
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy
2015 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
Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function
2015 Iommarini, Luisa; Peralta, Susana; Torraco, Alessandra; Diaz, Francisca
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function | Gasparre G; Kurelac I; Capristo M; Iommarini L; Ghelli A; Ceccarelli C; Nicoletti G; Nanni P; De ...Giovanni C; Scotlandi K; Betts CM; Carelli V; Lollini PL; Romeo G; Rugolo M; Porcelli AM | 2011-01-01 | CANCER RESEARCH | - | 1.01 Articolo in rivista | - |
| Mitochondrial complex I and cell death: a semi-automatic shogun model | Gonzalez-Halphen D; Ghelli A; Iommarini L; Carelli V; Degli Esposti M | 2011-01-01 | CELL DEATH & DISEASE | - | 1.01 Articolo in rivista | cddis2011107.pdf |
| A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. | Carelli V.; Schimpf S.; Fuhrmann N.; Valentino M.L.; Zanna C.; Iommarini L.; Papke M.; Schaich S....; Tippmann S.; Baumann B.; Barboni P.; Longanesi L.; Rugolo M.; Ghelli A.; Alavi M.V.; Youle R.J.; Bucchi L.; Carroccia R.; Giannoccaro M.P.; Tonon C.; Lodi R.; Cenacchi G.; Montagna P.; Liguori R.; Wissinger B. | 2011-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance | Leonardo Caporali;Carla Giordano;Luisa Iommarini;Alessandra Maresca;Pio D'adamo;Solange R. Saloma...o;Rubens Belfort;Alfredo Sadun;Valerio Carelli | 2012-01-01 | MITOCHONDRION | - | 1.06 Abstract in rivista | - |
| Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy. | Achilli A.; Iommarini L.; Olivieri A.; Pala M.; Hooshiar Kashani B.; Reynier P.; La Morgia C.; Va...lentino M.L.; Liguori R.; Pizza F.; Barboni P.; Sadun F.; De Negri A.M.; Zeviani M.; Dollfus H.; Moulignier A.; Ducos G.; Orssaud C.; Bonneau D.; Procaccio V.; Leo-Kottler B.; Fauser S.; Wissinger B.; Amati-Bonneau P.; Torroni A.; Carelli V. | 2012-01-01 | PLOS ONE | - | 1.01 Articolo in rivista | pone.0042242.pdf; pone.0042242.s001.pdf; pone.0042242.s002.pdf; pone.0042242.s003.pdf; pone.0042242.s004.pdf; pone.0042242.s005.pdf; pone.0042242.s006.pdf |
| Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies | Iommarini L.; Maresca A.; Caporali L.; Valentino M.L.; Liguori R.; Giordano C.; Carelli V. | 2012-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder | Ghelli A.; Tropeano C.V.; Calvaruso M.A.; Marchesini A.; Iommarini L.; Porcelli A.M.; Zanna C.; G...asparre G.; Kurelac I.; De Nardo V.; Martinuzzi A.; Vissing J.; Selamoglu N.; Daldal F.; Rugolo M. | 2012-01-01 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | - | 4.02 Riassunto (Abstract) | - |
| Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. | 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 | 2013-01-01 | CELL DEATH & DISEASE | - | 1.01 Articolo in rivista | cddis2013187.pdf |
| Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells | Calabrese C.; Iommarini L.; Kurelac I.; Calvaruso M.A.; Capristo M.; Lollini P.L.; Nanni P.; Berg...amini C.; Nicoletti G.; De Giovanni C.; Ghelli A.; Giorgio V.; Caratozzolo M.F.; Marzano F.; Manzari C.; Betts C.M.; Carelli V.; Ceccarelli C.; Attimonelli M.; Romeo G.; Fato R.; Rugolo M.; Tullo A.; Gasparre G.; Porcelli A.M. | 2013-01-01 | CANCER & METABOLISM | - | 1.01 Articolo in rivista | Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells.pdf; Electronic supplementary material.zip |
| Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways. | Mancini C;Roncaglia P;Brussino A;Stevanin G;Lo Buono N;Krmac H;Maltecca F;Gazzano E;Bartoletti St...ella 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 | 2013-01-01 | BMC MEDICAL GENOMICS | - | 1.01 Articolo in rivista | 1755-8794-6-22.pdf |
| The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes | Ghelli A.; Tropeano C.V.; Calvaruso M.A.; Marchesini A.; Iommarini L.; Porcelli A.M.; Zanna C.; D...e Nardo V.; Martinuzzi A.; Wibrand F.; Vissing J.; Kurelac I.; Gasparre G.; Selamoglu N.; Daldal F.; Rugolo M. | 2013-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| Complex I impairment in mitochondrial diseases and cancer: parallel roads leading to different outcomes. | Iommarini L.; Calvaruso M.A.; Kurelac I.; Gasparre G.; Porcelli A.M. | 2013-01-01 | THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY | - | 1.01 Articolo in rivista | - |
| Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. | Caporali L;Ghelli AM;Iommarini L;Maresca A;Valentino ML;La Morgia C;Liguori R;Zanna C;Barboni P;D...e Nardo V;Martinuzzi A;Rizzo G;Tonon C;Lodi R;Calvaruso MA;Cappelletti M;Porcelli AM;Achilli A;Pala M;Torroni A;Carelli V | 2013-01-01 | BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE | - | 1.01 Articolo in rivista | - |
| Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment | 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 | 2014-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. | 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 | 2014-01-01 | HUMAN MUTATION | - | 1.01 Articolo in rivista | - |
| Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. | 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 | 2014-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
| Analysis of Mitochondrial Proteome of Cybrid Cells Harbouring a Truncative Mitochondrial DNA Mutation in Respiratory Complex I | Clara Musicco;Antonella Cormio;Maria Antonietta Calvaruso;Luisa Iommarini;Giuseppe Gasparre;Anna ...Maria Porcelli;Anna Maria Timperio;Lello Zolla;Maria Nicola Gadaleta | 2014-01-01 | MOLECULAR BIOSYSTEMS | - | 1.01 Articolo in rivista | - |
| Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways | Giordano, L; Deceglie, S; D'Adamo, P; Valentino, M L; La Morgia, C; Fracasso, F; Roberti, M; Capp...ellari, 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 | 2015-01-01 | CELL DEATH & DISEASE | - | 1.01 Articolo in rivista | Cigarette toxicity triggers Leber's hereditary optic neuropathy.pdf; Supplementary information.zip |
| Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy | Pisano, Annalinda; Preziuso, Carmela; Iommarini, Luisa; Perli, Elena; Grazioli, Paola; Campese, A...ntonio F; Maresca, Alessandra; Montopoli, Monica; Masuelli, Laura; Sadun, Alfredo A; D'Amati, Giulia; Carelli, Valerio; Ghelli, Anna; Giordano, Carla | 2015-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function | Iommarini, Luisa; Peralta, Susana; Torraco, Alessandra; Diaz, Francisca | 2015-01-01 | MITOCHONDRION | - | 1.01 Articolo in rivista | - |
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