Sfoglia per Autore
The energetic failure caused by severe mutations in the mitochondrial genome is not rescued by Bcl-2 overexpression
2006 M. Hoque; A. M. Porcelli; A. Ghelli; L. Iommarini; M. Rugolo
Cybrids with mtDNA mutations causing Leber’s hereditary optic neuropathy are sensitized to apoptotic death induced by a mitochondrial oxidative stress
2006 A. M. Ghelli; C. Zanna; V. Carelli; A. Martinuzzi; M. Rugolo
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation
2006 C. Zanna; A. Ghelli; A. M.Porcelli; M. Karbowski; R.J. Youle; V. Carelli; M. Rugolo
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III
2006 BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G.
Effect of bcl-2 on the oxidative phosphorylation efficiency of cells with defective respiratory complex I.
2007 A.M. Porcelli ; A. Ghelli; L. Iommarini; G. Gasparre; M. Hoque; M. Rugolo
Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations.
2007 C. Zanna; A. Ghelli; A.M. Porcelli ; S. Vidoni; V. Carelli; M. Rugolo:
Dominant Optic Atrophy (DOA) and Sensorineural Hearing Loss: Clinical, Biochemical, Spectroscopic and Molecular Genetic Study of a Large Italian Pedigree Linked to a New Locus on Chromosome 16
2007 V. Carelli; S. Schimpf; M. L. Valentino; N. Fuhrmann; M. Papke; S. Schaich; S. Tippmann; B. Baumann; P. Barboni; A. Ghelli; L. Bucchi; R. Lodi; B. Barbiroli; R. Liguori; R. Carroccia; M. Villanova; P. Montagna; A. Baruzzi; B. Wissinger
OPA1 directly interacts with respiratory complexes and AIF.
2007 S. Vidoni; C. Zanna; A. Ghelli; A.M. Porcelli; V. Carelli; M. Rugolo
Green Tea Modulates Alpha-1-Adrenergic Stimulated Glucose Transport in Cultured Rat Cardiomyocytes
2007 C. Angeloni; T. Maraldi; A. Ghelli; M. Rugolo; E. Leoncini; G. Hakim; S. Hrelia
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours.
2007 Gasparre G.; Porcelli A.M.; Bonora E.; Pennisi L.F.; Toller M.; Iommarini L.; Ghelli A.; Moretti M.; Betts C.M.; Martinelli G.N.; Ceroni A.R.; Curcio F.; Carelli V.; Rugolo M.; Tallini G.; Romeo G.
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I.
2008 Porcelli A.M.; Ghelli A.; Iommarini L.; Mariani E.; Hoque M.; Zanna C.; Gasparre G.; Rugolo M.
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion.
2008 Zanna C.; Ghelli A.; Porcelli A.M.; Karbowski M.; Youle R.J.; Schimpf S.; Wissinger B.; Pinti M.; Cossarizza A.; Vidoni S.; Valentino M.L.; Rugolo M.; Carelli V.
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids.
2008 Ghelli A.; Porcelli A.M.; Zanna C.; Martinuzzi A.; Carelli V.; Rugolo M.
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells.
2009 G.Gasparre; L. Iommarini; A.M. Porcelli; M. Lang; G.G. Ferri; I.Kurelac; E. Mariani; L.F. Pennisi; E. Pasquini; G. Pasquinelli; A. Ghelli; E. Bonora; C. Ceccarelli; M. Rugolo; N. Salfi; G. Romeo; V. Carelli.
Modelling ND subunits of complex I: Leber’s Hereditary Optic Neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype-phenotype correlation
2009 Iommarini L.; Martelli P.L.; Ghelli A.; Rugolo M.; Casadio R.; Carelli V.
The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.
2009 Ghelli A.; Porcelli A.M.; Zanna C.; Vidoni S.; Mattioli S.; Barbieri A.; Iommarini L.; Pala M.; Achilli A.; Torroni A.; Rugolo M.; Carelli V.
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels
2009 A. M. Porcelli; A. Angelin; A. Ghelli; E. Mariani; A. Martinuzzi; V. Carelli; V. Petronilli; P. Bernardi; M. Rugolo
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization
2010 A.M.Porcelli ;A. Ghelli ;C. Ceccarelli ;M. Lang ;G. Cenacchi ; M.Capristo ;L.F. Pennisi ; I.Morra; E.Ciccarelli ; A.Melcarne ; A.;Bartoletti-Stella; N .Salfi ; G.Tallini ; A.Martinuzzi ; V.Carelli ; M.Attimonelli ; M.Rugolo ;G. Romeo ; G.Gasparre .
Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.
2011 Giordano C.; Montopoli M.; Perli E.; Orlandi M.; Fantin M.; Ross-Cisneros F.N.; Caparrotta L.; Martinuzzi A.; Ragazzi E.; Ghelli A.; Sadun A.A.; d'Amati G.; Carelli V.
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
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| The energetic failure caused by severe mutations in the mitochondrial genome is not rescued by Bcl-2 overexpression | M. Hoque; A. M. Porcelli; A. Ghelli; L. Iommarini; M. Rugolo | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Cybrids with mtDNA mutations causing Leber’s hereditary optic neuropathy are sensitized to apoptotic death induced by a mitochondrial oxidative stress | A. M. Ghelli; C. Zanna; V. Carelli; A. Martinuzzi; M. Rugolo | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation | C. Zanna; A. Ghelli; A. M.Porcelli; M. Karbowski; R.J. Youle; V. Carelli; M. Rugolo | 2006-01-01 | - | s. n. | 4.02 Riassunto (Abstract) | - |
| Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III | BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; ...MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G. | 2006-01-01 | CANCER RESEARCH | - | 1.01 Articolo in rivista | - |
| Effect of bcl-2 on the oxidative phosphorylation efficiency of cells with defective respiratory complex I. | A.M. Porcelli ; A. Ghelli; L. Iommarini; G. Gasparre; M. Hoque; M. Rugolo | 2007-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations. | C. Zanna; A. Ghelli; A.M. Porcelli ; S. Vidoni; V. Carelli; M. Rugolo: | 2007-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Dominant Optic Atrophy (DOA) and Sensorineural Hearing Loss: Clinical, Biochemical, Spectroscopic and Molecular Genetic Study of a Large Italian Pedigree Linked to a New Locus on Chromosome 16 | V. Carelli; S. Schimpf; M. L. Valentino; N. Fuhrmann; M. Papke; S. Schaich; S. Tippmann; B. Bauma...nn; P. Barboni; A. Ghelli; L. Bucchi; R. Lodi; B. Barbiroli; R. Liguori; R. Carroccia; M. Villanova; P. Montagna; A. Baruzzi; B. Wissinger | 2007-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| OPA1 directly interacts with respiratory complexes and AIF. | S. Vidoni; C. Zanna; A. Ghelli; A.M. Porcelli; V. Carelli; M. Rugolo | 2007-01-01 | - | University residential centre | 4.02 Riassunto (Abstract) | - |
| Green Tea Modulates Alpha-1-Adrenergic Stimulated Glucose Transport in Cultured Rat Cardiomyocytes | C. Angeloni; T. Maraldi; A. Ghelli; M. Rugolo; E. Leoncini; G. Hakim; S. Hrelia | 2007-01-01 | JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY | - | 1.01 Articolo in rivista | - |
| Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. | Gasparre G.; Porcelli A.M.; Bonora E.; Pennisi L.F.; Toller M.; Iommarini L.; Ghelli A.; Moretti ...M.; Betts C.M.; Martinelli G.N.; Ceroni A.R.; Curcio F.; Carelli V.; Rugolo M.; Tallini G.; Romeo G. | 2007-01-01 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | - | 1.01 Articolo in rivista | - |
| The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. | Porcelli A.M.; Ghelli A.; Iommarini L.; Mariani E.; Hoque M.; Zanna C.; Gasparre G.; Rugolo M. | 2008-01-01 | CELLULAR AND MOLECULAR LIFE SCIENCES | - | 1.01 Articolo in rivista | - |
| OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. | Zanna C.; Ghelli A.; Porcelli A.M.; Karbowski M.; Youle R.J.; Schimpf S.; Wissinger B.; Pinti M.;... Cossarizza A.; Vidoni S.; Valentino M.L.; Rugolo M.; Carelli V. | 2008-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
| Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. | Ghelli A.; Porcelli A.M.; Zanna C.; Martinuzzi A.; Carelli V.; Rugolo M. | 2008-01-01 | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | - | 1.01 Articolo in rivista | - |
| An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. | G.Gasparre; L. Iommarini; A.M. Porcelli; M. Lang; G.G. Ferri; I.Kurelac; E. Mariani; L.F. Pennisi...; E. Pasquini; G. Pasquinelli; A. Ghelli; E. Bonora; C. Ceccarelli; M. Rugolo; N. Salfi; G. Romeo; V. Carelli. | 2009-01-01 | HUMAN MUTATION | - | 1.01 Articolo in rivista | - |
| Modelling ND subunits of complex I: Leber’s Hereditary Optic Neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype-phenotype correlation | Iommarini L.; Martelli P.L.; Ghelli A.; Rugolo M.; Casadio R.; Carelli V. | 2009-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. | Ghelli A.; Porcelli A.M.; Zanna C.; Vidoni S.; Mattioli S.; Barbieri A.; Iommarini L.; Pala M.; A...chilli A.; Torroni A.; Rugolo M.; Carelli V. | 2009-01-01 | PLOS ONE | - | 1.01 Articolo in rivista | journal.pone.0007922.PDF |
| Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels | A. M. Porcelli; A. Angelin; A. Ghelli; E. Mariani; A. Martinuzzi; V. Carelli; V. Petronilli; P. B...ernardi; M. Rugolo | 2009-01-01 | THE JOURNAL OF BIOLOGICAL CHEMISTRY | - | 1.01 Articolo in rivista | - |
| The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization | A.M.Porcelli ;A. Ghelli ;C. Ceccarelli ;M. Lang ;G. Cenacchi ; M.Capristo ;L.F. Pennisi ; I.Morra...; E.Ciccarelli ; A.Melcarne ; A.;Bartoletti-Stella; N .Salfi ; G.Tallini ; A.Martinuzzi ; V.Carelli ; M.Attimonelli ; M.Rugolo ;G. Romeo ; G.Gasparre . | 2010-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy. | Giordano C.; Montopoli M.; Perli E.; Orlandi M.; Fantin M.; Ross-Cisneros F.N.; Caparrotta L.; Ma...rtinuzzi A.; Ragazzi E.; Ghelli A.; Sadun A.A.; d'Amati G.; Carelli V. | 2011-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
| 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 | - |
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