Sfoglia per Autore
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy.
2004 Carelli V.; Ghelli A.; Baracca A.; Zanna C.; Sgarbi G.; Solaini G.; Lenaz G.; Rugolo M.; Martinuzzi A.
Bioenergetic changes associated with the T8993G mutation of the mtDNA ATP6 gene.
2004 Baracca A.; Sgarbi G.; Lenaz G.; Carelli V.; Solaini G.
Increased state 4 mitochondrial respiration and swelling in early post-ischemic reperfusion of rat heart
2004 BOSETTI F.; BARACCA A.; LENAZ G.; SOLAINI G.
Biochemical analysis of respiratory function in cybrid cell lines harbouring mtDNA mutations
2004 PALLOTTI F.; BARACCA A.; HERNANDEZ-ROSA E.; WALKER W.F.; SOLAINI G.; LENAZ G.; MELZI D'ERIL G.V.; DIMAURO S.; SCHON E.A.; DAVIDSON M.
Mitochondrial quinone reductases: Complex I
2004 LENAZ G.; FATO R.; BARACCA A.; GENOVA M.L.
Bioenergetics of mitochondrial diseases associated with mtDNA mutations.
2004 Lenaz G.; Baracca A.; Carelli V.; D'Aurelio M.; Sgarbi G.; Solaini G.
Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration
2004 CARELLI V; RUGOLO M; SGARBI G; GHELLI A; ZANNA C; BARACCA A; LENAZ G; NAPOLI E; MARTINUZZI A; SOLAINI G.
Rhodamine 123 as a probe of mitochondrial membrane potential: Evaluation of proton flux through F0 during ATP synthesis
2004 Baracca A.; Sgarbi G.; Solaini G.; Lenaz G.
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma.
2005 Porcelli A.M.; Gasparre G.; Bonora E.; Ghelli A.; Iommarini L.; Biondi A.; Baracca A.; Rugolo M.; Lenaz G.; Romeo G.
mtDNA T>G mutation at the nt8993 of the ATP6 gene impairs the coupling mechanism of the F1F0-ATPase.
2005 Sgarbi G.; Baracca A.; Lenaz G.; Carelli V.; Solaini G.
Pathogenic role and biochemical dysfunctions associated with mtDNA ATP6 gene mutations.
2005 Solaini G.; Baracca A.; Sgarbi G.; Lenaz G.; Carelli V.
What can we learn from the study of the point mutations in the human mitochondrial ATP6 gene ?
2005 Solaini G.; Baracca A.; Sgarbi G.; Carelli V.; Lenaz G.
Severe impairment of Complex I-driven adenosine triphosphate synthesis in leber hereditarfy optic neuropathy cybrids
2005 Baracca A.; Solaini G.; Sgarbi G.; Lenaz G.; Baruzzi A.; Schapira A.H.; Martinuzzi A.; Carelli V.
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.
Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA
2006 Gianluca Sgarbi; Alessandra Baracca; Giorgio Lenaz; Lucia M. Valentino; Valerio Carelli; Giancarlo Solaini
New insights into structure and function of mitochondria and their role in aging and disease
2006 Lenaz G; Baracca A; Fato R; Genova ML; Solaini G.
Comparative bioenergetic studies of cells carrying the 8993T>G or 8993T>C mitochondrial DNA mutations.
2006 Sgarbi G.; Baracca A.; Mattiazzi M.; Carelli V.; Lenaz G.; Solaini G.
Biochemical dysfunction associated with mitochondrial DNA mutations at nt8993.
2006 Baracca A; Sgarbi G; Mattiazzi M; Casalena G; Lenaz G; Solaini G
Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation
2006 F. Squitieri; M. Cannella; G. Sgarbi; V. Maglione; A. Falleni; P. Lenzi; A. Baracca; G. Cislaghi; C. Saft; G. Ragona; M.A. Russo; L.M. Thompson; G. Solaini; F. Fornai
Mitochondrial Complex I: structure, function and implications in neurodegeneration
2006 Lenaz G.; Baracca A.; Fato R.; Genova M.L.; Solaini G.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. | Carelli V.; Ghelli A.; Baracca A.; Zanna C.; Sgarbi G.; Solaini G.; Lenaz G.; Rugolo M.; Martinuz...zi A. | 2004-01-01 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | - | 4.02 Riassunto (Abstract) | - |
| Bioenergetic changes associated with the T8993G mutation of the mtDNA ATP6 gene. | Baracca A.; Sgarbi G.; Lenaz G.; Carelli V.; Solaini G. | 2004-01-01 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | - | 4.02 Riassunto (Abstract) | - |
| Increased state 4 mitochondrial respiration and swelling in early post-ischemic reperfusion of rat heart | BOSETTI F.; BARACCA A.; LENAZ G.; SOLAINI G. | 2004-01-01 | FEBS LETTERS | - | 1.01 Articolo in rivista | - |
| Biochemical analysis of respiratory function in cybrid cell lines harbouring mtDNA mutations | PALLOTTI F.; BARACCA A.; HERNANDEZ-ROSA E.; WALKER W.F.; SOLAINI G.; LENAZ G.; MELZI D'ERIL G.V.;... DIMAURO S.; SCHON E.A.; DAVIDSON M. | 2004-01-01 | BIOCHEMICAL JOURNAL | - | 1.01 Articolo in rivista | - |
| Mitochondrial quinone reductases: Complex I | LENAZ G.; FATO R.; BARACCA A.; GENOVA M.L. | 2004-01-01 | - | Academic Press Incorporated | 2.01 Capitolo / saggio in libro | - |
| Bioenergetics of mitochondrial diseases associated with mtDNA mutations. | Lenaz G.; Baracca A.; Carelli V.; D'Aurelio M.; Sgarbi G.; Solaini G. | 2004-01-01 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | - | 1.01 Articolo in rivista | - |
| Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration | CARELLI V; RUGOLO M; SGARBI G; GHELLI A; ZANNA C; BARACCA A; LENAZ G; NAPOLI E; MARTINUZZI A; SOL...AINI G. | 2004-01-01 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | - | 1.01 Articolo in rivista | - |
| Rhodamine 123 as a probe of mitochondrial membrane potential: Evaluation of proton flux through F0 during ATP synthesis | Baracca A.; Sgarbi G.; Solaini G.; Lenaz G. | 2004-01-01 | BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | - | 1.01 Articolo in rivista | - |
| Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. | Porcelli A.M.; Gasparre G.; Bonora E.; Ghelli A.; Iommarini L.; Biondi A.; Baracca A.; Rugolo M.;... Lenaz G.; Romeo G. | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| mtDNA T>G mutation at the nt8993 of the ATP6 gene impairs the coupling mechanism of the F1F0-ATPase. | Sgarbi G.; Baracca A.; Lenaz G.; Carelli V.; Solaini G. | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Pathogenic role and biochemical dysfunctions associated with mtDNA ATP6 gene mutations. | Solaini G.; Baracca A.; Sgarbi G.; Lenaz G.; Carelli V. | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| What can we learn from the study of the point mutations in the human mitochondrial ATP6 gene ? | Solaini G.; Baracca A.; Sgarbi G.; Carelli V.; Lenaz G. | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Severe impairment of Complex I-driven adenosine triphosphate synthesis in leber hereditarfy optic neuropathy cybrids | Baracca A.; Solaini G.; Sgarbi G.; Lenaz G.; Baruzzi A.; Schapira A.H.; Martinuzzi A.; Carelli V. | 2005-01-01 | ARCHIVES OF NEUROLOGY | - | 1.01 Articolo in rivista | - |
| 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 | - |
| Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA | Gianluca Sgarbi; Alessandra Baracca; Giorgio Lenaz; Lucia M. Valentino; Valerio Carelli; Giancarl...o Solaini | 2006-01-01 | BIOCHEMICAL JOURNAL | - | 1.01 Articolo in rivista | - |
| New insights into structure and function of mitochondria and their role in aging and disease | Lenaz G; Baracca A; Fato R; Genova ML; Solaini G. | 2006-01-01 | ANTIOXIDANTS & REDOX SIGNALING | - | 1.01 Articolo in rivista | - |
| Comparative bioenergetic studies of cells carrying the 8993T>G or 8993T>C mitochondrial DNA mutations. | Sgarbi G.; Baracca A.; Mattiazzi M.; Carelli V.; Lenaz G.; Solaini G. | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Biochemical dysfunction associated with mitochondrial DNA mutations at nt8993. | Baracca A; Sgarbi G; Mattiazzi M; Casalena G; Lenaz G; Solaini G | 2006-01-01 | ITALIAN JOURNAL OF BIOCHEMISTRY | - | 4.02 Riassunto (Abstract) | - |
| Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation | F. Squitieri; M. Cannella; G. Sgarbi; V. Maglione; A. Falleni; P. Lenzi; A. Baracca; G. Cislaghi;... C. Saft; G. Ragona; M.A. Russo; L.M. Thompson; G. Solaini; F. Fornai | 2006-01-01 | MECHANISMS OF AGEING AND DEVELOPMENT | - | 1.01 Articolo in rivista | - |
| Mitochondrial Complex I: structure, function and implications in neurodegeneration | Lenaz G.; Baracca A.; Fato R.; Genova M.L.; Solaini G. | 2006-01-01 | ITALIAN JOURNAL OF BIOCHEMISTRY | - | 1.01 Articolo in rivista | - |
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