Sfoglia per Autore
Mitochondrial optic neuropathies: how two genomes may kill the same cell type?
2007 Carelli V.; La Morgia C.; Iommarini L.; Carroccia R.; Mattiazzi M.; Sangiorgi S.; Farné S.; Maresca A.; Foscarini B.; Lanzi L.; Amadori M.; Bellan M.; Valentino M.L.
Screening of candidate nuclear genes for modifying role in Leber's hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase
2010 Maresca A; Tagliavini F; Sangiorgi S; Mendieta L; Amadori M; Salomao S; Carelli V
Retinal nerve fiber layer thickness in dominant optic atrophy: measurements by optical coherence tomography and correlation with age.
2011 Barboni P.; Savini G.; Parisi V.; Carbonelli M.; La Morgia C.; Maresca A.; Sadun F.; De Negri A.M.; Carta A.; Sadun A.A.; Carelli V.
Functional investigation of the mitochondrial protein OPA3
2011 Maresca A.; Vidoni S.; Zanna C.; Rugolo M.; Carelli V.; Lenaers G.; Delettre C
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
OPA3, a new regulator of mitochondrial fission?
2012 Maresca A; Zanna C; Vidoni S; Rugolo M; Amati-Bonneau P; Carelli V; Lenaers G; Delettre C
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.
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION
2013 Maresca A; Zanna C; Vidoni S; Rugolo M; Amati-Bonneau P; Carelli V; Lenaers G; Delettre C
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
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
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy.
2013 T. Pippucci; A. Parmeggiani; F. Palombo; A. Maresca; A. Angius; L. Crisponi; F. Cucca; R. Liguori; M. L. Valentino; M. Seri; V. Carelli
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy.
2013 Barboni P;Valentino ML;La Morgia C;Carbonelli M;Savini G;De Negri A;Simonelli F;Sadun F;Caporali L;Maresca A;Liguori R;Baruzzi A;Zeviani M;Carelli V
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number
2013 Gianluca Marucci;Alessandra Maresca;Leonardo Caporali;Anna Farnedi;Christine Margaret Betts;Luca Morandi;Dario de Biase;Serenella Cerasoli;Maria Pia Foschini;Elena Bonora;Michele Vidone;Giovanni Romeo;Elena Perli;Carla Giordano;Giulia d'Amati;Giuseppe Gasparre;Agostino Baruzzi;Valerio Carelli;Vincenzo Eusebi
The optic nerve: a "mito-window" on mitochondrial neurodegeneration.
2013 Maresca A; la Morgia C; Caporali L; Valentino ML; 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
Genetic Basis of Mitochondrial Optic Neuropathies.
2014 Maresca A;Caporali L;Strobbe D;Zanna C;Malavolta D;La Morgia C;Valentino ML;Carelli V
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
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations
2014 Maresca A; Zanna C; Del Dotto V; Caporali L; Moghadam KK; Pizza F; La Morgia C; Melberg A; Mignot E; Plazzi G; Carelli V
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
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated?
2015 Maresca, Alessandra; Zaffagnini, Mirko; Caporali, Leonardo; Carelli, Valerio; Zanna, Claudia
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
Mitochondrial optic neuropathies: how two genomes may kill the same cell type? | Carelli V.; La Morgia C.; Iommarini L.; Carroccia R.; Mattiazzi M.; Sangiorgi S.; Farné S.; Mares...ca A.; Foscarini B.; Lanzi L.; Amadori M.; Bellan M.; Valentino M.L. | 2007-01-01 | BIOSCIENCE REPORTS | - | 1.01 Articolo in rivista | - |
Screening of candidate nuclear genes for modifying role in Leber's hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase |
Maresca A; Tagliavini F; Sangiorgi S; Mendieta L; Amadori M; Salomao S; Carelli V |
2010-01-01 | MITOCHONDRION | - | 1.06 Abstract in rivista | - |
Retinal nerve fiber layer thickness in dominant optic atrophy: measurements by optical coherence tomography and correlation with age. | Barboni P.; Savini G.; Parisi V.; Carbonelli M.; La Morgia C.; Maresca A.; Sadun F.; De Negri A.M....; Carta A.; Sadun A.A.; Carelli V. | 2011-01-01 | OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
Functional investigation of the mitochondrial protein OPA3 | Maresca A.; Vidoni S.; Zanna C.; Rugolo M.; Carelli V.; Lenaers G.; Delettre C | 2011-01-01 | - | - | 4.02 Riassunto (Abstract) | - |
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 | - |
OPA3, a new regulator of mitochondrial fission? | Maresca A; Zanna C; Vidoni S; Rugolo M; Amati-Bonneau P; Carelli V; Lenaers G; Delettre C | 2012-01-01 | MITOCHONDRION | - | 1.06 Abstract in rivista | - |
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 | - |
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION | Maresca A; Zanna C; Vidoni S; Rugolo M; Amati-Bonneau P; Carelli V; Lenaers G; Delettre C | 2013-01-01 | - | - | 4.02 Riassunto (Abstract) | - |
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 | - |
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 |
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. |
T. Pippucci; A. Parmeggiani; F. Palombo; A. Maresca; A. Angius; L. Crisponi; F. Cucca; R. Liguor...i; M. L. Valentino; M. Seri; V. Carelli |
2013-01-01 | PLOS ONE | - | 1.01 Articolo in rivista | journal.pone.0082154.PDF |
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy. | Barboni P;Valentino ML;La Morgia C;Carbonelli M;Savini G;De Negri A;Simonelli F;Sadun F;Caporali ...L;Maresca A;Liguori R;Baruzzi A;Zeviani M;Carelli V | 2013-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number | Gianluca Marucci;Alessandra Maresca;Leonardo Caporali;Anna Farnedi;Christine Margaret Betts;Luca ...Morandi;Dario de Biase;Serenella Cerasoli;Maria Pia Foschini;Elena Bonora;Michele Vidone;Giovanni Romeo;Elena Perli;Carla Giordano;Giulia d'Amati;Giuseppe Gasparre;Agostino Baruzzi;Valerio Carelli;Vincenzo Eusebi | 2013-01-01 | HUMAN PATHOLOGY | - | 1.01 Articolo in rivista | - |
The optic nerve: a "mito-window" on mitochondrial neurodegeneration. | Maresca A; la Morgia C; Caporali L; Valentino ML; Carelli V | 2013-01-01 | MOLECULAR AND CELLULAR NEUROSCIENCES | - | 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 | - |
Genetic Basis of Mitochondrial Optic Neuropathies. | Maresca A;Caporali L;Strobbe D;Zanna C;Malavolta D;La Morgia C;Valentino ML;Carelli V | 2014-01-01 | CURRENT MOLECULAR MEDICINE | - | 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 | - |
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations | Maresca A; Zanna C; Del Dotto V; Caporali L; Moghadam KK; Pizza F; La Morgia C; Melberg A; Mignot... E; Plazzi G; Carelli V | 2014-01-01 | - | - | 4.02 Riassunto (Abstract) | - |
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 | - |
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? | Maresca, Alessandra; Zaffagnini, Mirko; Caporali, Leonardo; Carelli, Valerio; Zanna, Claudia | 2015-01-01 | FRONTIERS IN GENETICS | - | 1.01 Articolo in rivista | Dna Methyltransferase 1 Mutations and Mitochondrial Pathology.pdf |
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