ZANNA, CLAUDIA

ZANNA, CLAUDIA  

DIPARTIMENTO DI SCIENZE BIOMEDICHE E NEUROMOTORIE  

Ricercatori a tempo determinato  

Risultati 1 - 20 di 55 (tempo di esecuzione: 0.136 secondi).
Titolo Autore(i) Anno Periodico Editore Tipo File
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 -
AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations A.M.Porcelli; C. Zanna; A. Montanaro; V.Carelli; A.Ghelli; M.Rugolo 2004-01-01 - s.n 4.02 Riassunto (Abstract) -
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.; Gasparre 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) -
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 -
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance A.M. PORCELLI; A. GHELLI; C. ZANNA; P. VALENTE; S. FERRONI; M. RUGOLO 2004-01-01 CELL DEATH AND DIFFERENTIATION - 1.01 Articolo in rivista -
ATP depletion and caspase independent death of cybrids bearing Leber's Hereditary Optic neuropathy MTDNA mutations incubated in galactose medium. A model for endonuclease G-mediated apoptosis A. Ghelli; C. Zanna; A.M. Porcelli; V. Carelli; M. Rugolo 2004-01-01 - Dipartimento Biologia Ev. SP. 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.; Achilli A.; Torroni A.; Rugolo M.; Carelli V. 2009-01-01 PLOS ONE - 1.01 Articolo in rivista journal.pone.0007922.PDF
'Behr syndrome' with OPA1 compound heterozygote mutations Carelli, Valerio; Sabatelli, Mario; Carrozzo, Rosalba; Rizza, Teresa; Schimpf, Simone; Wissinger, Bernd; Zanna, Claudia; Rugolo, Michela; La Morgia, Chiara; Caporali, Leonardo; Carbonelli, Michele; Barboni, Piero; Tonon, Caterina; Lodi, Raffaele; Bertini, Enrico 2015-01-01 BRAIN - 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; SOLAINI G. 2004-01-01 BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - 1.01 Articolo in rivista -
Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G. ZANNA C.; GHELLI A.; PORCELLI AM.; MARTINUZZI A.; Carelli V.; RUGOLO M. 2005-01-01 APOPTOSIS - 1.01 Articolo in rivista -
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations C.Zanna; A.M.Porcelli; A.Ghelli; V.Carelli; A.Martinuzzi; M.Rugolo 2004-01-01 - s.n 4.02 Riassunto (Abstract) -
Coenzyme Q biosynthesis inhibition induces HIF-1α stabilization and metabolic switch toward glycolysis Liparulo, Irene; Bergamini, Christian; Bortolus, Marco; Calonghi, Natalia; Gasparre, Giuseppe; Kurelac, Ivana; Masin, Luca; Rizzardi, Nicola; Rugolo, Michela; Wang, Wenping; Aleo, Serena J; Kiwan, Alisar; Torri, Cristian; Zanna, Claudia; Fato, Romana 2021-01-01 THE FEBS JOURNAL - 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;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 2013-01-01 BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE - 1.01 Articolo in rivista -
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) -
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models Del Dotto, Valentina; Fogazza, Mario; Musiani, Francesco; Maresca, Alessandra; Aleo, Serena J.; Caporali, Leonardo; La Morgia, Chiara; Nolli, Cecilia; Lodi, Tiziana; Goffrini, Paola; Chan, David; Carelli, Valerio; Rugolo, Michela; Baruffini, Enrico; Zanna, Claudia* 2018-01-01 BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE - 1.01 Articolo in rivista 56_2018_DelDotto_BBAMolBasisDisease.pdf
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) -
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
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism Maresca, Alessandra; Del Dotto, Valentina; Capristo, Mariantonietta; Scimonelli, Emanuela; Tagliavini, Francesca; Morandi, Luca; Tropeano, Concetta Valentina; Caporali, Leonardo; Mohamed, Susan; Roberti, Marina; Scandiffio, Letizia; Zaffagnini, Mirko; Rossi, Jacopo; Cappelletti, Martina; Musiani, Francesco; Contin, Manuela; Riva, Roberto; Liguori, Rocco; Pizza, Fabio; La Morgia, Chiara; Antelmi, Elena; Polosa, Paola Loguercio; Mignot, Emmanuel; Zanna, Claudia; Plazzi, Giuseppe; Carelli, Valerio 2020-01-01 HUMAN MOLECULAR GENETICS ONLINE - 1.01 Articolo in rivista ddaa014.pdfsupplementary_materials_rev_ddaa014.docx
Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics M.Rugolo; C.Zanna; A.Ghelli; A.M.Porcelli; V.Carelli 2005-01-01 ITALIAN JOURNAL OF BIOCHEMISTRY - 4.02 Riassunto (Abstract) -
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations Aleo, Serena J; Del Dotto, Valentina; Fogazza, Mario; Maresca, Alessandra; Lodi, Tiziana; Goffrini, Paola; Ghelli, Anna; Rugolo, Michela; Carelli, Valerio; Baruffini, Enrico; Zanna, Claudia 2020-01-01 HUMAN MOLECULAR GENETICS - 1.01 Articolo in rivista -