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Claudia Zanna
Claudia Zanna
Dip. Scienze Biomediche e Neuromotorie, Universitą di Bologna
Verified email at unibo.it
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Cited by
Cited by
Year
OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes
P Amati-Bonneau, ML Valentino, P Reynier, ME Gallardo, B Bornstein, ...
Brain 131 (2), 338-351, 2008
5612008
OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion
C Zanna, A Ghelli, AM Porcelli, M Karbowski, RJ Youle, S Schimpf, ...
Brain 131 (2), 352-367, 2008
4082008
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein mutant
AM Porcelli, A Ghelli, C Zanna, P Pinton, R Rizzuto, M Rugolo
Biochemical and biophysical research communications 326 (4), 799-804, 2005
3472005
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution
G Elachouri, S Vidoni, C Zanna, A Pattyn, H Boukhaddaoui, K Gaget, ...
Genome research 21 (1), 12-20, 2011
2562011
Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium
A Ghelli, C Zanna, AM Porcelli, AHV Schapira, A Martinuzzi, V Carelli, ...
Journal of Biological Chemistry 278 (6), 4145-4150, 2003
2182003
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
AJ Abrams, RB Hufnagel, A Rebelo, C Zanna, N Patel, MA Gonzalez, ...
Nature genetics 47 (8), 926-932, 2015
2052015
OPA1 isoforms in the hierarchical organization of mitochondrial functions
V Del Dotto, P Mishra, S Vidoni, M Fogazza, A Maresca, L Caporali, ...
Cell reports 19 (12), 2557-2571, 2017
1922017
Syndromic parkinsonism and dementia associated with OPA1 missense mutations
V Carelli, O Musumeci, L Caporali, C Zanna, C La Morgia, V Del Dotto, ...
Annals of neurology 78 (1), 21-38, 2015
1792015
Eight human OPA1 isoforms, long and short: What are they for?
V Del Dotto, M Fogazza, V Carelli, M Rugolo, C Zanna
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1859 (4), 263-269, 2018
1512018
Caspase-independent death of Leber’s hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G
C Zanna, A Ghelli, AM Porcelli, A Martinuzzi, V Carelli, M Rugolo
Apoptosis 10, 997-1007, 2005
1512005
Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration
V Carelli, M Rugolo, G Sgarbi, A Ghelli, C Zanna, A Baracca, G Lenaz, ...
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1658 (1-2), 172-179, 2004
1442004
The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2, 5-hexanedione toxicity
A Ghelli, AM Porcelli, C Zanna, S Vidoni, S Mattioli, A Barbieri, ...
PloS one 4 (11), e7922, 2009
902009
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus
CL Morgia, A Achilli, L Iommarini, P Barboni, M Pala, A Olivieri, C Zanna, ...
Neurology 70 (10), 762-770, 2008
852008
DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?
A Maresca, M Zaffagnini, L Caporali, V Carelli, C Zanna
Frontiers in genetics 6, 132809, 2015
832015
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations
V Carelli, A Maresca, L Caporali, S Trifunov, C Zanna, M Rugolo
The international journal of biochemistry & cell biology 63, 21-24, 2015
792015
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
V Del Dotto, F Ullah, I Di Meo, P Magini, M Gusic, A Maresca, L Caporali, ...
The Journal of clinical investigation 130 (1), 108-125, 2020
742020
Why mitochondria must fuse to maintain their genome integrity
S Vidoni, C Zanna, M Rugolo, E Sarzi, G Lenaers
Antioxidants & redox signaling 19 (4), 379-388, 2013
642013
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl− conductance
AM Porcelli, A Ghelli, C Zanna, P Valente, S Ferroni, M Rugolo
Cell Death & Differentiation 11 (6), 655-662, 2004
592004
‘Behr syndrome’ with OPA1 compound heterozygote mutations
V Carelli, M Sabatelli, R Carrozzo, T Rizza, S Schimpf, B Wissinger, ...
Brain 138 (1), e321-e321, 2015
562015
The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory …
A Ghelli, CV Tropeano, MA Calvaruso, A Marchesini, L Iommarini, ...
Human molecular genetics 22 (11), 2141-2151, 2013
562013
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