Anna Maria Ghelli
TitoloCitata daAnno
Mitochondrial cytochrome b: evolution and structure of the protein
M Degli Esposti, S De Vries, M Crimi, A Ghelli, T Patarnello, A Meyer
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1143 (3), 243-271, 1993
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
Natural substances (acetogenins) from the family Annonaceae are powerful inhibitors of mitochondrial NADH dehydrogenase (Complex I)
M Degli Esposti, A Ghelli, M Ratta, D Cortes, E Estornell
Biochemical Journal 301 (1), 161-167, 1994
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
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors
G Gasparre, AM Porcelli, E Bonora, LF Pennisi, M Toller, L Iommarini, ...
Proceedings of the National Academy of Sciences 104 (21), 9001-9006, 2007
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III
E Bonora, AM Porcelli, G Gasparre, A Biondi, A Ghelli, V Carelli, ...
Cancer research 66 (12), 6087-6096, 2006
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
Oestrogens ameliorate mitochondrial dysfunction in Leber’s hereditary optic neuropathy
C Giordano, M Montopoli, E Perli, M Orlandi, M Fantin, FN Ross-Cisneros, ...
Brain 134 (1), 220-234, 2011
Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy
V Carelli, A Ghelli, L Bucchi, P Montagna, A De Negri, V Leuzzi, ...
Annals of Neurology: Official Journal of the American Neurologicalá…, 1999
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 (5), 997-1007, 2005
Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype
V Carelli, A Ghelli, M Ratta, E Bacchilega, S Sangiorgi, R Mancini, ...
Neurology 48 (6), 1623-1632, 1997
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy
MD Esposti, V Carelli, A Ghelli, M Ratta, M Crimi, S Sangiorgi, ...
FEBS letters 352 (3), 375-379, 1994
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
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy
ML Valentino, P Barboni, A Ghelli, L Bucchi, C Rengo, A Achilli, A Torroni, ...
Annals of Neurology: Official Journal of the American Neurologicalá…, 2004
Complex I and complex III of mitochondria have common inhibitors acting as ubiquinone antagonists
M Degli Esposti, A Ghelli, M Crimi, E Estornell, R Fato, G Lenaz
Biochem. Biophys. Res. Commun 190, 1090-1096, 1993
The interaction of Q analogs, particularly hydroxydecyl benzoquinone (idebenone), with the respiratory complexes of heart mitochondria
M Degli Esposti, A Ngo, A Ghelli, B Benelli, V Carelli, H McLennan, ...
Archives of biochemistry and biophysics 330 (2), 395-400, 1996
The genetic and metabolic signature of oncocytic transformation implicates HIF1α destabilization
AM Porcelli, A Ghelli, C Ceccarelli, M Lang, G Cenacchi, M Capristo, ...
Human molecular genetics 19 (6), 1019-1032, 2010
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels
AM Porcelli, A Angelin, A Ghelli, E Mariani, A Martinuzzi, V Carelli, ...
Journal of Biological Chemistry 284 (4), 2045-2052, 2009
The effects of idebenone on mitochondrial bioenergetics
V Giorgio, V Petronilli, A Ghelli, V Carelli, M Rugolo, G Lenaz, P Bernardi
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1817 (2), 363-369, 2012
The specificity of mitochondrial complex I for ubiquinones
M ESPOSTI DEGLI, A Ngo, GL McMULLEN, A Ghelli, F Sparla, B Benelli, ...
Biochemical Journal 313 (1), 327-334, 1996
Il sistema al momento non pu˛ eseguire l'operazione. Riprova pi¨ tardi.
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