Alessandra Baracca
Alessandra Baracca
Dip. Scienze Biomediche e Neuromotorie, Università di Bologna, Italia
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TitoloCitata daAnno
Rhodamine 123 as a probe of mitochondrial membrane potential: evaluation of proton flux through F0 during ATP synthesis
A Baracca, G Sgarbi, G Solaini, G Lenaz
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1606 (1-3), 137-146, 2003
Hypoxia and mitochondrial oxidative metabolism
G Solaini, A Baracca, G Lenaz, G Sgarbi
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1797 (6-7), 1171-1177, 2010
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
Oxidative phosphorylation in cancer cells
G Solaini, G Sgarbi, A Baracca
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1807 (6), 534-542, 2011
Severe impairment of complex I–driven adenosine triphosphate synthesis in Leber hereditary optic neuropathy cybrids
A Baracca, G Solaini, G Sgarbi, G Lenaz, A Baruzzi, AHV Schapira, ...
Archives of neurology 62 (5), 730-736, 2005
Is supercomplex organization of the respiratory chain required for optimal electron transfer activity?
ML Genova, A Baracca, A Biondi, G Casalena, M Faccioli, AI Falasca, ...
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1777 (7-8), 740-746, 2008
Mitochondrial respiratory chain super-complex I–III in physiology and pathology
G Lenaz, A Baracca, G Barbero, C Bergamini, ME Dalmonte, M Del Sole, ...
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1797 (6-7), 633-640, 2010
Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit a
A Baracca, S Barogi, V Carelli, G Lenaz, G Solaini
Journal of Biological Chemistry 275 (6), 4177-4182, 2000
Mitochondrial Complex I decrease is responsible for bioenergetic dysfunction in K-ras transformed cells
A Baracca, F Chiaradonna, G Sgarbi, G Solaini, L Alberghina, G Lenaz
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1797 (2), 314-323, 2010
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
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function
M Spinazzi, S Cazzola, M Bortolozzi, A Baracca, E Loro, A Casarin, ...
Human molecular genetics 17 (21), 3291-3302, 2008
Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation
F Squitieri, M Cannella, G Sgarbi, V Maglione, A Falleni, P Lenzi, ...
Mechanisms of ageing and development 127 (2), 217-220, 2006
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
G Sgarbi, A Baracca, G Lenaz, LM Valentino, V Carelli, G Solaini
Biochemical Journal 395 (3), 493-500, 2006
New insights into structure and function of mitochondria and their role in aging and disease
G Lenaz, A Baracca, R Fato, ML Genova, G Solaini
Antioxidants & redox signaling 8 (3-4), 417-437, 2006
Bioenergetics of mitochondrial diseases associated with mtDNA mutations
G Lenaz, A Baracca, V Carelli, M D'Aurelio, G Sgarbi, G Solaini
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1658 (1-2), 89-94, 2004
Evaluating mitochondrial membrane potential in cells
G Solaini, G Sgarbi, G Lenaz, A Baracca
Bioscience reports 27 (1-3), 11-21, 2007
Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993
A Baracca, G Sgarbi, M Mattiazzi, G Casalena, E Pagnotta, ML Valentino, ...
Biochimica Et Biophysica Acta (BBA)-Bioenergetics 1767 (7), 913-919, 2007
Biochemical and immunological properties of alkaline invertase isolated from sprouting soybean hypocotyls
JQ Chen, CC Black
Archives of Biochemistry and Biophysics 295 (1), 61-69, 1992
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations
F Pallotti, A Baracca, E Hernandez-Rosa, WF Walker, G Solaini, G Lenaz, ...
Biochemical Journal 384 (2), 287-293, 2004
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation
V Carelli, A Baracca, S Barogi, F Pallotti, ML Valentino, P Montagna, ...
Archives of neurology 59 (2), 264-270, 2002
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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