Solaini G.; Sgarbi G.; Lenaz G.; Baracca A., Evaluating mitochondrial membrane potential in cells., «BIOSCIENCE REPORTS», 2007, 27, pp. 11 - 21 [Scientific article]
Baracca A; Sgarbi G; Mattiazzi M; Casalena G; Lenaz G; Solaini G, Biochemical dysfunction associated with mitochondrial DNA mutations at nt8993., in: ND, «ITALIAN JOURNAL OF BIOCHEMISTRY», 2006, 55, pp. 117 - 117 (atti di: SIB 2006, Riccione, 28-30 September 2006) [Abstract]
Sgarbi G.; Baracca A.; Mattiazzi M.; Carelli V.; Lenaz G.; Solaini G., Comparative bioenergetic studies of cells carrying the 8993T>G or 8993T>C mitochondrial DNA mutations., in: Abstracts GIBB 2006, s.l, s.n, 2006, pp. 33 - 33 (atti di: Riunione Annuale del Gruppo Italiano di Bioenergetica e Biomembrane, Bertinoro, Italy, 15-17 June 2006) [Abstract]
Gianluca Sgarbi; Alessandra Baracca; Giorgio Lenaz; Lucia M. Valentino; Valerio Carelli; Giancarlo Solaini, 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, «BIOCHEMICAL JOURNAL», 2006, 395, pp. 493 - 500 [Scientific article]
Lenaz G.; Baracca A.; Fato R.; Genova M.L.; Solaini G., Mitochondrial Complex I: structure, function and implications in neurodegeneration, «ITALIAN JOURNAL OF BIOCHEMISTRY», 2006, 55, pp. 232 - 253 [Scientific article]
Lenaz G; Baracca A; Fato R; Genova ML; Solaini G., New insights into structure and function of mitochondria and their role in aging and disease, «ANTIOXIDANTS & REDOX SIGNALING», 2006, 8, pp. 417 - 437 [Scientific article]
F. Squitieri; M. Cannella; G. Sgarbi; V. Maglione; A. Falleni; P. Lenzi; A. Baracca; G. Cislaghi; C. Saft; G. Ragona; M.A. Russo; L.M. Thompson; G. Solaini; F. Fornai, Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation, «MECHANISMS OF AGEING AND DEVELOPMENT», 2006, 127, pp. 217 - 220 [Scientific article]
SOLAINI G.; HARRIS D.A., Biochemical dysfunction in heart mitochondria exposed to ischaemia and reperfusion, «BIOCHEMICAL JOURNAL», 2005, 390, pp. 377 - 394 [Scientific article]
Squitieri F; Maglione V; Cannella M; Morgante E; Russo MA; Frati L; Solaini G; Fornai F, Genotype dependent abnormalities in Huntington’s disease lymphoblastoid cell lines, in: , «JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY», 2005, 76, pp. A31 - A31 (atti di: World Congress on Huntington's Disease-2005, Manchester, UK, 11-13th September 2005) [Abstract]
ALEARDI. AM; BENARD. G; AUGEREAU. O; MALGAT; TALBOT JC; MAZAT. JP; LETELLIER T; DACHARY-PRIGENT. J; SOLAINI G.; ROSSIGNOL. R, Gradual alteration of mitochondrial structure and function by β-amyloids: importance of membrane viscosity changes, energy deprivation, ROS production and cytochrome c release., «JOURNAL OF BIOENERGETICS AND BIOMEMBRANES», 2005, 37, pp. 207 - 225 [Scientific article]
Sgarbi G.; Baracca A.; Lenaz G.; Carelli V.; Solaini G., mtDNA T>G mutation at the nt8993 of the ATP6 gene impairs the coupling mechanism of the F1F0-ATPase., in: Abstracts GIBB 2005, s.l, s.n, 2005, pp. A28 - A28 (atti di: Riunione annuale del Gruppo Italiano di Biomembrane e Bioenergetica, Roma, Italy, 13-15 June, 2005) [Abstract]
Solaini G.; Baracca A.; Sgarbi G.; Lenaz G.; Carelli V., Pathogenic role and biochemical dysfunctions associated with mtDNA ATP6 gene mutations., in: XIII Convention Telethon, s.l, s.n, 2005, pp. 230 - 230 (atti di: Telethon Scientific Convention, Salsomaggiore Terme, Italy, 6-8 March 2005) [Abstract]
Baracca A.; Solaini G.; Sgarbi G.; Lenaz G.; Baruzzi A.; Schapira A.H.; Martinuzzi A.; Carelli V., Severe impairment of Complex I-driven adenosine triphosphate synthesis in leber hereditarfy optic neuropathy cybrids, «ARCHIVES OF NEUROLOGY», 2005, 62, pp. 730 - 736 [Scientific article]
Solaini G.; Baracca A.; Sgarbi G.; Carelli V.; Lenaz G., What can we learn from the study of the point mutations in the human mitochondrial ATP6 gene ?, in: Molecular Insight to Physiology and Pathology, s.l, s.n, 2005, pp. SC5.28 - SC5.28 (atti di: International Conference on Mitochondria, Bari, Italy, 17-22 December 2005) [Abstract]
PALLOTTI F.; BARACCA A.; HERNANDEZ-ROSA E.; WALKER W.F.; SOLAINI G.; LENAZ G.; MELZI D'ERIL G.V.; DIMAURO S.; SCHON E.A.; DAVIDSON M., Biochemical analysis of respiratory function in cybrid cell lines harbouring mtDNA mutations, «BIOCHEMICAL JOURNAL», 2004, 384, pp. 287 - 293 [Scientific article]
