Solaini G.; Baracca A.; Lenaz G.; Sgarbi G., Hypoxia and mitochondrial oxidative metabolism, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2010, 1797, pp. 1171 - 1177 [Scientific article]
Di Domenico F.; Casalena G.; Sultana R.; Cai J.; Pierce W.M.; Perluigi M.; Cini C.; Baracca A.; Solaini G.; Lenaz G.; Jia J.; Dziennis S.; Murphy S.J.; Alkayed N.J.; Butterfield D.A., Involvement of stat3 in mouse brain development and sexual
dimorphism: A proteomics approach, «BRAIN RESEARCH», 2010, 1362, pp. 1 - 12 [Scientific article]
A. Baracca; F. Chiaradonna; G. Sgarbi; G. Solaini; L. Alberghina; G. Lenaz, Mitochondrial Complex I decrease is responsible for bioenergetic dysfunction in K-ras transformed cells, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2010, 1797, pp. 314 - 323 [Scientific article]
G. Lenaz; A. Baracca; G. Barbero; C. Bergamini; M. E. Dalmonte; M. Del Sole; M. Faccioli; A. Falasca; R. Fato; M.L. Genova; G. Sgarbi; G. Solaini, MITOCHONDRIAL RESPIRATORY CHAIN SUPER-COMPLEX I-III IN PHYSIOLOGY AND PATHOLOGY, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2010, 1797, pp. 633 - 640 [Scientific article]
Sgarbi G; Casalena GA; Baracca A; Lenaz G; DiMauro S; Solaini G, Human NARP Mitochondrial Mutation Metabolism Corrected with Alpha-ketoglutarate/aspartarte: A Potential New Therapy, «ARCHIVES OF NEUROLOGY», 2009, 66, pp. 951 - 957 [Scientific article]
Spinazzi M; Cazzola S; Bortolozzi M; Baracca A; Loro E; Casarin A; Solaini G; Sgarbi G; Casalena G; Cenacchi G; Malena A; Frezza C; Carrara F; Angelini C; Scorrano L; Salviati L; Vergani L., A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function, «HUMAN MOLECULAR GENETICS», 2008, 17, pp. 3291 - 3302 [Scientific article]
Genova ML; Baracca A; Biondi A; Casalena G; Faccioli M; Falasca AI; Formiggini G; Sgarbi G; Solaini G; Lenaz G., Is supercomplex organization of the respiratory chain required for optimal electron transfer activity?, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2008, 1777, pp. 740 - 746 [Scientific article]
Solaini G; Harris DA; Lenaz G; Sgarbi G; Baracca A, The study of the pathogenic mechanism of mitochondrial diseases provides information on basic bioenergetics, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2008, 1777, pp. 941 - 945 [Scientific article]
Baracca A; Sgarbi G; Mattiazzi M; Casalena G; Pagnotta E; Valentino ML; Moggio M; Lenaz G; Carelli V; Solaini G., Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2007, 1767, pp. 913 - 919 [Scientific article]
Solaini G.; Sgarbi G.; Lenaz G.; Baracca A., Evaluating mitochondrial membrane potential in cells., «BIOSCIENCE REPORTS», 2007, 27, pp. 11 - 21 [Scientific article]
BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G., Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III, «CANCER RESEARCH», 2006, 66, pp. 6087 - 6096 [Scientific article]
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]
