A. Ghelli; C. Zanna; A.M. Porcelli; V. Carelli; M. Rugolo, ATP depletion and caspase independent death of cybrids bearing Leber's Hereditary Optic neuropathy MTDNA mutations incubated in galactose medium. A model for endonuclease G-mediated apoptosis, in: Programmed cell death across kingdoms similarities and differences, BOLOGNA, Dipartimento Biologia Ev. SP., 2004, pp. 10 - 10 (atti di: COST action 844: Apoptosis and programmed cell death: molecular mechanisms and applications in biotechnology and agricolture, Bertinoro (FO), 9-11 maggio 2004) [Abstract]
CARELLI V; RUGOLO M; SGARBI G; GHELLI A; ZANNA C; BARACCA A; LENAZ G; NAPOLI E; MARTINUZZI A; SOLAINI G., Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2004, 1658, pp. 172 - 179 [Scientific article]
C.Zanna; A.M.Porcelli; A.Ghelli; V.Carelli; A.Martinuzzi; M.Rugolo, Cell death of fibroblasts derived from patients with
Leber’s hereditary optic neuropathy mtDNA mutations, in: 12th Euroconference on Apoptosis, S.N., s.n, 2004, pp. 144 - 144 (atti di: 12th Euroconference on Apoptosis, Chania, 17-20 September, 2004) [Abstract]
Angeloni C.; Maraldi T.; Ghelli A.; Rugolo M.; Bordoni A.; Biagi P.L.; Hakim G.; Hrelia S., Green tea modulates a-1-adrenergic stimulated glucose transport in cultured cardiomyocytes via protein kinase C beta and delta isoforms, in: , «ITALIAN JOURNAL OF BIOCHEMISTRY», 2004, 53, pp. 144 - 144 (atti di: 49° Congresso Nazionale Societa' Italiana Biochimica e Biologia Molecolare, Riccione, 28 Settembre-1 Ottobre, 2004) [Abstract]
Carelli V.; Ghelli A.; Baracca A.; Zanna C.; Sgarbi G.; Solaini G.; Lenaz G.; Rugolo M.; Martinuzzi A., Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy., in: , «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2004, 1657, pp. 70 - 70 (atti di: Euromit 6-, Nijmegen, The Netherlands, 1-4 July 2004) [Abstract]
VALENTINO ML; BARBONI P; GHELLI A; BUCCHI L; RENGO C; ACHILLI A; TORRONI A; LUGARESI A; LODI R; BARBIROLI B; DOTTI M; FEDERICO A; BARUZZI A.; CARELLI V., The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy., «ANNALS OF NEUROLOGY», 2004, 56, pp. 631 - 641 [Scientific article]