Divisione Sistemi Agroalimentari Sostenibili

Found 7 results

Filtri: Autore is Carrì, M.T. and Parola Chiave is copper zinc superoxide dismutase [Clear All Filters]

2018

50-Hz magnetic field impairs the expression of iron-related genes in the in vitro SOD1G93A model of amyotrophic lateral sclerosis, Consales, Claudia, Panatta M., Butera Alessio, Filomeni G., Merla Caterina, Carrì M.T., Marino Carmela, and Benassi Barbara , International Journal of Radiation Biology, Jan-03-2019, Volume 95, Issue 3, Number 3, p.368-377, (2018)

2011

Astroglial inhibition of NF-κb does not ameliorate disease onset and progression in a mouse model for amyotrophic lateral sclerosis (ALS), Crosio, C., Valle C., Casciati Arianna, Iaccarino C., and Carrì M.T. , PLoS ONE, Volume 6, Number 3, (2011)

2006

Bcl2a1 serves as a switch in death of motor neurons in amyotrophic lateral sclerosis [1], Crosio, C., Casciati Arianna, Iaccarino C., Rotilio G., and Carrì M.T. , Cell Death and Differentiation, Volume 13, Number 12, p.2150-2153, (2006)

Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials, Ferri, A., Cozzolino M., Crosio C., Nencini M., Casciati Arianna, Gralla E.B., Rotilio G., Valentine J.S., and Carrì M.T. , Proceedings of the National Academy of Sciences of the United States of America, Volume 103, Number 37, p.13860-13865, (2006)

2004

Cell death in amyotrophic lateral sclerosis: Interplay between neuronal and glial cells, Ferri, A., Nencini M., Casciati Arianna, Cozzolino M., Angelini D.F., Longone P., Spalloni A., Rotilio G., and Carrì M.T. , FASEB Journal, Volume 18, Number 11, p.1261-1263, (2004)

2003

Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine, Beretta, S., Sala G., Mattavelli L., Ceresa C., Casciati Arianna, Ferri A., Carrì M.T., and Ferrarese C. , Neurobiology of Disease, Volume 13, Number 3, p.213-221, (2003)

2001

Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis, Ferri, A., Gabbianelli R., Casciati Arianna, Celsi F., Rotilio G., and Carrì M.T. , Journal of Neurochemistry, Volume 79, Number 3, p.531-538, (2001)