Arianna Casciati
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Oncogenic radiation abscopal effects in vivo: interrogating mouse skin.,
, Int J Radiat Oncol Biol Phys, 2013 Aug 01, Volume 86, Issue 5, p.993-9, (2013)
Oncogenic radiation abscopal effects in vivo: Interrogating mouse skin,
, International Journal of Radiation Oncology Biology Physics, Volume 86, Number 5, p.993-999, (2013)
Astroglial inhibition of NF-κb does not ameliorate disease onset and progression in a mouse model for amyotrophic lateral sclerosis (ALS),
, PLoS ONE, Volume 6, Number 3, (2011)
Bcl2a1 serves as a switch in death of motor neurons in amyotrophic lateral sclerosis [1],
, Cell Death and Differentiation, Volume 13, Number 12, p.2150-2153, (2006)
Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials,
, Proceedings of the National Academy of Sciences of the United States of America, Volume 103, Number 37, p.13860-13865, (2006)
Cell death in amyotrophic lateral sclerosis: Interplay between neuronal and glial cells,
, FASEB Journal, Volume 18, Number 11, p.1261-1263, (2004)
Overexpression of superoxide dismutase 1 protects against β-amyloid peptide toxicity: Effect of estrogen and copper chelators,
, Neurochemistry International, Volume 44, Number 1, p.25-33, (2004)
Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine,
, Neurobiology of Disease, Volume 13, Number 3, p.213-221, (2003)
Oxidative modulation of nuclear factor-κB in human cells expressing mutant fALS-typical superoxide dismutases,
, Journal of Neurochemistry, Volume 83, Number 5, p.1019-1029, (2002)
Copper-dependent oxidative stress, alteration of signal transduction and neurodegeneration in amyotrophic lateral sclerosis,
, Functional Neurology, Volume 16, Number 4 SUPPL., p.181-188, (2001)
Neurochemistry of SOD1 and familial amyotrophic lateral sclerosis,
, Functional Neurology, Volume 16, Number 1, p.73-82, (2001)
Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis,
, Journal of Neurochemistry, Volume 79, Number 3, p.531-538, (2001)
Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase,
, Journal of Neurochemistry, Volume 75, Number 2, p.606-613, (2000)