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Caterina Bendotti

Showing results (11-20 of 104) with videos related to

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Frontiers in Neuroscience|January 11, 2020
Spinal Cord Metabolic Signatures in Models of Fast- and Slow-Progressing SOD1<sup>G93A</sup> Amyotrophic Lateral SclerosisGabriel N Valbuena, Lavinia Cantoni, Massimo Tortarolo, et al.
Scientific Reports|March 2, 2017
Altered Metabolic Profiles Associate with Toxicity in SOD1<sup>G93A</sup> Astrocyte-Neuron Co-CulturesGabriel N Valbuena, Massimo Tortarolo, Caterina Bendotti, et al.
Journal of the Neurological Sciences|April 27, 2005
Low levels of ALS-linked Cu/Zn superoxide dismutase increase the production of reactive oxygen species and cause mitochondrial damage and death in motor neuron-like cellsMilena Rizzardini, Alessandra Mangolini, Monica Lupi, et al.
Journal of Proteome Research|March 4, 2014
Human SOD1-G93A specific distribution evidenced in murine brain of a transgenic model for amyotrophic lateral sclerosis by MALDI imaging mass spectrometryElena Acquadro, Ilaria Caron, Massimo Tortarolo, et al.
Journal of Neuroscience Methods|September 3, 2003
The densitometric physical fractionator for counting neuronal populations: application to a mouse model of familial amyotrophic lateral sclerosisGiuseppe Luca Ciavarro, Novella Calvaresi, Andrea Botturi, et al.
Cells|April 13, 2023
Intramuscular IL-10 Administration Enhances the Activity of Myogenic Precursor Cells and Improves Motor Function in ALS Mouse ModelPaola Fabbrizio, Cassandra Margotta, Jessica D'Agostino, et al.
Journal of Neuroscience Research|October 31, 2002
Expression of glutamate receptor subtypes in the spinal cord of control and mnd mice, a model of motor neuron disorderTiziana Mennini, Paolo Bigini, Teresa Ravizza, et al.
Journal of Neuroscience Research|February 14, 2003
Kif1Bbeta isoform is enriched in motor neurons but does not change in a mouse model of amyotrophic lateral sclerosisLaura Conforti, Carlotta Dell'Agnello, Novella Calvaresi, et al.
Plos One|May 30, 2018
Micro-computed tomography for non-invasive evaluation of muscle atrophy in mouse models of diseaseLaura Pasetto, Davide Olivari, Giovanni Nardo, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 25, 2009
Treatment with lithium carbonate does not improve disease progression in two different strains of SOD1 mutant miceChiara Pizzasegola, Ilaria Caron, Cristina Daleno, et al.
Pageof 11

Showing results (11-20 of 104) with videos related to

Sort By:
Pageof 11
Frontiers in Neuroscience|January 11, 2020
Spinal Cord Metabolic Signatures in Models of Fast- and Slow-Progressing SOD1<sup>G93A</sup> Amyotrophic Lateral SclerosisGabriel N Valbuena, Lavinia Cantoni, Massimo Tortarolo, et al.
Scientific Reports|March 2, 2017
Altered Metabolic Profiles Associate with Toxicity in SOD1<sup>G93A</sup> Astrocyte-Neuron Co-CulturesGabriel N Valbuena, Massimo Tortarolo, Caterina Bendotti, et al.
Journal of the Neurological Sciences|April 27, 2005
Low levels of ALS-linked Cu/Zn superoxide dismutase increase the production of reactive oxygen species and cause mitochondrial damage and death in motor neuron-like cellsMilena Rizzardini, Alessandra Mangolini, Monica Lupi, et al.
Journal of Proteome Research|March 4, 2014
Human SOD1-G93A specific distribution evidenced in murine brain of a transgenic model for amyotrophic lateral sclerosis by MALDI imaging mass spectrometryElena Acquadro, Ilaria Caron, Massimo Tortarolo, et al.
Journal of Neuroscience Methods|September 3, 2003
The densitometric physical fractionator for counting neuronal populations: application to a mouse model of familial amyotrophic lateral sclerosisGiuseppe Luca Ciavarro, Novella Calvaresi, Andrea Botturi, et al.
Cells|April 13, 2023
Intramuscular IL-10 Administration Enhances the Activity of Myogenic Precursor Cells and Improves Motor Function in ALS Mouse ModelPaola Fabbrizio, Cassandra Margotta, Jessica D'Agostino, et al.
Journal of Neuroscience Research|October 31, 2002
Expression of glutamate receptor subtypes in the spinal cord of control and mnd mice, a model of motor neuron disorderTiziana Mennini, Paolo Bigini, Teresa Ravizza, et al.
Journal of Neuroscience Research|February 14, 2003
Kif1Bbeta isoform is enriched in motor neurons but does not change in a mouse model of amyotrophic lateral sclerosisLaura Conforti, Carlotta Dell'Agnello, Novella Calvaresi, et al.
Plos One|May 30, 2018
Micro-computed tomography for non-invasive evaluation of muscle atrophy in mouse models of diseaseLaura Pasetto, Davide Olivari, Giovanni Nardo, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 25, 2009
Treatment with lithium carbonate does not improve disease progression in two different strains of SOD1 mutant miceChiara Pizzasegola, Ilaria Caron, Cristina Daleno, et al.
Pageof 11