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Caterina Bendotti

Showing results (51-60 of 104) with videos related to

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International Journal of Molecular Sciences|October 13, 2021
Novel P2X7 Antagonist Ameliorates the Early Phase of ALS Disease and Decreases Inflammation and Autophagy in SOD1-G93A Mouse ModelSavina Apolloni, Paola Fabbrizio, Susanna Amadio, et al.
The FEBS Journal|May 28, 2011
Reducing expression of NAD+ synthesizing enzyme NMNAT1 does not affect the rate of Wallerian degenerationLaura Conforti, Lucie Janeckova, Diana Wagner, et al.
Brain : a Journal of Neurology|September 26, 2013
Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosisGiovanni Nardo, Raffaele Iennaco, Nicolò Fusi, et al.
The Journal of Biological Chemistry|April 18, 2013
Mutant copper-zinc superoxide dismutase (SOD1) induces protein secretion pathway alterations and exosome release in astrocytes: implications for disease spreading and motor neuron pathology in amyotrophic lateral sclerosisManuela Basso, Silvia Pozzi, Massimo Tortarolo, et al.
Journal of Neurochemistry|June 12, 2026
Effects of Lysine Deacetylation Inhibition Alone or in Combination With Arimoclomol on TDP-43 ProteinopathySerena Scozzari, Stefano Fabrizio Columbro, Monica Favagrossa, et al.
Molecular Neurodegeneration|August 11, 2018
Counteracting roles of MHCI and CD8<sup>+</sup> T cells in the peripheral and central nervous system of ALS SOD1<sup>G93A</sup> miceGiovanni Nardo, Maria Chiara Trolese, Mattia Verderio, et al.
Cellular and Molecular Life Sciences : CMLS|December 22, 2021
Contingent intramuscular boosting of P2XR7 axis improves motor function in transgenic ALS micePaola Fabbrizio, Jessica D'Agostino, Cassandra Margotta, et al.
Human Molecular Genetics|October 2, 2008
Functional alterations of the ubiquitin-proteasome system in motor neurons of a mouse model of familial amyotrophic lateral sclerosisCristina Cheroni, Marianna Marino, Massimo Tortarolo, et al.
Current Medicinal Chemistry|January 29, 2008
The heterogeneity of amyotrophic lateral sclerosis: a possible explanation of treatment failureEttore Beghi, Tiziana Mennini, Caterina Bendotti, et al.
Journal of Neuroscience Research|December 3, 2005
Glutamate AMPA receptors change in motor neurons of SOD1G93A transgenic mice and their inhibition by a noncompetitive antagonist ameliorates the progression of amytrophic lateral sclerosis-like diseaseMassimo Tortarolo, Giuliano Grignaschi, Novella Calvaresi, et al.
Pageof 11

Showing results (51-60 of 104) with videos related to

Sort By:
Pageof 11
International Journal of Molecular Sciences|October 13, 2021
Novel P2X7 Antagonist Ameliorates the Early Phase of ALS Disease and Decreases Inflammation and Autophagy in SOD1-G93A Mouse ModelSavina Apolloni, Paola Fabbrizio, Susanna Amadio, et al.
The FEBS Journal|May 28, 2011
Reducing expression of NAD+ synthesizing enzyme NMNAT1 does not affect the rate of Wallerian degenerationLaura Conforti, Lucie Janeckova, Diana Wagner, et al.
Brain : a Journal of Neurology|September 26, 2013
Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosisGiovanni Nardo, Raffaele Iennaco, Nicolò Fusi, et al.
The Journal of Biological Chemistry|April 18, 2013
Mutant copper-zinc superoxide dismutase (SOD1) induces protein secretion pathway alterations and exosome release in astrocytes: implications for disease spreading and motor neuron pathology in amyotrophic lateral sclerosisManuela Basso, Silvia Pozzi, Massimo Tortarolo, et al.
Journal of Neurochemistry|June 12, 2026
Effects of Lysine Deacetylation Inhibition Alone or in Combination With Arimoclomol on TDP-43 ProteinopathySerena Scozzari, Stefano Fabrizio Columbro, Monica Favagrossa, et al.
Molecular Neurodegeneration|August 11, 2018
Counteracting roles of MHCI and CD8<sup>+</sup> T cells in the peripheral and central nervous system of ALS SOD1<sup>G93A</sup> miceGiovanni Nardo, Maria Chiara Trolese, Mattia Verderio, et al.
Cellular and Molecular Life Sciences : CMLS|December 22, 2021
Contingent intramuscular boosting of P2XR7 axis improves motor function in transgenic ALS micePaola Fabbrizio, Jessica D'Agostino, Cassandra Margotta, et al.
Human Molecular Genetics|October 2, 2008
Functional alterations of the ubiquitin-proteasome system in motor neurons of a mouse model of familial amyotrophic lateral sclerosisCristina Cheroni, Marianna Marino, Massimo Tortarolo, et al.
Current Medicinal Chemistry|January 29, 2008
The heterogeneity of amyotrophic lateral sclerosis: a possible explanation of treatment failureEttore Beghi, Tiziana Mennini, Caterina Bendotti, et al.
Journal of Neuroscience Research|December 3, 2005
Glutamate AMPA receptors change in motor neurons of SOD1G93A transgenic mice and their inhibition by a noncompetitive antagonist ameliorates the progression of amytrophic lateral sclerosis-like diseaseMassimo Tortarolo, Giuliano Grignaschi, Novella Calvaresi, et al.
Pageof 11