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Nereo Bresolin

Showing results (191-200 of 346) with videos related to

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Brain & Development|November 5, 2013
Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agentsChiara Vantaggiato, Orazio Cantoni, Andrea Guidarelli, et al.
Biomaterials|April 20, 2010
Ex vivo expansion of human circulating myogenic progenitors on cluster-assembled nanostructured TiO2Marzia Belicchi, Silvia Erratico, Paola Razini, et al.
Pediatric Research|February 7, 2004
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethalityMarco Crimi, Alexandros Papadimitriou, Sara Galbiati, et al.
Functional Neurology|April 20, 2013
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variantAnna Bersano, Michela Ranieri, Andrea Ciammola, et al.
Neurogenetics|October 20, 2005
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)Maria T Bassi, Umberto Balottin, Chris Panzeri, et al.
Experimental Neurology|May 1, 2007
Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expressionStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Neurobiology of Aging|August 21, 2003
High mutational burden in the mtDNA control region from aged muscles: a single-fiber studyRoberto Del Bo, Marco Crimi, Monica Sciacco, et al.
Brain : a Journal of Neurology|April 19, 2007
Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis modelStefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Neuroscience Letters|June 22, 2006
Candidate gene analysis of IP-10 gene in patients with Alzheimer's diseaseEliana Venturelli, Daniela Galimberti, Chiara Fenoglio, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 25, 2009
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1)Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Pageof 35

Showing results (191-200 of 346) with videos related to

Sort By:
Pageof 35
Brain & Development|November 5, 2013
Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agentsChiara Vantaggiato, Orazio Cantoni, Andrea Guidarelli, et al.
Biomaterials|April 20, 2010
Ex vivo expansion of human circulating myogenic progenitors on cluster-assembled nanostructured TiO2Marzia Belicchi, Silvia Erratico, Paola Razini, et al.
Pediatric Research|February 7, 2004
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethalityMarco Crimi, Alexandros Papadimitriou, Sara Galbiati, et al.
Functional Neurology|April 20, 2013
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variantAnna Bersano, Michela Ranieri, Andrea Ciammola, et al.
Neurogenetics|October 20, 2005
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)Maria T Bassi, Umberto Balottin, Chris Panzeri, et al.
Experimental Neurology|May 1, 2007
Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expressionStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Neurobiology of Aging|August 21, 2003
High mutational burden in the mtDNA control region from aged muscles: a single-fiber studyRoberto Del Bo, Marco Crimi, Monica Sciacco, et al.
Brain : a Journal of Neurology|April 19, 2007
Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis modelStefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Neuroscience Letters|June 22, 2006
Candidate gene analysis of IP-10 gene in patients with Alzheimer's diseaseEliana Venturelli, Daniela Galimberti, Chiara Fenoglio, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 25, 2009
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1)Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Pageof 35