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Nereo Bresolin

Showing results (81-90 of 346) with videos related to

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Journal of Neurology|October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literatureGauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS|April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translationIrene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
Journal of Cellular and Molecular Medicine|January 10, 2014
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)Chiara Zanetta, Giulietta Riboldi, Monica Nizzardo, et al.
Neurology Research International|June 20, 2013
Mitochondrial fusion proteins and human diseasesMichela Ranieri, Simona Brajkovic, Giulietta Riboldi, et al.
Developmental Medicine and Child Neurology|May 18, 2012
A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidanceRomina Romaniello, Alessandra Tonelli, Filippo Arrigoni, et al.
Human Genetics|February 22, 2003
Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spotManuela Sironi, Uberto Pozzoli, Rachele Cagliani, et al.
Genome Research|May 3, 2003
Comparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common featureUberto Pozzoli, Greg Elgar, Rachele Cagliani, et al.
Genome Biology|September 27, 2008
The signature of long-standing balancing selection at the human defensin beta-1 promoterRachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
BMC Evolutionary Biology|June 21, 2011
Balancing selection is common in the extended MHC region but most alleles with opposite risk profile for autoimmune diseases are neutrally evolvingRachele Cagliani, Stefania Riva, Uberto Pozzoli, et al.
BMC Neurology|August 4, 2014
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformationsSilvia Lanfranconi, Dario Ronchi, Naghia Ahmed, et al.
Pageof 35

Showing results (81-90 of 346) with videos related to

Sort By:
Pageof 35
Journal of Neurology|October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literatureGauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS|April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translationIrene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
Journal of Cellular and Molecular Medicine|January 10, 2014
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)Chiara Zanetta, Giulietta Riboldi, Monica Nizzardo, et al.
Neurology Research International|June 20, 2013
Mitochondrial fusion proteins and human diseasesMichela Ranieri, Simona Brajkovic, Giulietta Riboldi, et al.
Developmental Medicine and Child Neurology|May 18, 2012
A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidanceRomina Romaniello, Alessandra Tonelli, Filippo Arrigoni, et al.
Human Genetics|February 22, 2003
Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spotManuela Sironi, Uberto Pozzoli, Rachele Cagliani, et al.
Genome Research|May 3, 2003
Comparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common featureUberto Pozzoli, Greg Elgar, Rachele Cagliani, et al.
Genome Biology|September 27, 2008
The signature of long-standing balancing selection at the human defensin beta-1 promoterRachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
BMC Evolutionary Biology|June 21, 2011
Balancing selection is common in the extended MHC region but most alleles with opposite risk profile for autoimmune diseases are neutrally evolvingRachele Cagliani, Stefania Riva, Uberto Pozzoli, et al.
BMC Neurology|August 4, 2014
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformationsSilvia Lanfranconi, Dario Ronchi, Naghia Ahmed, et al.
Pageof 35