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Nucleic Acids Research|March 23, 2004
Silencer elements as possible inhibitors of pseudoexon splicingManuela Sironi, Giorgia Menozzi, Laura Riva, 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.
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