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

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Cellular and Molecular Life Sciences : CMLS|June 19, 2013
Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophyAlessandra Govoni, Francesca Magri, Simona Brajkovic, et al.
Molecular Biology and Evolution|March 19, 2010
Polymorphisms in the CPB2 gene are maintained by balancing selection and result in haplotype-preferential splicing of exon 7Rachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
Genome Research|November 11, 2008
Widespread balancing selection and pathogen-driven selection at blood group antigen genesMatteo Fumagalli, Rachele Cagliani, Uberto Pozzoli, et al.
Human Mutation|November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletionsAlessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Therapeutic Advances in Neurological Disorders|May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophiesDaniela Piga, Sabrina Salani, Francesca Magri, et al.
Journal of Cellular Biochemistry|August 14, 2001
Oxidative stress signalling in the apoptosis of Jurkat T-lymphocytesR Chiaramonte, E Bartolini, P Riso, et al.
Nucleic Acids Research|March 23, 2004
Silencer elements as possible inhibitors of pseudoexon splicingManuela Sironi, Giorgia Menozzi, Laura Riva, et al.
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.
European Journal of Biochemistry|January 1, 1983
Delta thalassemia: a non-deletion defectR Taramelli, B Giglioni, P Comi, et al.
Pageof 35

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

Sort By:
Pageof 35
Cellular and Molecular Life Sciences : CMLS|June 19, 2013
Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophyAlessandra Govoni, Francesca Magri, Simona Brajkovic, et al.
Molecular Biology and Evolution|March 19, 2010
Polymorphisms in the CPB2 gene are maintained by balancing selection and result in haplotype-preferential splicing of exon 7Rachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
Genome Research|November 11, 2008
Widespread balancing selection and pathogen-driven selection at blood group antigen genesMatteo Fumagalli, Rachele Cagliani, Uberto Pozzoli, et al.
Human Mutation|November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletionsAlessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Therapeutic Advances in Neurological Disorders|May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophiesDaniela Piga, Sabrina Salani, Francesca Magri, et al.
Journal of Cellular Biochemistry|August 14, 2001
Oxidative stress signalling in the apoptosis of Jurkat T-lymphocytesR Chiaramonte, E Bartolini, P Riso, et al.
Nucleic Acids Research|March 23, 2004
Silencer elements as possible inhibitors of pseudoexon splicingManuela Sironi, Giorgia Menozzi, Laura Riva, et al.
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.
European Journal of Biochemistry|January 1, 1983
Delta thalassemia: a non-deletion defectR Taramelli, B Giglioni, P Comi, et al.
Pageof 35