Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Giacomo P Comi

Showing results (11-20 of 224) with videos related to

Pageof 23
Sort By:
Cellular and Molecular Life Sciences : CMLS|March 12, 2026
RNA biomarkers in spinal muscular atrophy: enhancing pathogenesis understanding and guiding precision medicineClaudia Alberti, Angela Berardinelli, Giacomo P Comi, et al.
Molecular Neurobiology|July 27, 2018
R-Loops in Motor Neuron DiseasesMartina G L Perego, Michela Taiana, Nereo Bresolin, et al.
Trends in Genetics : TIG|October 31, 2006
Intron size in mammals: complexity comes to terms with economyUberto Pozzoli, Giorgia Menozzi, Giacomo P Comi, et al.
Genetics|February 28, 2002
Comparative analysis of the human dystrophin and utrophin gene structuresUberto Pozzoli, Manuela Sironi, Rachele Cagliani, et al.
Trends in Genetics : TIG|July 12, 2005
Fixation of conserved sequences shapes human intron size and influences transposon-insertion dynamicsManuela Sironi, Giorgia Menozzi, Giacomo P Comi, et al.
Human Molecular Genetics|July 23, 2005
Analysis of intronic conserved elements indicates that functional complexity might represent a major source of negative selection on non-coding sequencesManuela Sironi, Giorgia Menozzi, Giacomo P Comi, et al.
Molecular Neurobiology|March 5, 2019
Disease Modeling and Therapeutic Strategies in CMT2A: State of the ArtKordelia Barbullushi, Elena Abati, Federica Rizzo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 17, 2018
Novel Lys215Asn mutation in an Italian family with Thomsen myotoniaVittorio Mantero, Sabrina Lucchiari, Roberto Balgera, et al.
Journal of Cellular and Molecular Medicine|December 2, 2011
Generation of skeletal muscle cells from embryonic and induced pluripotent stem cells as an in vitro model and for therapy of muscular dystrophiesSabrina Salani, Chiara Donadoni, Federica Rizzo, et al.
Molecular Neurobiology|November 13, 2019
Molecular Approaches for the Treatment of Pompe DiseaseAnita Sofia Bellotti, Luca Andreoli, Dario Ronchi, et al.
Pageof 23

Showing results (11-20 of 224) with videos related to

Sort By:
Pageof 23
Cellular and Molecular Life Sciences : CMLS|March 12, 2026
RNA biomarkers in spinal muscular atrophy: enhancing pathogenesis understanding and guiding precision medicineClaudia Alberti, Angela Berardinelli, Giacomo P Comi, et al.
Molecular Neurobiology|July 27, 2018
R-Loops in Motor Neuron DiseasesMartina G L Perego, Michela Taiana, Nereo Bresolin, et al.
Trends in Genetics : TIG|October 31, 2006
Intron size in mammals: complexity comes to terms with economyUberto Pozzoli, Giorgia Menozzi, Giacomo P Comi, et al.
Genetics|February 28, 2002
Comparative analysis of the human dystrophin and utrophin gene structuresUberto Pozzoli, Manuela Sironi, Rachele Cagliani, et al.
Trends in Genetics : TIG|July 12, 2005
Fixation of conserved sequences shapes human intron size and influences transposon-insertion dynamicsManuela Sironi, Giorgia Menozzi, Giacomo P Comi, et al.
Human Molecular Genetics|July 23, 2005
Analysis of intronic conserved elements indicates that functional complexity might represent a major source of negative selection on non-coding sequencesManuela Sironi, Giorgia Menozzi, Giacomo P Comi, et al.
Molecular Neurobiology|March 5, 2019
Disease Modeling and Therapeutic Strategies in CMT2A: State of the ArtKordelia Barbullushi, Elena Abati, Federica Rizzo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 17, 2018
Novel Lys215Asn mutation in an Italian family with Thomsen myotoniaVittorio Mantero, Sabrina Lucchiari, Roberto Balgera, et al.
Journal of Cellular and Molecular Medicine|December 2, 2011
Generation of skeletal muscle cells from embryonic and induced pluripotent stem cells as an in vitro model and for therapy of muscular dystrophiesSabrina Salani, Chiara Donadoni, Federica Rizzo, et al.
Molecular Neurobiology|November 13, 2019
Molecular Approaches for the Treatment of Pompe DiseaseAnita Sofia Bellotti, Luca Andreoli, Dario Ronchi, et al.
Pageof 23