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

Pascale Guicheney

Showing results (1-10 of 121) with videos related to

Pageof 13
Sort By:
European Journal of Human Genetics : EJHG|April 9, 2002
Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin)Valérie Allamand, Pascale Guicheney
Neuromuscular Disorders : NMD|December 4, 2001
85th ENMC International Workshop on Congenital Muscular Dystrophy. 6th International CMD Workshop. 1st Workshop of the Myo-Cluster Project 'GENRE'. 27-28th October 2000, Naarden, The NetherlandsFrancesco Muntoni, Pascale Guicheney
Biology Open|November 22, 2016
Calcium homeostasis alterations in a mouse model of the Dynamin 2-related centronuclear myopathyBodvaël Fraysse, Pascale Guicheney, Marc Bitoun
Circulation. Arrhythmia and Electrophysiology|October 2, 2012
Catecholaminergic polymorphic ventricular tachycardiaAntoine Leenhardt, Isabelle Denjoy, Pascale Guicheney
Journal of Biomedical Science|March 8, 2022
The role of the M-band myomesin proteins in muscle integrity and cardiac diseaseEkaterina P Lamber, Pascale Guicheney, Nikos Pinotsis
Medecine Sciences : M/S|February 7, 2006
[Mutations in dynamin 2 cause dominant centronuclear myopathy]Marc Bitoun, Norma B Romero, Pascale Guicheney
Methods in Enzymology|September 7, 2010
POMGnT1, POMT1, and POMT2 mutations in congenital muscular dystrophiesTamao Endo, Hiroshi Manya, Nathalie Seta, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 25, 2012
Selenoprotein N in skeletal muscle: from diseases to functionPerrine Castets, Alain Lescure, Pascale Guicheney, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 4, 2010
Dynamin 2 and human diseasesAnne-Cécile Durieux, Bernard Prudhon, Pascale Guicheney, et al.
Frontiers in Bioscience (Landmark Edition)|July 22, 2022
Trafficking and Gating Cooperation Between Deficient Na<sub>v</sub>1.5-mutant Channels to Rescue I<sub>Na</sub>Jérôme Clatot, Alain Coulombe, Isabelle Deschênes, et al.
Pageof 13

Showing results (1-10 of 121) with videos related to

Sort By:
Pageof 13
European Journal of Human Genetics : EJHG|April 9, 2002
Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin)Valérie Allamand, Pascale Guicheney
Neuromuscular Disorders : NMD|December 4, 2001
85th ENMC International Workshop on Congenital Muscular Dystrophy. 6th International CMD Workshop. 1st Workshop of the Myo-Cluster Project 'GENRE'. 27-28th October 2000, Naarden, The NetherlandsFrancesco Muntoni, Pascale Guicheney
Biology Open|November 22, 2016
Calcium homeostasis alterations in a mouse model of the Dynamin 2-related centronuclear myopathyBodvaël Fraysse, Pascale Guicheney, Marc Bitoun
Circulation. Arrhythmia and Electrophysiology|October 2, 2012
Catecholaminergic polymorphic ventricular tachycardiaAntoine Leenhardt, Isabelle Denjoy, Pascale Guicheney
Journal of Biomedical Science|March 8, 2022
The role of the M-band myomesin proteins in muscle integrity and cardiac diseaseEkaterina P Lamber, Pascale Guicheney, Nikos Pinotsis
Medecine Sciences : M/S|February 7, 2006
[Mutations in dynamin 2 cause dominant centronuclear myopathy]Marc Bitoun, Norma B Romero, Pascale Guicheney
Methods in Enzymology|September 7, 2010
POMGnT1, POMT1, and POMT2 mutations in congenital muscular dystrophiesTamao Endo, Hiroshi Manya, Nathalie Seta, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 25, 2012
Selenoprotein N in skeletal muscle: from diseases to functionPerrine Castets, Alain Lescure, Pascale Guicheney, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 4, 2010
Dynamin 2 and human diseasesAnne-Cécile Durieux, Bernard Prudhon, Pascale Guicheney, et al.
Frontiers in Bioscience (Landmark Edition)|July 22, 2022
Trafficking and Gating Cooperation Between Deficient Na<sub>v</sub>1.5-mutant Channels to Rescue I<sub>Na</sub>Jérôme Clatot, Alain Coulombe, Isabelle Deschênes, et al.
Pageof 13