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 (11-20 of 121) with videos related to

Pageof 13
Sort By:
Journal of Molecular Medicine (Berlin, Germany)|April 24, 2013
Role of dynamin 2 in the disassembly of focal adhesionsLaura Briñas, Stéphane Vassilopoulos, Gisèle Bonne, et al.
Biochimica Et Biophysica Acta|March 17, 2009
Selenoprotein function and muscle diseaseAlain Lescure, Mathieu Rederstorff, Alain Krol, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|September 21, 2010
Germline and somatic mosaicism for a mutation of the ryanodine receptor type 2 gene: implication for genetic counselling and patient caringNathalie Roux-Buisson, Grégory Egéa, Isabelle Denjoy, et al.
Muscle & Nerve|February 3, 2004
EMG and nerve conduction studies in children with congenital muscular dystrophySusana Quijano-Roy, Francis Renault, Norma Romero, et al.
European Journal of Human Genetics : EJHG|September 1, 2005
Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy populationLaetitia Gouas, Viviane Nicaud, Myriam Berthet, et al.
International Journal of Molecular Sciences|July 26, 2020
Inter-Regulation of K<sub>v</sub>4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal ChannelopathiesJérôme Clatot, Nathalie Neyroud, Robert Cox, et al.
Neuromuscular Disorders : NMD|April 9, 2008
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findingsMarc Bitoun, Tanya Stojkovic, Bernard Prudhon, et al.
Stem Cell Research|October 25, 2025
Generation of a FAM189A2/ENTREP1 knockout human induced pluripotent stem cell line using CRISPR/Cas9 technologySibylle Marteau, Laetitia Duboscq-Bidot, Takanori Aizawa, et al.
Human Molecular Genetics|April 18, 2003
Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression patternNathalie Petit, Alain Lescure, Mathieu Rederstorff, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophySamira Makri, Nigel F Clarke, Pascale Richard, et al.
Pageof 13

Showing results (11-20 of 121) with videos related to

Sort By:
Pageof 13
Journal of Molecular Medicine (Berlin, Germany)|April 24, 2013
Role of dynamin 2 in the disassembly of focal adhesionsLaura Briñas, Stéphane Vassilopoulos, Gisèle Bonne, et al.
Biochimica Et Biophysica Acta|March 17, 2009
Selenoprotein function and muscle diseaseAlain Lescure, Mathieu Rederstorff, Alain Krol, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|September 21, 2010
Germline and somatic mosaicism for a mutation of the ryanodine receptor type 2 gene: implication for genetic counselling and patient caringNathalie Roux-Buisson, Grégory Egéa, Isabelle Denjoy, et al.
Muscle & Nerve|February 3, 2004
EMG and nerve conduction studies in children with congenital muscular dystrophySusana Quijano-Roy, Francis Renault, Norma Romero, et al.
European Journal of Human Genetics : EJHG|September 1, 2005
Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy populationLaetitia Gouas, Viviane Nicaud, Myriam Berthet, et al.
International Journal of Molecular Sciences|July 26, 2020
Inter-Regulation of K<sub>v</sub>4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal ChannelopathiesJérôme Clatot, Nathalie Neyroud, Robert Cox, et al.
Neuromuscular Disorders : NMD|April 9, 2008
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findingsMarc Bitoun, Tanya Stojkovic, Bernard Prudhon, et al.
Stem Cell Research|October 25, 2025
Generation of a FAM189A2/ENTREP1 knockout human induced pluripotent stem cell line using CRISPR/Cas9 technologySibylle Marteau, Laetitia Duboscq-Bidot, Takanori Aizawa, et al.
Human Molecular Genetics|April 18, 2003
Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression patternNathalie Petit, Alain Lescure, Mathieu Rederstorff, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophySamira Makri, Nigel F Clarke, Pascale Richard, et al.
Pageof 13