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

Patrick Vicart

Showing results (31-40 of 49) with videos related to

Pageof 5
Sort By:
Journal of the Neurological Sciences|March 31, 2004
Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studiesMontse Olivé, Lev Goldfarb, Dolores Moreno, et al.
Experimental Cell Research|August 2, 2019
Alterations of redox dynamics and desmin post-translational modifications in skeletal muscle models of desminopathiesFlorence Delort, Bertrand-David Segard, Coralie Hakibilen, et al.
Cell Stress & Chaperones|February 17, 2010
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3)Xiankui Sun, Jean-Marc Fontaine, Adam D Hoppe, et al.
Neuromuscular Disorders : NMD|February 6, 2010
Desmin myopathy with severe cardiomyopathy in a Uruguayan family due to a codon deletion in a new location within the desmin 1A rod domainLuis Vernengo, Oussama Chourbagi, Ana Panuncio, et al.
Human Molecular Genetics|December 20, 2014
The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophyNathalie Vadrot, Isabelle Duband-Goulet, Eva Cabet, et al.
Journal of Neurology|March 3, 2004
A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desminAyush Dagvadorj, Montse Olivé, Jean-Andoni Urtizberea, et al.
Experimental Cell Research|July 3, 2007
Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander diseaseCyril Mignot, Cécile Delarasse, Séverine Escaich, et al.
Human Genetics|December 3, 2003
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathyAnna Kaminska, Sergei V Strelkov, Bertrand Goudeau, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutationsMarinos C Dalakas, Ayush Dagvadorj, Bertrand Goudeau, et al.
Human Mutation|January 16, 2007
Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathiesHarald Bär, Bertrand Goudeau, Sarah Wälde, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Journal of the Neurological Sciences|March 31, 2004
Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studiesMontse Olivé, Lev Goldfarb, Dolores Moreno, et al.
Experimental Cell Research|August 2, 2019
Alterations of redox dynamics and desmin post-translational modifications in skeletal muscle models of desminopathiesFlorence Delort, Bertrand-David Segard, Coralie Hakibilen, et al.
Cell Stress & Chaperones|February 17, 2010
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3)Xiankui Sun, Jean-Marc Fontaine, Adam D Hoppe, et al.
Neuromuscular Disorders : NMD|February 6, 2010
Desmin myopathy with severe cardiomyopathy in a Uruguayan family due to a codon deletion in a new location within the desmin 1A rod domainLuis Vernengo, Oussama Chourbagi, Ana Panuncio, et al.
Human Molecular Genetics|December 20, 2014
The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophyNathalie Vadrot, Isabelle Duband-Goulet, Eva Cabet, et al.
Journal of Neurology|March 3, 2004
A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desminAyush Dagvadorj, Montse Olivé, Jean-Andoni Urtizberea, et al.
Experimental Cell Research|July 3, 2007
Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander diseaseCyril Mignot, Cécile Delarasse, Séverine Escaich, et al.
Human Genetics|December 3, 2003
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathyAnna Kaminska, Sergei V Strelkov, Bertrand Goudeau, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutationsMarinos C Dalakas, Ayush Dagvadorj, Bertrand Goudeau, et al.
Human Mutation|January 16, 2007
Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathiesHarald Bär, Bertrand Goudeau, Sarah Wälde, et al.
Pageof 5