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Pascale Guicheney

Showing results (71-80 of 121) with videos related to

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The Journal of Cell Biology|May 9, 2012
An alternative mechanism of clathrin-coated pit closure revealed by ion conductance microscopyAndrew I Shevchuk, Pavel Novak, Marcus Taylor, et al.
The Journal of Gene Medicine|December 13, 2007
Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubesValérie Allamand, Laure Bidou, Masayuki Arakawa, et al.
Molecular Biology of the Cell|January 3, 2019
Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscleAgathe Franck, Jeanne Lainé, Gilles Moulay, et al.
Annals of Neurology|May 4, 2004
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N geneAna Ferreiro, Chantal Ceuterick-de Groote, Jared J Marks, et al.
Journal of Personalized Medicine|July 2, 2021
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic ResponseMalorie Blancard, Zahia Touat-Hamici, Yuriana Aguilar-Sanchez, et al.
Acta Neuropathologica|December 17, 2008
"Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathyJorge A Bevilacqua, Marc Bitoun, Valérie Biancalana, et al.
Heart Rhythm|September 21, 2010
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillationDaniel C Bartos, Sabine Duchatelet, Don E Burgess, et al.
Circulation|April 29, 2009
Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardiaMeiso Hayashi, Isabelle Denjoy, Fabrice Extramiana, et al.
Annals of Neurology|September 1, 2005
Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophyBetti Giusti, Laura Lucarini, Valentina Pietroni, et al.
Nature Genetics|October 18, 2005
Mutations in dynamin 2 cause dominant centronuclear myopathyMarc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
The Journal of Cell Biology|May 9, 2012
An alternative mechanism of clathrin-coated pit closure revealed by ion conductance microscopyAndrew I Shevchuk, Pavel Novak, Marcus Taylor, et al.
The Journal of Gene Medicine|December 13, 2007
Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubesValérie Allamand, Laure Bidou, Masayuki Arakawa, et al.
Molecular Biology of the Cell|January 3, 2019
Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscleAgathe Franck, Jeanne Lainé, Gilles Moulay, et al.
Annals of Neurology|May 4, 2004
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N geneAna Ferreiro, Chantal Ceuterick-de Groote, Jared J Marks, et al.
Journal of Personalized Medicine|July 2, 2021
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic ResponseMalorie Blancard, Zahia Touat-Hamici, Yuriana Aguilar-Sanchez, et al.
Acta Neuropathologica|December 17, 2008
"Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathyJorge A Bevilacqua, Marc Bitoun, Valérie Biancalana, et al.
Heart Rhythm|September 21, 2010
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillationDaniel C Bartos, Sabine Duchatelet, Don E Burgess, et al.
Circulation|April 29, 2009
Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardiaMeiso Hayashi, Isabelle Denjoy, Fabrice Extramiana, et al.
Annals of Neurology|September 1, 2005
Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophyBetti Giusti, Laura Lucarini, Valentina Pietroni, et al.
Nature Genetics|October 18, 2005
Mutations in dynamin 2 cause dominant centronuclear myopathyMarc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, et al.
Pageof 13