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Bertrand Goudeau

Showing results (51-60 of 62) with videos related to

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Bioelectromagnetics|April 8, 2015
Effects of 50 Hz magnetic fields on gap junctional intercellular communication in NIH3T3 cellsYann Percherancier, Bertrand Goudeau, Renaud Charlet de Sauvage, et al.
International Journal of Cardiology|August 8, 2006
Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutationPiotr Pruszczyk, Anna Kostera-Pruszczyk, Alexey Shatunov, et al.
Muscle & Nerve|May 27, 2003
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segmentAyush Dagvadorj, Bertrand Goudeau, David Hilton-Jones, et al.
Biophysical Journal|January 12, 2017
Full-Spectral Multiplexing of Bioluminescence Resonance Energy Transfer in Three TRPV ChannelsHermanus Johannes Ruigrok, Guillaume Shahid, Bertrand Goudeau, 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.
Human Mutation|July 26, 2006
Variable pathogenic potentials of mutations located in the desmin alpha-helical domainBertrand Goudeau, Fernando Rodrigues-Lima, Dirk Fischer, et al.
FEBS Letters|June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathiesChristoph S Clemen, Dirk Fischer, Udo Roth, et al.
Human Molecular Genetics|March 7, 2003
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondriaRolf Schröder, Bertrand Goudeau, Monique Casteras Simon, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
Bioelectromagnetics|April 8, 2015
Effects of 50 Hz magnetic fields on gap junctional intercellular communication in NIH3T3 cellsYann Percherancier, Bertrand Goudeau, Renaud Charlet de Sauvage, et al.
International Journal of Cardiology|August 8, 2006
Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutationPiotr Pruszczyk, Anna Kostera-Pruszczyk, Alexey Shatunov, et al.
Muscle & Nerve|May 27, 2003
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segmentAyush Dagvadorj, Bertrand Goudeau, David Hilton-Jones, et al.
Biophysical Journal|January 12, 2017
Full-Spectral Multiplexing of Bioluminescence Resonance Energy Transfer in Three TRPV ChannelsHermanus Johannes Ruigrok, Guillaume Shahid, Bertrand Goudeau, 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.
Human Mutation|July 26, 2006
Variable pathogenic potentials of mutations located in the desmin alpha-helical domainBertrand Goudeau, Fernando Rodrigues-Lima, Dirk Fischer, et al.
FEBS Letters|June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathiesChristoph S Clemen, Dirk Fischer, Udo Roth, et al.
Human Molecular Genetics|March 7, 2003
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondriaRolf Schröder, Bertrand Goudeau, Monique Casteras Simon, et al.
Pageof 7