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Isabelle Richard

Showing results (61-70 of 182) with videos related to

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Human Mutation|November 19, 2011
Rescue of sarcoglycan mutations by inhibition of endoplasmic reticulum quality control is associated with minimal structural modificationsTayebeh Soheili, Evelyne Gicquel, Jérôme Poupiot, et al.
Human Gene Therapy|February 23, 2013
Prolonged gene expression in muscle is achieved without active immune tolerance using microrRNA 142.3p-regulated rAAV gene transferFlorence Boisgerault, David-Alexandre Gross, Maxime Ferrand, et al.
Family Practice|September 14, 2010
Psychosocial risk factors for chronic low back pain in primary care--a systematic reviewAline Ramond, Céline Bouton, Isabelle Richard, et al.
Research in Developmental Disabilities|April 16, 2013
Effect of observation of simple hand movement on brain activations in patients with unilateral cerebral palsy: an fMRI studyMickael Dinomais, Gregoire Lignon, Eva Chinier, et al.
Molecular Therapy. Methods & Clinical Development|June 2, 2015
A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequenceMarina Pryadkina, William Lostal, Nathalie Bourg, et al.
BMC Musculoskeletal Disorders|April 18, 2014
Effectiveness of three treatment strategies on occupational limitations and quality of life for patients with non-specific chronic low back pain: Is a multidisciplinary approach the key feature to success: study protocol for a randomized controlled trialAudrey Petit, Ghislaine Roche-Leboucher, Luc Bontoux, et al.
Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
The FEBS Journal|January 16, 2009
Cardiac ankyrin repeat protein is a marker of skeletal muscle pathological remodellingLydie Laure, Laurence Suel, Carinne Roudaut, et al.
Thrombosis Research|January 8, 2008
S35225 is a direct inhibitor of Plasminogen Activator Inhibitor type-1 activity in the bloodAlain Rupin, Roger Gaertner, Philippe Mennecier, et al.
Neuromuscular Disorders : NMD|March 20, 2021
Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletionMarco Spinazzi, Jerome Poupiot, Julien Cassereau, et al.
Pageof 19

Showing results (61-70 of 182) with videos related to

Sort By:
Pageof 19
Human Mutation|November 19, 2011
Rescue of sarcoglycan mutations by inhibition of endoplasmic reticulum quality control is associated with minimal structural modificationsTayebeh Soheili, Evelyne Gicquel, Jérôme Poupiot, et al.
Human Gene Therapy|February 23, 2013
Prolonged gene expression in muscle is achieved without active immune tolerance using microrRNA 142.3p-regulated rAAV gene transferFlorence Boisgerault, David-Alexandre Gross, Maxime Ferrand, et al.
Family Practice|September 14, 2010
Psychosocial risk factors for chronic low back pain in primary care--a systematic reviewAline Ramond, Céline Bouton, Isabelle Richard, et al.
Research in Developmental Disabilities|April 16, 2013
Effect of observation of simple hand movement on brain activations in patients with unilateral cerebral palsy: an fMRI studyMickael Dinomais, Gregoire Lignon, Eva Chinier, et al.
Molecular Therapy. Methods & Clinical Development|June 2, 2015
A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequenceMarina Pryadkina, William Lostal, Nathalie Bourg, et al.
BMC Musculoskeletal Disorders|April 18, 2014
Effectiveness of three treatment strategies on occupational limitations and quality of life for patients with non-specific chronic low back pain: Is a multidisciplinary approach the key feature to success: study protocol for a randomized controlled trialAudrey Petit, Ghislaine Roche-Leboucher, Luc Bontoux, et al.
Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
The FEBS Journal|January 16, 2009
Cardiac ankyrin repeat protein is a marker of skeletal muscle pathological remodellingLydie Laure, Laurence Suel, Carinne Roudaut, et al.
Thrombosis Research|January 8, 2008
S35225 is a direct inhibitor of Plasminogen Activator Inhibitor type-1 activity in the bloodAlain Rupin, Roger Gaertner, Philippe Mennecier, et al.
Neuromuscular Disorders : NMD|March 20, 2021
Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletionMarco Spinazzi, Jerome Poupiot, Julien Cassereau, et al.
Pageof 19