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Isabelle Marty

Showing results (11-20 of 65) with videos related to

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The Journal of Physiology|May 1, 2009
Triadin: what possible function 20 years later?Isabelle Marty, Julien Fauré, Anne Fourest-Lieuvin, et al.
Human Molecular Genetics|April 30, 2003
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegiaNicole Monnier, Ana Ferreiro, Isabelle Marty, et al.
Cells|February 12, 2025
RyR1 Is Involved in the Control of MyogenesisAmandine Tourel, Robin Reynaud-Dulaurier, Julie Brocard, et al.
Medecine Sciences : M/S|November 18, 2024
[From gene to cell: Functional validation of RYR1 variants]Robin Reynaud Dulaurier, Julie Brocard, John Rendu, et al.
Neuromuscular Disorders : NMD|September 8, 2009
First genomic rearrangement of the RYR1 gene associated with an atypical presentation of lethal neonatal hypotoniaNicole Monnier, Annie Laquerrière, Stéphane Marret, et al.
Journal of Visualized Experiments : Jove|July 5, 2022
Development of Knock-Out Muscle Cell Lines using Lentivirus-Mediated CRISPR/Cas9 Gene EditingMathilde Beaufils, Amandine Tourel, Anne Petiot, et al.
Journal of Experimental Botany|April 25, 2007
Physiological relationships among physical, sensory, and morphological attributes of texture in tomato fruitsJamila Chaïb, Marie-Françoise Devaux, Marie-Ghislaine Grotte, et al.
Neuromuscular Disorders : NMD|January 22, 2009
Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathyNicole Monnier, Joel Lunardi, Isabelle Marty, et al.
Journal of Cell Science|August 27, 2016
Triadin and CLIMP-63 form a link between triads and microtubules in muscle cellsAlexis Osseni, Muriel Sébastien, Oriana Sarrault, et al.
Human Molecular Genetics|December 23, 2020
SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteinsShiyu Luo, Qifei Li, Jasmine Lin, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
The Journal of Physiology|May 1, 2009
Triadin: what possible function 20 years later?Isabelle Marty, Julien Fauré, Anne Fourest-Lieuvin, et al.
Human Molecular Genetics|April 30, 2003
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegiaNicole Monnier, Ana Ferreiro, Isabelle Marty, et al.
Cells|February 12, 2025
RyR1 Is Involved in the Control of MyogenesisAmandine Tourel, Robin Reynaud-Dulaurier, Julie Brocard, et al.
Medecine Sciences : M/S|November 18, 2024
[From gene to cell: Functional validation of RYR1 variants]Robin Reynaud Dulaurier, Julie Brocard, John Rendu, et al.
Neuromuscular Disorders : NMD|September 8, 2009
First genomic rearrangement of the RYR1 gene associated with an atypical presentation of lethal neonatal hypotoniaNicole Monnier, Annie Laquerrière, Stéphane Marret, et al.
Journal of Visualized Experiments : Jove|July 5, 2022
Development of Knock-Out Muscle Cell Lines using Lentivirus-Mediated CRISPR/Cas9 Gene EditingMathilde Beaufils, Amandine Tourel, Anne Petiot, et al.
Journal of Experimental Botany|April 25, 2007
Physiological relationships among physical, sensory, and morphological attributes of texture in tomato fruitsJamila Chaïb, Marie-Françoise Devaux, Marie-Ghislaine Grotte, et al.
Neuromuscular Disorders : NMD|January 22, 2009
Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathyNicole Monnier, Joel Lunardi, Isabelle Marty, et al.
Journal of Cell Science|August 27, 2016
Triadin and CLIMP-63 form a link between triads and microtubules in muscle cellsAlexis Osseni, Muriel Sébastien, Oriana Sarrault, et al.
Human Molecular Genetics|December 23, 2020
SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteinsShiyu Luo, Qifei Li, Jasmine Lin, et al.
Pageof 7