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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 ophthalmoplegia
Nicole Monnier, Ana Ferreiro, Isabelle Marty, et al.
Cells
|
February 12, 2025
RyR1 Is Involved in the Control of Myogenesis
Amandine 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 hypotonia
Nicole 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 Editing
Mathilde 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 fruits
Jamila 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 myopathy
Nicole 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 cells
Alexis 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 proteins
Shiyu Luo, Qifei Li, Jasmine Lin, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 65) with videos related to
Sort By:
Page
of 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 ophthalmoplegia
Nicole Monnier, Ana Ferreiro, Isabelle Marty, et al.
Cells
|
February 12, 2025
RyR1 Is Involved in the Control of Myogenesis
Amandine 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 hypotonia
Nicole 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 Editing
Mathilde 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 fruits
Jamila 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 myopathy
Nicole 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 cells
Alexis 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 proteins
Shiyu Luo, Qifei Li, Jasmine Lin, et al.
Page
of 7