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Denis Furling

Showing results (51-60 of 80) with videos related to

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The Journal of Cell Biology|July 10, 2020
Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaquesGilles Moulay, Jeanne Lainé, Mégane Lemaître, et al.
Plos One|September 12, 2014
RBFOX1 cooperates with MBNL1 to control splicing in muscle, including events altered in myotonic dystrophy type 1Roscoe Klinck, Angélique Fourrier, Philippe Thibault, et al.
Molecular Therapy. Nucleic Acids|June 5, 2023
Specific Florent Porquet, Lin Weidong, Kévin Jehasse, et al.
Human Molecular Genetics|July 27, 2021
CRISPR gene editing in pluripotent stem cells reveals the function of MBNL proteins during human in vitro myogenesisAntoine Mérien, Julie Tahraoui-Bories, Michel Cailleret, et al.
Brain : a Journal of Neurology|October 26, 2024
MBNL deficiency in motor neurons disrupts neuromuscular junction maintenance and gait coordinationCharles Frison-Roche, Célia Martin Demier, Steve Cottin, et al.
Human Molecular Genetics|August 8, 2013
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1Morgane Gauthier, Antoine Marteyn, Jérôme Alexandre Denis, et al.
Iscience|January 15, 2019
Pluripotent Stem Cell-Based Drug Screening Reveals Cardiac Glycosides as Modulators of Myotonic Dystrophy Type 1Yves Maury, Pauline Poydenot, Benjamin Brinon, et al.
Circulation. Cardiovascular Genetics|June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart RegistryCaroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.
Journal of Proteomics|September 25, 2012
In-depth analysis of the secretome identifies three major independent secretory pathways in differentiating human myoblastsMarie-Catherine Le Bihan, Anne Bigot, Søren Skov Jensen, et al.
International Journal of Molecular Sciences|April 24, 2019
Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1Christine Voellenkle, Alessandra Perfetti, Matteo Carrara, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
The Journal of Cell Biology|July 10, 2020
Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaquesGilles Moulay, Jeanne Lainé, Mégane Lemaître, et al.
Plos One|September 12, 2014
RBFOX1 cooperates with MBNL1 to control splicing in muscle, including events altered in myotonic dystrophy type 1Roscoe Klinck, Angélique Fourrier, Philippe Thibault, et al.
Molecular Therapy. Nucleic Acids|June 5, 2023
Specific Florent Porquet, Lin Weidong, Kévin Jehasse, et al.
Human Molecular Genetics|July 27, 2021
CRISPR gene editing in pluripotent stem cells reveals the function of MBNL proteins during human in vitro myogenesisAntoine Mérien, Julie Tahraoui-Bories, Michel Cailleret, et al.
Brain : a Journal of Neurology|October 26, 2024
MBNL deficiency in motor neurons disrupts neuromuscular junction maintenance and gait coordinationCharles Frison-Roche, Célia Martin Demier, Steve Cottin, et al.
Human Molecular Genetics|August 8, 2013
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1Morgane Gauthier, Antoine Marteyn, Jérôme Alexandre Denis, et al.
Iscience|January 15, 2019
Pluripotent Stem Cell-Based Drug Screening Reveals Cardiac Glycosides as Modulators of Myotonic Dystrophy Type 1Yves Maury, Pauline Poydenot, Benjamin Brinon, et al.
Circulation. Cardiovascular Genetics|June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart RegistryCaroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.
Journal of Proteomics|September 25, 2012
In-depth analysis of the secretome identifies three major independent secretory pathways in differentiating human myoblastsMarie-Catherine Le Bihan, Anne Bigot, Søren Skov Jensen, et al.
International Journal of Molecular Sciences|April 24, 2019
Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1Christine Voellenkle, Alessandra Perfetti, Matteo Carrara, et al.
Pageof 8