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Ronald D Cohn

Showing results (41-50 of 100) with videos related to

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Pediatrics|May 3, 2006
Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T geneStacie B Peddy, Luca A Vricella, Jane E Crosson, et al.
Experimental Neurology|January 22, 2013
Hibernating squirrel muscle activates the endurance exercise pathway despite prolonged immobilizationRan Xu, Eva Andres-Mateos, Rebeca Mejias, et al.
The Journal of Pediatrics|January 31, 2016
Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1LGrace Yoon, Zeenat Malam, Tara Paton, et al.
Science Translational Medicine|May 13, 2011
Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopeniaTyesha N Burks, Eva Andres-Mateos, Ruth Marx, et al.
Nature Biotechnology|February 22, 2022
Saturation variant interpretation using CRISPR prime editingSteven Erwood, Teija M I Bily, Jason Lequyer, et al.
Disease Models & Mechanisms|February 8, 2014
Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibitionElizabeth M MacDonald, Eva Andres-Mateos, Rebeca Mejias, et al.
Disease Models & Mechanisms|August 5, 2024
Generation and characterization of a novel mouse model of Becker Muscular Dystrophy with a deletion of exons 52 to 55Lucie O M Perillat, Tatianna W Y Wong, Eleonora Maino, et al.
Molecular Genetics and Metabolism|January 27, 2017
Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type IIAmal Al Teneiji, Theodora U J Bruun, Sarah Sidky, et al.
Molecular Therapy. Methods & Clinical Development|August 7, 2023
Prevention of early-onset cardiomyopathy in <i>Dmd</i> exon 52-54 deletion mice by CRISPR-Cas9-mediated exon skippingMatthew Rok, Tatianna Wai Ying Wong, Eleonora Maino, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 9, 2025
Template-assisted sequence knockin rescues skeletal and cardiac muscle function in a deletion model of Duchenne muscular dystrophySina Fatehi, Matthew J Rok, Ryan M Marks, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
Pediatrics|May 3, 2006
Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T geneStacie B Peddy, Luca A Vricella, Jane E Crosson, et al.
Experimental Neurology|January 22, 2013
Hibernating squirrel muscle activates the endurance exercise pathway despite prolonged immobilizationRan Xu, Eva Andres-Mateos, Rebeca Mejias, et al.
The Journal of Pediatrics|January 31, 2016
Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1LGrace Yoon, Zeenat Malam, Tara Paton, et al.
Science Translational Medicine|May 13, 2011
Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopeniaTyesha N Burks, Eva Andres-Mateos, Ruth Marx, et al.
Nature Biotechnology|February 22, 2022
Saturation variant interpretation using CRISPR prime editingSteven Erwood, Teija M I Bily, Jason Lequyer, et al.
Disease Models & Mechanisms|February 8, 2014
Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibitionElizabeth M MacDonald, Eva Andres-Mateos, Rebeca Mejias, et al.
Disease Models & Mechanisms|August 5, 2024
Generation and characterization of a novel mouse model of Becker Muscular Dystrophy with a deletion of exons 52 to 55Lucie O M Perillat, Tatianna W Y Wong, Eleonora Maino, et al.
Molecular Genetics and Metabolism|January 27, 2017
Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type IIAmal Al Teneiji, Theodora U J Bruun, Sarah Sidky, et al.
Molecular Therapy. Methods & Clinical Development|August 7, 2023
Prevention of early-onset cardiomyopathy in <i>Dmd</i> exon 52-54 deletion mice by CRISPR-Cas9-mediated exon skippingMatthew Rok, Tatianna Wai Ying Wong, Eleonora Maino, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 9, 2025
Template-assisted sequence knockin rescues skeletal and cardiac muscle function in a deletion model of Duchenne muscular dystrophySina Fatehi, Matthew J Rok, Ryan M Marks, et al.
Pageof 10