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Life (Basel, Switzerland)|June 28, 2023
Serum Neurofilaments in Motor Neuron Disease and Their Utility in Differentiating ALS, PMA and PLSGavin McCluskey, Karen E Morrison, Colette Donaghy, et al.Skeletal Muscle|July 10, 2020
Optimized method for extraction of exosomes from human primary muscle cellsLaura Le Gall, Zamalou Gisele Ouandaogo, Ekene Anakor, et al.Journal of Cachexia, Sarcopenia and Muscle|October 23, 2021
RIPK3-mediated cell death is involved in DUX4-mediated toxicity in facioscapulohumeral dystrophyVirginie Mariot, Romain Joubert, Laura Le Gall, et al.Nucleic Acids Research|April 18, 2015
CellWhere: graphical display of interaction networks organized on subcellular localizationsLu Zhu, Apostolos Malatras, Matthew Thorley, et al.Skeletal Muscle|May 20, 2015
Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasiaWilliam Duddy, Stephanie Duguez, Helen Johnston, et al.Skeletal Muscle|December 10, 2016
Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell linesMatthew Thorley, Stéphanie Duguez, Emilia Maria Cristina Mazza, et al.Cellular and Molecular Life Sciences : CMLS|January 25, 2013
Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretionStephanie Duguez, William Duddy, Helen Johnston, et al.Human Molecular Genetics|March 24, 2017
Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscleAurelia Defour, Sushma Medikayala, Jack H Van der Meulen, et al.International Journal of Molecular Sciences|December 10, 2021
A <i>Dystrophin</i> Exon-52 Deleted Miniature Pig Model of Duchenne Muscular Dystrophy and Evaluation of Exon SkippingYusuke Echigoya, Nhu Trieu, William Duddy, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 17, 2019
Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD GeneYusuke Echigoya, Kenji Rowel Q Lim, Dyanna Melo, et al.Pageof 4