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European Journal of Preventive Cardiology|February 15, 2022
Cardiovascular disease in the elderly: proceedings of the European Society of Cardiology-Cardiovascular Round TableMaddalena Lettino, Julia Mascherbauer, Matias Nordaby, et al.
Disease Models & Mechanisms|January 8, 2026
A new dystrophin deficient rat model mirroring exon skipping in patients with DMD exon 45 deletionsTao Wang, Cynthia Daoud, Auriane Dubois, et al.
NPJ Regenerative Medicine|January 3, 2026
Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activityLaura Palmieri, Giorgia Bimbi, Maxime Ferrand, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 25, 2026
CRISPR-Cas9-Mediated Upregulation of Utrophin Ameliorates Duchenne Muscular DystrophyMaëlle Ralu, Simon Guiraud, Sumitava Dastidar, et al.
Nanomedicine (London, England)|June 10, 2014
Assessing dystrophies and other muscle diseases at the nanometer scale by atomic force microscopyRuthger W van Zwieten, Stefania Puttini, Małgorzata Lekka, et al.
Plos One|February 19, 2013
Distinctive serum miRNA profile in mouse models of striated muscular pathologiesNicolas Vignier, Fatima Amor, Paul Fogel, et al.
American Journal of Human Genetics|January 22, 2013
Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathyJohann Böhm, Frédéric Chevessier, André Maues De Paula, et al.
Annals of Clinical and Translational Neurology|April 21, 2020
A new congenital multicore titinopathy associated with fast myosin heavy chain deficiencyAurélien Perrin, Corinne Metay, Marcello Villanova, et al.
International Journal of Molecular Sciences|August 26, 2023
Modeling Sarcoglycanopathy in Danio rerioFrancesco Dalla Barba, Michela Soardi, Leila Mouhib, et al.
Genes|June 24, 2022
Genetic Profile of Patients with Limb-Girdle Muscle Weakness in the Chilean PopulationMathieu Cerino, Patricio González-Hormazábal, Mario Abaji, et al.
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