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Acta Neuropathologica|May 13, 2018
Collagen VI is required for the structural and functional integrity of the neuromuscular junctionMatilde Cescon, Ilaria Gregorio, Nane Eiber, et al.Autophagy|September 16, 2016
Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNAAdriana Malena, Boris Pantic, Doriana Borgia, et al.Human Molecular Genetics|June 9, 2017
SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cellsSara Vianello, Boris Pantic, Aurora Fusto, et al.Experimental Cell Research|February 25, 2016
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblastsBoris Pantic, Doriana Borgia, Silvia Giunco, et al.Human Molecular Genetics|January 15, 2017
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patientsDoriana Borgia, Adriana Malena, Marco Spinazzi, et al.Scientific Reports|January 25, 2017
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubesCarmelo Milioto, Adriana Malena, Eleonora Maino, et al.Acta Neuropathologica|March 14, 2016
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat dietAnna Rocchi, Carmelo Milioto, Sara Parodi, et al.Pageof 1