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Stem Cells and Development|November 18, 2015
Modeling Andersen's Syndrome in Human Induced Pluripotent Stem CellsJonathan Pini, Matthieu Rouleau, Claude Desnuelle, et al.Human Molecular Genetics|September 11, 2014
The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesisSonia Sacco, Serena Giuliano, Sabrina Sacconi, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 30, 2018
Osteogenic and Chondrogenic Master Genes Expression Is Dependent on the Kir2.1 Potassium Channel Through the Bone Morphogenetic Protein PathwayJonathan Pini, Serena Giuliano, Julia Matonti, et al.Biochimica Et Biophysica Acta|June 3, 2014
Facioscapulohumeral muscular dystrophySabrina Sacconi, Leonardo Salviati, Claude DesnuelleBulletin De L'Academie Nationale De Medecine|October 26, 2005
[The possible place of autologus cell therapy in facioscapulohumeral muscular dystrophy]Claude Desnuelle, Sabrina Sacconi, Jean-Pierre Marolleau, et al.Journal of Neurology|July 31, 2009
Do patients having a decrease in SNAP amplitude during the course of MMN present with a different condition?Emilien Delmont, Charles Benaïm, Mael Launay, et al.Journal of Neurology|June 19, 2010
Abnormalities of cerebral arteries are frequent in patients with late-onset Pompe diseaseSabrina Sacconi, Jonathan D Bocquet, Stéphane Chanalet, et al.Frontiers in Pharmacology|October 22, 2011
Skeletal muscle na channel disordersDina Simkin, Saïd BendahhouArchives of Physical Medicine and Rehabilitation|May 4, 2010
Neuromuscular electrical stimulation training: a safe and effective treatment for facioscapulohumeral muscular dystrophy patientsSerge S Colson, Michaël Benchortane, Véronique Tanant, et al.Plos Genetics|February 28, 2009
The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophyAlexandre Ottaviani, Sylvie Rival-Gervier, Amina Boussouar, et al.Pageof 26