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European Journal of Human Genetics : EJHG|April 9, 2002
Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin)Valérie Allamand, Pascale GuicheneyJournal of Molecular Medicine (Berlin, Germany)|April 25, 2012
Selenoprotein N in skeletal muscle: from diseases to functionPerrine Castets, Alain Lescure, Pascale Guicheney, et al.Trends in Molecular Medicine|October 23, 2012
Sense from nonsense: therapies for premature stop codon diseasesLaure Bidou, Valérie Allamand, Jean-Pierre Rousset, et al.Biochimica Et Biophysica Acta|March 17, 2009
Selenoprotein function and muscle diseaseAlain Lescure, Mathieu Rederstorff, Alain Krol, et al.Skeletal Muscle|September 28, 2011
ColVI myopathies: where do we stand, where do we go?Valérie Allamand, Laura Briñas, Pascale Richard, et al.The American Journal of Pathology|January 14, 2017
Elevated Expression of Moesin in Muscular DystrophiesMark Pines, Oshrat Levi, Olga Genin, et al.Antioxidants (Basel, Switzerland)|March 22, 2020
Antioxidants Reduce Muscular Dystrophy in the dy2J/dy2J Mouse Model of Laminin α2 Chain-Deficient Muscular DystrophyVahid M Harandi, Bernardo Moreira Soares Oliveira, Valérie Allamand, et al.BMC Developmental Biology|August 25, 2009
Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursorsPerrine Castets, Svetlana Maugenre, Corine Gartioux, et al.Proceedings of the National Academy of Sciences of the United States of America|July 10, 2003
Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophyMadeleine Durbeej, Shanna M Sawatzki, Rita Barresi, et al.Matrix Biology : Journal of the International Society for Matrix Biology|February 6, 2008
First molecular characterization and immunolocalization of keratoepithelin in adult human skeletal muscleFrancesca Sciandra, Simona Morlacchi, Valérie Allamand, et al.Pageof 5