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Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres.
Trollet C, Anvar SY, Venema A, Hargreaves IP, Foster K, Vignaud A, Ferry A, Negroni E, Hourde C, Baraibar MA, 't Hoen PA, Davies JE, Rubinsztein DC, Heales SJ, Mouly V, van der Maarel SM, Butler-Browne G, Raz V, Dickson G. Trollet C, et al. Hum Mol Genet. 2010 Jun 1;19(11):2191-207. doi: 10.1093/hmg/ddq098. Epub 2010 Mar 5. Hum Mol Genet. 2010. PMID: 20207626
Current advances in cell therapy strategies for muscular dystrophies.
Negroni E, Vallese D, Vilquin JT, Butler-Browne G, Mouly V, Trollet C. Negroni E, et al. Among authors: trollet c. Expert Opin Biol Ther. 2011 Feb;11(2):157-76. doi: 10.1517/14712598.2011.542748. Expert Opin Biol Ther. 2011. PMID: 21219234 Review.
57 results