Výsledky vyhledávání - Amanda M. Amell
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Wnt/β-catenin signaling suppresses DUX4 expression and prevents apoptosis of FSHD muscle cells Autor Gregory J. Block, Divya Narayanan, Amanda M. Amell, Lisa M. Petek, Kathryn C. Davidson, Thomas D. Bird, Rabi Tawil, Randall T. Moon, Daniel G. Miller
Vydáno 2013Artigo -
2
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2 Autor Richard J.L.F. Lemmers, Rabi Tawil, Lisa M. Petek, Judit Balog, Gregory J. Block, Gijs W.E. Santen, Amanda M. Amell, Patrick J. van der Vliet, Rowida Almomani, Kirsten R. Straasheijm, Yvonne D. Krom, Rinse Klooster, Yu Sun, Johan T. den Dunnen, Quinta Helmer, Colleen M. Donlin‐Smith, George W. Padberg, Baziel G.M. van Engelen, Jessica C. de Greef, Annemieke Aartsma‐Rus, Rune R. Frants, Marjolein Visser, Claude Desnuelle, Sabrina Sacconi, Galina N. Filippova, Egbert Bakker, Michael J. Bamshad, Stephen J. Tapscott, Daniel G. Miller, Silvère M. van der Maarel
Vydáno 2012Artigo