Wnt/β-catenin signaling suppresses DUX4 expression and prevents apoptosis of FSHD muscle cells

Por Block, Gregory J., Narayanan, Divya, Amell, Amanda M., Petek, Lisa M., Davidson, Kathryn C., Bird, Thomas D., Tawil, Rabi, Moon, Randall T., Miller, Daniel G.
Publicado em 2013

Asymmetric Bidirectional Transcription from the FSHD-Causing D4Z4 Array Modulates DUX4 Production

Por Block, Gregory J., Petek, Lisa M., Narayanan, Divya, Amell, Amanda M., Moore, James M., Rabaia, Natalia A., Tyler, Ashlee, van der Maarel, Silvere M., Tawil, Rabi, Filippova, Galina N., Miller, Daniel G.
Publicado em 2012

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

Por Lemmers, Richard J.L.F., Tawil, Rabi, Petek, Lisa M., Balog, Judit, Block, Gregory J., Santen, Gijs W.E., Amell, Amanda M., van der Vliet, Patrick J., Almomani, Rowida, Straasheijm, Kirsten R., Krom, Yvonne D., Klooster, Rinse, Sun, Yu, den Dunnen, Johan T., Helmer, Quinta, Donlin-Smith, Colleen M., Padberg, George W., van Engelen, Baziel G.M., de Greef, Jessica C., Aartsma-Rus, Annemieke M., Frants, Rune R., de Visser, Marianne, Desnuelle, Claude, Sacconi, Sabrina, Filippova, Galina N., Bakker, Bert, Bamshad, Michael J., Tapscott, Stephen J., Miller, Daniel G., van der Maarel, Silvère M.
Publicado em 2012