Postsynaptic Abnormalities at the Neuromuscular Junctions of Utrophin-deficient Mice

Por Deconinck, Anne E., Potter, Allyson C., Tinsley, Jonathon M., Wood, Sarah J., Vater, Ruth, Young, Carol, Metzinger, Laurent, Vincent, Angela, Slater, Clarke R., Davies, Kay E.
Publicado em 1997

Actin Nemaline Myopathy Mouse Reproduces Disease, Suggests Other Actin Disease Phenotypes and Provides Cautionary Note on Muscle Transgene Expression

Por Ravenscroft, Gianina, Jackaman, Connie, Sewry, Caroline A., McNamara, Elyshia, Squire, Sarah E., Potter, Allyson C., Papadimitriou, John, Griffiths, Lisa M., Bakker, Anthony J., Davies, Kay E., Laing, Nigel G., Nowak, Kristen J.
Publicado em 2011

Daily Treatment with SMTC1100, a Novel Small Molecule Utrophin Upregulator, Dramatically Reduces the Dystrophic Symptoms in the mdx Mouse

Por Tinsley, Jonathon M., Fairclough, Rebecca J., Storer, Richard, Wilkes, Fraser J., Potter, Allyson C., Squire, Sarah E., Powell, Dave S., Cozzoli, Anna, Capogrosso, Roberta F., Lambert, Adam, Wilson, Francis X., Wren, Stephen P., De Luca, Annamaria, Davies, Kay E.
Publicado em 2011

Rescue of skeletal muscle α-actin–null mice by cardiac (fetal) α-actin

Por Nowak, Kristen J., Ravenscroft, Gianina, Jackaman, Connie, Filipovska, Aleksandra, Davies, Stefan M., Lim, Esther M., Squire, Sarah E., Potter, Allyson C., Baker, Elizabeth, Clément, Sophie, Sewry, Caroline A., Fabian, Victoria, Crawford, Kelly, Lessard, James L., Griffiths, Lisa M., Papadimitriou, John M., Shen, Yun, Morahan, Grant, Bakker, Anthony J., Davies, Kay E., Laing, Nigel G.
Publicado em 2009