Biography and Research Interest

Publications

Non-Zebrafish Publications

Miller, G., Moore, C.J., Terry, R., La Riviere, T., Mitchell, A., Piggott, R., Dear, T.N., Wells, D.J. and Winder, S.J. (2012) Preventing phosphorylation of dystroglycan ameliorates the dystrophic phenotype in mdx mouse. Hum Mol Genet, 21, 4508–4520.

Moore, C.J. and Winder, S.J. (2012) The inside and out of dystroglycan post-translational modification. Neuromuscul Disord, 22, 959–965.

Thompson, O., Moore, C.J., Hussain, S.-A., Kleino, I., Peckham, M., Hohenester, E., Ayscough, K.R., Saksela, K. and Winder, S.J. (2010) Modulation of cell spreading and cell-substrate adhesion dynamics by dystroglycan. Journal of Cell Science, 123, 118–127.

Moore, C.J. and Winder, S.J. (2010) Dystroglycan versatility in cell adhesion: a tale of multiple motifs. Cell Commun. Signal, 8, 3.

Moore, C.J. and Hewitt, J.E. (2009) Dystroglycan glycosylation and muscular dystrophy. Glycoconj J, 26, 349–357.

Moore, C.J., Goh, H.T. and Hewitt, J.E. (2008) Genes required for functional glycosylation of dystroglycan are conserved in zebrafish. Genomics, 92, 159–167.

Grewal, P.K., McLaughlan, J.M., Moore, C.J., Browning, C.A. and Hewitt, J.E. (2005) Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies. Glycobiology, 15, 912–923.

Browning, C.A., Grewal, P.K., Moore, C.J. and Hewitt, J.E. (2005) A rapid PCR method for genotyping the Large(myd) mouse, a model of glycosylation-deficient congenital muscular dystrophy. Neuromuscul Disord, 15, 331–335.