Derek Blake - Publications

Publications

• Blake D.J., Hawkes R., Benson M.A. and Beesley P. (1999) Different dystrophin-like complexes are found in neurons and glia. J. Cell Biol. 147: 645-657.
• Blake D.J. and Kröger S. (2000) The molecular neurobiology of muscular dystrophy: Learning lessons from muscle? Trends Neurosci. 23: 92-99.
• Newey S.E., Benson, M.A., Ponting C.P., Davies K.E. and Blake D.J. (2000) Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex. Curr. Biol. 10: 12951298.
• Benson M.A., Newey S.E., Martin-Rendon E., Hawkes R. and Blake D.J. (2001) Dysbindin, a novel coiled-coil containing protein that interacts with the dystrobrevins in muscle and brain. J. Biol. Chem. 276: 24232-24241.
• Brockington M., Blake D. J., Prandini P., Brown S. C., Torelli S., Benson M. A., Ponting C. P., Estournet B., Romero N. B., Mercuri E., Voit T., Sewry C. A., Guicheney P. and Muntoni F. (2001) Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin a2 deficiency and abnormal glycosylation of a-dystroglycan. Am J. Hum. Genet. 69: 1198-1209.
• Brockington M., Yuva Y., Prandini P., Brown S. C., Torelli S., Benson M. A., Herrmann R., Anderson L. V. B., Bashir R., Burgunder J-M., Fallet S., Romero, N., Guicheney P., Fardeau M., Straub V., Reynolds G., Pollitt C., Sewry C. A., Bushby K., Voit T., Blake D. J. and Muntoni F. (2001) Mutations in the Fukutin Related-Protein gene (FKRP) identifies Limb Girdle Muscular Dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Hum. Mol. Genet. 10: 2851-2859.
• Blake D. J, Weir A., Newey S. E. and Davies K. E. (2002) Function and genetics of dystrophin and dystrophin-related proteins in muscle. Phys. Rev. 82: 291-329.