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Biochemical Society Transactions|November 23, 2011
Nuclear envelope disease and chromatin organizationJuliet A Ellis, Sue ShackletonExpert Reviews in Molecular Medicine|October 31, 2003
Muscular dystrophies, dilated cardiomyopathy, lipodystrophy and neuropathy: the nuclear connectionStephen L Maidment, Juliet A EllisBiochemical Society Transactions|November 22, 2008
Molecular signatures of Emery-Dreifuss muscular dystrophyMatthew A Wheeler, Juliet A EllisBiochemical Society Transactions|November 22, 2008
Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?Viola F Gnocchi, Juliet A Ellis, Peter S ZammitBiochemical Society Transactions|January 16, 2010
Genotype-phenotype correlations in laminopathies: how does fate translate?Juergen Scharner, Viola F Gnocchi, Juliet A Ellis, et al.Journal of Cell Science|February 13, 2002
The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotypeElizabeth A L Fairley, Andrew Riddell, Juliet A Ellis, et al.Proteins|December 31, 2013
Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathiesJuergen Scharner, Hui-Chun Lu, Franca Fraternali, et al.Cellular and Molecular Life Sciences : CMLS|December 10, 2009
Identification of an emerin-beta-catenin complex in the heart important for intercalated disc architecture and beta-catenin localisationMatthew A Wheeler, Alice Warley, Roland G Roberts, et al.Plos One|April 17, 2009
Further characterisation of the molecular signature of quiescent and activated mouse muscle satellite cellsViola F Gnocchi, Robert B White, Yusuke Ono, et al.Biochimica Et Biophysica Acta|June 16, 2009
Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutationsLindsay J Emerson, Mark R Holt, Matthew A Wheeler, et al.Pageof 3