PubRank

Juliet A Ellis

Author PubWeight™ 25.00‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity. Hum Mol Genet 2007 3.26
2 Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle. J Cell Sci 2005 2.47
3 Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes. J Biol Chem 2009 1.79
4 The inner nuclear membrane protein emerin regulates beta-catenin activity by restricting its accumulation in the nucleus. EMBO J 2006 1.61
5 Further characterisation of the molecular signature of quiescent and activated mouse muscle satellite cells. PLoS One 2009 1.30
6 Distinct functional domains in nesprin-1alpha and nesprin-2beta bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy. Exp Cell Res 2007 1.29
7 The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype. J Cell Sci 2002 0.98
8 Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations. Hum Mutat 2011 0.96
9 Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutations. Biochim Biophys Acta 2009 0.92
10 Genotype-phenotype correlations in laminopathies: how does fate translate? Biochem Soc Trans 2010 0.89
11 The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A. FEBS J 2006 0.85
12 Identification of an emerin-beta-catenin complex in the heart important for intercalated disc architecture and beta-catenin localisation. Cell Mol Life Sci 2009 0.84
13 Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α. Hum Mol Genet 2013 0.84
14 Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy. Eur J Cell Biol 2005 0.83
15 Molecular signatures of Emery-Dreifuss muscular dystrophy. Biochem Soc Trans 2008 0.82
16 Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy. PLoS One 2011 0.82
17 NEP-A and NEP-B both contribute to nuclear pore formation in Xenopus eggs and oocytes. J Cell Sci 2008 0.81
18 Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy? Biochem Soc Trans 2008 0.81
19 Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies. Proteins 2013 0.79
20 Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot. J Hum Genet 2011 0.78
21 Cell biology: Patches for wounded muscle. Nature 2003 0.77
22 Muscular dystrophies, dilated cardiomyopathy, lipodystrophy and neuropathy: the nuclear connection. Expert Rev Mol Med 2002 0.77