Search Results - "Emerson, Lindsay"

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  1. 1

    Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutations by Emerson, Lindsay J., Holt, Mark R., Wheeler, Matthew A., Wehnert, Manfred, Parsons, Maddy, Ellis, Juliet A.

    Published in Biochimica et biophysica acta (01-08-2009)
    “…In-frame mutations in nuclear lamin A/C lead to a multitude of tissue-specific degenerative diseases known as the ‘laminopathies’. Previous studies have…”
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    Journal Article
  2. 2

    The Emery–Dreifuss muscular dystrophy associated‐protein emerin is phosphorylated on serine 49 by protein kinase A by Roberts, Rhys C., Sutherland‐Smith, Andrew J., Wheeler, Matthew A., Norregaard Jensen, Ole, Emerson, Lindsay J., Spiliotis, Ioannis I., Tate, Christopher G., Kendrick‐Jones, John, Ellis, Juliet A.

    Published in The FEBS journal (01-10-2006)
    “…Emerin is a ubiquitously expressed inner nuclear membrane protein of unknown function. Mutations in its gene give rise to X‐linked Emery–Dreifuss muscular…”
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  3. 3

    Id Proteins Negatively Regulate Basic Helix-Loop-Helix Transcription Factor Function by Disrupting Subnuclear Compartmentalization by O'Toole, Peter J., Inoue, Toshiaki, Emerson, Lindsay, Morrison, Ian E.G., Mackie, Alan R., Cherry, Richard J., Norton, John D.

    Published in The Journal of biological chemistry (14-11-2003)
    “…Id helix-loop-helix (HLH) proteins act as global regulators of metazoan cell fate, cell growth, and differentiation. They heterodimerize with and inhibit the…”
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  4. 4

    Distinct functional domains in nesprin-1[alpha] and nesprin-2[beta] bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy by Wheeler, Matthew A, Davies, John D, Zhang, Qiuping, Emerson, Lindsay J, Hunt, James, Shanahan, Catherine M, Ellis, Juliet A

    Published in Experimental cell research (01-08-2007)
    “…Emerin and specific isoforms of nesprin-1 and -2 are nuclear membrane proteins which are binding partners in multi-protein complexes spanning the nuclear…”
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    Journal Article
  5. 5

    Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy by Motsch, Isabell, Kaluarachchi, Manuja, Emerson, Lindsay J., Brown, Charlotte A., Brown, Susan C., Dabauvalle, Marie-Christine, Ellis, Juliet A.

    Published in European journal of cell biology (01-09-2005)
    “…Mutations in the LMNA gene, which encodes nuclear lamins A and C by alternative splicing, can give rise to Emery–Dreifuss muscular dystrophy. The mechanism by…”
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    Journal Article
  6. 6

    Distinct functional domains in nesprin-1α and nesprin-2β bind directly to emerin and both interactions are disrupted in X-linked Emery–Dreifuss muscular dystrophy by Wheeler, Matthew A., Davies, John D., Zhang, Qiuping, Emerson, Lindsay J., Hunt, James, Shanahan, Catherine M., Ellis, Juliet A.

    Published in Experimental cell research (01-08-2007)
    “…Emerin and specific isoforms of nesprin-1 and -2 are nuclear membrane proteins which are binding partners in multi-protein complexes spanning the nuclear…”
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    Journal Article
  7. 7

    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 by Wheeler, Matthew A, Davies, John D, Zhang, Qiuping, Emerson, Lindsay J, Hunt, James, Shanahan, Catherine M, Ellis, Juliet A

    Published in Experimental cell research (01-08-2007)
    “…Emerin and specific isoforms of nesprin-1 and -2 are nuclear membrane proteins which are binding partners in multi-protein complexes spanning the nuclear…”
    Get full text
    Journal Article