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Cx43

  • RESEARCH ARTICLE
    Identification of serine residues in the connexin43 carboxyl tail important for BCR-mediated spreading of B-lymphocytes
    Farnaz Pournia, May Dang-Lawson, Kate Choi, Victor Mo, Paul D. Lampe, Linda Matsuuchi
    Journal of Cell Science 2020 133: jcs237925 doi: 10.1242/jcs.237925 Published 10 March 2020

    Summary: Mutation of specific serine residues of connexin43 affects B-cell spreading, suggesting that this protein can be considered as a regulator of B-cell responses.

  • RESEARCH ARTICLE
    Mice harbouring an oculodentodigital dysplasia-linked Cx43 G60S mutation have severe hearing loss
    Julia M. Abitbol, John J. Kelly, Kevin J. Barr, Brian L. Allman, Dale W. Laird
    Journal of Cell Science 2018 131: jcs214635 doi: 10.1242/jcs.214635 Published 4 May 2018

    Summary: Mutant mice harbouring a severe loss-of-function mutation in Gja1, encoding Cx43, that is associated with the human-linked disease oculodentodigital dysplasia, leads to severe hearing loss and central auditory defects.

  • RESEARCH ARTICLE
    Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms
    Tao Huang, Qing Shao, Andrew MacDonald, Li Xin, Robert Lorentz, Donglin Bai, Dale W. Laird
    Journal of Cell Science 2013 126: 2857-2866; doi: 10.1242/jcs.123315

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