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  1. Article

    Open Access

    Phenotypes induced by NM causing α-skeletal muscle actin mutants in fibroblasts, Sol 8 myoblasts and myotubes

    Nemaline myopathy is a neuromuscular disorder characterized by the presence of nemaline bodies in patient muscles. 20% of the cases are associated with α-skeletal muscle actin mutations. We previously showed t...

    Drieke Vandamme, Ellen Lambert, Davy Waterschoot, Davina Tondeleir… in BMC Research Notes (2009)

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    Article

    A method for rapidly screening functionality of actin mutants and tagged actins

    Recombinant production and biochemical analysis of actin mutants has been hampered by the fact that actin has an absolute requirement for the eukaryotic chaperone CCT to reach its native state. We therefore ha...

    Heidi Rommelaere, Davy Waterschoot, Katrien Neirynck… in Biological Procedures Online (2004)