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Cells lacking β-actin are genetically reprogrammed and maintain conditional migratory capacity
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- journalArticle
- A1
- open access
Identification and expression analysis of splice variants of mouse enabled homologue during development and in adult tissues
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alpha-Skeletal Muscle Actin Mutants Causing Different Congenital Myopathies Induce Similar Cytoskeletal Defects in Cell Line Cultures
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The Mouse Thymosin Beta15 Gene Family Displays Unique Complexity and Encodes A Functional Thymosin Repeat
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Unbalancing the phosphatidylinositol-4,5-bisphosphate-cofilin interaction impairs cell steering
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alpha-Skeletal muscle actin nemaline myopathy mutants cause cell death in cultured muscle cells.
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- journalArticle
- A2
- open access
Phenotypes induced by NM causing α-skeletal muscle actin mutants in fibroblasts, Sol 8 myoblasts and myotubes
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Impaired neural crest migration contributes to midgestation lethality of beta-actin knock-out mouse
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Actin interacts with CCT via discrete binding sites: A binding transition-release model for CCT-mediated actin folding
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Structural plasticity of functional actin: Pictures of actin binding protein and polymer interfaces (vol 11, pg 1279, 2004)