Do actin isoforms have unique functionalities at the protein level? by James M. Ervasti, Anna S. Kashina, Benjamin J. Perrin

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Skeletal muscle-specific ablation of gamma(cyto)-actin does not exacerbate the mdx phenotype. by Kurt W Prins, Dawn A Lowe, James M Ervasti

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β-actin and γ-actin are each dispensable for auditory hair cell development but required for Stereocilia maintenance. by Benjamin J Perrin, Kevin J Sonnemann, James M Ervasti

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Loss of β-Cytoplasmic Actin in the Intestinal Epithelium Increases Gut Barrier Permeability in vivo and Exaggerates the Severity of Experimental Colitis by Susana Lechuga, Nayden G. Naydenov, Alex Feygin, Michael Cruise, James M. Ervasti, Andrei I. Ivanov

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Destabilization of the dystrophin-glycoprotein complex without functional deficits in alpha-dystrobrevin null muscle. by Tina M Bunnell, Michele A Jaeger, Daniel P Fitzsimons, Kurt W Prins, James M Ervasti

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Deletion of exons 2 and 3 from Actb and cell immortalization lead to widespread, β-actin independent alterations in gene expression associated with cell cycle control by Lauren J. Sundby, William M. Southern, Jiao Sun, Xiaobai Patrinostro, Wei Zhang, Jeongsik Yong, James M. Ervasti

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Rapid, redox-mediated mechanical susceptibility of the cortical microtubule lattice in skeletal muscle by D'anna M. Nelson, Elizabeth K. Fasbender, Margurite C. Jakubiak, Angus Lindsay, Dawn A. Lowe, James M. Ervasti

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Functional substitution by TAT-utrophin in dystrophin-deficient mice. by Kevin J Sonnemann, Hanke Heun-Johnson, Amy J Turner, Kristen A Baltgalvis, Dawn A Lowe, James M Ervasti

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Mitochondrial bioenergetic dysfunction in the D2.mdx model of Duchenne muscular dystrophy is associated with microtubule disorganization in skeletal muscle by Sofhia V. Ramos, Meghan C. Hughes, Luca J. Delfinis, Catherine A. Bellissimo, Christopher G. R. Perry, James M. Ervasti

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High Frequency Hearing Loss and Hyperactivity in DUX4 Transgenic Mice. by Abhijit Dandapat, Benjamin J Perrin, Christine Cabelka, Maria Razzoli, James M Ervasti, Alessandro Bartolomucci, Dawn A Lowe, Michael Kyba

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Contraction-Induced Loss of Plasmalemmal Electrophysiological Function Is Dependent on the Dystrophin Glycoprotein Complex by Cory W. Baumann, Cory W. Baumann, Angus Lindsay, Angus Lindsay, Sylvia R. Sidky, James M. Ervasti, Gordon L. Warren, Dawn A. Lowe

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Mechanical factors tune the sensitivity of mdx muscle to eccentric strength loss and its protection by antioxidant and calcium modulators by Angus Lindsay, Cory W. Baumann, Robyn T. Rebbeck, Samantha L. Yuen, William M. Southern, James S. Hodges, Razvan L. Cornea, David D. Thomas, James M. Ervasti, Dawn A. Lowe

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Social stress is lethal in the mdx model of Duchenne muscular dystrophy by Maria Razzoli, Angus Lindsay, Michelle L. Law, Christopher M. Chamberlain, William M. Southern, Madeleine Berg, John Osborn, William C. Engeland, Joseph M. Metzger, James M. Ervasti, Alessandro Bartolomucci

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Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle by John T. Olthoff, Angus Lindsay, Reem Abo-Zahrah, Kristen A. Baltgalvis, Xiaobai Patrinostro, Joseph J. Belanto, Dae-Yeul Yu, Benjamin J. Perrin, Daniel J. Garry, George G. Rodney, Dawn A. Lowe, James M. Ervasti

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PFKFB3-mediated glycolysis rescues myopathic outcomes in the ischemic limb by Terence E. Ryan, Cameron A. Schmidt, Michael D. Tarpey, Adam J. Amorese, Dean J. Yamaguchi, Emma J. Goldberg, Melissa M.R. Iñigo, Reema Karnekar, Allison O’Rourke, James M. Ervasti, Patricia Brophy, Thomas D. Green, P. Darrell Neufer, Kelsey Fisher-Wellman, Espen E. Spangenburg, Joseph M. McClung

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