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Journal of Neuromuscular Diseases|December 23, 2025
Identification of myokines associated with the pathological stress response in the mdx mouse model of Duchenne muscular dystrophyErynn E Johnson, Jacob Powers, James M ErvastiPlos One|March 10, 2012
Restricted morphological and behavioral abnormalities following ablation of β-actin in the brainThomas R Cheever, Bin Li, James M ErvastiProceedings of the National Academy of Sciences of the United States of America|May 12, 2010
Disease-causing missense mutations in actin binding domain 1 of dystrophin induce thermodynamic instability and protein aggregationDavin M Henderson, Ann Lee, James M ErvastiMolecular Biology of the Cell|June 7, 2018
The stable actin core of mechanosensory stereocilia features continuous turnover of actin cross-linkersPallabi Roy, Benjamin J PerrinCurrent Biology : CB|February 5, 2020
Cell Biology: Function Guides Form of Auditory Sensory CellsJamis McGrath, Benjamin J PerrinProceedings of the National Academy of Sciences of the United States of America|September 23, 2015
Disease-proportional proteasomal degradation of missense dystrophinsDana M Talsness, Joseph J Belanto, James M ErvastiJournal of Applied Physiology (Bethesda, Md. : 1985)|May 14, 2011
TAT-μUtrophin mitigates the pathophysiology of dystrophin and utrophin double-knockout miceJarrod A Call, James M Ervasti, Dawn A LowePlos One|March 30, 2011
Axonal regeneration and neuronal function are preserved in motor neurons lacking ß-actin in vivoThomas R Cheever, Emily A Olson, James M ErvastiPlos One|June 12, 2008
Skeletal muscle-specific ablation of gamma(cyto)-actin does not exacerbate the mdx phenotypeKurt W Prins, Dawn A Lowe, James M ErvastiThe Journal of Biological Chemistry|September 4, 2003
Core 1 glycans on alpha-dystroglycan mediate laminin-induced acetylcholine receptor clustering but not laminin bindingErin L McDearmon, Ariana C Combs, James M ErvastiPageof 12