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Plos Medicine|May 30, 2009
Functional substitution by TAT-utrophin in dystrophin-deficient miceKevin J Sonnemann, Hanke Heun-Johnson, Amy J Turner, et al.Skeletal Muscle|May 9, 2015
In vitro stability of therapeutically relevant, internally truncated dystrophinsJackie L McCourt, Katrina K Rhett, Michele A Jaeger, et al.Skeletal Muscle|October 15, 2011
Transgenic overexpression of γ-cytoplasmic actin protects against eccentric contraction-induced force loss in mdx miceKristen A Baltgalvis, Michele A Jaeger, Daniel P Fitzsimons, et al.Scientific Reports|September 13, 2018
Integrative effects of dystrophin loss on metabolic function of the mdx mouseJana Strakova, Forum Kamdar, Debra Kulhanek, et al.Human Molecular Genetics|April 5, 2018
Variable rescue of microtubule and physiological phenotypes in mdx muscle expressing different miniaturized dystrophinsD'anna M Nelson, Angus Lindsay, Luke M Judge, et al.Stem Cell Reports|June 10, 2022
Fibroblast fate determination during cardiac reprogramming by remodeling of actin filamentsZhentao Zhang, Wenhui Zhang, Robert Blakes, et al.The FEBS Journal|April 4, 2019
Variable cytoplasmic actin expression impacts the sensitivity of different dystrophin-deficient mdx skeletal muscles to eccentric contractionAngus Lindsay, William M Southern, Preston M McCourt, et al.Developmental Cell|September 5, 2006
Cytoplasmic gamma-actin is not required for skeletal muscle development but its absence leads to a progressive myopathyKevin J Sonnemann, Daniel P Fitzsimons, Jitandrakumar R Patel, et al.Human Molecular Genetics|April 30, 2002
Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin-glycoprotein complex and partially prevents dystrophyLaura E Warner, Christiana DelloRusso, Robert W Crawford, et al.Journal of Leukocyte Biology|September 12, 2006
Resolution of inflammation by retrograde chemotaxis of neutrophils in transgenic zebrafishJonathan R Mathias, Benjamin J Perrin, Ting-Xi Liu, et al.Pageof 12