Jamie L. Marshall, Ph.D.
Affiliations: | 2012 | University of California, Los Angeles, Los Angeles, CA |
Area:
Molecular Biology, Physiology Biology, Cell BiologyGoogle:
"Jamie Marshall"Parents
Sign in to add mentor| Rachelle H. Crosbie | grad student | 2012 | UCLA | |
| (The Role of Sarcospan in the Adhesion Glycoprotein Complexes at the Sarcolemma in Murine Models of Muscular Dystrophy.) | ||||
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| Gibbs EM, McCourt JL, Shin KM, et al. (2021) Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease. Human Molecular Genetics |
| Parvatiyar MS, Brownstein AJ, Kanashiro-Takeuchi RM, et al. (2019) Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy. Jci Insight. 5 |
| Gibbs EM, Marshall JL, Ma E, et al. (2016) High levels of sarcospan are well tolerated and act as a sarcolemmal stabilizer to address skeletal muscle and pulmonary dysfunction in DMD. Human Molecular Genetics |
| McMorran BJ, McCarthy FE, Gibbs EM, et al. (2016) Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx. Glycobiology |
| Parvatiyar MS, Marshall JL, Nguyen RT, et al. (2015) Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy. Journal of the American Heart Association. 4 |
| Vieira NM, Elvers I, Alexander MS, et al. (2015) Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype. Cell. 163: 1204-13 |
| Marshall JL, Oh J, Chou E, et al. (2015) Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin. Human Molecular Genetics. 24: 2011-22 |
| Alexander MS, Casar JC, Motohashi N, et al. (2014) MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms. The Journal of Clinical Investigation. 124: 2651-67 |
| Marshall JL, Kwok Y, McMorran BJ, et al. (2013) The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy. The Febs Journal. 280: 4210-29 |
| Marshall JL, Crosbie-Watson RH. (2013) Sarcospan: a small protein with large potential for Duchenne muscular dystrophy. Skeletal Muscle. 3: 1 |