| Year |
Citation |
Score |
| 2021 |
Gibbs EM, McCourt JL, Shin KM, Hammond KG, Marshall JL, Crosbie RH. Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease. Human Molecular Genetics. PMID 33432327 DOI: 10.1093/hmg/ddaa264 |
0.712 |
|
| 2019 |
Parvatiyar MS, Brownstein AJ, Kanashiro-Takeuchi RM, Collado JR, Dieseldorff Jones KM, Gopal J, Hammond KG, Marshall JL, Ferrel A, Beedle AM, Chamberlain JS, Pinto JR, Crosbie RH. Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy. Jci Insight. 5. PMID 31039133 DOI: 10.1172/Jci.Insight.123855 |
0.678 |
|
| 2016 |
Gibbs EM, Marshall JL, Ma E, Nguyen TM, Hong G, Lam J, Spencer MJ, Crosbie-Watson RH. 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. PMID 27798107 DOI: 10.1093/Hmg/Ddw356 |
0.591 |
|
| 2016 |
McMorran BJ, McCarthy FE, Gibbs EM, Pang M, Marshall JL, Nairn AV, Moremen KW, Crosbie-Watson RH, Baum LG. Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx. Glycobiology. PMID 27236198 DOI: 10.1093/Glycob/Cww061 |
0.353 |
|
| 2015 |
Parvatiyar MS, Marshall JL, Nguyen RT, Jordan MC, Richardson VA, Roos KP, Crosbie-Watson RH. Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy. Journal of the American Heart Association. 4. PMID 26702077 DOI: 10.1161/Jaha.115.002481 |
0.699 |
|
| 2015 |
Vieira NM, Elvers I, Alexander MS, Moreira YB, Eran A, Gomes JP, Marshall JL, Karlsson EK, Verjovski-Almeida S, Lindblad-Toh K, Kunkel LM, Zatz M. Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype. Cell. 163: 1204-13. PMID 26582133 DOI: 10.1016/J.Cell.2015.10.049 |
0.424 |
|
| 2015 |
Marshall JL, Oh J, Chou E, Lee JA, Holmberg J, Burkin DJ, Crosbie-Watson RH. Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin. Human Molecular Genetics. 24: 2011-22. PMID 25504048 DOI: 10.1093/Hmg/Ddu615 |
0.514 |
|
| 2014 |
Alexander MS, Casar JC, Motohashi N, Vieira NM, Eisenberg I, Marshall JL, Gasperini MJ, Lek A, Myers JA, Estrella EA, Kang PB, Shapiro F, Rahimov F, Kawahara G, Widrick JJ, et al. MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms. The Journal of Clinical Investigation. 124: 2651-67. PMID 24789910 DOI: 10.1172/Jci73579 |
0.434 |
|
| 2013 |
Marshall JL, Kwok Y, McMorran BJ, Baum LG, Crosbie-Watson RH. The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy. The Febs Journal. 280: 4210-29. PMID 23601082 DOI: 10.1111/Febs.12295 |
0.449 |
|
| 2013 |
Marshall JL, Crosbie-Watson RH. Sarcospan: a small protein with large potential for Duchenne muscular dystrophy. Skeletal Muscle. 3: 1. PMID 23282144 DOI: 10.1186/2044-5040-3-1 |
0.624 |
|
| 2012 |
Marshall JL, Chou E, Oh J, Kwok A, Burkin DJ, Crosbie-Watson RH. Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice. Human Molecular Genetics. 21: 4378-93. PMID 22798625 DOI: 10.1093/Hmg/Dds271 |
0.636 |
|
| 2012 |
Marshall JL, Holmberg J, Chou E, Ocampo AC, Oh J, Lee J, Peter AK, Martin PT, Crosbie-Watson RH. Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration. The Journal of Cell Biology. 197: 1009-27. PMID 22734004 DOI: 10.1083/Jcb.201110032 |
0.698 |
|
| 2012 |
Cabrera PV, Pang M, Marshall JL, Kung R, Nelson SF, Stalnaker SH, Wells L, Crosbie-Watson RH, Baum LG. High throughput screening for compounds that alter muscle cell glycosylation identifies new role for N-glycans in regulating sarcolemmal protein abundance and laminin binding. The Journal of Biological Chemistry. 287: 22759-70. PMID 22570487 DOI: 10.1074/Jbc.M111.334581 |
0.348 |
|
| 2008 |
Peter AK, Marshall JL, Crosbie RH. Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex. The Journal of Cell Biology. 183: 419-27. PMID 18981229 DOI: 10.1083/Jcb.200808027 |
0.66 |
|
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