| Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies DE Michele, R Barresi, M Kanagawa, F Saito, RD Cohn, JS Satz, J Dollar, ... Nature 418 (6896), 417-421, 2002 | 883 | 2002 |
| Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy SA Moore, F Saito, J Chen, DE Michele, MD Henry, A Messing, RD Cohn, ... Nature 418 (6896), 422-425, 2002 | 604 | 2002 |
| Dystrophin-Glycoprotein Complex: Post-translational Processing and Dystroglycan Function* 210 DE Michele, KP Campbell Journal of Biological Chemistry 278 (18), 15457-15460, 2003 | 515 | 2003 |
| Dystrophic heart failure blocked by membrane sealant poloxamer S Yasuda, DW Townsend, DE Michele, EG Favre, SM Day, JM Metzger Nature 436 (7053), 1025-1029, 2005 | 360 | 2005 |
| Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration RD Cohn, MD Henry, DE Michele, R Barresi, F Saito, SA Moore, ... Cell 110 (5), 639-648, 2002 | 326 | 2002 |
| LARGE can functionally bypass α-dystroglycan glycosylation defects in distinct congenital muscular dystrophies R Barresi, DE Michele, M Kanagawa, HA Harper, SA Dovico, JS Satz, ... Nature medicine 10 (7), 696-703, 2004 | 300 | 2004 |
| Molecular recognition by LARGE is essential for expression of functional dystroglycan M Kanagawa, F Saito, S Kunz, T Yoshida-Moriguchi, R Barresi, ... Cell 117 (7), 953-964, 2004 | 295 | 2004 |
| Lateral transmission of force is impaired in skeletal muscles of dystrophic mice and very old rats KS Ramaswamy, ML Palmer, JH van der Meulen, A Renoux, ... The Journal of physiology 589 (5), 1195-1208, 2011 | 261 | 2011 |
| Expression of peroxisomal proliferator-activated receptors and retinoid X receptors in the kidney T Yang, DE Michele, J Park, AM Smart, Z Lin, FC Brosius III, ... American Journal of Physiology-Renal Physiology 277 (6), F966-F973, 1999 | 209 | 1999 |
| Limb-girdle muscular dystrophy in the United States SA Moore, CJ Shilling, S Westra, C Wall, MP Wicklund, C Stolle, ... Journal of Neuropathology & Experimental Neurology 65 (10), 995-1003, 2006 | 199 | 2006 |
| Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of α-dystroglycan R Han, M Kanagawa, T Yoshida-Moriguchi, EP Rader, RA Ng, ... Proceedings of the National Academy of Sciences 106 (31), 12573-12579, 2009 | 155 | 2009 |
| COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans C Labelle-Dumais, DJ Dilworth, EP Harrington, M de Leau, D Lyons, ... PLoS genetics 7 (5), e1002062, 2011 | 139 | 2011 |
| The dystrophin-glycoprotein complex in the prevention of muscle damage JD Gumerson, DE Michele BioMed Research International 2011, 2011 | 133 | 2011 |
| Interactions of intermediate filament protein synemin with dystrophin and utrophin RC Bhosle, DE Michele, KP Campbell, Z Li, RM Robson Biochemical and biophysical research communications 346 (3), 768-777, 2006 | 127 | 2006 |
| Direct, convergent hypersensitivity of calcium-activated force generation produced by hypertrophic cardiomyopathy mutant α-tropomyosins in adult cardiac myocytes DE Michele, FP Albayya, JM Metzger Nature medicine 5 (12), 1413-1417, 1999 | 119 | 1999 |
| Cardiac dysfunction in hypertrophic cardiomyopathy mutant tropomyosin mice is transgene-dependent, hypertrophy-independent, and improved by β-blockade DE Michele, CA Gomez, KE Hong, MV Westfall, JM Metzger Circulation research 91 (3), 255-262, 2002 | 107 | 2002 |
| Blebbistatin extends culture life of adult mouse cardiac myocytes and allows efficient and stable transgene expression Z Kabaeva, M Zhao, DE Michele American Journal of Physiology-Heart and Circulatory Physiology 294 (4 …, 2008 | 106 | 2008 |
| Effects of Myosin Heavy Chain Isoform Switching on Ca2+-Activated Tension Development in Single Adult Cardiac Myocytes JM Metzger, PA Wahr, DE Michele, F Albayya, MV Westfall Circulation research 84 (11), 1310-1317, 1999 | 105 | 1999 |
| POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in α-DG DS Kim, YK Hayashi, H Matsumoto, M Ogawa, S Noguchi, N Murakami, ... Neurology 62 (6), 1009-1011, 2004 | 97 | 2004 |
| ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies S Cirak, AR Foley, R Herrmann, T Willer, S Yau, E Stevens, S Torelli, ... Brain 136 (1), 269-281, 2013 | 96 | 2013 |
