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| A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin JM Ervasti, KP Campbell The Journal of cell biology 122 (4), 809-823, 1993 | 1689 | 1993 |
| Membrane organization of the dystrophin-glycoprotein complex JM Ervasti, KP Campbell Cell 66 (6), 1121-1131, 1991 | 1627 | 1991 |
| Nomenclature of voltage-gated calcium channels EA Ertel, KP Campbell, MM Harpold, F Hofmann, Y Mori, E Perez-Reyes, ... Neuron 25 (3), 533-535, 2000 | 1419 | 2000 |
| Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle JM Ervasti, K Ohlendieck, SD Kahl, MG Gaver, KP Campbell Nature 345 (6273), 315-319, 1990 | 1237 | 1990 |
| Defective membrane repair in dysferlin-deficient muscular dystrophy D Bansal, K Miyake, SS Vogel, S Groh, CC Chen, R Williamson, ... Nature 423 (6936), 168-172, 2003 | 1167 | 2003 |
| Three muscular dystrophies: review loss of cytoskeleton-extracellular matrix linkage KP Campbell Cell 80, 675-679, 1995 | 1069 | 1995 |
| Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle. BA Block, T Imagawa, KP Campbell, C Franzini-Armstrong The Journal of cell biology 107 (6), 2587-2600, 1988 | 945 | 1988 |
| Association of dystrophin and an integral membrane glycoprotein KP Campbell, SD Kahl Nature 338 (6212), 259-262, 1989 | 942 | 1989 |
| 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 | 886 | 2002 |
| Calcium channel β-subunit binds to a conserved motif in the I–II cytoplasmic linker of the α1-subunit M Pragnell, M De Waard, Y Mori, T Tanabe, TP Snutch, KP Campbell Nature 368 (6466), 67-70, 1994 | 883 | 1994 |
| Identification of α-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus W Cao, MD Henry, P Borrow, H Yamada, JH Elder, EV Ravkov, ST Nichol, ... Science 282 (5396), 2079-2081, 1998 | 867 | 1998 |
| The mouse stargazer gene encodes a neuronal Ca2+-channel γ subunit VA Letts, R Felix, GH Biddlecome, J Arikkath, CL Mahaffey, A Valenzuela, ... Nature genetics 19 (4), 340-347, 1998 | 789 | 1998 |
| Cell therapy of α-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblasts M Sampaolesi, Y Torrente, A Innocenzi, R Tonlorenzi, G D'Antona, ... Science 301 (5632), 487-492, 2003 | 777 | 2003 |
| Sequence and Expression of mRNAs Encoding the α1 and α2 Subunits of a DHP-Sensitive Calcium Channel SB Ellis, ME Williams, NR Ways, R Brenner, AH Sharp, AT Leung, ... Science 241 (4873), 1661-1664, 1988 | 773 | 1988 |
| Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy C Badorff, GH Lee, BJ Lamphear, ME Martone, KP Campbell, RE Rhoads, ... Nature medicine 5 (3), 320-326, 1999 | 768 | 1999 |
| Auxiliary subunits: essential components of the voltage-gated calcium channel complex J Arikkath, KP Campbell Current opinion in neurobiology 13 (3), 298-307, 2003 | 717 | 2003 |
| Molecular basis of muscular dystrophies RD Cohn, KP Campbell Muscle & nerve 23 (10), 1456-1471, 2000 | 681 | 2000 |
| Dystroglycan: from biosynthesis to pathogenesis of human disease R Barresi, KP Campbell Journal of cell science 119 (2), 199-207, 2006 | 661 | 2006 |
| Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice RA Williamson, MD Henry, KJ Daniels, RF Hrstka, JC Lee, Y Sunada, ... Human molecular genetics 6 (6), 831-841, 1997 | 641 | 1997 |
