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Kevin P Campbell
Kevin P Campbell
Chair, Molecular Physiology and Biophysics, Howard Hughes Medical Institute, Carver College of
Preverjeni e-poštni naslov na uiowa.edu
Naslov
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Leto
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
O Ibraghimov-Beskrovnaya, JM Ervasti, CJ Leveille, CA Slaughter, ...
Nature 355 (6362), 696-702, 1992
17101992
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
16821993
Membrane organization of the dystrophin-glycoprotein complex
JM Ervasti, KP Campbell
Cell 66 (6), 1121-1131, 1991
16221991
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
14132000
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
12311990
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
11552003
Three muscular dystrophies: review loss of cytoskeleton-extracellular matrix linkage
KP Campbell
Cell 80, 675-679, 1995
10661995
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
9431988
Association of dystrophin and an integral membrane glycoprotein
KP Campbell, SD Kahl
Nature 338 (6212), 259-262, 1989
9391989
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
8832002
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
8791994
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
8621998
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
7871998
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
7772003
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
7711988
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
7661999
Auxiliary subunits: essential components of the voltage-gated calcium channel complex
J Arikkath, KP Campbell
Current opinion in neurobiology 13 (3), 298-307, 2003
7152003
Molecular basis of muscular dystrophies
RD Cohn, KP Campbell
Muscle & nerve 23 (10), 1456-1471, 2000
6782000
Dystroglycan: from biosynthesis to pathogenesis of human disease
R Barresi, KP Campbell
Journal of cell science 119 (2), 199-207, 2006
6572006
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
6401997
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