Kevin P. Campbell, Ph.D, University of Rochester 1976 - Publications

Affiliations: 
Physiology & Biophysics and Neurology University of Iowa, Iowa City, IA 
Area:
Ion channels, muscle pathology
Website:
http://www.physiology.uiowa.edu/campbell/

302 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Cox ML, Evans JM, Davis AG, Guo LT, Levy JR, Starr-Moss AN, Salmela E, Hytönen MK, Lohi H, Campbell KP, Clark LA, Shelton GD. Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers. Skeletal Muscle. 7: 15. PMID 28702169 DOI: 10.1186/s13395-017-0131-0  0.32
2017 Cox ML, Evans JM, Davis AG, Guo LT, Levy JR, Starr-Moss AN, Salmela E, Hytönen MK, Lohi H, Campbell KP, Clark LA, Shelton GD. Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers. Skeletal Muscle. 7: 15. PMID 28697784 DOI: 10.1186/s13395-017-0131-0  0.32
2016 Rader EP, Turk R, Willer T, Beltrán D, Inamori KI, Peterson TA, Engle J, Prouty S, Matsumura K, Saito F, Anderson ME, Campbell KP. Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle. Proceedings of the National Academy of Sciences of the United States of America. PMID 27625424 DOI: 10.1073/pnas.1605265113  1
2016 de Greef JC, Hamlyn R, Jensen BS, O'Campo Landa R, Levy JR, Kobuke K, Campbell KP. Collagen VI deficiency reduces muscle pathology, but does not improve muscle function, in the γ-sarcoglycan-null mouse. Human Molecular Genetics. PMID 26908621 DOI: 10.1093/hmg/ddw018  1
2015 Wiktorowicz T, Kinter J, Kobuke K, Campbell KP, Sinnreich M. Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf (tm1Kcam). Skeletal Muscle. 5: 32. PMID 26464793 DOI: 10.1186/s13395-015-0057-3  1
2015 Yoshida-Moriguchi T, Campbell KP. Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane. Glycobiology. 25: 702-13. PMID 25882296 DOI: 10.1093/glycob/cwv021  1
2015 Hara Y, Campbell KP. Dystroglycan: Extracellular Matrix Receptor that Links to Cytoskeleton Glycoscience: Biology and Medicine. 1245-1251. DOI: 10.1007/978-4-431-54841-6_173  1
2014 Inamori K, Willer T, Hara Y, Venzke D, Anderson ME, Clarke NF, Guicheney P, Bönnemann CG, Moore SA, Campbell KP. Endogenous glucuronyltransferase activity of LARGE or LARGE2 required for functional modification of α-dystroglycan in cells and tissues. The Journal of Biological Chemistry. 289: 28138-48. PMID 25138275 DOI: 10.1074/jbc.M114.597831  1
2014 Lin SS, Tzeng BH, Lee KR, Smith RJ, Campbell KP, Chen CC. Cav3.2 T-type calcium channel is required for the NFAT-dependent Sox9 expression in tracheal cartilage. Proceedings of the National Academy of Sciences of the United States of America. 111: E1990-8. PMID 24778262 DOI: 10.1073/pnas.1323112111  1
2014 Wallace SE, Conta JH, Winder TL, Willer T, Eskuri JM, Haas R, Patterson K, Campbell KP, Moore SA, Gospe SM. A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations. Neuromuscular Disorders : Nmd. 24: 312-20. PMID 24491487 DOI: 10.1016/j.nmd.2014.01.001  1
2014 Glass DJ, Campbell KP, Rudnicki MA. Skeletal muscle's 3rd year anniversary. Skeletal Muscle. 4: 3. PMID 24456943 DOI: 10.1186/2044-5040-4-3  1
2013 Nguyen H, Ostendorf AP, Satz JS, Westra S, Ross-Barta SE, Campbell KP, Moore SA. Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteins. Acta Neuropathologica Communications. 1: 58. PMID 24252195 DOI: 10.1186/2051-5960-1-58  1
2013 Levy JR, Campbell KP, Glass DJ. MG53's new identity. Skeletal Muscle. 3: 25. PMID 24175977 DOI: 10.1186/2044-5040-3-25  1
2013 Goddeeris MM, Wu B, Venzke D, Yoshida-Moriguchi T, Saito F, Matsumura K, Moore SA, Campbell KP. LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy. Nature. 503: 136-40. PMID 24132234 DOI: 10.1038/nature12605  1
2013 Yoshida-Moriguchi T, Willer T, Anderson ME, Venzke D, Whyte T, Muntoni F, Lee H, Nelson SF, Yu L, Campbell KP. SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function. Science (New York, N.Y.). 341: 896-9. PMID 23929950 DOI: 10.1126/science.1239951  1
2013 Yang AC, Ng BG, Moore SA, Rush J, Waechter CJ, Raymond KM, Willer T, Campbell KP, Freeze HH, Mehta L. Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy. Molecular Genetics and Metabolism. 110: 345-51. PMID 23856421 DOI: 10.1016/j.ymgme.2013.06.016  1
2013 Carss KJ, Stevens E, Foley AR, Cirak S, Riemersma M, Torelli S, Hoischen A, Willer T, van Scherpenzeel M, Moore SA, Messina S, Bertini E, Bönnemann CG, Abdenur JE, Grosmann CM, ... ... Campbell KP, et al. Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. American Journal of Human Genetics. 93: 29-41. PMID 23768512 DOI: 10.1016/j.ajhg.2013.05.009  1
2013 Levy JR, Campbell KP. Illuminating regeneration: noninvasive imaging of disease progression in muscular dystrophy. The Journal of Clinical Investigation. 123: 1931-4. PMID 23619358 DOI: 10.1172/JCI69568  1
2013 Stevens E, Carss KJ, Cirak S, Foley AR, Torelli S, Willer T, Tambunan DE, Yau S, Brodd L, Sewry CA, Feng L, Haliloglu G, Orhan D, Dobyns WB, Enns GM, ... ... Campbell KP, et al. Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan. American Journal of Human Genetics. 92: 354-65. PMID 23453667 DOI: 10.1016/j.ajhg.2013.01.016  1
2013 Cirak S, Foley AR, Herrmann R, Willer T, Yau S, Stevens E, Torelli S, Brodd L, Kamynina A, Vondracek P, Roper H, Longman C, Korinthenberg R, Marrosu G, Nürnberg P, ... ... Campbell KP, et al. ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies. Brain : a Journal of Neurology. 136: 269-81. PMID 23288328 DOI: 10.1093/brain/aws312  1
2013 Moraz ML, Pythoud C, Turk R, Rothenberger S, Pasquato A, Campbell KP, Kunz S. Cell entry of Lassa virus induces tyrosine phosphorylation of dystroglycan. Cellular Microbiology. 15: 689-700. PMID 23279385 DOI: 10.1111/cmi.12078  1
2013 Esser AK, Miller MR, Huang Q, Meier MM, Beltran-Valero de Bernabé D, Stipp CS, Campbell KP, Lynch CF, Smith BJ, Cohen MB, Henry MD. Loss of LARGE2 disrupts functional glycosylation of α-dystroglycan in prostate cancer. The Journal of Biological Chemistry. 288: 2132-42. PMID 23223448 DOI: 10.1074/jbc.M112.432807  1
2013 Inamori K, Hara Y, Willer T, Anderson ME, Zhu Z, Yoshida-Moriguchi T, Campbell KP. Xylosyl- and glucuronyltransferase functions of LARGE in α-dystroglycan modification are conserved in LARGE2. Glycobiology. 23: 295-302. PMID 23125099 DOI: 10.1093/glycob/cws152  1
2012 Li Z, Gilbert JA, Zhang Y, Zhang M, Qiu Q, Ramanujan K, Shavlakadze T, Eash JK, Scaramozza A, Goddeeris MM, Kirsch DG, Campbell KP, Brack AS, Glass DJ. An HMGA2-IGF2BP2 axis regulates myoblast proliferation and myogenesis. Developmental Cell. 23: 1176-88. PMID 23177649 DOI: 10.1016/j.devcel.2012.10.019  1
2012 Myshrall TD, Moore SA, Ostendorf AP, Satz JS, Kowalczyk T, Nguyen H, Daza RA, Lau C, Campbell KP, Hevner RF. Dystroglycan on radial glia end feet is required for pial basement membrane integrity and columnar organization of the developing cerebral cortex. Journal of Neuropathology and Experimental Neurology. 71: 1047-63. PMID 23147502 DOI: 10.1097/NEN.0b013e318274a128  1
2012 Beedle AM, Turner AJ, Saito Y, Lueck JD, Foltz SJ, Fortunato MJ, Nienaber PM, Campbell KP. Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy. The Journal of Clinical Investigation. 122: 3330-42. PMID 22922256 DOI: 10.1172/JCI63004  1
2012 Willer T, Lee H, Lommel M, Yoshida-Moriguchi T, de Bernabe DB, Venzke D, Cirak S, Schachter H, Vajsar J, Voit T, Muntoni F, Loder AS, Dobyns WB, Winder TL, Strahl S, ... ... Campbell KP, et al. ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome. Nature Genetics. 44: 575-80. PMID 22522420 DOI: 10.1038/ng.2252  1
2012 Rojek JM, Moraz ML, Pythoud C, Rothenberger S, Van der Goot FG, Campbell KP, Kunz S. Binding of Lassa virus perturbs extracellular matrix-induced signal transduction via dystroglycan. Cellular Microbiology. 14: 1122-34. PMID 22405130 DOI: 10.1111/j.1462-5822.2012.01784.x  1
2012 Inamori K, Yoshida-Moriguchi T, Hara Y, Anderson ME, Yu L, Campbell KP. Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE. Science (New York, N.Y.). 335: 93-6. PMID 22223806 DOI: 10.1126/science.1214115  1
2012 Kobayashi YM, Rader EP, Crawford RW, Campbell KP. Endpoint measures in the mdx mouse relevant for muscular dystrophy pre-clinical studies. Neuromuscular Disorders : Nmd. 22: 34-42. PMID 22154712 DOI: 10.1016/j.nmd.2011.08.001  1
2012 Kobayashi YM, Campbell KP. Skeletal muscle dystrophin-glycoprotein complex and muscular dystrophy Muscle. 2: 935-942. DOI: 10.1016/B978-0-12-381510-1.00066-1  1
2011 Di Blasi C, Bellafiore E, Salih MA, Manzini MC, Moore SA, Seidahmed MZ, Mukhtar MM, Karrar ZA, Walsh CA, Campbell KP, Mantegazza R, Morandi L, Mora M. Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2. Bmc Research Notes. 4: 534. PMID 22166137 DOI: 10.1186/1756-0500-4-534  1
2011 Han R, Rader EP, Levy JR, Bansal D, Campbell KP. Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice. Skeletal Muscle. 1: 35. PMID 22132688 DOI: 10.1186/2044-5040-1-35  1
2011 Hara Y, Kanagawa M, Kunz S, Yoshida-Moriguchi T, Satz JS, Kobayashi YM, Zhu Z, Burden SJ, Oldstone MB, Campbell KP. Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection. Proceedings of the National Academy of Sciences of the United States of America. 108: 17426-31. PMID 21987822 DOI: 10.1073/pnas.1114836108  1
2011 Lancioni A, Rotundo IL, Kobayashi YM, D'Orsi L, Aurino S, Nigro G, Piluso G, Acampora D, Cacciottolo M, Campbell KP, Nigro V. Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex. Human Molecular Genetics. 20: 4644-54. PMID 21890494 DOI: 10.1093/hmg/ddr398  1
2011 Alnawaiseh M, Albanna W, Chen CC, Campbell KP, Hescheler J, Lüke M, Schneider T. Two separate Ni(2+) -sensitive voltage-gated Ca(2+) channels modulate transretinal signalling in the isolated murine retina. Acta Ophthalmologica. 89: e579-90. PMID 21883984 DOI: 10.1111/j.1755-3768.2011.02167.x  1
2011 Glass DJ, Campbell KP, Rudnicki MA. Welcome to skeletal muscle. Skeletal Muscle. 1: 1. PMID 21798079 DOI: 10.1186/2044-5040-1-1  1
2011 Lei D, Gao X, Perez P, Ohlemiller KK, Chen CC, Campbell KP, Hood AY, Bao J. Anti-epileptic drugs delay age-related loss of spiral ganglion neurons via T-type calcium channel. Hearing Research. 278: 106-12. PMID 21640179 DOI: 10.1016/j.heares.2011.05.010  1
2011 Noell S, Wolburg-Buchholz K, Mack AF, Beedle AM, Satz JS, Campbell KP, Wolburg H, Fallier-Becker P. Evidence for a role of dystroglycan regulating the membrane architecture of astroglial endfeet. The European Journal of Neuroscience. 33: 2179-86. PMID 21501259 DOI: 10.1111/j.1460-9568.2011.07688.x  1
2011 Stalnaker SH, Aoki K, Lim JM, Porterfield M, Liu M, Satz JS, Buskirk S, Xiong Y, Zhang P, Campbell KP, Hu H, Live D, Tiemeyer M, Wells L. Glycomic analyses of mouse models of congenital muscular dystrophy. The Journal of Biological Chemistry. 286: 21180-90. PMID 21460210 DOI: 10.1074/jbc.M110.203281  1
2011 Hara Y, Balci-Hayta B, Yoshida-Moriguchi T, Kanagawa M, Beltrán-Valero de Bernabé D, Günde?li H, Willer T, Satz JS, Crawford RW, Burden SJ, Kunz S, Oldstone MB, Accardi A, Talim B, Muntoni F, ... ... Campbell KP, et al. A dystroglycan mutation associated with limb-girdle muscular dystrophy. The New England Journal of Medicine. 364: 939-46. PMID 21388311 DOI: 10.1056/NEJMoa1006939  1
2011 Wu J, Ruas JL, Estall JL, Rasbach KA, Choi JH, Ye L, Boström P, Tyra HM, Crawford RW, Campbell KP, Rutkowski DT, Kaufman RJ, Spiegelman BM. The unfolded protein response mediates adaptation to exercise in skeletal muscle through a PGC-1α/ATF6α complex. Cell Metabolism. 13: 160-9. PMID 21284983 DOI: 10.1016/j.cmet.2011.01.003  1
2011 Sullivan BM, Emonet SF, Welch MJ, Lee AM, Campbell KP, de la Torre JC, Oldstone MB. Point mutation in the glycoprotein of lymphocytic choriomeningitis virus is necessary for receptor binding, dendritic cell infection, and long-term persistence. Proceedings of the National Academy of Sciences of the United States of America. 108: 2969-74. PMID 21270335 DOI: 10.1073/pnas.1019304108  1
2011 Clarke NF, Maugenre S, Vandebrouck A, Urtizberea JA, Willer T, Peat RA, Gray F, Bouchet C, Manya H, Vuillaumier-Barrot S, Endo T, Chouery E, Campbell KP, Mégarbané A, Guicheney P. Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene. European Journal of Human Genetics : Ejhg. 19: 452-7. PMID 21248746 DOI: 10.1038/ejhg.2010.212  1
2011 Mathews KD, Stephan CM, Laubenthal K, Winder TL, Michele DE, Moore SA, Campbell KP. Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I. Neurology. 76: 194-5. PMID 21220724 DOI: 10.1212/WNL.0b013e3182061ad4  1
2011 Oldstone MB, Campbell KP. Decoding arenavirus pathogenesis: essential roles for alpha-dystroglycan-virus interactions and the immune response. Virology. 411: 170-9. PMID 21185048 DOI: 10.1016/j.virol.2010.11.023  1
2011 Lueck JD, Rossi AE, Thornton CA, Campbell KP, Dirksen RT. Response to the letter: "On the localization of ClC-1 in skeletal muscle fibers" Journal of General Physiology. 137: 331-333. DOI: 10.1085/jgp.201010589  1
2010 Lueck JD, Rossi AE, Thornton CA, Campbell KP, Dirksen RT. Sarcolemmal-restricted localization of functional ClC-1 channels in mouse skeletal muscle. The Journal of General Physiology. 136: 597-613. PMID 21078869 DOI: 10.1085/jgp.201010526  1
2010 Han R, Frett EM, Levy JR, Rader EP, Lueck JD, Bansal D, Moore SA, Ng R, Beltrán-Valero de Bernabé D, Faulkner JA, Campbell KP. Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice. The Journal of Clinical Investigation. 120: 4366-74. PMID 21060153 DOI: 10.1172/JCI42390  1
2010 Satz JS, Ostendorf AP, Hou S, Turner A, Kusano H, Lee JC, Turk R, Nguyen H, Ross-Barta SE, Westra S, Hoshi T, Moore SA, Campbell KP. Distinct functions of glial and neuronal dystroglycan in the developing and adult mouse brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 14560-72. PMID 20980614 DOI: 10.1523/JNEUROSCI.3247-10.2010  1
2010 Leonoudakis D, Singh M, Mohajer R, Mohajer P, Fata JE, Campbell KP, Muschler JL. Dystroglycan controls signaling of multiple hormones through modulation of STAT5 activity. Journal of Cell Science. 123: 3683-92. PMID 20940259 DOI: 10.1242/jcs.070680  1
2010 Weiss RM, Kerber RE, Jones JK, Stephan CM, Trout CJ, Lindower PD, Staffey KS, Campbell KP, Mathews KD. Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathy. Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography. 23: 848-53. PMID 20646909 DOI: 10.1016/j.echo.2010.05.007  1
2010 Vassilopoulos S, Oddoux S, Groh S, Cacheux M, Fauré J, Brocard J, Campbell KP, Marty I. Caveolin 3 is associated with the calcium release complex and is modified via in vivo triadin modification. Biochemistry. 49: 6130-5. PMID 20565104 DOI: 10.1021/bi100796v  1
2010 Uriu Y, Kiyonaka S, Miki T, Yagi M, Akiyama S, Mori E, Nakao A, Beedle AM, Campbell KP, Wakamori M, Mori Y. Rab3-interacting molecule gamma isoforms lacking the Rab3-binding domain induce long lasting currents but block neurotransmitter vesicle anchoring in voltage-dependent P/Q-type Ca2+ channels. The Journal of Biological Chemistry. 285: 21750-67. PMID 20452978 DOI: 10.1074/jbc.M110.101311  1
2010 Wang R, Urso ML, Zambraski EJ, Rader EP, Campbell KP, Liang BT. Adenosine A(3) receptor stimulation induces protection of skeletal muscle from eccentric exercise-mediated injury. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 299: R259-67. PMID 20427727 DOI: 10.1152/ajpregu.00060.2010  1
2010 Liou LY, Walsh KB, Vartanian AR, Beltran-Valero de Bernabe D, Welch M, Campbell KP, Oldstone MB, Kunz S. Functional glycosylation of dystroglycan is crucial for thymocyte development in the mouse. Plos One. 5: e9915. PMID 20369005 DOI: 10.1371/journal.pone.0009915  1
2010 Watanabe H, Yamashita T, Saitoh N, Kiyonaka S, Iwamatsu A, Campbell KP, Mori Y, Takahashi T. Involvement of Ca2+ channel synprint site in synaptic vesicle endocytosis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 655-60. PMID 20071530 DOI: 10.1523/JNEUROSCI.3214-09.2010  1
2010 Yoshida-Moriguchi T, Yu L, Stalnaker SH, Davis S, Kunz S, Madson M, Oldstone MB, Schachter H, Wells L, Campbell KP. O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding. Science (New York, N.Y.). 327: 88-92. PMID 20044576 DOI: 10.1126/science.1180512  1
2010 Vogtländer NP, van der Vlag J, Bakker MA, Dijkman HB, Wevers RA, Campbell KP, Wetzels JF, Berden JH. Expression of sialidase and dystroglycan in human glomerular diseases. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 25: 478-84. PMID 19755471 DOI: 10.1093/ndt/gfp465  1
2010 Satz JS, Philp AR, Nguyen H, Kusano H, Lee J, Turk R, Riker MJ, Hernández J, Weiss RM, Anderson MG, Mullins RF, Moore SA, Stone EM, Campbell KP. Visual impairment in the absence of dystroglycan (The Journal of Neuroscience (2009) (13136-13146)) Journal of Neuroscience. 30: 1983.  1
2010 Satz JS, Philip AR, Nguyen H, Kusano H, Lee J, Turk R, Riker MJ, Hernández J, Weiss RM, Anderson MG, Mullins RF, Moore SA, Stone EM, Campbell KP. Visual impairment in the absence of dystroglycan (Journal of Neuroscience (2010) 30, (13136-13146)) Journal of Neuroscience. 30: 797.  1
2009 Satz JS, Philp AR, Nguyen H, Kusano H, Lee J, Turk R, Riker MJ, Hernández J, Weiss RM, Anderson MG, Mullins RF, Moore SA, Stone EM, Campbell KP. Visual impairment in the absence of dystroglycan. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 13136-46. PMID 19846701 DOI: 10.1523/JNEUROSCI.0474-09.2009  1
2009 Michele DE, Kabaeva Z, Davis SL, Weiss RM, Campbell KP. Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage. Circulation Research. 105: 984-93. PMID 19797173 DOI: 10.1161/CIRCRESAHA.109.199489  1
2009 Andrade A, Sandoval A, González-Ramírez R, Lipscombe D, Campbell KP, Felix R. The alpha(2)delta subunit augments functional expression and modifies the pharmacology of Ca(V)1.3 L-type channels. Cell Calcium. 46: 282-92. PMID 19796812 DOI: 10.1016/j.ceca.2009.08.006  1
2009 Han R, Kanagawa M, Yoshida-Moriguchi T, Rader EP, Ng RA, Michele DE, Muirhead DE, Kunz S, Moore SA, Iannaccone ST, Miyake K, McNeil PL, Mayer U, Oldstone MB, Faulkner JA, ... Campbell KP, et al. Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan. Proceedings of the National Academy of Sciences of the United States of America. 106: 12573-9. PMID 19633189 DOI: 10.1073/pnas.0906545106  1
2009 Groh S, Zong H, Goddeeris MM, Lebakken CS, Venzke D, Pessin JE, Campbell KP. Sarcoglycan complex: implications for metabolic defects in muscular dystrophies. The Journal of Biological Chemistry. 284: 19178-82. PMID 19494113 DOI: 10.1074/jbc.C109.010728  1
2009 Puckett RL, Moore SA, Winder TL, Willer T, Romansky SG, Covault KK, Campbell KP, Abdenur JE. Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardation. Neuromuscular Disorders : Nmd. 19: 352-6. PMID 19342235 DOI: 10.1016/j.nmd.2009.03.001  1
2009 de Bernabé DB, Inamori K, Yoshida-Moriguchi T, Weydert CJ, Harper HA, Willer T, Henry MD, Campbell KP. Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE. The Journal of Biological Chemistry. 284: 11279-84. PMID 19244252 DOI: 10.1074/jbc.C900007200  1
2009 Chiang CS, Huang CH, Chieng H, Chang YT, Chang D, Chen JJ, Chen YC, Chen YH, Shin HS, Campbell KP, Chen CC. The Ca(v)3.2 T-type Ca(2+) channel is required for pressure overload-induced cardiac hypertrophy in mice. Circulation Research. 104: 522-30. PMID 19122177 DOI: 10.1161/CIRCRESAHA.108.184051  1
2009 Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, ... ... Campbell KP, et al. Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy. Human Molecular Genetics. 18: 621-31. PMID 19017726 DOI: 10.1093/hmg/ddn387  1
2009 Murakami T, Hayashi YK, Ogawa M, Noguchi S, Campbell KP, Togawa M, Inoue T, Oka A, Ohno K, Nonaka I, Nishino I. A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI. Brain & Development. 31: 465-8. PMID 18804929 DOI: 10.1016/j.braindev.2008.08.005  1
2009 Jimenez-Mallebrera C, Torelli S, Feng L, Kim J, Godfrey C, Clement E, Mein R, Abbs S, Brown SC, Campbell KP, Kröger S, Talim B, Topaloglu H, Quinlivan R, Roper H, et al. A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity. Brain Pathology (Zurich, Switzerland). 19: 596-611. PMID 18691338 DOI: 10.1111/j.1750-3639.2008.00198.x  1
2008 Becker AJ, Pitsch J, Sochivko D, Opitz T, Staniek M, Chen CC, Campbell KP, Schoch S, Yaari Y, Beck H. Transcriptional upregulation of Cav3.2 mediates epileptogenesis in the pilocarpine model of epilepsy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 13341-53. PMID 19052226 DOI: 10.1523/JNEUROSCI.1421-08.2008  1
2008 Kobayashi YM, Rader EP, Crawford RW, Iyengar NK, Thedens DR, Faulkner JA, Parikh SV, Weiss RM, Chamberlain JS, Moore SA, Campbell KP. Sarcolemma-localized nNOS is required to maintain activity after mild exercise. Nature. 456: 511-5. PMID 18953332 DOI: 10.1038/nature07414  1
2008 Satz JS, Barresi R, Durbeej M, Willer T, Turner A, Moore SA, Campbell KP. Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblast. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 10567-75. PMID 18923033 DOI: 10.1523/JNEUROSCI.2457-08.2008  1
2008 Satz JS, Campbell KP. Unraveling the ribbon synapse. Nature Neuroscience. 11: 857-9. PMID 18660835 DOI: 10.1038/nn0808-857  1
2008 Nodari A, Previtali SC, Dati G, Occhi S, Court FA, Colombelli C, Zambroni D, Dina G, Del Carro U, Campbell KP, Quattrini A, Wrabetz L, Feltri ML. Alpha6beta4 integrin and dystroglycan cooperate to stabilize the myelin sheath. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 6714-9. PMID 18579745 DOI: 10.1523/JNEUROSCI.0326-08.2008  1
2008 Dylla DE, Michele DE, Campbell KP, McCray PB. Basolateral entry and release of New and Old World arenaviruses from human airway epithelia. Journal of Virology. 82: 6034-8. PMID 18417570 DOI: 10.1128/JVI.00100-08  1
2008 Kobuke K, Piccolo F, Garringer KW, Moore SA, Sweezer E, Yang B, Campbell KP. A common disease-associated missense mutation in alpha-sarcoglycan fails to cause muscular dystrophy in mice. Human Molecular Genetics. 17: 1201-13. PMID 18252746 DOI: 10.1093/hmg/ddn009  1
2007 Miki T, Kiyonaka S, Uriu Y, De Waard M, Wakamori M, Beedle AM, Campbell KP, Mori Y. Mutation associated with an autosomal dominant cone-rod dystrophy CORD7 modifies RIM1-mediated modulation of voltage-dependent Ca2+ channels. Channels (Austin, Tex.). 1: 144-7. PMID 18690027  1
2007 Kabosova A, Azar DT, Bannikov GA, Campbell KP, Durbeej M, Ghohestani RF, Jones JC, Kenney MC, Koch M, Ninomiya Y, Patton BL, Paulsson M, Sado Y, Sage EH, Sasaki T, et al. Compositional differences between infant and adult human corneal basement membranes. Investigative Ophthalmology & Visual Science. 48: 4989-99. PMID 17962449 DOI: 10.1167/iovs.07-0654  1
2007 Sandoval A, Arikkath J, Monjaraz E, Campbell KP, Felix R. gamma1-dependent down-regulation of recombinant voltage-gated Ca2+ channels. Cellular and Molecular Neurobiology. 27: 901-8. PMID 17934806 DOI: 10.1007/s10571-007-9210-9  1
2007 Rojek JM, Campbell KP, Oldstone MB, Kunz S. Old World arenavirus infection interferes with the expression of functional alpha-dystroglycan in the host cell. Molecular Biology of the Cell. 18: 4493-507. PMID 17761532 DOI: 10.1091/mbc.E07-04-0374  1
2007 Jethwaney D, Islam MR, Leidal KG, de Bernabe DB, Campbell KP, Nauseef WM, Gibson BW. Proteomic analysis of plasma membrane and secretory vesicles from human neutrophils. Proteome Science. 5: 12. PMID 17692124 DOI: 10.1186/1477-5956-5-12  1
2007 Han R, Campbell KP. Dysferlin and muscle membrane repair. Current Opinion in Cell Biology. 19: 409-16. PMID 17662592 DOI: 10.1016/j.ceb.2007.07.001  1
2007 Pacak CA, Walter GA, Gaidosh G, Bryant N, Lewis MA, Germain S, Mah CS, Campbell KP, Byrne BJ. Long-term skeletal muscle protection after gene transfer in a mouse model of LGMD-2D. Molecular Therapy : the Journal of the American Society of Gene Therapy. 15: 1775-81. PMID 17653106 DOI: 10.1038/sj.mt.6300246  1
2007 Han R, Bansal D, Miyake K, Muniz VP, Weiss RM, McNeil PL, Campbell KP. Dysferlin-mediated membrane repair protects the heart from stress-induced left ventricular injury. The Journal of Clinical Investigation. 117: 1805-13. PMID 17607357 DOI: 10.1172/JCI30848  1
2007 Figueroa XF, Chen CC, Campbell KP, Damon DN, Day KH, Ramos S, Duling BR. Are voltage-dependent ion channels involved in the endothelial cell control of vasomotor tone? American Journal of Physiology. Heart and Circulatory Physiology. 293: H1371-83. PMID 17513486 DOI: 10.1152/ajpheart.01368.2006  1
2007 Kiyonaka S, Wakamori M, Miki T, Uriu Y, Nonaka M, Bito H, Beedle AM, Mori E, Hara Y, De Waard M, Kanagawa M, Itakura M, Takahashi M, Campbell KP, Mori Y. RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca2+ channels. Nature Neuroscience. 10: 691-701. PMID 17496890 DOI: 10.1038/nn1904  1
2007 Beedle AM, Nienaber PM, Campbell KP. Fukutin-related protein associates with the sarcolemmal dystrophin-glycoprotein complex. The Journal of Biological Chemistry. 282: 16713-7. PMID 17452335 DOI: 10.1074/jbc.C700061200  1
2007 Escoffier J, Boisseau S, Serres C, Chen CC, Kim D, Stamboulian S, Shin HS, Campbell KP, De Waard M, Arnoult C. Expression, localization and functions in acrosome reaction and sperm motility of Ca(V)3.1 and Ca(V)3.2 channels in sperm cells: an evaluation from Ca(V)3.1 and Ca(V)3.2 deficient mice. Journal of Cellular Physiology. 212: 753-63. PMID 17450521 DOI: 10.1002/jcp.21075  1
2007 Carmignac V, Salih MA, Quijano-Roy S, Marchand S, Al Rayess MM, Mukhtar MM, Urtizberea JA, Labeit S, Guicheney P, Leturcq F, Gautel M, Fardeau M, Campbell KP, Richard I, Estournet B, et al. C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy. Annals of Neurology. 61: 340-51. PMID 17444505 DOI: 10.1002/ana.21089  1
2007 Handschin C, Kobayashi YM, Chin S, Seale P, Campbell KP, Spiegelman BM. PGC-1alpha regulates the neuromuscular junction program and ameliorates Duchenne muscular dystrophy. Genes & Development. 21: 770-83. PMID 17403779 DOI: 10.1101/gad.1525107  1
2007 Sandoval A, Andrade A, Beedle AM, Campbell KP, Felix R. Inhibition of recombinant N-type Ca(V) channels by the gamma 2 subunit involves unfolded protein response (UPR)-dependent and UPR-independent mechanisms. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 3317-27. PMID 17376992 DOI: 10.1523/JNEUROSCI.4566-06.2007  1
2007 Rojek JM, Spiropoulou CF, Campbell KP, Kunz S. Old World and clade C New World arenaviruses mimic the molecular mechanism of receptor recognition used by alpha-dystroglycan's host-derived ligands. Journal of Virology. 81: 5685-95. PMID 17360738 DOI: 10.1128/JVI.02574-06  1
2007 Choi S, Na HS, Kim J, Lee J, Lee S, Kim D, Park J, Chen CC, Campbell KP, Shin HS. Attenuated pain responses in mice lacking Ca(V)3.2 T-type channels. Genes, Brain, and Behavior. 6: 425-31. PMID 16939637 DOI: 10.1111/j.1601-183X.2006.00268.x  1
2006 Murakami T, Hayashi YK, Noguchi S, Ogawa M, Nonaka I, Tanabe Y, Ogino M, Takada F, Eriguchi M, Kotooka N, Campbell KP, Osawa M, Nishino I. Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness. Annals of Neurology. 60: 597-602. PMID 17036286 DOI: 10.1002/ana.20973  1
2006 Moore SA, Shilling CJ, Westra S, Wall C, Wicklund MP, Stolle C, Brown CA, Michele DE, Piccolo F, Winder TL, Stence A, Barresi R, King N, King W, Florence J, ... Campbell KP, et al. Limb-girdle muscular dystrophy in the United States. Journal of Neuropathology and Experimental Neurology. 65: 995-1003. PMID 17021404 DOI: 10.1097/01.jnen.0000235854.77716.6c  1
2006 Weir ML, Oppizzi ML, Henry MD, Onishi A, Campbell KP, Bissell MJ, Muschler JL. Dystroglycan loss disrupts polarity and beta-casein induction in mammary epithelial cells by perturbing laminin anchoring. Journal of Cell Science. 119: 4047-58. PMID 16968749 DOI: 10.1242/jcs.03103  1
2006 Bhosle RC, Michele DE, Campbell KP, Li Z, Robson RM. Interactions of intermediate filament protein synemin with dystrophin and utrophin. Biochemical and Biophysical Research Communications. 346: 768-77. PMID 16777071 DOI: 10.1016/j.bbrc.2006.05.192  1
2006 Vogtländer NP, Tamboer WP, Bakker MA, Campbell KP, van der Vlag J, Berden JH. Reactive oxygen species deglycosilate glomerular alpha-dystroglycan. Kidney International. 69: 1526-34. PMID 16672922 DOI: 10.1038/sj.ki.5000138  1
2006 Joksovic PM, Nelson MT, Jevtovic-Todorovic V, Patel MK, Perez-Reyes E, Campbell KP, Chen CC, Todorovic SM. CaV3.2 is the major molecular substrate for redox regulation of T-type Ca2+ channels in the rat and mouse thalamus. The Journal of Physiology. 574: 415-30. PMID 16644797 DOI: 10.1113/jphysiol.2006.110395  1
2006 Kang MG, Chen CC, Wakamori M, Hara Y, Mori Y, Campbell KP. A functional AMPA receptor-calcium channel complex in the postsynaptic membrane. Proceedings of the National Academy of Sciences of the United States of America. 103: 5561-6. PMID 16567654 DOI: 10.1073/pnas.0601289103  1
2006 Barresi R, Campbell KP. Dystroglycan: from biosynthesis to pathogenesis of human disease. Journal of Cell Science. 119: 199-207. PMID 16410545 DOI: 10.1242/jcs.02814  1
2006 Turk R, Sterrenburg E, van der Wees CG, de Meijer EJ, de Menezes RX, Groh S, Campbell KP, Noguchi S, van Ommen GJ, den Dunnen JT, 't Hoen PA. Common pathological mechanisms in mouse models for muscular dystrophies. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 20: 127-9. PMID 16306063 DOI: 10.1096/fj.05-4678fje  1
2005 Kunz S, Rojek JM, Kanagawa M, Spiropoulou CF, Barresi R, Campbell KP, Oldstone MB. Posttranslational modification of alpha-dystroglycan, the cellular receptor for arenaviruses, by the glycosyltransferase LARGE is critical for virus binding. Journal of Virology. 79: 14282-96. PMID 16254363 DOI: 10.1128/JVI.79.22.14282-14296.2005  1
2005 Occhi S, Zambroni D, Del Carro U, Amadio S, Sirkowski EE, Scherer SS, Campbell KP, Moore SA, Chen ZL, Strickland S, Di Muzio A, Uncini A, Wrabetz L, Feltri ML. Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 9418-27. PMID 16221851 DOI: 10.1523/JNEUROSCI.2068-05.2005  1
2005 Nakagawa O, Arnold M, Nakagawa M, Hamada H, Shelton JM, Kusano H, Harris TM, Childs G, Campbell KP, Richardson JA, Nishino I, Olson EN. Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2. Genes & Development. 19: 2066-77. PMID 16140986 DOI: 10.1101/gad.1338705  1
2005 Kanagawa M, Michele DE, Satz JS, Barresi R, Kusano H, Sasaki T, Timpl R, Henry MD, Campbell KP. Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function. Febs Letters. 579: 4792-6. PMID 16098969 DOI: 10.1016/j.febslet.2005.07.059  1
2005 Vogtländer NP, Dijkman H, Bakker MA, Campbell KP, van der Vlag J, Berden JH. Localization of alpha-dystroglycan on the podocyte: from top to toe. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 53: 1345-53. PMID 15956031 DOI: 10.1369/jhc.4A6596.2005  1
2005 Consolino CM, Duclos F, Lee J, Williamson RA, Campbell KP, Brooks SV. Muscles of mice deficient in alpha-sarcoglycan maintain large masses and near control force values throughout the life span. Physiological Genomics. 22: 244-56. PMID 15886330 DOI: 10.1152/physiolgenomics.00311.2004  1
2005 Saito F, Blank M, Schröder J, Manya H, Shimizu T, Campbell KP, Endo T, Mizutani M, Kröger S, Matsumura K. Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy. Febs Letters. 579: 2359-63. PMID 15848172 DOI: 10.1016/j.febslet.2005.03.033  1
2005 Matsumoto H, Hayashi YK, Kim DS, Ogawa M, Murakami T, Noguchi S, Nonaka I, Nakazawa T, Matsuo T, Futagami S, Campbell KP, Nishino I. Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan. Neuromuscular Disorders : Nmd. 15: 342-8. PMID 15833426 DOI: 10.1016/j.nmd.2005.01.009  1
2005 Huang H, Sylvan J, Jonas M, Barresi R, So PT, Campbell KP, Lee RT. Cell stiffness and receptors: evidence for cytoskeletal subnetworks. American Journal of Physiology. Cell Physiology. 288: C72-80. PMID 15385268 DOI: 10.1152/ajpcell.00056.2004  1
2004 Saito F, Matsumura K, Campbell KP. [Function of dystroglycan in the nervous system]. Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme. 49: 2437-44. PMID 15552998  1
2004 Kikkawa Y, Yu H, Genersch E, Sanzen N, Sekiguchi K, Fässler R, Campbell KP, Talts JF, Ekblom P. Laminin isoforms differentially regulate adhesion, spreading, proliferation, and ERK activation of beta1 integrin-null cells. Experimental Cell Research. 300: 94-108. PMID 15383318 DOI: 10.1016/j.yexcr.2004.06.031  1
2004 Singh J, Itahana Y, Knight-Krajewski S, Kanagawa M, Campbell KP, Bissell MJ, Muschler J. Proteolytic enzymes and altered glycosylation modulate dystroglycan function in carcinoma cells. Cancer Research. 64: 6152-9. PMID 15342399 DOI: 10.1158/0008-5472.CAN-04-1638  1
2004 Kanagawa M, Saito F, Kunz S, Yoshida-Moriguchi T, Barresi R, Kobayashi YM, Muschler J, Dumanski JP, Michele DE, Oldstone MB, Campbell KP. Molecular recognition by LARGE is essential for expression of functional dystroglycan. Cell. 117: 953-64. PMID 15210115 DOI: 10.1016/j.cell.2004.06.003  1
2004 Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP. LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nature Medicine. 10: 696-703. PMID 15184894 DOI: 10.1038/nm1059  1
2004 Opatowsky Y, Chen CC, Campbell KP, Hirsch JA. Structural analysis of the voltage-dependent calcium channel beta subunit functional core and its complex with the alpha 1 interaction domain. Neuron. 42: 387-99. PMID 15134636 DOI: 10.1016/S0896-6273(04)00250-8  1
2004 Bansal D, Campbell KP. Dysferlin and the plasma membrane repair in muscular dystrophy. Trends in Cell Biology. 14: 206-13. PMID 15066638 DOI: 10.1016/j.tcb.2004.03.001  1
2004 Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, Sakuta R, Mochizuki M, Michele DE, Campbell KP, Nonaka I, Nishino I. POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG. Neurology. 62: 1009-11. PMID 15037715  1
2003 Rambukkana A, Kunz S, Min J, Campbell KP, Oldstone MB. Targeting Schwann cells by nonlytic arenaviral infection selectively inhibits myelination. Proceedings of the National Academy of Sciences of the United States of America. 100: 16071-6. PMID 14657400 DOI: 10.1073/pnas.2232366100  1
2003 Kunz S, Campbell KP, Oldstone MB. Alpha-dystroglycan can mediate arenavirus infection in the absence of beta-dystroglycan. Virology. 316: 213-20. PMID 14644604 DOI: 10.1016/j.virol.2003.07.002  1
2003 Chen CC, Lamping KG, Nuno DW, Barresi R, Prouty SJ, Lavoie JL, Cribbs LL, England SK, Sigmund CD, Weiss RM, Williamson RA, Hill JA, Campbell KP. Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels. Science (New York, N.Y.). 302: 1416-8. PMID 14631046 DOI: 10.1126/science.1089268  1
2003 Opatowsky Y, Chomsky-Hecht O, Kang MG, Campbell KP, Hirsch JA. The voltage-dependent calcium channel beta subunit contains two stable interacting domains. The Journal of Biological Chemistry. 278: 52323-32. PMID 14559910 DOI: 10.1074/jbc.M303564200  1
2003 Letts VA, Kang MG, Mahaffey CL, Beyer B, Tenbrink H, Campbell KP, Frankel WN. Phenotypic heterogeneity in the stargazin allelic series. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 506-13. PMID 12925883 DOI: 10.1007/s00335-003-2268-x  1
2003 Muntoni F, Valero de Bernabe B, Bittner R, Blake D, van Bokhoven H, Brockington M, Brown S, Bushby K, Campbell KP, Fiszman M, Gruenewald S, Merlini L, Quijano-Roy S, Romero N, Sabatelli P, et al. 114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE). Neuromuscular Disorders : Nmd. 13: 579-88. PMID 12921796 DOI: 10.1016/S0960-8966(03)00072-5  1
2003 Murakami M, Yamamura H, Suzuki T, Kang MG, Ohya S, Murakami A, Miyoshi I, Sasano H, Muraki K, Hano T, Kasai N, Nakayama S, Campbell KP, Flockerzi V, Imaizumi Y, et al. Modified cardiovascular L-type channels in mice lacking the voltage-dependent Ca2+ channel beta3 subunit. The Journal of Biological Chemistry. 278: 43261-7. PMID 12920136 DOI: 10.1074/jbc.M211380200  1
2003 Sampaolesi M, Torrente Y, Innocenzi A, Tonlorenzi R, D'Antona G, Pellegrino MA, Barresi R, Bresolin N, De Angelis MG, Campbell KP, Bottinelli R, Cossu G. Cell therapy of alpha-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblasts. Science (New York, N.Y.). 301: 487-92. PMID 12855815 DOI: 10.1126/science.1082254  1
2003 Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP. Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 100: 8910-5. PMID 12851463 DOI: 10.1073/pnas.1537554100  1
2003 Arikkath J, Campbell KP. Auxiliary subunits: essential components of the voltage-gated calcium channel complex. Current Opinion in Neurobiology. 13: 298-307. PMID 12850214 DOI: 10.1016/S0959-4388(03)00066-7  1
2003 Ferletta M, Kikkawa Y, Yu H, Talts JF, Durbeej M, Sonnenberg A, Timpl R, Campbell KP, Ekblom P, Genersch E. Opposing roles of integrin alpha6Abeta1 and dystroglycan in laminin-mediated extracellular signal-regulated kinase activation. Molecular Biology of the Cell. 14: 2088-103. PMID 12802077 DOI: 10.1091/mbc.E03-01-0852  1
2003 Saito F, Moore SA, Barresi R, Henry MD, Messing A, Ross-Barta SE, Cohn RD, Williamson RA, Sluka KA, Sherman DL, Brophy PJ, Schmelzer JD, Low PA, Wrabetz L, Feltri ML, ... Campbell KP, et al. Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization. Neuron. 38: 747-58. PMID 12797959 DOI: 10.1016/S0896-6273(03)00301-5  1
2003 Bansal D, Miyake K, Vogel SS, Groh S, Chen CC, Williamson R, McNeil PL, Campbell KP. Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature. 423: 168-72. PMID 12736685 DOI: 10.1038/nature01573  1
2003 Kang MG, Campbell KP. Gamma subunit of voltage-activated calcium channels. The Journal of Biological Chemistry. 278: 21315-8. PMID 12676943 DOI: 10.1074/jbc.R300004200  1
2003 Campbell KP, Stull JT. Skeletal muscle basement membrane-sarcolemma-cytoskeleton interaction minireview series. The Journal of Biological Chemistry. 278: 12599-600. PMID 12556456 DOI: 10.1074/jbc.R300005200  1
2003 Michele DE, Campbell KP. Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function. The Journal of Biological Chemistry. 278: 15457-60. PMID 12556455 DOI: 10.1074/jbc.R200031200  1
2003 Arikkath J, Chen CC, Ahern C, Allamand V, Flanagan JD, Coronado R, Gregg RG, Campbell KP. Gamma 1 subunit interactions within the skeletal muscle L-type voltage-gated calcium channels. The Journal of Biological Chemistry. 278: 1212-9. PMID 12409298 DOI: 10.1074/jbc.M208689200  1
2002 Arikkath J, Felix R, Ahern C, Chen CC, Mori Y, Song I, Shin HS, Coronado R, Campbell KP. Molecular characterization of a two-domain form of the neuronal voltage-gated P/Q-type calcium channel alpha(1)2.1 subunit. Febs Letters. 532: 300-8. PMID 12482583 DOI: 10.1016/S0014-5793(02)03693-1  1
2002 Crosbie RH, Barresi R, Campbell KP. Loss of sarcolemma nNOS in sarcoglycan-deficient muscle. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 16: 1786-91. PMID 12409321 DOI: 10.1096/fj.02-0519com  1
2002 Kang MG, Felix R, Campbell KP. Long-term regulation of voltage-gated Ca(2+) channels by gabapentin. Febs Letters. 528: 177-82. PMID 12297300 DOI: 10.1016/S0014-5793(02)03295-7  1
2002 Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, Williamson RA, Campbell KP. Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration. Cell. 110: 639-48. PMID 12230980 DOI: 10.1016/S0092-8674(02)00907-8  1
2002 Moore SA, Saito F, Chen J, Michele DE, Henry MD, Messing A, Cohn RD, Ross-Barta SE, Westra S, Williamson RA, Hoshi T, Campbell KP. Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. Nature. 418: 422-5. PMID 12140559 DOI: 10.1038/nature00838  1
2002 Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP. Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature. 418: 417-22. PMID 12140558 DOI: 10.1038/nature00837  1
2002 Crosbie RH, Dovico SA, Flanagan JD, Chamberlain JS, Ownby CL, Campbell KP. Characterization of aquaporin-4 in muscle and muscular dystrophy. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 16: 943-9. PMID 12087055 DOI: 10.1096/fj.01-0327com  1
2002 Durbeej M, Campbell KP. Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models. Current Opinion in Genetics & Development. 12: 349-61. PMID 12076680 DOI: 10.1016/S0959-437X(02)00309-X  1
2002 Lévi S, Grady RM, Henry MD, Campbell KP, Sanes JR, Craig AM. Dystroglycan is selectively associated with inhibitory GABAergic synapses but is dispensable for their differentiation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 4274-85. PMID 12040032  1
2002 Spiropoulou CF, Kunz S, Rollin PE, Campbell KP, Oldstone MB. New World arenavirus clade C, but not clade A and B viruses, utilizes alpha-dystroglycan as its major receptor. Journal of Virology. 76: 5140-6. PMID 11967329 DOI: 10.1128/JVI.76.10.5140-5146.2002  1
2002 Piccolo F, Moore SA, Mathews KD, Campbell KP. Limb-girdle muscular dystrophies. Advances in Neurology. 88: 273-91. PMID 11908231  1
2001 Kunz S, Sevilla N, McGavern DB, Campbell KP, Oldstone MB. Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan. The Journal of Cell Biology. 155: 301-10. PMID 11604425 DOI: 10.1083/jcb.200104103  1
2001 Henry MD, Cohen MB, Campbell KP. Reduced expression of dystroglycan in breast and prostate cancer. Human Pathology. 32: 791-5. PMID 11521221 DOI: 10.1053/hupa.2001.26468  1
2001 Ahern CA, Powers PA, Biddlecome GH, Roethe L, Vallejo P, Mortenson L, Strube C, Campbell KP, Coronado R, Gregg RG. Modulation of L-type Ca2+ current but not activation of Ca2+ release by the gamma1 subunit of the dihydropyridine receptor of skeletal muscle. Bmc Physiology. 1: 8. PMID 11495636  1
2001 Kang MG, Chen CC, Felix R, Letts VA, Frankel WN, Mori Y, Campbell KP. Biochemical and biophysical evidence for gamma 2 subunit association with neuronal voltage-activated Ca2+ channels. The Journal of Biological Chemistry. 276: 32917-24. PMID 11441000 DOI: 10.1074/jbc.M100787200  0.32
2001 Ahern CA, Arikkath J, Vallejo P, Gurnett CA, Powers PA, Campbell KP, Coronado R. Intramembrane charge movements and excitation- contraction coupling expressed by two-domain fragments of the Ca2+ channel. Proceedings of the National Academy of Sciences of the United States of America. 98: 6935-40. PMID 11371610 DOI: 10.1073/pnas.111001898  1
2001 Henry MD, Satz JS, Brakebusch C, Costell M, Gustafsson E, Fässler R, Campbell KP. Distinct roles for dystroglycan, beta1 integrin and perlecan in cell surface laminin organization. Journal of Cell Science. 114: 1137-44. PMID 11228157  1
2000 Piccolo F, Moore SA, Ford GC, Campbell KP. Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb--girdle muscular dystrophies. Annals of Neurology. 48: 902-12. PMID 11117547 DOI: 10.1002/1531-8249(200012)48:6<902::AID-ANA11>3.0.CO;2-Z  1
2000 Heathcote RD, Ekman JM, Campbell KP, Godfrey EW. Dystroglycan overexpression in vivo alters acetylcholine receptor aggregation at the neuromuscular junction. Developmental Biology. 227: 595-605. PMID 11071777 DOI: 10.1006/dbio.2000.9906  1
2000 Straub V, Donahue KM, Allamand V, Davisson RL, Kim YR, Campbell KP. Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy. Magnetic Resonance in Medicine : Official Journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine. 44: 655-9. PMID 11025524 DOI: 10.1002/1522-2594(200010)44:4<655::AID-MRM22>3.0.CO;2-T  1
2000 Allamand V, Campbell KP. Animal models for muscular dystrophy: valuable tools for the development of therapies. Human Molecular Genetics. 9: 2459-67. PMID 11005802  1
2000 Cohn RD, Campbell KP. Molecular basis of muscular dystrophies. Muscle & Nerve. 23: 1456-71. PMID 11003781 DOI: 10.1002/1097-4598(200010)23:10<1456::AID-MUS2>3.0.CO;2-T  1
2000 Crawford GE, Faulkner JA, Crosbie RH, Campbell KP, Froehner SC, Chamberlain JS. Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain. The Journal of Cell Biology. 150: 1399-410. PMID 10995444 DOI: 10.1083/jcb.150.6.1399  1
2000 Barresi R, Moore SA, Stolle CA, Mendell JR, Campbell KP. Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex. The Journal of Biological Chemistry. 275: 38554-60. PMID 10993904 DOI: 10.1074/jbc.M007799200  1
2000 Allamand V, Donahue KM, Straub V, Davisson RL, Davidson BL, Campbell KP. Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice. Gene Therapy. 7: 1385-91. PMID 10981665 DOI: 10.1038/sj.gt.3301247  1
2000 Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tomé FM, Campbell KP. Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions. Human Molecular Genetics. 9: 2019-27. PMID 10942431  1
2000 Ertel EA, Campbell KP, Harpold MM, Hofmann F, Mori Y, Perez-Reyes E, Schwartz A, Snutch TP, Tanabe T, Birnbaumer L, Tsien RW, Catterall WA. Nomenclature of voltage-gated calcium channels. Neuron. 25: 533-5. PMID 10774722  1
2000 Grady RM, Zhou H, Cunningham JM, Henry MD, Campbell KP, Sanes JR. Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex. Neuron. 25: 279-93. PMID 10719885  1
2000 Holt KH, Crosbie RH, Venzke DP, Campbell KP. Biosynthesis of dystroglycan: processing of a precursor propeptide. Febs Letters. 468: 79-83. PMID 10683445 DOI: 10.1016/S0014-5793(00)01195-9  1
2000 Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP. Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E. Molecular Cell. 5: 141-51. PMID 10678176  0.32
2000 Lebakken CS, Venzke DP, Hrstka RF, Consolino CM, Faulkner JA, Williamson RA, Campbell KP. Sarcospan-deficient mice maintain normal muscle function. Molecular and Cellular Biology. 20: 1669-77. PMID 10669744 DOI: 10.1128/MCB.20.5.1669-1677.2000  1
2000 Flanigan KM, Kerr L, Bromberg MB, Leonard C, Tsuruda J, Zhang P, Gonzalez-Gomez I, Cohn R, Campbell KP, Leppert M. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study. Annals of Neurology. 47: 152-61. PMID 10665485 DOI: 10.1002/1531-8249(200002)47:2<152::AID-ANA4>3.0.CO;2-U  1
2000 Leschziner A, Moukhles H, Lindenbaum M, Gee SH, Butterworth J, Campbell KP, Carbonetto S. Neural regulation of alpha-dystroglycan biosynthesis and glycosylation in skeletal muscle. Journal of Neurochemistry. 74: 70-80. PMID 10617107 DOI: 10.1046/j.1471-4159.2000.0740070.x  1
1999 Henry MD, Campbell KP. Dystroglycan inside and out. Current Opinion in Cell Biology. 11: 602-7. PMID 10508656 DOI: 10.1016/S0955-0674(99)00024-1  1
1999 Straub V, Ettinger AJ, Durbeej M, Venzke DP, Cutshall S, Sanes JR, Campbell KP. epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex. The Journal of Biological Chemistry. 274: 27989-96. PMID 10488149 DOI: 10.1074/jbc.274.39.27989  1
1999 Coral-Vazquez R, Cohn RD, Moore SA, Hill JA, Weiss RM, Davisson RL, Straub V, Barresi R, Bansal D, Hrstka RF, Williamson R, Campbell KP. Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy. Cell. 98: 465-74. PMID 10481911 DOI: 10.1016/S0092-8674(00)81975-3  1
1999 Durbeej M, Campbell KP. Biochemical characterization of the epithelial dystroglycan complex. The Journal of Biological Chemistry. 274: 26609-16. PMID 10473626 DOI: 10.1074/jbc.274.37.26609  1
1999 Burgess DL, Biddlecome GH, McDonough SI, Diaz ME, Zilinski CA, Bean BP, Campbell KP, Noebels JL. beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain. Molecular and Cellular Neurosciences. 13: 293-311. PMID 10328888 DOI: 10.1006/mcne.1999.0748  1
1999 Johnston JC, Gasmi M, Lim LE, Elder JH, Yee JK, Jolly DJ, Campbell KP, Davidson BL, Sauter SL. Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. Journal of Virology. 73: 4991-5000. PMID 10233961  1
1999 Crosbie RH, Lebakken CS, Holt KH, Venzke DP, Straub V, Lee JC, Grady RM, Chamberlain JS, Sanes JR, Campbell KP. Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex. The Journal of Cell Biology. 145: 153-65. PMID 10189375 DOI: 10.1083/jcb.145.1.153  1
1999 Badorff C, Lee GH, Lamphear BJ, Martone ME, Campbell KP, Rhoads RE, Knowlton KU. Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy. Nature Medicine. 5: 320-6. PMID 10086389 DOI: 10.1038/6543  1
1999 Brown SC, Fassati A, Popplewell L, Page AM, Henry MD, Campbell KP, Dickson G. Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan-laminin interaction. Journal of Cell Science. 112: 209-16. PMID 9858474  1
1998 Henry MD, Williamson RA, Campbell KP. Analysis of the role of dystroglycan in early postimplantation mouse development. Annals of the New York Academy of Sciences. 857: 256-9. PMID 9917851  1
1998 Henry MD, Campbell KP. A role for dystroglycan in basement membrane assembly. Cell. 95: 859-70. PMID 9865703 DOI: 10.1016/S0092-8674(00)81708-0  1
1998 Holt KH, Campbell KP. Assembly of the sarcoglycan complex. Insights for muscular dystrophy. The Journal of Biological Chemistry. 273: 34667-70. PMID 9856984 DOI: 10.1074/jbc.273.52.34667  1
1998 Cao W, Henry MD, Borrow P, Yamada H, Elder JH, Ravkov EV, Nichol ST, Compans RW, Campbell KP, Oldstone MB. Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus. Science (New York, N.Y.). 282: 2079-81. PMID 9851928 DOI: 10.1126/science.282.5396.2079  1
1998 Rambukkana A, Yamada H, Zanazzi G, Mathus T, Salzer JL, Yurchenco PD, Campbell KP, Fischetti VA. Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae. Science (New York, N.Y.). 282: 2076-9. PMID 9851927 DOI: 10.1126/science.282.5396.2076  1
1998 Lim LE, Campbell KP. The sarcoglycan complex in limb-girdle muscular dystrophy. Current Opinion in Neurology. 11: 443-52. PMID 9847993 DOI: 10.1097/00019052-199810000-00006  1
1998 Durbeej M, Henry MD, Campbell KP. Dystroglycan in development and disease. Current Opinion in Cell Biology. 10: 594-601. PMID 9818169 DOI: 10.1016/S0955-0674(98)80034-3  1
1998 Duclos F, Straub V, Moore SA, Venzke DP, Hrstka RF, Crosbie RH, Durbeej M, Lebakken CS, Ettinger AJ, van der Meulen J, Holt KH, Lim LE, Sanes JR, Davidson BL, Faulkner JA, ... ... Campbell KP, et al. Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice. The Journal of Cell Biology. 142: 1461-71. PMID 9744877 DOI: 10.1083/jcb.142.6.1461  1
1998 Letts VA, Felix R, Biddlecome GH, Arikkath J, Mahaffey CL, Valenzuela A, Bartlett FS, Mori Y, Campbell KP, Frankel WN. The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit. Nature Genetics. 19: 340-7. PMID 9697694 DOI: 10.1038/1228  1
1998 Ding JM, Buchanan GF, Tischkau SA, Chen D, Kuriashkina L, Faiman LE, Alster JM, McPherson PS, Campbell KP, Gillette MU. A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock. Nature. 394: 381-4. PMID 9690474 DOI: 10.1038/28639  1
1998 Scott VE, Gurnett CA, Campbell KP. Overlay and bead assay. Determination of calcium channel subunit interaction domains. Methods in Molecular Biology (Clifton, N.J.). 88: 71-85. PMID 9664299 DOI: 10.1385/0-89603-487-9:71  1
1998 Holt KH, Lim LE, Straub V, Venzke DP, Duclos F, Anderson RD, Davidson BL, Campbell KP. Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer. Molecular Cell. 1: 841-8. PMID 9660967  0.76
1998 Crosbie RH, Yamada H, Venzke DP, Lisanti MP, Campbell KP. Caveolin-3 is not an integral component of the dystrophin glycoprotein complex. Febs Letters. 427: 279-82. PMID 9607328 DOI: 10.1016/S0014-5793(98)00442-6  1
1998 Duclos F, Broux O, Bourg N, Straub V, Feldman GL, Sunada Y, Lim LE, Piccolo F, Cutshall S, Gary F, Quetier F, Kaplan JC, Jackson CE, Beckmann JS, Campbell KP. Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. Neuromuscular Disorders : Nmd. 8: 30-8. PMID 9565988 DOI: 10.1016/S0960-8966(97)00135-1  1
1998 Crosbie RH, Straub V, Yun HY, Lee JC, Rafael JA, Chamberlain JS, Dawson VL, Dawson TM, Campbell KP. mdx muscle pathology is independent of nNOS perturbation. Human Molecular Genetics. 7: 823-9. PMID 9536086 DOI: 10.1093/hmg/7.5.823  1
1998 Durbeej M, Henry MD, Ferletta M, Campbell KP, Ekblom P. Distribution of dystroglycan in normal adult mouse tissues. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 46: 449-57. PMID 9524190  1
1998 Walker D, Bichet D, Campbell KP, De Waard M. A beta 4 isoform-specific interaction site in the carboxyl-terminal region of the voltage-dependent Ca2+ channel alpha 1A subunit. The Journal of Biological Chemistry. 273: 2361-7. PMID 9442082 DOI: 10.1074/jbc.273.4.2361  1
1998 Scott VE, Felix R, Arikkath J, Campbell KP. Evidence for a 95 kDa short form of the alpha1A subunit associated with the omega-conotoxin MVIIC receptor of the P/Q-type Ca2+ channels. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 641-7. PMID 9425006  1
1997 Bies RD, Maeda M, Roberds SL, Holder E, Bohlmeyer T, Young JB, Campbell KP. A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy. Journal of Molecular and Cellular Cardiology. 29: 3175-88. PMID 9441825 DOI: 10.1006/jmcc.1997.0568  0.32
1997 Crosbie RH, Heighway J, Venzke DP, Lee JC, Campbell KP. Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex. The Journal of Biological Chemistry. 272: 31221-4. PMID 9395445 DOI: 10.1074/jbc.272.50.31221  1
1997 Straub V, Rafael JA, Chamberlain JS, Campbell KP. Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. The Journal of Cell Biology. 139: 375-85. PMID 9334342 DOI: 10.1083/jcb.139.2.375  1
1997 Felix R, Gurnett CA, De Waard M, Campbell KP. Dissection of functional domains of the voltage-dependent Ca2+ channel alpha2delta subunit. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 6884-91. PMID 9278523  1
1997 Dinçer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, de Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea JA, Jung D, Tan E, Jeanpierre M, ... Campbell KP, et al. A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Annals of Neurology. 42: 222-9. PMID 9266733 DOI: 10.1002/ana.410420214  0.32
1997 Gurnett CA, Felix R, Campbell KP. Extracellular interaction of the voltage-dependent Ca2+ channel alpha2delta and alpha1 subunits. The Journal of Biological Chemistry. 272: 18508-12. PMID 9218497 DOI: 10.1074/jbc.272.29.18508  1
1997 Carrié A, Piccolo F, Leturcq F, de Toma C, Azibi K, Beldjord C, Vallat JM, Merlini L, Voit T, Sewry C, Urtizberea JA, Romero N, Tomé FM, Fardeau M, Sunada Y, ... Campbell KP, et al. Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). Journal of Medical Genetics. 34: 470-5. PMID 9192266  0.32
1997 Williamson RA, Henry MD, Daniels KJ, Hrstka RF, Lee JC, Sunada Y, Ibraghimov-Beskrovnaya O, Campbell KP. Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice. Human Molecular Genetics. 6: 831-41. PMID 9175728 DOI: 10.1093/hmg/6.6.831  1
1997 Allamand V, Sunada Y, Salih MA, Straub V, Ozo CO, Al-Turaiki MH, Akbar M, Kolo T, Colognato H, Zhang X, Sorokin LM, Yurchenco PD, Tryggvason K, Campbell KP. Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain. Human Molecular Genetics. 6: 747-52. PMID 9158149  0.32
1997 Eymard B, Romero NB, Leturcq F, Piccolo F, Carrié A, Jeanpierre M, Collin H, Deburgrave N, Azibi K, Chaouch M, Merlini L, Thémar-Noël C, Penisson I, Mayer M, Tanguy O, ... Campbell KP, et al. Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy. Neurology. 48: 1227-34. PMID 9153448  0.32
1997 Straub V, Campbell KP. Muscular dystrophies and the dystrophin-glycoprotein complex. Current Opinion in Neurology. 10: 168-75. PMID 9146999  1
1997 Durbeej M, Jung D, Hjalt T, Campbell KP, Ekblom P. Transient expression of Dp140, a product of the Duchenne muscular dystrophy locus, during kidney tubulogenesis. Developmental Biology. 181: 156-67. PMID 9013927 DOI: 10.1006/dbio.1996.8430  1
1997 De Waard M, Liu H, Walker D, Scott VE, Gurnett CA, Campbell KP. Direct binding of G-protein betagamma complex to voltage-dependent calcium channels. Nature. 385: 446-50. PMID 9009193 DOI: 10.1038/385446a0  1
1997 Fahlke C, Knittle T, Gurnett CA, Campbell KP, George AL. Subunit stoichiometry of human muscle chloride channels. The Journal of General Physiology. 109: 93-104. PMID 8997668 DOI: 10.1085/jgp.109.1.93  1
1996 Jeanpierre M, Carrié A, Piccolo F, Leturcq F, Azibi K, De Toma C, Beldjord C, Merlini L, Voit T, Romero N, Sunada Y, Tomé FM, Fardeau M, Campbell KP, Kaplan JC. From adhalinopathies to alpha-sarcoglycanopathies: an overview. Neuromuscular Disorders : Nmd. 6: 463-5. PMID 9027856  0.32
1996 Beckmann JS, Richard I, Broux O, Fougerousse F, Allamand V, Chiannilkulchai N, Lim LE, Duclos F, Bourg N, Brenguier L, Pasturaud P, Quétier F, Roudaut C, Sunada Y, Meyer J, ... ... Campbell KP, et al. Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies. Neuromuscular Disorders : Nmd. 6: 455-62. PMID 9027855 DOI: 10.1016/S0960-8966(96)00386-0  1
1996 Tian M, Jacobson C, Gee SH, Campbell KP, Carbonetto S, Jucker M. Dystroglycan in the cerebellum is a laminin alpha 2-chain binding protein at the glial-vascular interface and is expressed in Purkinje cells. The European Journal of Neuroscience. 8: 2739-47. PMID 8996823 DOI: 10.1111/j.1460-9568.1996.tb01568.x  1
1996 Piccolo F, Jeanpierre M, Leturcq F, Dodé C, Azibi K, Toutain A, Merlini L, Jarre L, Navarro C, Krishnamoorthy R, Tomé FM, Urtizberea JA, Beckmann JS, Campbell KP, Kaplan JC. A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India. Human Molecular Genetics. 5: 2019-22. PMID 8968757  0.32
1996 Jung D, Duclos F, Apostol B, Straub V, Lee JC, Allamand V, Venzke DP, Sunada Y, Moomaw CR, Leveille CJ, Slaughter CA, Crawford TO, McPherson JD, Campbell KP. Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy. The Journal of Biological Chemistry. 271: 32321-9. PMID 8943294  0.32
1996 Clemens PR, Kochanek S, Sunada Y, Chan S, Chen HH, Campbell KP, Caskey CT. In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes. Gene Therapy. 3: 965-72. PMID 8940636  1
1996 Henry MD, Campbell KP. Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton. Current Opinion in Cell Biology. 8: 625-31. PMID 8939660 DOI: 10.1016/S0955-0674(96)80103-7  1
1996 Campbell KP, Crosbie RH. Muscular dystrophy. Utrophin to the rescue. Nature. 384: 308-9. PMID 8934508 DOI: 10.1038/384308a0  1
1996 Liu H, Felix R, Gurnett CA, De Waard M, Witcher DR, Campbell KP. Expression and subunit interaction of voltage-dependent Ca2+ channels in PC12 cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 16: 7557-65. PMID 8922412  1
1996 Gurnett CA, Campbell KP. Transmembrane auxiliary subunits of voltage-dependent ion channels. The Journal of Biological Chemistry. 271: 27975-8. PMID 8910401 DOI: 10.1074/jbc.271.45.27975  1
1996 Cullen MJ, Walsh J, Roberds SL, Campbell KP. Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscle. Neuropathology and Applied Neurobiology. 22: 30-7. PMID 8866780  1
1996 Guo W, Jorgensen AO, Campbell KP. Triadin, a linker for calsequestrin and the ryanodine receptor. Society of General Physiologists Series. 51: 19-28. PMID 8809931  1
1996 Gurnett CA, De Waard M, Campbell KP. Dual function of the voltage-dependent Ca2+ channel alpha 2 delta subunit in current stimulation and subunit interaction. Neuron. 16: 431-40. PMID 8789958 DOI: 10.1016/S0896-6273(00)80061-6  1
1996 De Waard M, Gurnett CA, Campbell KP. Structural and functional diversity of voltage-activated calcium channels. Ion Channels. 4: 41-87. PMID 8744206  1
1996 Cullen MJ, Walsh J, Roberds SL, Campbell KP. Immunogold localization of adhalin, alpha-dystroglycan and laminin in normal and dystrophic skeletal muscle. Biochemical Society Transactions. 24: 274S. PMID 8736932  1
1996 Rafael JA, Cox GA, Corrado K, Jung D, Campbell KP, Chamberlain JS. Forced expression of dystrophin deletion constructs reveals structure-function correlations. The Journal of Cell Biology. 134: 93-102. PMID 8698825 DOI: 10.1083/jcb.134.1.93  1
1996 Oexle K, Herrmann R, Dodé C, Leturcq F, Hübner C, Kaplan JC, Mizuno Y, Ozawa E, Campbell KP, Voit T. Neurosensory hearing loss in secondary adhalinopathy. Neuropediatrics. 27: 32-6. PMID 8677023 DOI: 10.1055/s-2007-973744  0.32
1996 Liu H, De Waard M, Scott VE, Gurnett CA, Lennon VA, Campbell KP. Identification of three subunits of the high affinity omega-conotoxin MVIIC-sensitive Ca2+ channel. The Journal of Biological Chemistry. 271: 13804-10. PMID 8662888  1
1996 Jung D, Leturcq F, Sunada Y, Duclos F, Tomé FM, Moomaw C, Merlini L, Azibi K, Chaouch M, Slaughter C, Fardeau M, Kaplan JC, Campbell KP. Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12. Febs Letters. 381: 15-20. PMID 8641426  0.32
1996 Salih MA, Mahdi AH, al-Rikabi AC, al-Bunyan M, Roberds SL, Anderson RD, Campbell KP. Clinical and molecular pathological features of severe childhood autosomal recessive muscular dystrophy in Saudi Arabia. Developmental Medicine and Child Neurology. 38: 262-70. PMID 8631523  0.32
1996 Scott VE, De Waard M, Liu H, Gurnett CA, Venzke DP, Lennon VA, Campbell KP. Beta subunit heterogeneity in N-type Ca2+ channels. The Journal of Biological Chemistry. 271: 3207-12. PMID 8621722  1
1996 De Waard M, Scott VE, Pragnell M, Campbell KP. Identification of critical amino acids involved in alpha1-beta interaction in voltage-dependent Ca2+ channels. Febs Letters. 380: 272-6. PMID 8601439 DOI: 10.1016/0014-5793(96)00007-5  1
1996 Guo W, Jorgensen AO, Jones LR, Campbell KP. Biochemical characterization and molecular cloning of cardiac triadin. The Journal of Biological Chemistry. 271: 458-65. PMID 8550602 DOI: 10.1074/jbc.271.1.458  1
1995 Montanaro F, Carbonetto S, Campbell KP, Lindenbaum M. Dystroglycan expression in the wild type and mdx mouse neural retina: synaptic colocalization with dystrophin, dystrophin-related protein but not laminin. Journal of Neuroscience Research. 42: 528-38. PMID 8568939 DOI: 10.1002/jnr.490420411  1
1995 Sunada Y, Campbell KP. Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle. Current Opinion in Neurology. 8: 379-84. PMID 8542044  1
1995 Mills KA, Sunada Y, Campbell KP, Mathews KD. A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 664-5. PMID 8535078 DOI: 10.1007/BF00352377  1
1995 Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Human Molecular Genetics. 4: 1163-7. PMID 8528203  0.32
1995 Yang B, Jung D, Rafael JA, Chamberlain JS, Campbell KP. Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin. The Journal of Biological Chemistry. 270: 4975-8. PMID 7890602 DOI: 10.1074/jbc.270.10.4975  1
1995 Campbell KP. Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. Cell. 80: 675-9. PMID 7889563 DOI: 10.1016/0092-8674(95)90344-5  1
1995 Durbeej M, Larsson E, Ibraghimov-Beskrovnaya O, Roberds SL, Campbell KP, Ekblom P. Non-muscle alpha-dystroglycan is involved in epithelial development. The Journal of Cell Biology. 130: 79-91. PMID 7790379 DOI: 10.1083/jcb.130.1.79  1
1995 Kawai H, Inui T, Mitsui T, Campbell KP, Shimizu T, Matsumura K. [Complete deficiency of adhalin (50 kDa DAG) in skeletal muscle of malignant limb-girdle muscular dystrophy]. Rinshō Shinkeigaku = Clinical Neurology. 35: 184-9. PMID 7781237  1
1995 Roberds SL, Campbell KP. Adhalin mRNA and cDNA sequence are normal in the cardiomyopathic hamster. Febs Letters. 364: 245-9. PMID 7758576 DOI: 10.1016/0014-5793(95)00395-P  1
1995 Cohen MW, Jacobson C, Godfrey EW, Campbell KP, Carbonetto S. Distribution of alpha-dystroglycan during embryonic nerve-muscle synaptogenesis. The Journal of Cell Biology. 129: 1093-101. PMID 7744958  1
1995 De Waard M, Witcher DR, Pragnell M, Liu H, Campbell KP. Properties of the alpha 1-beta anchoring site in voltage-dependent Ca2+ channels. The Journal of Biological Chemistry. 270: 12056-64. PMID 7744854  1
1995 Yang B, Jung D, Motto D, Meyer J, Koretzky G, Campbell KP. SH3 domain-mediated interaction of dystroglycan and Grb2. The Journal of Biological Chemistry. 270: 11711-4. PMID 7744812 DOI: 10.1074/jbc.270.20.11711  1
1995 Gurnett CA, Kahl SD, Anderson RD, Campbell KP. Absence of the skeletal muscle sarcolemma chloride channel ClC-1 in myotonic mice. The Journal of Biological Chemistry. 270: 9035-8. PMID 7721815 DOI: 10.1074/jbc.270.16.9035  1
1995 Guo W, Campbell KP. Association of triadin with the ryanodine receptor and calsequestrin in the lumen of the sarcoplasmic reticulum. The Journal of Biological Chemistry. 270: 9027-30. PMID 7721813 DOI: 10.1074/jbc.270.16.9027  1
1995 Campbell KP. Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy. Annals of Neurology. 38: 353-4. PMID 7668818 DOI: 10.1002/ana.410380302  1
1995 Sunada Y, Bernier SM, Utani A, Yamada Y, Campbell KP. Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice. Human Molecular Genetics. 4: 1055-61. PMID 7655459 DOI: 10.1093/hmg/4.6.1055  1
1995 Fritz JD, Danko I, Roberds SL, Campbell KP, Latendresse JS, Wolff JA. Expression of deletion-containing dystrophins in mdx muscle: implications for gene therapy and dystrophin function. Pediatric Research. 37: 693-700. PMID 7651751 DOI: 10.1203/00006450-199506000-00004  0.32
1995 Witcher DR, De Waard M, Liu H, Pragnell M, Campbell KP. Association of native Ca2+ channel beta subunits with the alpha 1 subunit interaction domain. The Journal of Biological Chemistry. 270: 18088-93. PMID 7629119  1
1995 Apel ED, Roberds SL, Campbell KP, Merlie JP. Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex. Neuron. 15: 115-26. PMID 7619516 DOI: 10.1016/0896-6273(95)90069-1  1
1995 Vater R, Harris JB, Anderson VB, Roberds SL, Campbell KP, Cullen MJ. The expression of dystrophin-associated glycoproteins during skeletal muscle degeneration and regeneration. An immunofluorescence study. Journal of Neuropathology and Experimental Neurology. 54: 557-69. PMID 7602329  0.32
1995 Jung D, Yang B, Meyer J, Chamberlain JS, Campbell KP. Identification and characterization of the dystrophin anchoring site on beta-dystroglycan. The Journal of Biological Chemistry. 270: 27305-10. PMID 7592992 DOI: 10.1074/jbc.270.45.27305  1
1995 Wells DJ, Wells KE, Asante EA, Turner G, Sunada Y, Campbell KP, Walsh FS, Dickson G. Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Human Molecular Genetics. 4: 1245-50. PMID 7581360  1
1995 De Waard M, Campbell KP. Subunit regulation of the neuronal alpha 1A Ca2+ channel expressed in Xenopus oocytes. The Journal of Physiology. 485: 619-34. PMID 7562605  1
1995 Sunada Y, Edgar TS, Lotz BP, Rust RS, Campbell KP. Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities. Neurology. 45: 2084-9. PMID 7501163  1
1994 Parys JB, McPherson SM, Mathews L, Campbell KP, Longo FJ. Presence of inositol 1,4,5-trisphosphate receptor, calreticulin, and calsequestrin in eggs of sea urchins and Xenopus laevis. Developmental Biology. 161: 466-76. PMID 8313995 DOI: 10.1006/dbio.1994.1045  1
1994 Matsumura K, Campbell KP. Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies. Muscle & Nerve. 17: 2-15. PMID 8264699 DOI: 10.1002/mus.880170103  1
1994 Campanelli JT, Roberds SL, Campbell KP, Scheller RH. A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering. Cell. 77: 663-74. PMID 8205616  1
1994 Sunada Y, Bernier SM, Kozak CA, Yamada Y, Campbell KP. Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. The Journal of Biological Chemistry. 269: 13729-32. PMID 8188645  1
1994 De Waard M, Witcher DR, Campbell KP. Functional properties of the purified N-type Ca2+ channel from rabbit brain. The Journal of Biological Chemistry. 269: 6716-24. PMID 8120030  1
1994 Ervasti JM, Roberds SL, Anderson RD, Sharp NJ, Kornegay JN, Campbell KP. Alpha-dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophy. Febs Letters. 350: 173-6. PMID 8070559 DOI: 10.1016/0014-5793(94)00748-9  1
1994 De Waard M, Pragnell M, Campbell KP. Ca2+ channel regulation by a conserved beta subunit domain. Neuron. 13: 495-503. PMID 8060623  1
1994 Mickelson JR, Ervasti JM, Litterer LA, Campbell KP, Louis CF. Skeletal muscle junctional membrane protein content in pigs with different ryanodine receptor genotypes. The American Journal of Physiology. 267: C282-92. PMID 8048487  1
1994 Higuchi I, Yamada H, Fukunaga H, Iwaki H, Okubo R, Nakagawa M, Osame M, Roberds SL, Shimizu T, Campbell KP. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. The Journal of Clinical Investigation. 94: 601-6. PMID 8040315 DOI: 10.1172/JCI117375  0.32
1994 Sewry CA, Sansome A, Matsumura K, Campbell KP, Dubowitz V. Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy. Neuromuscular Disorders : Nmd. 4: 121-9. PMID 8012192 DOI: 10.1016/0960-8966(94)90003-5  1
1994 Romero NB, Tomé FM, Leturcq F, el Kerch FE, Azibi K, Bachner L, Anderson RD, Roberds SL, Campbell KP, Fardeau M. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency. Comptes Rendus De L'AcadéMie Des Sciences. SéRie Iii, Sciences De La Vie. 317: 70-6. PMID 7987694  0.32
1994 Tomé FM, Matsumura K, Chevallay M, Campbell KP, Fardeau M. Expression of dystrophin-associated glycoproteins during human fetal muscle development: a preliminary immunocytochemical study. Neuromuscular Disorders : Nmd. 4: 343-8. PMID 7981591 DOI: 10.1016/0960-8966(94)90070-1  1
1994 Guo W, Jorgensen AO, Campbell KP. Characterization and ultrastructural localization of a novel 90-kDa protein unique to skeletal muscle junctional sarcoplasmic reticulum. The Journal of Biological Chemistry. 269: 28359-65. PMID 7961775  1
1994 Yamada H, Shimizu T, Tanaka T, Campbell KP, Matsumura K. Dystroglycan is a binding protein of laminin and merosin in peripheral nerve. Febs Letters. 352: 49-53. PMID 7925941 DOI: 10.1016/0014-5793(94)00917-1  1
1994 Birnbaumer L, Campbell KP, Catterall WA, Harpold MM, Hofmann F, Horne WA, Mori Y, Schwartz A, Snutch TP, Tanabe T. The naming of voltage-gated calcium channels. Neuron. 13: 505-6. PMID 7917287  1
1994 Greenberg DS, Sunada Y, Campbell KP, Yaffe D, Nudel U. Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice. Nature Genetics. 8: 340-4. PMID 7894483 DOI: 10.1038/ng1294-340  1
1994 Cox GA, Sunada Y, Campbell KP, Chamberlain JS. Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy. Nature Genetics. 8: 333-9. PMID 7894482 DOI: 10.1038/ng1294-333  1
1994 Allamand V, Leturcq F, Piccolo F, Jeanpierre M, Azibi K, Roberds SL, Lim LE, Campbell KP, Beckmann JS, Kaplan JC. Adhalin gene polymorphism. Human Molecular Genetics. 3: 2269. PMID 7881446 DOI: 10.1093/hmg/3.12.2269  1
1994 Sewry CA, Matsumura K, Campbell KP, Dubowitz V. Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 4: 401-9. PMID 7881285 DOI: 10.1016/0960-8966(94)90079-5  1
1994 Rafael JA, Sunada Y, Cole NM, Campbell KP, Faulkner JA, Chamberlain JS. Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform. Human Molecular Genetics. 3: 1725-33. PMID 7849695  1
1994 Witcher DR, De Waard M, Kahl SD, Campbell KP. Purification and reconstitution of N-type calcium channel complex from rabbit brain. Methods in Enzymology. 238: 335-48. PMID 7799800 DOI: 10.1016/0076-6879(94)38030-9  1
1994 Matsumura K, Tomé FM, Collin H, Leturcq F, Jeanpierre M, Kaplan JC, Fardeau M, Campbell KP. Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 4: 115-20. PMID 7516752  0.32
1994 Pragnell M, De Waard M, Mori Y, Tanabe T, Snutch TP, Campbell KP. Calcium channel beta-subunit binds to a conserved motif in the I-II cytoplasmic linker of the alpha 1-subunit. Nature. 368: 67-70. PMID 7509046 DOI: 10.1038/368067a0  1
1993 Ibraghimov-Beskrovnaya O, Sheffield VC, Campbell KP. Single base polymorphism in the DAG1 gene detected by DGGE and mismatch PCR. Human Molecular Genetics. 2: 1983. PMID 8281174 DOI: 10.1093/hmg/2.11.1983-a  1
1993 Matsumura K, Yamada H, Shimizu T, Campbell KP. Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve. Febs Letters. 334: 281-5. PMID 8243633 DOI: 10.1016/0014-5793(93)80695-Q  1
1993 Phillips WD, Noakes PG, Roberds SL, Campbell KP, Merlie JP. Clustering and immobilization of acetylcholine receptors by the 43-kD protein: a possible role for dystrophin-related protein. The Journal of Cell Biology. 123: 729-40. PMID 8227135  1
1993 Roberds SL, Anderson RD, Ibraghimov-Beskrovnaya O, Campbell KP. Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin). The Journal of Biological Chemistry. 268: 23739-42. PMID 8226900  1
1993 Witcher DR, De Waard M, Campbell KP. Characterization of the purified N-type Ca2+ channel and the cation sensitivity of omega-conotoxin GVIA binding. Neuropharmacology. 32: 1127-39. PMID 8107967 DOI: 10.1016/0028-3908(93)90007-P  1
1993 Stea A, Dubel SJ, Pragnell M, Leonard JP, Campbell KP, Snutch TP. A beta-subunit normalizes the electrophysiological properties of a cloned N-type Ca2+ channel alpha 1-subunit. Neuropharmacology. 32: 1103-16. PMID 8107965 DOI: 10.1016/0028-3908(93)90005-N  1
1990 Leberer E, Timms BG, Campbell KP, MacLennan DH. Purification, calcium binding properties, and ultrastructural localization of the 53,000- and 160,000 (sarcalumenin)-dalton glycoproteins of the sarcoplasmic reticulum. The Journal of Biological Chemistry. 265: 10118-24. PMID 2112542  1
1984 MacLennan DH, Campbell KP, Takisawa H, Tuana BS. A calmodulin-dependent protein kinase system from skeletal muscle sarcoplasmic reticulum. Advances in Cyclic Nucleotide and Protein Phosphorylation Research. 17: 393-401. PMID 6328928  1
1983 Campbell KP, MacLennan DH. Labeling of high affinity ATP binding sites on the 53,000- and 160,000-dalton glycoproteins of the sarcoplasmic reticulum with the photoaffinity probe 8-N3-[alpha-32P]ATP. The Journal of Biological Chemistry. 258: 1391-4. PMID 6687385  1
1983 Jorgensen AO, Shen AC, Campbell KP, MacLennan DH. Ultrastructural localization of calsequestrin in rat skeletal muscle by immunoferritin labeling of ultrathin frozen sections. The Journal of Cell Biology. 97: 1573-81. PMID 6355123  1
1983 Campbell KP, MacLennan DH, Jorgensen AO, Mintzer MC. Purification and characterization of calsequestrin from canine cardiac sarcoplasmic reticulum and identification of the 53,000 dalton glycoprotein. The Journal of Biological Chemistry. 258: 1197-204. PMID 6337133  1
1983 Campbell KP, MacLennan DH, Jorgensen AO. Staining of the Ca2+-binding proteins, calsequestrin, calmodulin, troponin C, and S-100, with the cationic carbocyanine dye "Stains-all". The Journal of Biological Chemistry. 258: 11267-73. PMID 6193121  1
1983 Zubrzycka-Gaarn E, Campbell KP, MacLennan DH, Jorgensen AO. Biosynthesis of intrinsic sarcoplasmic reticulum proteins during differentiation of the myogenic cell line L6. The Journal of Biological Chemistry. 258: 4576-81. PMID 6131896  1
1982 Campbell KP, MacLennan DH. A calmodulin-dependent protein kinase system from skeletal muscle sarcoplasmic reticulum. Phosphorylation of a 60,000-dalton protein. The Journal of Biological Chemistry. 257: 1238-46. PMID 6799504  1
1981 Campbell KP, MacLennan DH. Purification and characterization of the 53,000-dalton glycoprotein from the sarcoplasmic reticulum. The Journal of Biological Chemistry. 256: 4626-32. PMID 6260806  1
1980 Campbell KP, MacLennan DH. DIDS inhibition of sarcoplasmic reticulum anion efflux and calcium transport. Annals of the New York Academy of Sciences. 358: 328-31. PMID 6938153  1
1980 Michalak M, Campbell KP, MacLennan DH. Localization of the high affinity calcium binding protein and an intrinsic glycoprotein in sarcoplasmic reticulum membranes. The Journal of Biological Chemistry. 255: 1317-26. PMID 6766447  1
1980 Shoshan V, Campbell KP, MacLennan DH, Frodis W, Britt BA. Quercetin inhibits Ca2+ uptake but not Ca2+ release by sarcoplasmic reticulum in skinned muscle fibers. Proceedings of the National Academy of Sciences of the United States of America. 77: 4435-8. PMID 6449007  1
1980 MacLennan DH, Reithmeier RA, Shoshan V, Campbell KP, LeBel D, Herrmann TR, Shamoo AE. Ion pathways in proteins of the sarcoplasmic reticulum. Annals of the New York Academy of Sciences. 358: 138-48. PMID 6259987 DOI: 10.1111/j.1749-6632.1980.tb15392.x  1
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