| Year |
Citation |
Score |
| 2021 |
Shelton GD, Minor KM, Guo LT, Friedenberg SG, Cullen JN, Hord JM, Venzke D, Anderson ME, Devereaux M, Prouty SJ, Handelman C, Campbell KP, Mickelson JR. Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation. Neuromuscular Disorders : Nmd. PMID 34654610 DOI: 10.1016/j.nmd.2021.07.016 |
0.323 |
|
| 2020 |
Bez Batti Angulski A, Bauer J, Cohen H, Kobuke K, Campbell KP, Metzger JM. Investigations of an inducible intact dystrophin gene excision system in cardiac and skeletal muscle in vivo. Scientific Reports. 10: 10967. PMID 32620803 DOI: 10.1038/S41598-020-67372-0 |
0.404 |
|
| 2019 |
Beltrán D, Anderson ME, Bharathy N, Settelmeyer TP, Svalina MN, Bajwa Z, Shern JF, Gultekin SH, Cuellar MA, Yonekawa T, Keller C, Campbell KP. Exogenous expression of the glycosyltransferase LARGE1 restores α-dystroglycan matriglycan and laminin binding in rhabdomyosarcoma. Skeletal Muscle. 9: 11. PMID 31054580 DOI: 10.1186/S13395-019-0195-0 |
0.332 |
|
| 2018 |
González Coraspe JA, Weis J, Anderson ME, Münchberg U, Lorenz K, Buchkremer S, Carr S, Zahedi RP, Brauers E, Michels H, Sunada Y, Lochmüller H, Campbell KP, Freier E, Hathazi D, et al. Biochemical and pathological changes result from mutated Caveolin-3 in muscle. Skeletal Muscle. 8: 28. PMID 30153853 DOI: 10.1186/S13395-018-0173-Y |
0.401 |
|
| 2018 |
Brun BN, Willer T, Darbro BW, Gonorazky HD, Naumenko S, Dowling JJ, Campbell KP, Moore SA, Mathews KD. Uniparental disomy unveils a novel recessive mutation in POMT2. Neuromuscular Disorders : Nmd. PMID 29759639 DOI: 10.1016/J.Nmd.2018.04.003 |
0.395 |
|
| 2017 |
Clements R, Turk R, Campbell KP, Wright KM. Dystroglycan Maintains Inner Limiting Membrane Integrity to Coordinate Retinal Development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 28760865 DOI: 10.1523/Jneurosci.0946-17.2017 |
0.314 |
|
| 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 |
0.385 |
|
| 2016 |
Jerber J, Zaki MS, Al-Aama JY, Rosti RO, Ben-Omran T, Dikoglu E, Silhavy JL, Caglar C, Musaev D, Albrecht B, Campbell KP, Willer T, Almuriekhi M, Çağlayan AO, Vajsar J, et al. Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly. American Journal of Human Genetics. PMID 27773428 DOI: 10.1016/J.Ajhg.2016.09.007 |
0.431 |
|
| 2016 |
Früh S, Romanos J, Panzanelli P, Bürgisser D, Tyagarajan SK, Campbell KP, Santello M, Fritschy JM. Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 10296-10313. PMID 27707967 DOI: 10.1523/Jneurosci.1823-16.2016 |
0.325 |
|
| 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 |
0.429 |
|
| 2016 |
Briggs DC, Yoshida-Moriguchi T, Zheng T, Venzke D, Anderson ME, Strazzulli A, Moracci M, Yu L, Hohenester E, Campbell KP. Structural basis of laminin binding to the LARGE glycans on dystroglycan. Nature Chemical Biology. PMID 27526028 DOI: 10.1038/Nchembio.2146 |
0.351 |
|
| 2016 |
Inamori KI, Beedle AM, de Bernabé DB, Wright ME, Campbell KP. LARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans. Glycobiology. PMID 27496765 DOI: 10.1093/Glycob/Cww075 |
0.331 |
|
| 2016 |
Praissman JL, Willer T, Sheikh MO, Toi A, Chitayat D, Lin YY, Lee H, Stalnaker SH, Wang S, Prabhakar PK, Nelson SF, Stemple DL, Moore SA, Moremen KW, Campbell KP, et al. The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition. Elife. 5. PMID 27130732 DOI: 10.7554/Elife.14473 |
0.386 |
|
| 2016 |
Turk R, Hsiao JJ, Smits MM, Ng BH, Pospisil TC, Jones KS, Campbell KP, Wright ME. Molecular signatures of membrane protein complexes underlying muscular dystrophy. Molecular & Cellular Proteomics : McP. PMID 27099343 DOI: 10.1074/Mcp.M116.059188 |
0.445 |
|
| 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 |
0.422 |
|
| 2015 |
Jensen BS, Willer T, Saade DN, Cox MO, Mozaffar T, Scavina M, Stefans VA, Winder TL, Campbell KP, Moore SA, Mathews KD. Gmppb-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation. Human Mutation. PMID 26310427 DOI: 10.1002/Humu.22898 |
0.305 |
|
| 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 |
0.412 |
|
| 2014 |
Willer T, Inamori K, Venzke D, Harvey C, Morgensen G, Hara Y, Beltrán Valero de Bernabé D, Yu L, Wright KM, Campbell KP. The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation. Elife. 3. PMID 25279699 DOI: 10.7554/Elife.03941 |
0.311 |
|
| 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 |
0.334 |
|
| 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 |
0.302 |
|
| 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 |
0.369 |
|
| 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 |
0.779 |
|
| 2013 |
Levy JR, Campbell KP, Glass DJ. MG53's new identity. Skeletal Muscle. 3: 25. PMID 24175977 DOI: 10.1186/2044-5040-3-25 |
0.324 |
|
| 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 |
0.436 |
|
| 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 |
0.316 |
|
| 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 |
0.398 |
|
| 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 |
0.402 |
|
| 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 |
0.376 |
|
| 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 |
0.399 |
|
| 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 |
0.687 |
|
| 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 |
0.305 |
|
| 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 |
0.395 |
|
| 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 |
0.749 |
|
| 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 |
0.651 |
|
| 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 |
0.338 |
|
| 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 |
0.303 |
|
| 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 |
0.37 |
|
| 2012 |
Cirak S, Foley RA, Herrmann R, Willer T, Elisabeth S, Yau M, Brodd L, Torelli S, Kamynina A, Vondracek P, Roper H, Longman C, Korinthenberg R, Marrosu G, Nurnberg P, ... ... Campbell KP, et al. G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies Neuromuscular Disorders. 22: 812. DOI: 10.1016/J.Nmd.2012.06.036 |
0.394 |
|
| 2012 |
Willer T, Lee H, Lommel M, Yoshida-Moriguchi T, Beltran Valero de Bernabe D, Venzke D, Cirak S, Schachter H, Vajsar J, Voit T, Muntoni F, Strahl S, Mathews K, Nelson S, Moore S, ... Campbell K, et al. D.I.4 Patient fibroblast functional complementation studies: A valuable tool in the identification of novel Walker–Warburg syndrome disease genes Neuromuscular Disorders. 22: 805. DOI: 10.1016/J.Nmd.2012.06.014 |
0.377 |
|
| 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 |
0.467 |
|
| 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 |
0.313 |
|
| 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 |
0.774 |
|
| 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 |
0.755 |
|
| 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 |
0.429 |
|
| 2011 |
Glass DJ, Campbell KP, Rudnicki MA. Welcome to skeletal muscle. Skeletal Muscle. 1: 1. PMID 21798079 DOI: 10.1186/2044-5040-1-1 |
0.405 |
|
| 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 |
0.776 |
|
| 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 |
0.741 |
|
| 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 |
0.783 |
|
| 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 |
0.352 |
|
| 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 |
0.326 |
|
| 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 |
0.667 |
|
| 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 |
0.697 |
|
| 2011 |
Campbell K, Han R, Kobuke K, Anderson M, Bernabé DBd, Kobayashi Y, Yang B. Improved genotyping of the dysferlin null mouse Protocol Exchange. DOI: 10.1038/Protex.2011.232 |
0.61 |
|
| 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: 10.1083/Jcb1916Oia16 |
0.712 |
|
| 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 |
0.811 |
|
| 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 |
0.763 |
|
| 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 |
0.302 |
|
| 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 |
0.421 |
|
| 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 |
0.383 |
|
| 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 |
0.331 |
|
| 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 |
0.317 |
|
| 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 |
0.313 |
|
| 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 |
0.402 |
|
| 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 |
0.305 |
|
| 2010 |
Chou M, Krause KH, Campbell KP, Jensen KG, Sjolund RD. Antibodies against the Calcium-Binding Protein: Calsequestrin from Streptanthus tortuosus (Brassicaceae). Plant Physiology. 91: 1259-61. PMID 16667172 DOI: 10.1104/Pp.91.4.1259 |
0.349 |
|
| 2010 |
Beltran D, Inamori K, Moriguchi T, Weydert CJ, Harper HA, Willer T, Muller WJ, Henry MD, Campbell KP. Abstract 996: Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing ofLARGE Cancer Research. 70: 996-996. DOI: 10.1158/1538-7445.Am10-996 |
0.33 |
|
| 2010 |
Rader EP, Willer T, Eyberg BA, Prouty SJ, Campbell KP. Functional Consequences of Large1 Overexpression in Two Distinct Forms of Muscular Dystrophy Biophysical Journal. 98: 543a. DOI: 10.1016/J.Bpj.2009.12.2947 |
0.411 |
|
| 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. |
0.699 |
|
| 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. |
0.699 |
|
| 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 |
0.763 |
|
| 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 |
0.679 |
|
| 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 |
0.332 |
|
| 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 |
0.809 |
|
| 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 |
0.414 |
|
| 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 |
0.42 |
|
| 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 |
0.338 |
|
| 2009 |
Zong H, Bastie CC, Xu J, Fassler R, Campbell KP, Kurland IJ, Pessin JE. Insulin resistance in striated muscle-specific integrin receptor beta1-deficient mice. The Journal of Biological Chemistry. 284: 4679-88. PMID 19064993 DOI: 10.1074/Jbc.M807408200 |
0.309 |
|
| 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 |
0.406 |
|
| 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 |
0.389 |
|
| 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 |
0.367 |
|
| 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 |
0.513 |
|
| 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 |
0.756 |
|
| 2008 |
Satz JS, Campbell KP. Unraveling the ribbon synapse. Nature Neuroscience. 11: 857-9. PMID 18660835 DOI: 10.1038/Nn0808-857 |
0.741 |
|
| 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 |
0.631 |
|
| 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 |
0.432 |
|
| 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 DOI: 10.4161/Chan.4660 |
0.314 |
|
| 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 |
0.711 |
|
| 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 |
0.355 |
|
| 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 |
0.666 |
|
| 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 |
0.436 |
|
| 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 |
0.744 |
|
| 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 |
0.301 |
|
| 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 |
0.431 |
|
| 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 |
0.417 |
|
| 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 |
0.414 |
|
| 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 |
0.318 |
|
| 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 |
0.332 |
|
| 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 |
0.459 |
|
| 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 |
0.658 |
|
| 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 |
0.327 |
|
| 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 |
0.701 |
|
| 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 |
0.336 |
|
| 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 |
0.315 |
|
| 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 |
0.371 |
|
| 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 |
0.385 |
|
| 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 |
0.334 |
|
| 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 |
0.425 |
|
| 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 |
0.787 |
|
| 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 |
0.332 |
|
| 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 |
0.41 |
|
| 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 |
0.43 |
|
| 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 |
0.421 |
|
| 2005 |
Méhes E, Czirók A, Hegedüs B, Szabó B, Vicsek T, Satz J, Campbell K, Jancsik V. Dystroglycan is involved in laminin-1-stimulated motility of Müller glial cells: Combined velocity and directionality analysis Glia. 49: 492-500. PMID 15578661 DOI: 10.1002/Glia.20135 |
0.753 |
|
| 2005 |
Pacak CA, Mah C, Gaidosh G, Lewis M, Torres R, Campbell K, Walter GA, Byrne BJ. 44. Development of AAV-Mediated Gene Therapy for Murine Models of Genetic Diseases Affecting the Heart Molecular Therapy. 11. DOI: 10.1016/J.Ymthe.2005.06.072 |
0.37 |
|
| 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 |
0.315 |
|
| 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 |
0.347 |
|
| 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 |
0.7 |
|
| 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 |
0.802 |
|
| 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 |
0.359 |
|
| 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 |
0.626 |
|
| 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 DOI: 10.1212/01.Wnl.0000115386.28769.65 |
0.674 |
|
| 2004 |
Yurchenco PD, Cheng YS, Campbell K, Li S. Loss of basement membrane, receptor and cytoskeletal lattices in a laminin-deficient muscular dystrophy. Journal of Cell Science. 117: 735-42. PMID 14734655 DOI: 10.1242/Jcs.00911 |
0.417 |
|
| 2004 |
Dylla DE, Hickey MA, Michele DE, Davidson BL, Campbell KP, McCray PB. 491. Improved Apical Airway Epithelia Targeting Properties of FIV Vector Pseudotyped with Envelopes from LCMV Molecular Therapy. 9. DOI: 10.1016/J.Ymthe.2004.06.405 |
0.654 |
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| 2004 |
Pacak CA, Cloutier D, Zolotukhin I, Gaidosh GS, Campbell K, Walter GA, Byrne BJ. 251. rAAV-Mediated Gene Therapy To Treat Limb Girdle Muscular Dystrophy Type 2D (LGMD-2D) Molecular Therapy. 9. DOI: 10.1016/J.Ymthe.2004.06.192 |
0.39 |
|
| 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 |
0.372 |
|
| 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 |
0.356 |
|
| 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 |
0.335 |
|
| 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 |
0.344 |
|
| 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 |
0.4 |
|
| 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 |
0.707 |
|
| 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 |
0.715 |
|
| 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 |
0.643 |
|
| 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 |
0.382 |
|
| 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 |
0.394 |
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| 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 |
0.624 |
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| 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 |
0.696 |
|
| 2003 |
Feltri M, Saito F, Moore S, Nodari A, Previtali S, Quattrini A, Messing A, Campbell K, Wrabetz L. Abstracts of the 8th Meeting of the Italian Peripheral Nerve Study Group: 23 Journal of the Peripheral Nervous System. 8: 29-58. DOI: 10.1046/J.1529-8027.2003.00034.X |
0.307 |
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| 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 |
0.717 |
|
| 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 |
0.751 |
|
| 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 |
0.305 |
|
| 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 |
0.703 |
|
| 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 |
0.679 |
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| 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 |
0.824 |
|
| 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 |
0.78 |
|
| 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 |
0.388 |
|
| 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 |
0.318 |
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| 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 |
0.355 |
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| 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 DOI: 10.1186/1472-6793-1-8 |
0.368 |
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| 2001 |
Sugita S, Saito F, Tang J, Satz J, Campbell K, Südhof TC. A stoichiometric complex of neurexins and dystroglycan in brain. The Journal of Cell Biology. 154: 435-45. PMID 11470830 DOI: 10.1083/Jcb.200105003 |
0.77 |
|
| 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 |
0.343 |
|
| 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 |
0.689 |
|
| 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 |
0.739 |
|
| 2001 |
Cohn RD, Durbeej M, Moore SA, Coral-Vazquez R, Prouty S, Campbell KP. Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex. The Journal of Clinical Investigation. 107: R1-7. PMID 11160141 DOI: 10.1172/Jci11642 |
0.398 |
|
| 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 |
0.459 |
|
| 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 |
0.374 |
|
| 2000 |
Sevilla N, Kunz S, Holz A, Lewicki H, Homann D, Yamada H, Campbell KP, de La Torre JC, Oldstone MB. Immunosuppression and resultant viral persistence by specific viral targeting of dendritic cells. The Journal of Experimental Medicine. 192: 1249-60. PMID 11067874 DOI: 10.1084/Jem.192.9.1249 |
0.308 |
|
| 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 |
0.377 |
|
| 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 |
0.452 |
|
| 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 |
0.761 |
|
| 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 |
0.441 |
|
| 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 |
0.407 |
|
| 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 DOI: 10.1093/Hmg/9.13.2019 |
0.813 |
|
| 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 DOI: 10.1016/S0896-6273(00)80894-6 |
0.394 |
|
| 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 |
0.686 |
|
| 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 DOI: 10.1016/S1097-2765(00)80410-4 |
0.446 |
|
| 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 |
0.466 |
|
| 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 |
0.349 |
|
| 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 |
0.42 |
|
| 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 |
0.459 |
|
| 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 |
0.634 |
|
| 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 |
0.431 |
|
| 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 |
0.335 |
|
| 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 DOI: 10.1128/Jvi.73.6.4991-5000.1999 |
0.66 |
|
| 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 |
0.735 |
|
| 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 |
0.312 |
|
| 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 |
0.353 |
|
| 1999 |
Moore SA, Coral R, Cohn RD, Straub V, Williamson R, Campbell KP. SEVERE MUSCULAR DYSTROPHY AND CARDIOMYOPATHY IN MICE DEFICIENT IN DELTA-SARCOGLYCAN Journal of Neuropathology and Experimental Neurology. 58: 527. DOI: 10.1097/00005072-199905000-00085 |
0.304 |
|
| 1998 |
Salih MA, Al Rayess M, Cutshall S, Urtizberea JA, Al-Turaiki MH, Ozo CO, Straub V, Akbar M, Abid M, Andeejani A, Campbell KP. A novel form of familial congenital muscular dystrophy in two adolescents. Neuropediatrics. 29: 289-93. PMID 10029346 DOI: 10.1055/S-2007-973579 |
0.423 |
|
| 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 |
0.319 |
|
| 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 |
0.364 |
|
| 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 |
0.337 |
|
| 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 |
0.336 |
|
| 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 |
0.694 |
|
| 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 |
0.307 |
|
| 1998 |
Straub V, Duclos F, Venzke DP, Lee JC, Cutshall S, Leveille CJ, Campbell KP. Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster. The American Journal of Pathology. 153: 1623-30. PMID 9811355 DOI: 10.1016/S0002-9440(10)65751-3 |
0.466 |
|
| 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 |
0.819 |
|
| 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 |
0.718 |
|
| 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 DOI: 10.1016/S1097-2765(00)80083-0 |
0.725 |
|
| 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 |
0.712 |
|
| 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 |
0.687 |
|
| 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 |
0.76 |
|
| 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 DOI: 10.1177/002215549804600404 |
0.398 |
|
| 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 |
0.333 |
|
| 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 |
0.688 |
|
| 1998 |
Scott VES, Felix R, Arikkath J, Campbell KP. Evidence for a 95 kDa Short Form of the α1ASubunit Associated with the ω-Conotoxin MVIIC Receptor of the P/Q-type Ca2+Channels The Journal of Neuroscience. 18: 641-647. DOI: 10.1523/Jneurosci.18-02-00641.1998 |
0.331 |
|
| 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 |
0.347 |
|
| 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 |
0.726 |
|
| 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 |
0.606 |
|
| 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 |
0.338 |
|
| 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 |
0.361 |
|
| 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 DOI: 10.1136/Jmg.34.6.470 |
0.35 |
|
| 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 |
0.337 |
|
| 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 DOI: 10.1093/Hmg/6.5.747 |
0.38 |
|
| 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 DOI: 10.1212/Wnl.48.5.1227 |
0.391 |
|
| 1997 |
Matsumura K, Chiba A, Yamada H, Fukuta-Ohi H, Fujita S, Endo T, Kobata A, Anderson LV, Kanazawa I, Campbell KP, Shimizu T. A role of dystroglycan in schwannoma cell adhesion to laminin. The Journal of Biological Chemistry. 272: 13904-10. PMID 9153251 DOI: 10.1074/Jbc.272.21.13904 |
0.382 |
|
| 1997 |
Straub V, Campbell KP. Muscular dystrophies and the dystrophin-glycoprotein complex. Current Opinion in Neurology. 10: 168-75. PMID 9146999 DOI: 10.1097/00019052-199704000-00016 |
0.372 |
|
| 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 |
0.368 |
|
| 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 |
0.366 |
|
| 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 |
0.319 |
|
| 1997 |
Felix R, Gurnett CA, De Waard M, Campbell KP. Dissection of Functional Domains of the Voltage-Dependent Ca2+Channel α2δ Subunit The Journal of Neuroscience. 17: 6884-6891. DOI: 10.1523/Jneurosci.17-18-06884.1997 |
0.309 |
|
| 1996 |
Seidahmed MZ, Sunada Y, Ozo CO, Hamid F, Campbell KP, Salih MA. Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome? Neuropediatrics. 27: 305-10. PMID 9050048 DOI: 10.1055/S-2007-973799 |
0.353 |
|
| 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 |
0.712 |
|
| 1996 |
Salih MA, Sunada Y, Al-Nasser M, Ozo CO, Al-Turaiki MH, Akbar M, Campbell KP. Muscular dystrophy associated with beta-Dystroglycan deficiency. Annals of Neurology. 40: 925-8. PMID 9007100 DOI: 10.1002/Ana.410400617 |
0.398 |
|
| 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 |
0.441 |
|
| 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 DOI: 10.1093/Hmg/5.12.2019 |
0.332 |
|
| 1996 |
Morandi L, Barresi R, Di Blasi C, Jung D, Sunada Y, Confalonieri V, Dworzak F, Mantegazza R, Antozzi C, Jarre L, Pini A, Gobbi G, Bianchi C, Cornelio F, Campbell KP, et al. Clinical heterogeneity of adhalin deficiency. Annals of Neurology. 39: 196-202. PMID 8967751 DOI: 10.1002/Ana.410390209 |
0.358 |
|
| 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 DOI: 10.1074/Jbc.271.50.32321 |
0.43 |
|
| 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 |
0.445 |
|
| 1996 |
Campbell KP, Crosbie RH. Muscular dystrophy. Utrophin to the rescue. Nature. 384: 308-9. PMID 8934508 DOI: 10.1038/384308A0 |
0.714 |
|
| 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 DOI: 10.1523/Jneurosci.16-23-07557.1996 |
0.333 |
|
| 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 |
0.301 |
|
| 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 |
0.347 |
|
| 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 DOI: 10.1042/Bst024274S |
0.418 |
|
| 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 |
0.605 |
|
| 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 DOI: 10.1016/0014-5793(96)00056-7 |
0.429 |
|
| 1996 |
Yamada H, Chiba A, Endo T, Kobata A, Anderson LV, Hori H, Fukuta-Ohi H, Kanazawa I, Campbell KP, Shimizu T, Matsumura K. Characterization of dp6troglycan-laminin interaction in peripheral nerve. Journal of Neurochemistry. 66: 1518-24. PMID 8627307 DOI: 10.1046/J.1471-4159.1996.66041518.X |
0.362 |
|
| 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 DOI: 10.1074/Jbc.271.6.3207 |
0.32 |
|
| 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 |
0.322 |
|
| 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 |
0.411 |
|
| 1996 |
Fadic R, Sunada Y, Waclawik AJ, Buck S, Lewandoski PJ, Campbell KP, Lotz BP. Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy. The New England Journal of Medicine. 334: 362-6. PMID 8538707 DOI: 10.1056/Nejm199602083340604 |
0.445 |
|
| 1996 |
Cullen MJ, Walsh J, Roberds SL, Campbell KP. Ultrastructural localization of adhalin, α‐dystroglycan and merosin in normal and dystrophic muscle Neuropathology and Applied Neurobiology. 22: 30-37. DOI: 10.1111/J.1365-2990.1996.Tb00843.X |
0.374 |
|
| 1996 |
Liu H, Waard MD, Scott VES, Gurnett CA, Lennon VA, Campbell KP. Identification of Three Subunits of the High Affinity ω-Conotoxin MVIIC-sensitive Ca2+ Channel Journal of Biological Chemistry. 271: 13804-13810. DOI: 10.1074/Jbc.271.23.13804 |
0.315 |
|
| 1996 |
Broux O, Duclos F, Lim LE, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C, Tomé FMS, Fardeau M, Jackson CE, Campbell KP, Beckmann JS. β-sarcoglycan : Characterization and role in limb-girdle muscular dystrophy linked to 4q12 Neuromuscular Disorders. 6. DOI: 10.1016/0960-8966(96)88965-6 |
0.651 |
|
| 1996 |
Kaplan J-, Piccolo F, Azibi K, Carrié A, Leturcq F, Toma Cd, Beldjord C, Chaouch M, Sefiani A, Merlini L, Voit T, Sewry C, Sunada Y, Beckmann JS, Rornero N, ... ... Campbell KP, et al. Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan) Neuromuscular Disorders. 6. DOI: 10.1016/0960-8966(96)88959-0 |
0.318 |
|
| 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 |
0.415 |
|
| 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 DOI: 10.1097/00019052-199510000-00010 |
0.381 |
|
| 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 DOI: 10.1093/Hmg/4.7.1163 |
0.513 |
|
| 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 |
0.603 |
|
| 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 |
0.454 |
|
| 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 |
0.307 |
|
| 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 |
0.389 |
|
| 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 DOI: 10.1074/Jbc.270.20.12056 |
0.337 |
|
| 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 |
0.454 |
|
| 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 |
0.451 |
|
| 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 |
0.423 |
|
| 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 |
0.312 |
|
| 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 |
0.393 |
|
| 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 |
0.41 |
|
| 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 DOI: 10.1074/Jbc.270.30.18088 |
0.364 |
|
| 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 DOI: 10.1097/00005072-199507000-00010 |
0.427 |
|
| 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 |
0.562 |
|
| 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 DOI: 10.1093/Hmg/4.8.1245 |
0.33 |
|
| 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 DOI: 10.1113/Jphysiol.1995.Sp020757 |
0.32 |
|
| 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 DOI: 10.1212/Wnl.45.11.2084 |
0.426 |
|
| 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 |
0.381 |
|
| 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 DOI: 10.1016/0092-8674(94)90051-5 |
0.375 |
|
| 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 |
0.312 |
|
| 1994 |
Yang B, Ibraghimov-Beskrovnaya O, Moomaw CR, Slaughter CA, Campbell KP. Heterogeneity of the 59-kDa dystrophin-associated protein revealed by cDNA cloning and expression. The Journal of Biological Chemistry. 269: 6040-4. PMID 8119949 |
0.326 |
|
| 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 |
0.658 |
|
| 1994 |
Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RC, Marie SK, Campbell KP. Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences. 123: 122-8. PMID 8064304 DOI: 10.1016/0022-510X(94)90213-5 |
0.334 |
|
| 1994 |
De Waard M, Pragnell M, Campbell KP. Ca2+ channel regulation by a conserved beta subunit domain. Neuron. 13: 495-503. PMID 8060623 DOI: 10.1016/0896-6273(94)90363-8 |
0.318 |
|
| 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 DOI: 10.1152/Ajpcell.1994.267.1.C282 |
0.75 |
|
| 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 |
0.415 |
|
| 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 |
0.361 |
|
| 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 |
0.431 |
|
| 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 |
0.31 |
|
| 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 |
0.342 |
|
| 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 |
0.433 |
|
| 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 |
0.598 |
|
| 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 |
0.633 |
|
| 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 |
0.363 |
|
| 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 DOI: 10.1093/Hmg/3.10.1725 |
0.604 |
|
| 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 DOI: 10.1016/0960-8966(94)90002-7 |
0.423 |
|
| 1993 |
Ohlendieck K, Matsumura K, Ionasescu VV, Towbin JA, Bosch EP, Weinstein SL, Sernett SW, Campbell KP. Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma. Neurology. 43: 795-800. PMID 8469343 DOI: 10.1212/Wnl.43.4.795 |
0.435 |
|
| 1993 |
Matsumura K, Lee CC, Caskey CT, Campbell KP. Restoration of dystrophin-associated proteins in skeletal muscle of mdx mice transgenic for dystrophin gene. Febs Letters. 320: 276-80. PMID 8462697 DOI: 10.1016/0014-5793(93)80602-Q |
0.45 |
|
| 1993 |
Ervasti JM, Campbell KP. Dystrophin and the membrane skeleton. Current Opinion in Cell Biology. 5: 82-7. PMID 8448034 DOI: 10.1016/S0955-0674(05)80012-2 |
0.632 |
|
| 1993 |
Klietsch R, Ervasti JM, Arnold W, Campbell KP, Jorgensen AO. Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle. Circulation Research. 72: 349-60. PMID 8418988 DOI: 10.1161/01.Res.72.2.349 |
0.654 |
|
| 1993 |
Witcher DR, De Waard M, Sakamoto J, Franzini-Armstrong C, Pragnell M, Kahl SD, Campbell KP. Subunit identification and reconstitution of the N-type Ca2+ channel complex purified from brain. Science (New York, N.Y.). 261: 486-9. PMID 8392754 DOI: 10.1126/Science.8392754 |
0.316 |
|
| 1993 |
Jorgensen AO, Shen AC, Arnold W, McPherson PS, Campbell KP. The Ca2+-release channel/ryanodine receptor is localized in junctional and corbular sarcoplasmic reticulum in cardiac muscle. The Journal of Cell Biology. 120: 969-80. PMID 8381786 DOI: 10.1083/Jcb.120.4.969 |
0.329 |
|
| 1993 |
Matsumura K, Campbell KP. Deficiency of dystrophin-associated proteins: A common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies Neuromuscular Disorders. 3: 109-118. PMID 8358236 DOI: 10.1016/0960-8966(93)90002-2 |
0.451 |
|
| 1993 |
Cox GA, Cole NM, Matsumura K, Phelps SF, Hauschka SD, Campbell KP, Faulkner JA, Chamberlain JS. Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature. 364: 725-9. PMID 8355788 DOI: 10.1038/364725A0 |
0.591 |
|
| 1993 |
Ervasti JM, Campbell KP. A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. The Journal of Cell Biology. 122: 809-23. PMID 8349731 DOI: 10.1083/Jcb.122.4.809 |
0.637 |
|
| 1993 |
Matsumura K, Shasby DM, Campbell KP. Purification of dystrophin-related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells Febs Letters. 326: 289-293. PMID 8325382 DOI: 10.1016/0014-5793(93)81810-M |
0.33 |
|
| 1993 |
Ibraghimov-Beskrovnaya O, Milatovich A, Ozcelik T, Yang B, Koepnick K, Francke U, Campbell KP. Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization. Human Molecular Genetics. 2: 1651-7. PMID 8268918 DOI: 10.1093/Hmg/2.10.1651 |
0.366 |
|
| 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 |
0.416 |
|
| 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 |
0.331 |
|
| 1993 |
Matsumura K, Ohlendieck K, Ionasescu VV, Tomé FM, Nonaka I, Burghes AH, Mora M, Kaplan JC, Fardeau M, Campbell KP. The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies. Neuromuscular Disorders : Nmd. 3: 533-5. PMID 8186706 DOI: 10.1016/0960-8966(93)90110-6 |
0.44 |
|
| 1993 |
Matsumura K, Nonaka I, Arahata K, Campbell KP. Partial deficiency of dystrophin-associated proteins in a young girl with sporadic myopathy and normal karyotype Neurology. 43: 1267-1268. PMID 8170583 DOI: 10.1212/Wnl.43.6.1267 |
0.312 |
|
| 1993 |
Ervasti JM, Campbell KP. Dystrophin-associated glycoproteins: their possible roles in the pathogenesis of Duchenne muscular dystrophy. Molecular and Cell Biology of Human Diseases Series. 3: 139-66. PMID 8111538 DOI: 10.1007/978-94-011-1528-5_6 |
0.646 |
|
| 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 |
0.339 |
|
| 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 |
0.323 |
|
| 1993 |
Matsumura K, Campbell KP, Nonaka I. Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy The Lancet. 341: 521-522. PMID 8094772 DOI: 10.1016/0140-6736(93)90279-P |
0.415 |
|
| 1992 |
Ibraghimov-Beskrovnaya O, Ervasti JM, Leveille CJ, Slaughter CA, Sernett SW, Campbell KP. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature. 355: 696-702. PMID 1741056 DOI: 10.1038/355696A0 |
0.593 |
|
| 1992 |
Matsumura K, Ervasti JM, Ohlendieck K, Kahl SD, Campbell KP. Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle. Nature. 360: 588-91. PMID 1461282 DOI: 10.1038/360588A0 |
0.669 |
|
| 1992 |
Matsumura K, Tomé FM, Collin H, Azibi K, Chaouch M, Kaplan JC, Fardeau M, Campbell KP. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy. Nature. 359: 320-2. PMID 1406935 DOI: 10.1038/359320A0 |
0.421 |
|
| 1992 |
Mickelson JR, Knudson CM, Kennedy CFH, Yang DI, Litterer LA, Rempel WE, Campbell KP, Louis CF. Structural and functional correlates of a mutation in the malignant hyperthermia-susceptible pig ryanodine receptor Febs Letters. 301: 49-52. PMID 1333412 DOI: 10.1016/0014-5793(92)80208-X |
0.617 |
|
| 1991 |
Movsesian MA, Leveille C, Krall J, Colyer J, Wang JH, Campbell KP. Identification and characterization of proteins in sarcoplasmic reticulum from normal and failing human left ventricles. Journal of Molecular and Cellular Cardiology. 22: 1477-85. PMID 2089160 DOI: 10.1016/0022-2828(90)90990-J |
0.348 |
|
| 1991 |
Ohlendieck K, Ervasti JM, Snook JB, Campbell KP. Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma. The Journal of Cell Biology. 112: 135-48. PMID 1986002 DOI: 10.1083/Jcb.112.1.135 |
0.678 |
|
| 1991 |
Ervasti JM, Campbell KP. Membrane organization of the dystrophin-glycoprotein complex. Cell. 66: 1121-31. PMID 1913804 DOI: 10.1016/0092-8674(91)90035-W |
0.635 |
|
| 1991 |
McLeod AG, Shen ACY, Campbell KP, Michalak M, Jorgensen AO. Frog cardiac calsequestrin: Identification, characterization, and subcellular distribution in two structurally distinct regions of peripheral sarcoplasmic reticulum in frog ventricular myocardium Circulation Research. 69: 344-359. PMID 1860177 DOI: 10.1161/01.Res.69.2.344 |
0.339 |
|
| 1991 |
Ohlendieck K, Campbell KP. Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice Journal of Cell Biology. 115: 1685-1694. PMID 1757468 DOI: 10.1083/Jcb.115.6.1685 |
0.453 |
|
| 1991 |
Ohlendieck K, Briggs FN, Lee KF, Wechsler AW, Campbell KP. Analysis of excitation-contraction-coupling components in chronically stimulated canine skeletal muscle. European Journal of Biochemistry / Febs. 202: 739-47. PMID 1662614 DOI: 10.1111/J.1432-1033.1991.Tb16428.X |
0.413 |
|
| 1991 |
Pragnell M, Sakamoto J, Jay SD, Campbell KP. Cloning and tissue-specific expression of the brain calcium channel β-subunit Febs Letters. 291: 253-258. PMID 1657644 DOI: 10.1016/0014-5793(91)81296-K |
0.36 |
|
| 1991 |
Ohlendieck K, Ervasti JM, Matsumura K, Kahl SD, Leveille CJ, Campbell KP. Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle. Neuron. 7: 499-508. PMID 1654951 DOI: 10.1016/0896-6273(91)90301-F |
0.667 |
|
| 1991 |
McPherson PS, Kim YK, Valdivia H, Knudson CM, Takekura H, Franzini-Armstrong C, Coronado R, Campbell KP. The brain ryanodine receptor: a caffeine-sensitive calcium release channel. Neuron. 7: 17-25. PMID 1648939 DOI: 10.1016/0896-6273(91)90070-G |
0.325 |
|
| 1990 |
Fischer TH, Barton DW, Krause KH, White TE, Campbell KP, White GC. The identification of sarcoplasmic reticulum terminal cisternae proteins in platelets. The Biochemical Journal. 263: 605-8. PMID 2512909 DOI: 10.1042/Bj2630605 |
0.345 |
|
| 1990 |
Krause KH, Simmerman HKB, Jones LR, Campbell KP. Sequence similarity of calreticulin with a Ca2+-binding protein that co-purifies with an Ins(1,4,5)P3-sensitive Ca2+ store in HL-60 cells Biochemical Journal. 270: 545-548. PMID 2400400 DOI: 10.1042/Bj2700545 |
0.315 |
|
| 1990 |
Ervasti JM, Ohlendieck K, Kahl SD, Gaver MG, Campbell KP. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature. 345: 315-9. PMID 2188135 DOI: 10.1038/345315A0 |
0.653 |
|
| 1990 |
Chu A, Sumbilla C, Inesi G, Jay SD, Campbell KP. Specific association of calmodulin-dependent protein kinase and related substrates with the junctional sarcoplasmic reticulum of skeletal muscle Biochemistry. 29: 5899-5905. PMID 2166564 DOI: 10.1021/Bi00477A003 |
0.342 |
|
| 1990 |
Jay SD, Ellis SB, McCue AF, Williams ME, Vedvick TS, Harpold MM, Campbell KP. Primary structure of the gamma subunit of the DHP-sensitive calcium channel from skeletal muscle. Science (New York, N.Y.). 248: 490-2. PMID 2158672 DOI: 10.1126/SCIENCE.2158672 |
0.301 |
|
| 1990 |
Jorgensen AO, Arnold W, Shen AC, Yuan SH, Gaver M, Campbell KP. Identification of novel proteins unique to either transverse tubules (TS28) or the sarcolemma (SL50) in rabbit skeletal muscle. The Journal of Cell Biology. 110: 1173-85. PMID 2157716 DOI: 10.1083/Jcb.110.4.1173 |
0.393 |
|
| 1990 |
Briggs FN, Lee KF, Feher JJ, Wechsler AS, Ohlendieck K, Campbell K. Ca-ATPase isozyme expression in sarcoplasmic reticulum is altered by chronic stimulation of skeletal muscle. Febs Letters. 259: 269-72. PMID 2136731 DOI: 10.1016/0014-5793(90)80025-E |
0.376 |
|
| 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 |
0.481 |
|
| 1989 |
Fill M, Ma JJ, Knudson CM, Imagawa T, Campbell KP, Coronado R. Role of the ryanodine receptor of skeletal muscle in excitation-contraction coupling. Annals of the New York Academy of Sciences. 560: 155-62. PMID 2662857 DOI: 10.1111/J.1749-6632.1989.Tb24092.X |
0.327 |
|
| 1989 |
Jorgensen AO, Shen ACY, Arnold W, Leung AT, Campbell KP. Subcellular distribution of the 1,4-dihydropyridine receptor in rabbit skeletal muscle in situ: An immunofluorescence and immunocolloidal gold-labeling study Journal of Cell Biology. 109: 135-147. PMID 2545725 DOI: 10.1083/Jcb.109.1.135 |
0.35 |
|
| 1989 |
Campbell KP, Kahl SD. Association of dystrophin and an integral membrane glycoprotein Nature. 338: 259-262. PMID 2493582 DOI: 10.1038/338259A0 |
0.44 |
|
| 1989 |
Perez-Reyes E, Kim HS, Lacerda AE, Horne W, Wei XY, Rampe D, Campbell KP, Brown AM, Birnbaumer L. Induction of calcium currents by the expression of the alpha 1-subunit of the dihydropyridine receptor from skeletal muscle. Nature. 340: 233-6. PMID 2474131 DOI: 10.1038/340233A0 |
0.391 |
|
| 1988 |
Jorgensen AO, Arnold W, Pepper DR, Kahl SD, Mandel F, Campbell KP. A monoclonal antibody to the Ca2+-ATPase of cardiac sarcoplasmic reticulum cross-reacts with slow type I but not with fast type II canine skeletal muscle fibers: an immunocytochemical and immunochemical study. Cell Motility and the Cytoskeleton. 9: 164-74. PMID 2965994 DOI: 10.1002/Cm.970090208 |
0.34 |
|
| 1988 |
Block BA, Imagawa T, Campbell KP, Franzini-Armstrong C. Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle. The Journal of Cell Biology. 107: 2587-600. PMID 2849609 DOI: 10.1083/Jcb.107.6.2587 |
0.365 |
|
| 1988 |
Campbell KP, Leung AT, Sharp AH. The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel Trends in Neurosciences. 11: 425-430. PMID 2469159 DOI: 10.1016/0166-2236(88)90193-2 |
0.327 |
|
| 1988 |
Campbell KP, Leung AT, Imagawa T. Structural characterization of the nitrendipine receptor of the voltage-dependent Ca2+ channel: Evidence for a 52,000 dalton subunit Journal of Cardiovascular Pharmacology. 12. PMID 2468882 DOI: 10.1097/00005344-198806124-00017 |
0.306 |
|
| 1988 |
Ma J, Fill M, Knudson CM, Campbell KP, Coronado R. Ryanodine receptor of skeletal muscle is a gap junction-type channel Science. 242: 99-102. PMID 2459777 DOI: 10.1126/Science.2459777 |
0.373 |
|
| 1988 |
Smith JS, Imagawa T, Ma J, Fill M, Campbell KP, Coronado R. Purified ryanodine receptor from rabbit skeletal muscle is the calcium-release channel of sarcoplasmic reticulum Journal of General Physiology. 92: 1-26. PMID 2459298 DOI: 10.1085/Jgp.92.1.1 |
0.31 |
|
| 1988 |
Ellis SB, Williams ME, Ways NR, Brenner R, Sharp AH, Leung AT, Campbell KP, McKenna E, Koch WJ, Hui A, Schwartz A, Harpold MM. Sequence and expression of mRNAs encoding the α1 and α2 subunits of a DHP-sensitive calcium channel Science. 241: 1661-1664. PMID 2458626 DOI: 10.1126/Science.2458626 |
0.364 |
|
| 1988 |
LEUNG AT, IMAGAWA T, CAMPBELL KP. Monoclonal Antibody Characterization of the 1,4-Dihydropyridine Receptor of Rabbit Skeletal Muscle Annals of the New York Academy of Sciences. 522: 43-46. DOI: 10.1111/J.1749-6632.1988.Tb33341.X |
0.37 |
|
| 1987 |
Hoffman EP, Knudson CM, Campbell KP, Kunkel LM. Subcellular fractionation of dystrophin to the triads of skeletal muscle Nature. 330: 754-758. PMID 2447503 DOI: 10.1038/330754A0 |
0.429 |
|
| 1985 |
Jorgensen AO, Shen ACY, Campbell KP. Ultrastructural localization of calsequestrin in adult rat atrial and ventricular muscle cells Journal of Cell Biology. 101: 257-268. PMID 4008530 DOI: 10.1083/Jcb.101.1.257 |
0.318 |
|
| 1984 |
Jorgensen AO, Campbell KP. Evidence for the presence of calsequestrin in two structurally different regions of myocardial sarcoplasmic reticulum Journal of Cell Biology. 98: 1597-1602. PMID 6371026 DOI: 10.1083/Jcb.98.4.1597 |
0.381 |
|
| 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 |
0.522 |
|
| 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 |
0.454 |
|
| 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 DOI: 10.1083/Jcb.97.5.1573 |
0.554 |
|
| 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 |
0.42 |
|
| 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 |
0.474 |
|
| 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 |
0.468 |
|
| 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 |
0.467 |
|
| 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 |
0.472 |
|
| 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 DOI: 10.1111/J.1749-6632.1980.Tb15406.X |
0.465 |
|
| 1980 |
Campbell KP, Shamoo AE. Phosphorylation of heavy sarcoplasmic reticulum vesicles: Identification and characterization of three phosphorylated proteins The Journal of Membrane Biology. 56: 241-248. PMID 6779012 DOI: 10.1007/Bf01869479 |
0.569 |
|
| 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 |
0.483 |
|
| 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 DOI: 10.1073/Pnas.77.8.4435 |
0.504 |
|
| 1980 |
Campbell KP, Franzini-Armstrong C, Shamoo AE. Further characterization of light and heavy sarcoplasmic reticulum vesicles. Identification of the 'sarcoplasmic reticulum feet' associated with heavy sarcoplasmic reticulum vesicles. Biochimica Et Biophysica Acta. 602: 97-116. PMID 6448074 DOI: 10.1016/0005-2736(80)90293-X |
0.604 |
|
| 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 |
0.655 |
|
| 1980 |
Campbell KP, Shamoo AE. Chloride-induced release of actively loaded calcium from light and heavy sarcoplasmic reticulum vesicles The Journal of Membrane Biology. 54: 73-80. PMID 6259360 DOI: 10.1007/Bf01875378 |
0.566 |
|
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