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Kevin Campbell
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18
Moore, Steven
17
Straub, Volker
17
De Waard, Michel
16
Sunada, Y
16
Henry, Michael
15
Barresi, Rita
14
Durbeej, Madeleine
14
Kaplan, Jean-Claude
13
Leturcq, France
13
Tomé, Fernando
12
Michele, Daniel
11
Venzke, DP
11
Piccolo, Federica
11
Gurnett, Christina
11
Ervasti, James
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All Publications
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2009: Michele Daniel E; Kabaeva Zhyldyz; Davis Sarah L; Weiss Robert M; Campbell Kevin P
Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage.
Circulation research 2009;105(10):984-93.
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2009: Satz Jakob S; Philp Alisdair R; Nguyen Huy; Kusano Hajime; Lee Jane; Turk Rolf; Riker Megan J; Hernández Jasmine; Weiss Robert M; Anderson Michael G; Mullins Robert F; Moore Steven A; Stone Edwin M; Campbell Kevin P
Visual impairment in the absence of dystroglycan.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2009;29(42):13136-46.
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2009: Han Renzhi; Kanagawa Motoi; Yoshida-Moriguchi Takako; Rader Erik P; Ng Rainer A; Michele Daniel E; Muirhead David E; Kunz Stefan; Moore Steven A; Iannaccone Susan T; Miyake Katsuya; McNeil Paul L; Mayer Ulrike; Oldstone Michael B A; Faulkner John A; Campbell Kevin P
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 2009;106(31):12573-9.
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2009: de Bernabé Daniel Beltrán-Valero; Inamori Kei-Ichiro; Yoshida-Moriguchi Takako; Weydert Christine J; Harper Hollie A; Willer Tobias; Henry Michael D; Campbell Kevin P
Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE.
The Journal of biological chemistry 2009;284(17):11279-84.
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2008: Satz Jakob S; Barresi Rita; Durbeej Madeleine; Willer Tobias; Turner Amy; Moore Steven A; Campbell Kevin P
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 2008;28(42):10567-75.
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2008: Satz Jakob S; Campbell Kevin P
Unraveling the ribbon synapse.
Nature neuroscience 2008;11(8):857-9.
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2008: Dylla Douglas E; Michele Daniel E; Campbell Kevin P; McCray Paul B
Basolateral entry and release of New and Old World arenaviruses from human airway epithelia.
Journal of virology 2008;82(12):6034-8.
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2008: Kobuke Kazuhiro; Piccolo Federica; Garringer Keith W; Moore Steven A; Sweezer Eileen; Yang Baoli; Campbell Kevin P
A common disease-associated missense mutation in alpha-sarcoglycan fails to cause muscular dystrophy in mice.
Human molecular genetics 2008;17(9):1201-13.
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2007: Sandoval Alejandro; Arikkath Jyothi; Monjaraz Eduardo; Campbell Kevin P; Felix Ricardo
gamma1-dependent down-regulation of recombinant voltage-gated Ca2+ channels.
Cellular and molecular neurobiology 2007;27(7):901-8.
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2007: Rojek Jillian M; Campbell Kevin P; Oldstone Michael B A; Kunz Stefan
Old World arenavirus infection interferes with the expression of functional alpha-dystroglycan in the host cell.
Molecular biology of the cell 2007;18(11):4493-507.
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2007: Han Renzhi; Campbell Kevin P
Dysferlin and muscle membrane repair.
Current opinion in cell biology 2007;19(4):409-16.
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2007: Han Renzhi; Bansal Dimple; Miyake Katsuya; Muniz Viviane P; Weiss Robert M; McNeil Paul L; Campbell Kevin P
Dysferlin-mediated membrane repair protects the heart from stress-induced left ventricular injury.
The Journal of clinical investigation 2007;117(7):1805-13.
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2007: Kiyonaka Shigeki; Wakamori Minoru; Miki Takafumi; Uriu Yoshitsugu; Nonaka Mio; Bito Haruhiko; Beedle Aaron M; Mori Emiko; Hara Yuji; De Waard Michel; Kanagawa Motoi; Itakura Makoto; Takahashi Masami; Campbell Kevin P; Mori Yasuo
RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca2+ channels.
Nature neuroscience 2007;10(6):691-701.
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2007: Beedle Aaron M; Nienaber Patricia M; Campbell Kevin P
Fukutin-related protein associates with the sarcolemmal dystrophin-glycoprotein complex.
The Journal of biological chemistry 2007;282(23):16713-7.
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2007: Rojek Jillian M; Spiropoulou Christina F; Campbell Kevin P; Kunz Stefan
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 2007;81(11):5685-95.
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2007: Miki Takafumi; Kiyonaka Shigeki; Uriu Yoshitsugu; De Waard Michel; Wakamori Minoru; Beedle Aaron M; Campbell Kevin P; Mori Yasuo
Mutation associated with an autosomal dominant cone-rod dystrophy CORD7 modifies RIM1-mediated modulation of voltage-dependent Ca2+ channels.
Channels (Austin, Tex.) 2007;1(3):144-7.
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2007: Carmignac Virginie; Salih Mustafa A M; Quijano-Roy Susana; Marchand Sylvie; Al Rayess Molham M; Mukhtar Maowia M; Urtizberea Jon A; Labeit Siegfried; Guicheney Pascale; Leturcq France; Gautel Mathias; Fardeau Michel; Campbell Kevin P; Richard Isabelle; Estournet Brigitte; Ferreiro Ana
C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy.
Annals of neurology 2007;61(4):340-51.
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2007: Sandoval Alejandro; Andrade Arturo; Beedle Aaron M; Campbell Kevin P; Felix Ricardo
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 2007;27(12):3317-27.
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2006: Moore Steven A; Shilling Christopher J; Westra Steven; Wall Cheryl; Wicklund Matthew P; Stolle Catherine; Brown Charlotte A; Michele Daniel E; Piccolo Federica; Winder Thomas L; Stence Aaron; Barresi Rita; King Nick; King Wendy; Florence Julaine; Campbell Kevin P; Fenichel Gerald M; Stedman Hansell H; Kissel John T; Griggs Robert C; Pandya Shree; Mathews Katherine D; Pestronk Alan; Serrano Carmen; Darvish Daniel; Mendell Jerry R
Limb-girdle muscular dystrophy in the United States.
Journal of neuropathology and experimental neurology 2006;65(10):995-1003.
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2006: Weir M Lynn; Oppizzi Maria Luisa; Henry Michael D; Onishi Akiko; Campbell Kevin P; Bissell Mina J; Muschler John L
Dystroglycan loss disrupts polarity and beta-casein induction in mammary epithelial cells by perturbing laminin anchoring.
Journal of cell science 2006;119(Pt 19):4047-58.
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2006: Kang Myoung-Goo; Chen Chien-Chang; Wakamori Minoru; Hara Yuji; Mori Yasuo; Campbell Kevin P
A functional AMPA receptor-calcium channel complex in the postsynaptic membrane.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(14):5561-6.
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2006: Barresi Rita; Campbell Kevin P
Dystroglycan: from biosynthesis to pathogenesis of human disease.
Journal of cell science 2006;119(Pt 2):199-207.
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2005: Kunz Stefan; Rojek Jillian M; Kanagawa Motoi; Spiropoulou Christina F; Barresi Rita; Campbell Kevin P; Oldstone Michael B A
Posttranslational modification of alpha-dystroglycan, the cellular receptor for arenaviruses, by the glycosyltransferase LARGE is critical for virus binding.
Journal of virology 2005;79(22):14282-96.
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2005: Kanagawa Motoi; Michele Daniel E; Satz Jakob S; Barresi Rita; Kusano Hajime; Sasaki Takako; Timpl Rupert; Henry Michael D; Campbell Kevin P
Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function.
FEBS letters 2005;579(21):4792-6.
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2005: Consolino Christina M; Duclos Franck; Lee Jane; Williamson Roger A; Campbell Kevin P; Brooks Susan V
Muscles of mice deficient in alpha-sarcoglycan maintain large masses and near control force values throughout the life span.
Physiological genomics 2005;22(2):244-56.
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2004: Kikkawa Yamato; Yu Hao; Genersch Elke; Sanzen Noriko; Sekiguchi Kiyotoshi; Fässler Reinhard; Campbell Kevin P; Talts Jan F; Ekblom Peter
Laminin isoforms differentially regulate adhesion, spreading, proliferation, and ERK activation of beta1 integrin-null cells.
Experimental cell research 2004;300(1):94-108.
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2004: Singh Jarnail; Itahana Yoko; Knight-Krajewski Selena; Kanagawa Motoi; Campbell Kevin P; Bissell Mina J; Muschler John
Proteolytic enzymes and altered glycosylation modulate dystroglycan function in carcinoma cells.
Cancer research 2004;64(17):6152-9.
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2004: Barresi Rita; Michele Daniel E; Kanagawa Motoi; Harper Hollie A; Dovico Sherri A; Satz Jakob S; Moore Steven A; Zhang Wenli; Schachter Harry; Dumanski Jan P; Cohn Ronald D; Nishino Ichizo; Campbell Kevin P
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.
Nature medicine 2004;10(7):696-703.
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2004: Kanagawa Motoi; Saito Fumiaki; Kunz Stefan; Yoshida-Moriguchi Takako; Barresi Rita; Kobayashi Yvonne M; Muschler John; Dumanski Jan P; Michele Daniel E; Oldstone Michael B A; Campbell Kevin P
Molecular recognition by LARGE is essential for expression of functional dystroglycan.
Cell 2004;117(7):953-64.
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2004: Opatowsky Yarden; Chen Chien-Chang; Campbell Kevin P; Hirsch Joel A
Structural analysis of the voltage-dependent calcium channel beta subunit functional core and its complex with the alpha 1 interaction domain.
Neuron 2004;42(3):387-99.
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2004: Bansal Dimple; Campbell Kevin P
Dysferlin and the plasma membrane repair in muscular dystrophy.
Trends in cell biology 2004;14(4):206-13.
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2003: Opatowsky Yarden; Chomsky-Hecht Orna; Kang Myoung-Goo; Campbell Kevin P; Hirsch Joel A
The voltage-dependent calcium channel beta subunit contains two stable interacting domains.
The Journal of biological chemistry 2003;278(52):52323-32.
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2003: Kunz Stefan; Campbell Kevin P; Oldstone Michael B A
Alpha-dystroglycan can mediate arenavirus infection in the absence of beta-dystroglycan.
Virology 2003;316(2):213-20.
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2003: Chen Chien-Chang; Lamping Kathryn G; Nuno Daniel W; Barresi Rita; Prouty Sally J; Lavoie Julie L; Cribbs Leanne L; England Sarah K; Sigmund Curt D; Weiss Robert M; Williamson Roger A; Hill Joseph A; Campbell Kevin P
Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels.
Science (New York, N.Y.) 2003;302(5649):1416-8.
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2003: Murakami Manabu; Yamamura Hisao; Suzuki Takashi; Kang Myoung-Goo; Ohya Susumu; Murakami Agnieszka; Miyoshi Ichiro; Sasano Hironobu; Muraki Katsuhiko; Hano Takuzou; Kasai Noriyuki; Nakayama Shinnsuke; Campbell Kevin P; Flockerzi Veit; Imaizumi Yuji; Yanagisawa Teruyuki; Iijima Toshihiko
Modified cardiovascular L-type channels in mice lacking the voltage-dependent Ca2+ channel beta3 subunit.
The Journal of biological chemistry 2003;278(44):43261-7.
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2003: Muntoni F; Valero de Bernabe B; Bittner R; Blake D; van Bokhoven H; Brockington M; Brown S; Bushby K; Campbell K P; Fiszman M; Gruenewald S; Merlini L; Quijano-Roy S; Romero N; Sabatelli P; Sewry C A; Straub V; Talim B; Topaloglu H; Voit T; Yurchenco P D; Urtizberea J A; Wewer U M; Guicheney P
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE).
Neuromuscular disorders : NMD 2003;13(7-8):579-88.
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2003: Letts Verity A; Kang Myoung-Goo; Mahaffey Connie L; Beyer Barbara; Tenbrink Heather; Campbell Kevin P; Frankel Wayne N
Phenotypic heterogeneity in the stargazin allelic series.
Mammalian genome : official journal of the International Mammalian Genome Society 2003;14(8):506-13.
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2003: Durbeej Madeleine; Sawatzki Shanna M; Barresi Rita; Schmainda Kathleen M; Allamand Valérie; Michele Daniel E; Campbell Kevin P
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 2003;100(15):8910-5.
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2003: Arikkath Jyothi; Campbell Kevin P
Auxiliary subunits: essential components of the voltage-gated calcium channel complex.
Current opinion in neurobiology 2003;13(3):298-307.
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2003: Saito Fumiaki; Moore Steven A; Barresi Rita; Henry Michael D; Messing Albee; Ross-Barta Susan E; Cohn Ronald D; Williamson Roger A; Sluka Kathleen A; Sherman Diane L; Brophy Peter J; Schmelzer James D; Low Phillip A; Wrabetz Lawrence; Feltri M Laura; Campbell Kevin P
Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization.
Neuron 2003;38(5):747-58.
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2003: Kang Myoung-Goo; Campbell Kevin P
Gamma subunit of voltage-activated calcium channels.
The Journal of biological chemistry 2003;278(24):21315-8.
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2003: Ferletta Maria; Kikkawa Yamato; Yu Hao; Talts Jan F; Durbeej Madeleine; Sonnenberg Arnoud; Timpl Rupert; Campbell Kevin P; Ekblom Peter; Genersch Elke
Opposing roles of integrin alpha6Abeta1 and dystroglycan in laminin-mediated extracellular signal-regulated kinase activation.
Molecular biology of the cell 2003;14(5):2088-103.
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2003: Bansal Dimple; Miyake Katsuya; Vogel Steven S; Groh Séverine; Chen Chien-Chang; Williamson Roger; McNeil Paul L; Campbell Kevin P
Defective membrane repair in dysferlin-deficient muscular dystrophy.
Nature 2003;423(6936):168-72.
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2003: Michele Daniel E; Campbell Kevin P
Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.
The Journal of biological chemistry 2003;278(18):15457-60.
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2003: Campbell Kevin P; Stull James T
Skeletal muscle basement membrane-sarcolemma-cytoskeleton interaction minireview series.
The Journal of biological chemistry 2003;278(15):12599-600.
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2003: Arikkath Jyothi; Chen Chien-Chang; Ahern Christopher; Allamand Valérie; Flanagan Jason D; Coronado Roberto; Gregg Ronald G; Campbell Kevin P
Gamma 1 subunit interactions within the skeletal muscle L-type voltage-gated calcium channels.
The Journal of biological chemistry 2003;278(2):1212-9.
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2002: Arikkath Jyothi; Felix Ricardo; Ahern Christopher; Chen Chien-Chang; Mori Yasuo; Song Inseon; Shin Hee-Sup; Coronado Roberto; Campbell Kevin P
Molecular characterization of a two-domain form of the neuronal voltage-gated P/Q-type calcium channel alpha(1)2.1 subunit.
FEBS letters 2002;532(3):300-8.
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2002: Crosbie Rachelle H; Barresi Rita; Campbell Kevin P
Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2002;16(13):1786-91.
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2002: Kang Myoung-Goo; Felix Ricardo; Campbell Kevin P
Long-term regulation of voltage-gated Ca(2+) channels by gabapentin.
FEBS letters 2002;528(1-3):177-82.
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2002: Cohn Ronald D; Henry Michael D; Michele Daniel E; Barresi Rita; Saito Fumiaki; Moore Steven A; Flanagan Jason D; Skwarchuk Mark W; Robbins Michael E; Mendell Jerry R; Williamson Roger A; Campbell Kevin P
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.
Cell 2002;110(5):639-48.
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2002: Moore Steven A; Saito Fumiaki; Chen Jianguo; Michele Daniel E; Henry Michael D; Messing Albee; Cohn Ronald D; Ross-Barta Susan E; Westra Steve; Williamson Roger A; Hoshi Toshinori; Campbell Kevin P
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.
Nature 2002;418(6896):422-5.
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2002: Michele Daniel E; Barresi Rita; Kanagawa Motoi; Saito Fumiaki; Cohn Ronald D; Satz Jakob S; Dollar James; Nishino Ichizo; Kelley Richard I; Somer Hannu; Straub Volker; Mathews Katherine D; Moore Steven A; Campbell Kevin P
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.
Nature 2002;418(6896):417-22.
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2002: Crosbie Rachelle H; Dovico Sherri A; Flanagan Jason D; Chamberlain Jeffrey S; Ownby Charlotte L; Campbell Kevin P
Characterization of aquaporin-4 in muscle and muscular dystrophy.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2002;16(9):943-9.
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2002: Durbeej Madeleine; Campbell Kevin P
Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.
Current opinion in genetics & development 2002;12(3):349-61.
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2002: Spiropoulou Christina F; Kunz Stefan; Rollin Pierre E; Campbell Kevin P; Oldstone Michael B A
New World arenavirus clade C, but not clade A and B viruses, utilizes alpha-dystroglycan as its major receptor.
Journal of virology 2002;76(10):5140-6.
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2002: Piccolo Federica; Moore Steven A; Mathews Katherine D; Campbell Kevin P
Limb-girdle muscular dystrophies.
Advances in neurology 2002;88():273-91.
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2001: Durbeej M; Talts J F; Henry M D; Yurchenco P D; Campbell K P; Ekblom P
Dystroglycan binding to laminin alpha1LG4 module influences epithelial morphogenesis of salivary gland and lung in vitro.
Differentiation; research in biological diversity 2001;69(2-3):121-34.
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2001: Kunz S; Sevilla N; McGavern D B; Campbell K P; Oldstone M B
Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan.
The Journal of cell biology 2001;155(2):301-10.
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2001: Henry M D; Cohen M B; Campbell K P
Reduced expression of dystroglycan in breast and prostate cancer.
Human pathology 2001;32(8):791-5.
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2001: Kang M G; Chen C C; Felix R; Letts V A; Frankel W N; Mori Y; Campbell K P
Biochemical and biophysical evidence for gamma 2 subunit association with neuronal voltage-activated Ca2+ channels.
The Journal of biological chemistry 2001;276(35):32917-24.
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2001: Ahern C A; Arikkath J; Vallejo P; Gurnett C A; Powers P A; Campbell K P; 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 2001;98(12):6935-40.
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2001: Henry M D; Satz J S; Brakebusch C; Costell M; Gustafsson E; Fässler R; Campbell K P
Distinct roles for dystroglycan, beta1 integrin and perlecan in cell surface laminin organization.
Journal of cell science 2001;114(Pt 6):1137-44.
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2001: Cohn R D; Durbeej M; Moore S A; Coral-Vazquez R; Prouty S; Campbell K P
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex.
The Journal of clinical investigation 2001;107(2):R1-7.
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2001: Smelt S C; Borrow P; Kunz S; Cao W; Tishon A; Lewicki H; Campbell K P; Oldstone M B
Differences in affinity of binding of lymphocytic choriomeningitis virus strains to the cellular receptor alpha-dystroglycan correlate with viral tropism and disease kinetics.
Journal of virology 2001;75(1):448-57.
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2001: Ahern C A; Powers P A; Biddlecome G H; Roethe L; Vallejo P; Mortenson L; Strube C; Campbell K P; Coronado R; Gregg R G
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 2001;1():8.
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2000: Piccolo F; Moore S A; Ford G C; Campbell K P
Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb--girdle muscular dystrophies.
Annals of neurology 2000;48(6):902-12.
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2000: Barresi R; Moore S A; Stolle C A; Mendell J R; Campbell K P
Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.
The Journal of biological chemistry 2000;275(49):38554-60.
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2000: Sevilla N; Kunz S; Holz A; Lewicki H; Homann D; Yamada H; Campbell K P; de La Torre J C; Oldstone M B
Immunosuppression and resultant viral persistence by specific viral targeting of dendritic cells.
The Journal of experimental medicine 2000;192(9):1249-60.
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2000: Straub V; Donahue K M; Allamand V; Davisson R L; Kim Y R; Campbell K P
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 2000;44(4):655-9.
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2000: Allamand V; Campbell K P
Animal models for muscular dystrophy: valuable tools for the development of therapies.
Human molecular genetics 2000;9(16):2459-67.
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2000: Cohn R D; Campbell K P
Molecular basis of muscular dystrophies.
Muscle & nerve 2000;23(10):1456-71.
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2000: Crawford G E; Faulkner J A; Crosbie R H; Campbell K P; Froehner S C; Chamberlain J S
Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain.
The Journal of cell biology 2000;150(6):1399-410.
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2000: Allamand V; Donahue K M; Straub V; Davisson R L; Davidson B L; Campbell K P
Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice.
Gene therapy 2000;7(16):1385-91.
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2000: Crosbie R H; Lim L E; Moore S A; Hirano M; Hays A P; Maybaum S W; Collin H; Dovico S A; Stolle C A; Fardeau M; Tomé F M; Campbell K P
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.
Human molecular genetics 2000;9(13):2019-27.
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2000: Lebakken C S; Venzke D P; Hrstka R F; Consolino C M; Faulkner J A; Williamson R A; Campbell K P
Sarcospan-deficient mice maintain normal muscle function.
Molecular and cellular biology 2000;20(5):1669-77.
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2000: Holt K H; Crosbie R H; Venzke D P; Campbell K P
Biosynthesis of dystroglycan: processing of a precursor propeptide.
FEBS letters 2000;468(1):79-83.
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2000: Durbeej M; Cohn R D; Hrstka R F; Moore S A; Allamand V; Davidson B L; Williamson R A; Campbell K P
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.
Molecular cell 2000;5(1):141-51.
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1999: Henry M D; Campbell K P
Dystroglycan inside and out.
Current opinion in cell biology 1999;11(5):602-7.
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1999: Straub V; Ettinger A J; Durbeej M; Venzke D P; Cutshall S; Sanes J R; Campbell K P
epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex.
The Journal of biological chemistry 1999;274(39):27989-96.
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1999: Durbeej M; Campbell K P
Biochemical characterization of the epithelial dystroglycan complex.
The Journal of biological chemistry 1999;274(37):26609-16.
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1999: Coral-Vazquez R; Cohn R D; Moore S A; Hill J A; Weiss R M; Davisson R L; Straub V; Barresi R; Bansal D; Hrstka R F; Williamson R; Campbell K P
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy.
Cell 1999;98(4):465-74.
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1999: Crosbie R H; Lebakken C S; Holt K H; Venzke D P; Straub V; Lee J C; Grady R M; Chamberlain J S; Sanes J R; Campbell K P
Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex.
The Journal of cell biology 1999;145(1):153-65.
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1998: Salih M A; Al Rayess M; Cutshall S; Urtizberea J A; Al-Turaiki M H; Ozo C O; Straub V; Akbar M; Abid M; Andeejani A; Campbell K P
A novel form of familial congenital muscular dystrophy in two adolescents.
Neuropediatrics 1998;29(6):289-93.
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1998: Henry M D; Campbell K P
A role for dystroglycan in basement membrane assembly.
Cell 1998;95(6):859-70.
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1998: Holt K H; Campbell K P
Assembly of the sarcoglycan complex. Insights for muscular dystrophy.
The Journal of biological chemistry 1998;273(52):34667-70.
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1998: Cao W; Henry M D; Borrow P; Yamada H; Elder J H; Ravkov E V; Nichol S T; Compans R W; Campbell K P; Oldstone M B
Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus.
Science (New York, N.Y.) 1998;282(5396):2079-81.
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1998: Straub V; Duclos F; Venzke D P; Lee J C; Cutshall S; Leveille C J; Campbell K P
Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster.
The American journal of pathology 1998;153(5):1623-30.
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1998: Henry M D; Williamson R A; Campbell K P
Analysis of the role of dystroglycan in early postimplantation mouse development.
Annals of the New York Academy of Sciences 1998;857():256-9.
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1998: Lim L E; Campbell K P
The sarcoglycan complex in limb-girdle muscular dystrophy.
Current opinion in neurology 1998;11(5):443-52.
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1998: Durbeej M; Henry M D; Campbell K P
Dystroglycan in development and disease.
Current opinion in cell biology 1998;10(5):594-601.
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1998: Duclos F; Straub V; Moore S A; Venzke D P; Hrstka R F; Crosbie R H; Durbeej M; Lebakken C S; Ettinger A J; van der Meulen J; Holt K H; Lim L E; Sanes J R; Davidson B L; Faulkner J A; Williamson R; Campbell K P
Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice.
The Journal of cell biology 1998;142(6):1461-71.
-
1998: Letts V A; Felix R; Biddlecome G H; Arikkath J; Mahaffey C L; Valenzuela A; Bartlett F S; Mori Y; Campbell K P; Frankel W N
The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
Nature genetics 1998;19(4):340-7.
-
1998: Holt K H; Lim L E; Straub V; Venzke D P; Duclos F; Anderson R D; Davidson B L; Campbell K P
Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer.
Molecular cell 1998;1(6):841-8.
-
1998: Crosbie R H; Yamada H; Venzke D P; Lisanti M P; Campbell K P
Caveolin-3 is not an integral component of the dystrophin glycoprotein complex.
FEBS letters 1998;427(2):279-82.
-
1998: Crosbie R H; Straub V; Yun H Y; Lee J C; Rafael J A; Chamberlain J S; Dawson V L; Dawson T M; Campbell K P
mdx muscle pathology is independent of nNOS perturbation.
Human molecular genetics 1998;7(5):823-9.
-
1998: Durbeej M; Henry M D; Ferletta M; Campbell K P; Ekblom P
Distribution of dystroglycan in normal adult mouse tissues.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1998;46(4):449-57.
-
1998: Duclos F; Broux O; Bourg N; Straub V; Feldman G L; Sunada Y; Lim L E; Piccolo F; Cutshall S; Gary F; Quetier F; Kaplan J C; Jackson C E; Beckmann J S; Campbell K P
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.
Neuromuscular disorders : NMD 1998;8(1):30-8.
-
1998: Scott V E; Felix R; Arikkath J; Campbell K P
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 1998;18(2):641-7.
-
1998: Scott V E; Gurnett C A; Campbell K P
Overlay and bead assay. Determination of calcium channel subunit interaction domains.
Methods in molecular biology (Clifton, N.J.) 1998;88():71-85.
-
1997: Crosbie R H; Heighway J; Venzke D P; Lee J C; Campbell K P
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex.
The Journal of biological chemistry 1997;272(50):31221-4.
-
1997: Straub V; Rafael J A; Chamberlain J S; Campbell K P
Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.
The Journal of cell biology 1997;139(2):375-85.
-
1997: Felix R; Gurnett C A; De Waard M; Campbell K P
Dissection of functional domains of the voltage-dependent Ca2+ channel alpha2delta subunit.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1997;17(18):6884-91.
-
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 J A; Jung D; Tan E; Jeanpierre M; Campbell K P; Kaplan J C; Beckmann J S; Topaloglu H
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
Annals of neurology 1997;42(2):222-9.
-
1997: Gurnett C A; Felix R; Campbell K P
Extracellular interaction of the voltage-dependent Ca2+ channel alpha2delta and alpha1 subunits.
The Journal of biological chemistry 1997;272(29):18508-12.
-
1997: Carrié A; Piccolo F; Leturcq F; de Toma C; Azibi K; Beldjord C; Vallat J M; Merlini L; Voit T; Sewry C; Urtizberea J A; Romero N; Tomé F M; Fardeau M; Sunada Y; Campbell K P; Kaplan J C; Jeanpierre M
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).
Journal of medical genetics 1997;34(6):470-5.
-
1997: Williamson R A; Henry M D; Daniels K J; Hrstka R F; Lee J C; Sunada Y; Ibraghimov-Beskrovnaya O; Campbell K P
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice.
Human molecular genetics 1997;6(6):831-41.
-
1997: Allamand V; Sunada Y; Salih M A; Straub V; Ozo C O; Al-Turaiki M H; Akbar M; Kolo T; Colognato H; Zhang X; Sorokin L M; Yurchenco P D; Tryggvason K; Campbell K P
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain.
Human molecular genetics 1997;6(5):747-52.
-
1997: Eymard B; Romero N B; 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 K P; Kaplan J C; Tomé F M; Fardeau M
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.
Neurology 1997;48(5):1227-34.
-
1997: Straub V; Campbell K P
Muscular dystrophies and the dystrophin-glycoprotein complex.
Current opinion in neurology 1997;10(2):168-75.
-
1997: Durbeej M; Jung D; Hjalt T; Campbell K P; Ekblom P
Transient expression of Dp140, a product of the Duchenne muscular dystrophy locus, during kidney tubulogenesis.
Developmental biology 1997;181(2):156-67.
-
1997: De Waard M; Liu H; Walker D; Scott V E; Gurnett C A; Campbell K P
Direct binding of G-protein betagamma complex to voltage-dependent calcium channels.
Nature 1997;385(6615):446-50.
-
1996: Seidahmed M Z; Sunada Y; Ozo C O; Hamid F; Campbell K P; Salih M A
Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?
Neuropediatrics 1996;27(6):305-10.
-
1996: Jeanpierre M; Carrié A; Piccolo F; Leturcq F; Azibi K; De Toma C; Beldjord C; Merlini L; Voit T; Romero N; Sunada Y; Tomé F M; Fardeau M; Campbell K P; Kaplan J C
From adhalinopathies to alpha-sarcoglycanopathies: an overview.
Neuromuscular disorders : NMD 1996;6(6):463-5.
-
1996: Beckmann J S; Richard I; Broux O; Fougerousse F; Allamand V; Chiannilkulchai N; Lim L E; Duclos F; Bourg N; Brenguier L; Pasturaud P; Quétier F; Roudaut C; Sunada Y; Meyer J; Dinçer P; Lefranc G; Merlini L; Topaloglu H; Tomé F M; Cohen D; Jackson C E; Campbell K P; Fardeau M
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies.
Neuromuscular disorders : NMD 1996;6(6):455-62.
-
1996: Salih M A; Sunada Y; Al-Nasser M; Ozo C O; Al-Turaiki M H; Akbar M; Campbell K P
Muscular dystrophy associated with beta-Dystroglycan deficiency.
Annals of neurology 1996;40(6):925-8.
-
1996: Piccolo F; Jeanpierre M; Leturcq F; Dodé C; Azibi K; Toutain A; Merlini L; Jarre L; Navarro C; Krishnamoorthy R; Tomé F M; Urtizberea J A; Beckmann J S; Campbell K P; Kaplan J C
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India.
Human molecular genetics 1996;5(12):2019-22.
-
1996: Jung D; Duclos F; Apostol B; Straub V; Lee J C; Allamand V; Venzke D P; Sunada Y; Moomaw C R; Leveille C J; Slaughter C A; Crawford T O; McPherson J D; Campbell K P
Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy.
The Journal of biological chemistry 1996;271(50):32321-9.
-
1996: Liu H; Felix R; Gurnett C A; De Waard M; Witcher D R; Campbell K P
Expression and subunit interaction of voltage-dependent Ca2+ channels in PC12 cells.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1996;16(23):7557-65.
-
1996: Gurnett C A; Campbell K P
Transmembrane auxiliary subunits of voltage-dependent ion channels.
The Journal of biological chemistry 1996;271(45):27975-8.
-
1996: Henry M D; Campbell K P
Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton.
Current opinion in cell biology 1996;8(5):625-31.
-
1996: Rafael J A; Cox G A; Corrado K; Jung D; Campbell K P; Chamberlain J S
Forced expression of dystrophin deletion constructs reveals structure-function correlations.
The Journal of cell biology 1996;134(1):93-102.
-
1996: Liu H; De Waard M; Scott V E; Gurnett C A; Lennon V A; Campbell K P
Identification of three subunits of the high affinity omega-conotoxin MVIIC-sensitive Ca2+ channel.
The Journal of biological chemistry 1996;271(23):13804-10.
-
1996: Salih M A; Mahdi A H; al-Rikabi A C; al-Bunyan M; Roberds S L; Anderson R D; Campbell K P
Clinical and molecular pathological features of severe childhood autosomal recessive muscular dystrophy in Saudi Arabia.
Developmental medicine and child neurology 1996;38(3):262-70.
-
1996: Gurnett C A; De Waard M; Campbell K P
Dual function of the voltage-dependent Ca2+ channel alpha 2 delta subunit in current stimulation and subunit interaction.
Neuron 1996;16(2):431-40.
-
1996: Oexle K; Herrmann R; Dodé C; Leturcq F; Hübner C; Kaplan J C; Mizuno Y; Ozawa E; Campbell K P; Voit T
Neurosensory hearing loss in secondary adhalinopathy.
Neuropediatrics 1996;27(1):32-6.
-
1996: Jung D; Leturcq F; Sunada Y; Duclos F; Tomé F M; Moomaw C; Merlini L; Azibi K; Chaouch M; Slaughter C; Fardeau M; Kaplan J C; Campbell K P
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.
FEBS letters 1996;381(1-2):15-20.
-
1996: Scott V E; De Waard M; Liu H; Gurnett C A; Venzke D P; Lennon V A; Campbell K P
Beta subunit heterogeneity in N-type Ca2+ channels.
The Journal of biological chemistry 1996;271(6):3207-12.
-
1996: De Waard M; Scott V E; Pragnell M; Campbell K P
Identification of critical amino acids involved in alpha1-beta interaction in voltage-dependent Ca2+ channels.
FEBS letters 1996;380(3):272-6.
-
1996: Fadic R; Sunada Y; Waclawik A J; Buck S; Lewandoski P J; Campbell K P; Lotz B P
Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy.
The New England journal of medicine 1996;334(6):362-6.
-
1996: Guo W; Jorgensen A O; Jones L R; Campbell K P
Biochemical characterization and molecular cloning of cardiac triadin.
The Journal of biological chemistry 1996;271(1):458-65.
-
1996: Guo W; Jorgensen A O; Campbell K P
Triadin, a linker for calsequestrin and the ryanodine receptor.
Society of General Physiologists series 1996;51():19-28.
-
1996: De Waard M; Gurnett C A; Campbell K P
Structural and functional diversity of voltage-activated calcium channels.
Ion channels 1996;4():41-87.
-
1995: Jung D; Yang B; Meyer J; Chamberlain J S; Campbell K P
Identification and characterization of the dystrophin anchoring site on beta-dystroglycan.
The Journal of biological chemistry 1995;270(45):27305-10.
-
1995: Sunada Y; Edgar T S; Lotz B P; Rust R S; Campbell K P
Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities.
Neurology 1995;45(11):2084-9.
-
1995: Sunada Y; Campbell K P
Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle.
Current opinion in neurology 1995;8(5):379-84.
-
1995: Mills K A; Sunada Y; Campbell K P; Mathews K D
A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(9):664-5.
-
1995: Bueno M R; Moreira E S; Vainzof M; Chamberlain J; Marie S K; Pereira L; Akiyama J; Roberds S L; Campbell K P; 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 1995;4(7):1163-7.
-
1995: Durbeej M; Larsson E; Ibraghimov-Beskrovnaya O; Roberds S L; Campbell K P; Ekblom P
Non-muscle alpha-dystroglycan is involved in epithelial development.
The Journal of cell biology 1995;130(1):79-91.
-
1995: Witcher D R; De Waard M; Liu H; Pragnell M; Campbell K P
Association of native Ca2+ channel beta subunits with the alpha 1 subunit interaction domain.
The Journal of biological chemistry 1995;270(30):18088-93.
-
1995: Sunada Y; Bernier S M; Utani A; Yamada Y; Campbell K P
Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice.
Human molecular genetics 1995;4(6):1055-61.
-
1995: De Waard M; Campbell K P
Subunit regulation of the neuronal alpha 1A Ca2+ channel expressed in Xenopus oocytes.
The Journal of physiology 1995;485 ( Pt 3)():619-34.
-
1995: Roberds S L; Campbell K P
Adhalin mRNA and cDNA sequence are normal in the cardiomyopathic hamster.
FEBS letters 1995;364(3):245-9.
-
1995: De Waard M; Witcher D R; Pragnell M; Liu H; Campbell K P
Properties of the alpha 1-beta anchoring site in voltage-dependent Ca2+ channels.
The Journal of biological chemistry 1995;270(20):12056-64.
-
1995: Yang B; Jung D; Motto D; Meyer J; Koretzky G; Campbell K P
SH3 domain-mediated interaction of dystroglycan and Grb2.
The Journal of biological chemistry 1995;270(20):11711-4.
-
1995: Gurnett C A; Kahl S D; Anderson R D; Campbell K P
Absence of the skeletal muscle sarcolemma chloride channel ClC-1 in myotonic mice.
The Journal of biological chemistry 1995;270(16):9035-8.
-
1995: Guo W; Campbell K P
Association of triadin with the ryanodine receptor and calsequestrin in the lumen of the sarcoplasmic reticulum.
The Journal of biological chemistry 1995;270(16):9027-30.
-
1995: Yang B; Jung D; Rafael J A; Chamberlain J S; Campbell K P
Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin.
The Journal of biological chemistry 1995;270(10):4975-8.
-
1995: Campbell K P
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
Cell 1995;80(5):675-9.
-
1994: Cox G A; Sunada Y; Campbell K P; Chamberlain J S
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy.
Nature genetics 1994;8(4):333-9.
-
1994: Allamand V; Leturcq F; Piccolo F; Jeanpierre M; Azibi K; Roberds S L; Lim L E; Campbell K P; Beckmann J S; Kaplan J C
Adhalin gene polymorphism.
Human molecular genetics 1994;3(12):2269.
-
1994: Guo W; Jorgensen A O; Campbell K P
Characterization and ultrastructural localization of a novel 90-kDa protein unique to skeletal muscle junctional sarcoplasmic reticulum.
The Journal of biological chemistry 1994;269(45):28359-65.
-
1994: Rafael J A; Sunada Y; Cole N M; Campbell K P; Faulkner J A; Chamberlain J S
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.
Human molecular genetics 1994;3(10):1725-33.
-
1994: Ervasti J M; Roberds S L; Anderson R D; Sharp N J; Kornegay J N; Campbell K P
Alpha-dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophy.
FEBS letters 1994;350(2-3):173-6.
-
1994: De Waard M; Pragnell M; Campbell K P
Ca2+ channel regulation by a conserved beta subunit domain.
Neuron 1994;13(2):495-503.
-
1994: Mickelson J R; Ervasti J M; Litterer L A; Campbell K P; Louis C F
Skeletal muscle junctional membrane protein content in pigs with different ryanodine receptor genotypes.
The American journal of physiology 1994;267(1 Pt 1):C282-92.
-
1994: Campanelli J T; Roberds S L; Campbell K P; Scheller R H
A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering.
Cell 1994;77(5):663-74.
-
1994: Sunada Y; Bernier S M; Kozak C A; Yamada Y; Campbell K P
Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus.
The Journal of biological chemistry 1994;269(19):13729-32.
-
1994: Witcher D R; McPherson P S; Kahl S D; Lewis T; Bentley P; Mullinnix M J; Windass J D; Campbell K P
Photoaffinity labeling of the ryanodine receptor/Ca2+ release channel with an azido derivative of ryanodine.
The Journal of biological chemistry 1994;269(18):13076-9.
-
1994: Zatz M; Matsumura K; Vainzof M; Passos-Bueno M R; Pavanello R C; Marie S K; Campbell K P
Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.
Journal of the neurological sciences 1994;123(1-2):122-8.
-
1994: Kahl S D; McPherson P S; Lewis T; Bentley P; Mullinnix M J; Windass J D; Campbell K P
Radioimmunoassay for the calcium release channel agonist ryanodine.
Analytical biochemistry 1994;218(1):55-62.
-
1994: De Waard M; Witcher D R; Campbell K P
Functional properties of the purified N-type Ca2+ channel from rabbit brain.
The Journal of biological chemistry 1994;269(9):6716-24.
-
1994: Matsumura K; Tomé F M; Collin H; Leturcq F; Jeanpierre M; Kaplan J C; Fardeau M; Campbell K P
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1994;4(2):115-20.
-
1994: Pragnell M; De Waard M; Mori Y; Tanabe T; Snutch T P; Campbell K P
Calcium channel beta-subunit binds to a conserved motif in the I-II cytoplasmic linker of the alpha 1-subunit.
Nature 1994;368(6466):67-70.
-
1994: Parys J B; McPherson S M; Mathews L; Campbell K P; Longo F J
Presence of inositol 1,4,5-trisphosphate receptor, calreticulin, and calsequestrin in eggs of sea urchins and Xenopus laevis.
Developmental biology 1994;161(2):466-76.
-
1994: Yang B; Ibraghimov-Beskrovnaya O; Moomaw C R; Slaughter C A; Campbell K P
Heterogeneity of the 59-kDa dystrophin-associated protein revealed by cDNA cloning and expression.
The Journal of biological chemistry 1994;269(8):6040-4.
-
1994: Matsumura K; Campbell K P
Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.
Muscle & nerve 1994;17(1):2-15.
-
1994: Romero N B; Tomé F M; Leturcq F; el Kerch F E; Azibi K; Bachner L; Anderson R D; Roberds S L; Campbell K P; Fardeau M
Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1994;317(1):70-6.
-
1994: Witcher D R; De Waard M; Kahl S D; Campbell K P
Purification and reconstitution of N-type calcium channel complex from rabbit brain.
Methods in enzymology 1994;238():335-48.
-
1993: Ibraghimov-Beskrovnaya O; Sheffield V C; Campbell K P
Single base polymorphism in the DAG1 gene detected by DGGE and mismatch PCR.
Human molecular genetics 1993;2(11):1983.
-
1993: Passos-Bueno M R; Oliveira J R; Bakker E; Anderson R D; Marie S K; Vainzof M; Roberds S; Campbell K P; Zatz M
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.
Human molecular genetics 1993;2(11):1945-7.
-
1993: Roberds S L; Anderson R D; Ibraghimov-Beskrovnaya O; Campbell K P
Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin).
The Journal of biological chemistry 1993;268(32):23739-42.
-
1993: Witcher D R; De Waard M; Campbell K P
Characterization of the purified N-type Ca2+ channel and the cation sensitivity of omega-conotoxin GVIA binding.
Neuropharmacology 1993;32(11):1127-39.
-
1993: Stea A; Dubel S J; Pragnell M; Leonard J P; Campbell K P; Snutch T P
A beta-subunit normalizes the electrophysiological properties of a cloned N-type Ca2+ channel alpha 1-subunit.
Neuropharmacology 1993;32(11):1103-16.
-
1993: Ibraghimov-Beskrovnaya O; Milatovich A; Ozcelik T; Yang B; Koepnick K; Francke U; Campbell K P
Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization.
Human molecular genetics 1993;2(10):1651-7.
-
1993: Matsumura K; Ohlendieck K; Ionasescu V V; Tomé F M; Nonaka I; Burghes A H; Mora M; Kaplan J C; Fardeau M; Campbell K P
The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies.
Neuromuscular disorders : NMD 1993;3(5-6):533-5.
-
1993: McPherson P S; Campbell K P
Characterization of the major brain form of the ryanodine receptor/Ca2+ release channel.
The Journal of biological chemistry 1993;268(26):19785-90.
-
1993: Cox G A; Cole N M; Matsumura K; Phelps S F; Hauschka S D; Campbell K P; Faulkner J A; Chamberlain J S
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity.
Nature 1993;364(6439):725-9.
-
1993: Ervasti J M; Campbell K P
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.
The Journal of cell biology 1993;122(4):809-23.
-
1993: Matsumura K; Nonaka I; Tomé F M; Arahata K; Collin H; Leturcq F; Récan D; Kaplan J C; Fardeau M; Campbell K P
Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.
American journal of human genetics 1993;53(2):409-16.
-
1993: Fardeau M; Matsumura K; Tomé F M; Collin H; Leturcq F; Kaplan J C; Campbell K P
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1993;316(8):799-804.
-
1993: Witcher D R; De Waard M; Sakamoto J; Franzini-Armstrong C; Pragnell M; Kahl S D; Campbell K P
Subunit identification and reconstitution of the N-type Ca2+ channel complex purified from brain.
Science (New York, N.Y.) 1993;261(5120):486-9.
-
1993: McPherson P S; Campbell K P
The ryanodine receptor/Ca2+ release channel.
The Journal of biological chemistry 1993;268(19):13765-8.
-
1993: Matsumura K; Shasby D M; Campbell K P
Purification of dystrophin-related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells.
FEBS letters 1993;326(1-3):289-93.
-
1993: Roberds S L; Ervasti J M; Anderson R D; Ohlendieck K; Kahl S D; Zoloto D; Campbell K P
Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster.
The Journal of biological chemistry 1993;268(16):11496-9.
-
1993: Knudson C M; Stang K K; Jorgensen A O; Campbell K P
Biochemical characterization of ultrastructural localization of a major junctional sarcoplasmic reticulum glycoprotein (triadin).
The Journal of biological chemistry 1993;268(17):12637-45.
-
1993: Matsumura K; Nonaka I; Arahata K; Campbell K P
Partial deficiency of dystrophin-associated proteins in a young girl with sporadic myopathy and normal karyotype.
Neurology 1993;43(6):1267-8.
-
1993: Ohlendieck K; Matsumura K; Ionasescu V V; Towbin J A; Bosch E P; Weinstein S L; Sernett S W; Campbell K P
Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma.
Neurology 1993;43(4):795-800.
-
1993: Matsumura K; Lee C C; Caskey C T; Campbell K P
Restoration of dystrophin-associated proteins in skeletal muscle of mdx mice transgenic for dystrophin gene.
FEBS letters 1993;320(3):276-80.
-
1993: Matsumura K; Campbell K P
Deficiency of dystrophin-associated proteins: a common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies.
Neuromuscular disorders : NMD 1993;3(2):109-18.
-
1993: Matsumura K; Nonaka I; Campbell K P
Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy.
Lancet 1993;341(8844):521-2.
-
1993: Ervasti J M; Campbell K P
Dystrophin-associated glycoproteins: their possible roles in the pathogenesis of Duchenne muscular dystrophy.
Molecular and cell biology of human diseases series 1993;3():139-66.
-
1992: Matsumura K; Ervasti J M; Ohlendieck K; Kahl S D; Campbell K P
Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle.
Nature 1992;360(6404):588-91.
-
1992: Matsumura K; Tomé F M; Collin H; Azibi K; Chaouch M; Kaplan J C; Fardeau M; Campbell K P
Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy.
Nature 1992;359(6393):320-2.
-
1992: Parys J B; Sernett S W; DeLisle S; Snyder P M; Welsh M J; Campbell K P
Isolation, characterization, and localization of the inositol 1,4,5-trisphosphate receptor protein in Xenopus laevis oocytes.
The Journal of biological chemistry 1992;267(26):18776-82.
-
1992: Mickelson J R; Knudson C M; Kennedy C F; Yang D I; Litterer L A; Rempel W E; Campbell K P; Louis C F
Structural and functional correlates of a mutation in the malignant hyperthermia-susceptible pig ryanodine receptor.
FEBS letters 1992;301(1):49-52.
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1992: McPherson S M; McPherson P S; Mathews L; Campbell K P; Longo F J
Cortical localization of a calcium release channel in sea urchin eggs.
The Journal of cell biology 1992;116(5):1111-21.
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1992: Ibraghimov-Beskrovnaya O; Ervasti J M; Leveille C J; Slaughter C A; Sernett S W; Campbell K P
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix.
Nature 1992;355(6362):696-702.
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1991: Ohlendieck K; Campbell K P
Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice.
The Journal of cell biology 1991;115(6):1685-94.
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1991: Ohlendieck K; Briggs F N; Lee K F; Wechsler A W; Campbell K P
Analysis of excitation-contraction-coupling components in chronically stimulated canine skeletal muscle.
European journal of biochemistry / FEBS 1991;202(3):739-47.
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1991: Pragnell M; Sakamoto J; Jay S D; Campbell K P
Cloning and tissue-specific expression of the brain calcium channel beta-subunit.
FEBS letters 1991;291(2):253-8.
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1991: Sakamoto J; Campbell K P
A monoclonal antibody to the beta subunit of the skeletal muscle dihydropyridine receptor immunoprecipitates the brain omega-conotoxin GVIA receptor.
The Journal of biological chemistry 1991;266(28):18914-9.
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1991: Ervasti J M; Campbell K P
Membrane organization of the dystrophin-glycoprotein complex.
Cell 1991;66(6):1121-31.
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1991: Ohlendieck K; Ervasti J M; Matsumura K; Kahl S D; Leveille C J; Campbell K P
Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle.
Neuron 1991;7(3):499-508.
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1991: McPherson P S; Kim Y K; Valdivia H; Knudson C M; Takekura H; Franzini-Armstrong C; Coronado R; Campbell K P
The brain ryanodine receptor: a caffeine-sensitive calcium release channel.
Neuron 1991;7(1):17-25.
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1991: Ohlendieck K; Campbell K P
Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscle.
FEBS letters 1991;283(2):230-4.
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1991: Ervasti J M; Kahl S D; Campbell K P
Purification of dystrophin from skeletal muscle.
The Journal of biological chemistry 1991;266(14):9161-5.
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1991: Jay S D; Sharp A H; Kahl S D; Vedvick T S; Harpold M M; Campbell K P
Structural characterization of the dihydropyridine-sensitive calcium channel alpha 2-subunit and the associated delta peptides.
The Journal of biological chemistry 1991;266(5):3287-93.
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1991: Ohlendieck K; Ervasti J M; Snook J B; Campbell K P
Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma.
The Journal of cell biology 1991;112(1):135-48.
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1990: McPherson P S; Campbell K P
Solubilization and biochemical characterization of the high affinity [3H]ryanodine receptor from rabbit brain membranes.
The Journal of biological chemistry 1990;265(30):18454-60.
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1990: Ervasti J M; Ohlendieck K; Kahl S D; Gaver M G; Campbell K P
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle.
Nature 1990;345(6273):315-9.
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1990: Jay S D; Ellis S B; McCue A F; Williams M E; Vedvick T S; Harpold M M; Campbell K P
Primary structure of the gamma subunit of the DHP-sensitive calcium channel from skeletal muscle.
Science (New York, N.Y.) 1990;248(4954):490-2.
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1990: Knudson C M; Mickelson J R; Louis C F; Campbell K P
Distinct immunopeptide maps of the sarcoplasmic reticulum Ca2+ release channel in malignant hyperthermia.
The Journal of biological chemistry 1990;265(5):2421-4.
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1989: Perez-Reyes E; Kim H S; Lacerda A E; Horne W; Wei X Y; Rampe D; Campbell K P; Brown A M; Birnbaumer L
Induction of calcium currents by the expression of the alpha 1-subunit of the dihydropyridine receptor from skeletal muscle.
Nature 1989;340(6230):233-6.
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1989: Knudson C M; Campbell K P
Albumin is a major protein component of transverse tubule vesicles isolated from skeletal muscle.
The Journal of biological chemistry 1989;264(18):10795-8.
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1989: Krause K H; Chou M; Thomas M A; Sjolund R D; Campbell K P
Plant cells contain calsequestrin.
The Journal of biological chemistry 1989;264(8):4269-72.
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1989: Campbell K P; Kahl S D
Association of dystrophin and an integral membrane glycoprotein.
Nature 1989;338(6212):259-62.
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1989: Sharp A H; Campbell K P
Characterization of the 1,4-dihydropyridine receptor using subunit-specific polyclonal antibodies. Evidence for a 32,000-Da subunit.
The Journal of biological chemistry 1989;264(5):2816-25.
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1989: Knudson C M; Chaudhari N; Sharp A H; Powell J A; Beam K G; Campbell K P
Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis.
The Journal of biological chemistry 1989;264(3):1345-8.
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1989: Fill M; Ma J J; Knudson C M; Imagawa T; Campbell K P; Coronado R
Role of the ryanodine receptor of skeletal muscle in excitation-contraction coupling.
Annals of the New York Academy of Sciences 1989;560():155-62.
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1989: Campbell K P; Sharp A H; Leung A T
32,000-Dalton subunit of the 1,4-dihydropyridine receptor.
Annals of the New York Academy of Sciences 1989;560():251-7.
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1988: Campbell K P; Leung A T; Sharp A H
The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel.
Trends in neurosciences 1988;11(10):425-30.
-
1988: Ma J; Fill M; Knudson C M; Campbell K P; Coronado R
Ryanodine receptor of skeletal muscle is a gap junction-type channel.
Science (New York, N.Y.) 1988;242(4875):99-102.
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1988: Ellis S B; Williams M E; Ways N R; Brenner R; Sharp A H; Leung A T; Campbell K P; McKenna E; Koch W J; Hui A
Sequence and expression of mRNAs encoding the alpha 1 and alpha 2 subunits of a DHP-sensitive calcium channel.
Science (New York, N.Y.) 1988;241(4873):1661-4.
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1988: Smith J S; Imagawa T; Ma J; Fill M; Campbell K P; Coronado R
Purified ryanodine receptor from rabbit skeletal muscle is the calcium-release channel of sarcoplasmic reticulum.
The Journal of general physiology 1988;92(1):1-26.
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1988: Knudson C M; Hoffman E P; Kahl S D; Kunkel L M; Campbell K P
Evidence for the association of dystrophin with the transverse tubular system in skeletal muscle.
The Journal of biological chemistry 1988;263(17):8480-4.
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1988: Leung A T; Imagawa T; Block B; Franzini-Armstrong C; Campbell K P
Biochemical and ultrastructural characterization of the 1,4-dihydropyridine receptor from rabbit skeletal muscle. Evidence for a 52,000 Da subunit.
The Journal of biological chemistry 1988;263(2):994-1001.
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1988: Campbell K P; Leung A T; 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 1988;12 Suppl 4():S86-90.
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1987: Imagawa T; Smith J S; Coronado R; Campbell K P
Purified ryanodine receptor from skeletal muscle sarcoplasmic reticulum is the Ca2+-permeable pore of the calcium release channel.
The Journal of biological chemistry 1987;262(34):16636-43.
-
1987: Sharp A H; Campbell K P
Affinity purification of antibodies specific for 1,4-dihydropyridine Ca2+ channel blockers.
Circulation research 1987;61(4 Pt 2):I37-45.
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1987: Sharp A H; Imagawa T; Leung A T; Campbell K P
Identification and characterization of the dihydropyridine-binding subunit of the skeletal muscle dihydropyridine receptor.
The Journal of biological chemistry 1987;262(25):12309-15.
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1987: Campbell K P; Knudson C M; Imagawa T; Leung A T; Sutko J L; Kahl S D; Raab C R; Madson L
Identification and characterization of the high affinity [3H]ryanodine receptor of the junctional sarcoplasmic reticulum Ca2+ release channel.
The Journal of biological chemistry 1987;262(14):6460-3.
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