J M Ervasti, K P Campbell. J Cell Biol 1993
Times Cited: 1117
Times Cited: 1117
Times Cited
Times Co-cited
Similarity
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix.
O Ibraghimov-Beskrovnaya, J M Ervasti, C J Leveille, C A Slaughter, S W Sernett, K P Campbell. Nature 1992
O Ibraghimov-Beskrovnaya, J M Ervasti, C J Leveille, C A Slaughter, S W Sernett, K P Campbell. Nature 1992
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Dystrophin: the protein product of the Duchenne muscular dystrophy locus.
E P Hoffman, R H Brown, L M Kunkel. Cell 1987
E P Hoffman, R H Brown, L M Kunkel. Cell 1987
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Dystrophin protects the sarcolemma from stresses developed during muscle contraction.
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Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy.
Motoi Kanagawa, Kazuhiro Kobayashi, Michiko Tajiri, Hiroshi Manya, Atsushi Kuga, Yoshiki Yamaguchi, Keiko Akasaka-Manya, Jun-Ichi Furukawa, Mamoru Mizuno, Hiroko Kawakami,[...]. Cell Rep 2016
Motoi Kanagawa, Kazuhiro Kobayashi, Michiko Tajiri, Hiroshi Manya, Atsushi Kuga, Yoshiki Yamaguchi, Keiko Akasaka-Manya, Jun-Ichi Furukawa, Mamoru Mizuno, Hiroko Kawakami,[...]. Cell Rep 2016
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Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.
Daniel E Michele, Rita Barresi, Motoi Kanagawa, Fumiaki Saito, Ronald D Cohn, Jakob S Satz, James Dollar, Ichizo Nishino, Richard I Kelley, Hannu Somer,[...]. Nature 2002
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ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan.
Isabelle Gerin, Benoît Ury, Isabelle Breloy, Céline Bouchet-Seraphin, Jennifer Bolsée, Mathias Halbout, Julie Graff, Didier Vertommen, Giulio G Muccioli, Nathalie Seta,[...]. Nat Commun 2016
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Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.
Takako Yoshida-Moriguchi, Kevin P Campbell. Glycobiology 2015
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Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle.
J M Ervasti, K Ohlendieck, S D Kahl, M G Gaver, K P Campbell. Nature 1990
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Dystroglycan: from biosynthesis to pathogenesis of human disease.
Rita Barresi, Kevin P Campbell. J Cell Sci 2006
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Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE.
Kei-ichiro Inamori, Takako Yoshida-Moriguchi, Yuji Hara, Mary E Anderson, Liping Yu, Kevin P Campbell. Science 2012
Kei-ichiro Inamori, Takako Yoshida-Moriguchi, Yuji Hara, Mary E Anderson, Liping Yu, Kevin P Campbell. Science 2012
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Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.
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The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition.
Jeremy L Praissman, Tobias Willer, M Osman Sheikh, Ants Toi, David Chitayat, Yung-Yao Lin, Hane Lee, Stephanie H Stalnaker, Shuo Wang, Pradeep Kumar Prabhakar,[...]. Elife 2016
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Association of dystrophin and an integral membrane glycoprotein.
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Evidence-based path to newborn screening for Duchenne muscular dystrophy.
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Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.
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Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor.
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Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.
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Ribitol restores functionally glycosylated α-dystroglycan and improves muscle function in dystrophic FKRP-mutant mice.
Marcela P Cataldi, Peijuan Lu, Anthony Blaeser, Qi Long Lu. Nat Commun 2018
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A stoichiometric complex of neurexins and dystroglycan in brain.
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The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy.
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Structural basis of laminin binding to the LARGE glycans on dystroglycan.
David C Briggs, Takako Yoshida-Moriguchi, Tianqing Zheng, David Venzke, Mary E Anderson, Andrea Strazzulli, Marco Moracci, Liping Yu, Erhard Hohenester, Kevin P Campbell. Nat Chem Biol 2016
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O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.
Takako Yoshida-Moriguchi, Liping Yu, Stephanie H Stalnaker, Sarah Davis, Stefan Kunz, Michael Madson, Michael B A Oldstone, Harry Schachter, Lance Wells, Kevin P Campbell. Science 2010
Takako Yoshida-Moriguchi, Liping Yu, Stephanie H Stalnaker, Sarah Davis, Stefan Kunz, Michael Madson, Michael B A Oldstone, Harry Schachter, Lance Wells, Kevin P Campbell. Science 2010
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Dystrophin, its interactions with other proteins, and implications for muscular dystrophy.
James M Ervasti. Biochim Biophys Acta 2007
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Microtubule binding distinguishes dystrophin from utrophin.
Joseph J Belanto, Tara L Mader, Michael D Eckhoff, Dana M Strandjord, Glen B Banks, Melissa K Gardner, Dawn A Lowe, James M Ervasti. Proc Natl Acad Sci U S A 2014
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Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy.
J E Brenman, D S Chao, H Xia, K Aldape, D S Bredt. Cell 1995
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B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan.
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The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation.
Tobias Willer, Kei-Ichiro Inamori, David Venzke, Corinne Harvey, Greg Morgensen, Yuji Hara, Daniel Beltrán Valero de Bernabé, Liping Yu, Kevin M Wright, Kevin P Campbell. Elife 2014
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Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation.
Shigeru Sato, Yoshihiro Omori, Kimiko Katoh, Mineo Kondo, Motoi Kanagawa, Kentaro Miyata, Kazuo Funabiki, Toshiyuki Koyasu, Naoko Kajimura, Tomomitsu Miyoshi,[...]. Nat Neurosci 2008
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Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.
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Efficacy of Gene Therapy Is Dependent on Disease Progression in Dystrophic Mice with Mutations in the FKRP Gene.
Charles Harvey Vannoy, Will Xiao, Peijuan Lu, Xiao Xiao, Qi Long Lu. Mol Ther Methods Clin Dev 2017
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Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies.
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The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein.
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The Dystrophin Complex: Structure, Function, and Implications for Therapy.
Quan Q Gao, Elizabeth M McNally. Compr Physiol 2015
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A Single CRISPR-Cas9 Deletion Strategy that Targets the Majority of DMD Patients Restores Dystrophin Function in hiPSC-Derived Muscle Cells.
Courtney S Young, Michael R Hicks, Natalia V Ermolova, Haruko Nakano, Majib Jan, Shahab Younesi, Saravanan Karumbayaram, Chino Kumagai-Cresse, Derek Wang, Jerome A Zack,[...]. Cell Stem Cell 2016
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Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.
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ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome.
Tobias Willer, Hane Lee, Mark Lommel, Takako Yoshida-Moriguchi, Daniel Beltran Valero de Bernabe, David Venzke, Sebahattin Cirak, Harry Schachter, Jiri Vajsar, Thomas Voit,[...]. Nat Genet 2012
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Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy.
Douglas P Millay, Michelle A Sargent, Hanna Osinska, Christopher P Baines, Elisabeth R Barton, Grégoire Vuagniaux, H Lee Sweeney, Jeffrey Robbins, Jeffery D Molkentin. Nat Med 2008
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Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection.
Yuji Hara, Motoi Kanagawa, Stefan Kunz, Takako Yoshida-Moriguchi, Jakob S Satz, Yvonne M Kobayashi, Zihan Zhu, Steven J Burden, Michael B A Oldstone, Kevin P Campbell. Proc Natl Acad Sci U S A 2011
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Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins.
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Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
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Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation.
Moniek Riemersma, D Sean Froese, Walinka van Tol, Udo F Engelke, Jolanta Kopec, Monique van Scherpenzeel, Angel Ashikov, Tobias Krojer, Frank von Delft, Marco Tessari,[...]. Chem Biol 2015
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SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function.
Takako Yoshida-Moriguchi, Tobias Willer, Mary E Anderson, David Venzke, Tamieka Whyte, Francesco Muntoni, Hane Lee, Stanley F Nelson, Liping Yu, Kevin P Campbell. Science 2013
Takako Yoshida-Moriguchi, Tobias Willer, Mary E Anderson, David Venzke, Tamieka Whyte, Francesco Muntoni, Hane Lee, Stanley F Nelson, Liping Yu, Kevin P Campbell. Science 2013
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The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan.
Hiroshi Manya, Yoshiki Yamaguchi, Motoi Kanagawa, Kazuhiro Kobayashi, Michiko Tajiri, Keiko Akasaka-Manya, Hiroko Kawakami, Mamoru Mizuno, Yoshinao Wada, Tatsushi Toda,[...]. J Biol Chem 2016
Hiroshi Manya, Yoshiki Yamaguchi, Motoi Kanagawa, Kazuhiro Kobayashi, Michiko Tajiri, Keiko Akasaka-Manya, Hiroko Kawakami, Mamoru Mizuno, Yoshinao Wada, Tatsushi Toda,[...]. J Biol Chem 2016
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Expression of full-length utrophin prevents muscular dystrophy in mdx mice.
J Tinsley, N Deconinck, R Fisher, D Kahn, S Phelps, J M Gillis, K Davies. Nat Med 1998
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The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma.
Karen A Lapidos, Rahul Kakkar, Elizabeth M McNally. Circ Res 2004
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Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.
M Brockington, Y Yuva, P Prandini, S C Brown, S Torelli, M A Benson, R Herrmann, L V Anderson, R Bashir, J M Burgunder,[...]. Hum Mol Genet 2001
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Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.