A citation-based method for searching scientific literature


List of co-cited articles
981 articles co-cited >1



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
26


Dystrophin protects the sarcolemma from stresses developed during muscle contraction.
B J Petrof, J B Shrager, H H Stedman, A M Kelly, H L Sweeney. Proc Natl Acad Sci U S A 1993
21


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
121
16

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
618
15

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
72
19

Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.
Takako Yoshida-Moriguchi, Kevin P Campbell. Glycobiology 2015
109
14

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
848
14

Dystroglycan: from biosynthesis to pathogenesis of human disease.
Rita Barresi, Kevin P Campbell. J Cell Sci 2006
404
13

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
192
13

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.
M Brockington, D J Blake, P Prandini, S C Brown, S Torelli, M A Benson, C P Ponting, B Estournet, N B Romero, E Mercuri,[...]. Am J Hum Genet 2001
437
12

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
64
17


Evidence-based path to newborn screening for Duchenne muscular dystrophy.
Jerry R Mendell, Chris Shilling, Nancy D Leslie, Kevin M Flanigan, Roula al-Dahhak, Julie Gastier-Foster, Kelley Kneile, Diane M Dunn, Brett Duval, Alexander Aoyagi,[...]. Ann Neurol 2012
466
10


Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor.
S H Gee, F Montanaro, M H Lindenbaum, S Carbonetto. Cell 1994
450
10

Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.
D Beltran-Valero de Bernabé, T Voit, C Longman, A Steinbrecher, V Straub, Y Yuva, R Herrmann, J Sperner, C Korenke, C Diesen,[...]. J Med Genet 2004
185
10


A stoichiometric complex of neurexins and dystroglycan in brain.
S Sugita, F Saito, J Tang, J Satz, K Campbell, T C Südhof. J Cell Biol 2001
330
9

The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy.
G Nigro, L I Comi, L Politano, R J Bain. Int J Cardiol 1990
408
9

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
60
15

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
240
9


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
84
9


B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan.
Jeremy L Praissman, David H Live, Shuo Wang, Annapoorani Ramiah, Zoeisha S Chinoy, Geert-Jan Boons, Kelley W Moremen, Lance Wells. Elife 2014
56
14

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
65
12

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
191
8



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
18
44

Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies.
Yiumo Michael Chan, Elizabeth Keramaris-Vrantsis, Hart G Lidov, James H Norton, Natalia Zinchenko, Helen E Gruber, Randy Thresher, Derek J Blake, Jignya Ashar, Jeffrey Rosenfeld,[...]. Hum Mol Genet 2010
72
11


The Dystrophin Complex: Structure, Function, and Implications for Therapy.
Quan Q Gao, Elizabeth M McNally. Compr Physiol 2015
141
8

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
211
8


Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.
Katharine Bushby, Richard Finkel, David J Birnkrant, Laura E Case, Paula R Clemens, Linda Cripe, Ajay Kaul, Kathi Kinnett, Craig McDonald, Shree Pandya,[...]. Lancet Neurol 2010
7

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
162
7

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
254
7

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
77
9



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
49
14

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
137
7

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
38
18

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
441
7

The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma.
Karen A Lapidos, Rahul Kakkar, Elizabeth M McNally. Circ Res 2004
336
7

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
348
7

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.
Ronald D Cohn, Michael D Henry, Daniel E Michele, Rita Barresi, Fumiaki Saito, Steven A Moore, Jason D Flanagan, Mark W Skwarchuk, Michael E Robbins, Jerry R Mendell,[...]. Cell 2002
204
7


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.