A citation-based method for searching scientific literature

Michael J Parsons, Isabel Campos, Elizabeth M A Hirst, Derek L Stemple. Development 2002
Times Cited: 124







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



Times Cited
  Times     Co-cited
Similarity


Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo.
David I Bassett, Robert J Bryson-Richardson, David F Daggett, Philippe Gautier, David G Keenan, Peter D Currie. Development 2003
172
40

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice.
R A Williamson, M D Henry, K J Daniels, R F Hrstka, J C Lee, Y Sunada, O Ibraghimov-Beskrovnaya, K P Campbell. Hum Mol Genet 1997
422
30

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.
Thomas E Hall, Robert J Bryson-Richardson, Silke Berger, Arie S Jacoby, Nicholas J Cole, Georgina E Hollway, Joachim Berger, Peter D Currie. Proc Natl Acad Sci U S A 2007
125
29


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
616
24

Dystroglycan: from biosynthesis to pathogenesis of human disease.
Rita Barresi, Kevin P Campbell. J Cell Sci 2006
395
22

The dystrophin associated protein complex in zebrafish.
J R Guyon, A N Mosley, Y Zhou, K F O'Brien, X Sheng, K Chiang, A J Davidson, J M Volinski, L I Zon, L M Kunkel. Hum Mol Genet 2003
78
26

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
21

Stages of embryonic development of the zebrafish.
C B Kimmel, W W Ballard, S R Kimmel, B Ullmann, T F Schilling. Dev Dyn 1995
21


Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.
Steven A Moore, Fumiaki Saito, Jianguo Chen, Daniel E Michele, Michael D Henry, Albee Messing, Ronald D Cohn, Susan E Ross-Barta, Steve Westra, Roger A Williamson,[...]. Nature 2002
424
20

Genes controlling and mediating locomotion behavior of the zebrafish embryo and larva.
M Granato, F J van Eeden, U Schach, T Trowe, M Brand, M Furutani-Seiki, P Haffter, M Hammerschmidt, C P Heisenberg, Y J Jiang,[...]. Development 1996
417
19

Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP).
Paul Thornhill, David Bassett, Hanns Lochmüller, Kate Bushby, Volker Straub. Brain 2008
53
35

Zebrafish mutants identify an essential role for laminins in notochord formation.
Michael J Parsons, Steven M Pollard, Leonor Saúde, Benjamin Feldman, Pedro Coutinho, Elizabeth M A Hirst, Derek L Stemple. Development 2002
173
18

Delta-sarcoglycan is required for early zebrafish muscle organization.
Jeffrey R Guyon, Alycia N Mosley, Susan J Jun, Federica Montanaro, Leta S Steffen, Yi Zhou, Vincenzo Nigro, Len I Zon, Louis M Kunkel. Exp Cell Res 2005
38
47

The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies.
Vandana Gupta, Genri Kawahara, Stacey R Gundry, Aye T Chen, Wayne I Lencer, Yi Zhou, Leonard I Zon, Louis M Kunkel, Alan H Beggs. Hum Mol Genet 2011
79
22

Zebrafish Fukutin family proteins link the unfolded protein response with dystroglycanopathies.
Yung-Yao Lin, Richard J White, Silvia Torelli, Sebahattin Cirak, Francesco Muntoni, Derek L Stemple. Hum Mol Genet 2011
59
30

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
A Yoshida, K Kobayashi, H Manya, K Taniguchi, H Kano, M Mizuno, T Inazu, H Mitsuhashi, S Takahashi, M Takeuchi,[...]. Dev Cell 2001
521
17

Modeling human muscle disease in zebrafish.
Jeffrey R Guyon, Leta S Steffen, Melanie H Howell, Timothy J Pusack, Christian Lawrence, Louis M Kunkel. Biochim Biophys Acta 2007
67
25

The zebrafish as a model for muscular dystrophy and congenital myopathy.
David I Bassett, Peter D Currie. Hum Mol Genet 2003
94
17

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
200
15

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
60
25

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
433
14

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.
Daniel Beltrán-Valero de Bernabé, Sophie Currier, Alice Steinbrecher, Jacopo Celli, Ellen van Beusekom, Bert van der Zwaag, Hülya Kayserili, Luciano Merlini, David Chitayat, William B Dobyns,[...]. Am J Hum Genet 2002
503
14

Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality.
Tobias Willer, Belén Prados, Juan Manuel Falcón-Pérez, Ingrid Renner-Müller, Gerhard K H Przemeck, Mark Lommel, Antonio Coloma, M Carmen Valero, Martin Hrabé de Angelis, Widmar Tanner,[...]. Proc Natl Acad Sci U S A 2004
114
14

A dystroglycan mutation associated with limb-girdle muscular dystrophy.
Yuji Hara, Burcu Balci-Hayta, Takako Yoshida-Moriguchi, Motoi Kanagawa, Daniel Beltrán-Valero de Bernabé, Hülya Gündeşli, Tobias Willer, Jakob S Satz, Robert W Crawford, Steven J Burden,[...]. N Engl J Med 2011
166
14

Biosynthesis of dystroglycan: processing of a precursor propeptide.
K H Holt, R H Crosbie, D P Venzke, K P Campbell. FEBS Lett 2000
135
13

POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome.
J van Reeuwijk, M Janssen, C van den Elzen, D Beltran-Valero de Bernabé, P Sabatelli, L Merlini, M Boon, H Scheffer, M Brockington, F Muntoni,[...]. J Med Genet 2005
291
13

Zebrafish orthologs of human muscular dystrophy genes.
Leta S Steffen, Jeffrey R Guyon, Emily D Vogel, Rosanna Beltre, Timothy J Pusack, Yi Zhou, Leonard I Zon, Louis M Kunkel. BMC Genomics 2007
47
27

Effective targeted gene 'knockdown' in zebrafish.
A Nasevicius, S C Ekker. Nat Genet 2000
12


Molecular basis of muscular dystrophies.
R D Cohn, K P Campbell. Muscle Nerve 2000
348
12

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.
K Kobayashi, Y Nakahori, M Miyake, K Matsumura, E Kondo-Iida, Y Nomura, M Segawa, M Yoshioka, K Saito, M Osawa,[...]. Nature 1998
600
12

Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor.
S H Gee, F Montanaro, M H Lindenbaum, S Carbonetto. Cell 1994
447
12


Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization.
O Ibraghimov-Beskrovnaya, A Milatovich, T Ozcelik, B Yang, K Koepnick, U Francke, K P Campbell. Hum Mol Genet 1993
204
11

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.
Rita Barresi, Daniel E Michele, Motoi Kanagawa, Hollie A Harper, Sherri A Dovico, Jakob S Satz, Steven A Moore, Wenli Zhang, Harry Schachter, Jan P Dumanski,[...]. Nat Med 2004
188
11


Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.
A Helbling-Leclerc, X Zhang, H Topaloglu, C Cruaud, F Tesson, J Weissenbach, F M Tomé, K Schwartz, M Fardeau, K Tryggvason. Nat Genet 1995
512
11


Activity and distribution of paxillin, focal adhesion kinase, and cadherin indicate cooperative roles during zebrafish morphogenesis.
Bryan D Crawford, Clarissa A Henry, Todd A Clason, Amanda L Becker, Merrill B Hille. Mol Biol Cell 2003
100
11

Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning.
Susan J Nixon, Jeremy Wegner, Charles Ferguson, Pierre-François Méry, John F Hancock, Peter D Currie, Brian Key, Monte Westerfield, Robert G Parton. Hum Mol Genet 2005
72
15

Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation.
Steven M Pollard, Michael J Parsons, Makoto Kamei, Ross N W Kettleborough, Kevin A Thomas, Van N Pham, Moon-Kyoung Bae, Annabelle Scott, Brant M Weinstein, Derek L Stemple. Dev Biol 2006
78
14

Identification of separate slow and fast muscle precursor cells in vivo, prior to somite formation.
S H Devoto, E Melançon, J S Eisen, M Westerfield. Development 1996
483
11

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.
Jeffrey R Guyon, Julie Goswami, Susan J Jun, Marielle Thorne, Melanie Howell, Timothy Pusack, Genri Kawahara, Leta S Steffen, Michal Galdzicki, Louis M Kunkel. Hum Mol Genet 2009
48
22

Genes required for functional glycosylation of dystroglycan are conserved in zebrafish.
Christopher J Moore, Huey Tse Goh, Jane E Hewitt. Genomics 2008
31
35

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan.
Tony Roscioli, Erik-Jan Kamsteeg, Karen Buysse, Isabelle Maystadt, Jeroen van Reeuwijk, Christa van den Elzen, Ellen van Beusekom, Moniek Riemersma, Rolph Pfundt, Lisenka E L M Vissers,[...]. Nat Genet 2012
139
11

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
Cheryl Longman, Martin Brockington, Silvia Torelli, Cecilia Jimenez-Mallebrera, Colin Kennedy, Nofal Khalil, Lucy Feng, Ravindra K Saran, Thomas Voit, Luciano Merlini,[...]. Hum Mol Genet 2003
304
10

Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity.
Hiroshi Manya, Atsuro Chiba, Aruto Yoshida, Xiaohui Wang, Yasunori Chiba, Yoshifumi Jigami, Richard U Margolis, Tamao Endo. Proc Natl Acad Sci U S A 2004
266
10

Molecular recognition by LARGE is essential for expression of functional dystroglycan.
Motoi Kanagawa, Fumiaki Saito, Stefan Kunz, Takako Yoshida-Moriguchi, Rita Barresi, Yvonne M Kobayashi, John Muschler, Jan P Dumanski, Daniel E Michele, Michael B A Oldstone,[...]. Cell 2004
196
10


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.