A citation-based method for searching scientific literature

Johan Holmberg, Madeleine Durbeej. Cell Adh Migr 2013
Times Cited: 70







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



Times Cited
  Times     Co-cited
Similarity


Laminins.
Madeleine Durbeej. Cell Tissue Res 2010
289
15

Laminins in basement membrane assembly.
Erhard Hohenester, Peter D Yurchenco. Cell Adh Migr 2013
222
15

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
509
15

Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.
Kinga I Gawlik, Madeleine Durbeej. Skelet Muscle 2011
72
12



Absence of integrin alpha 7 causes a novel form of muscular dystrophy.
U Mayer, G Saher, R Fässler, A Bornemann, F Echtermeyer, H von der Mark, N Miosge, E Pöschl, K von der Mark. Nat Genet 1997
342
11

Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.
Y Miyagoe, K Hanaoka, I Nonaka, M Hayasaka, Y Nabeshima, K Arahata, Y Nabeshima, S Takeda. FEBS Lett 1997
202
11

The laminin family.
Monique Aumailley. Cell Adh Migr 2013
158
10

Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy.
Jachinta E Rooney, Jolie R Knapp, Bradley L Hodges, Ryan D Wuebbles, Dean J Burkin. Am J Pathol 2012
67
10

The alpha7beta1 integrin in muscle development and disease.
D J Burkin, S J Kaufman. Cell Tissue Res 1999
205
10


Structure and function of the skeletal muscle extracellular matrix.
Allison R Gillies, Richard L Lieber. Muscle Nerve 2011
405
10

Satellite cells and the muscle stem cell niche.
Hang Yin, Feodor Price, Michael A Rudnicki. Physiol Rev 2013
899
10



Laminin-111 restores regenerative capacity in a mouse model for alpha7 integrin congenital myopathy.
Jachinta E Rooney, Praveen B Gurpur, Zipora Yablonka-Reuveni, Dean J Burkin. Am J Pathol 2009
55
10

A simplified laminin nomenclature.
Monique Aumailley, Leena Bruckner-Tuderman, William G Carter, Rainer Deutzmann, David Edgar, Peter Ekblom, Jürgen Engel, Eva Engvall, Erhard Hohenester, Jonathan C R Jones,[...]. Matrix Biol 2005
558
8

Merosin, a tissue-specific basement membrane protein, is a laminin-like protein.
K Ehrig, I Leivo, W S Argraves, E Ruoslahti, E Engvall. Proc Natl Acad Sci U S A 1990
387
8


Matrix elasticity directs stem cell lineage specification.
Adam J Engler, Shamik Sen, H Lee Sweeney, Dennis E Discher. Cell 2006
8


Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.
W Kuang, H Xu, P H Vachon, L Liu, F Loechel, U M Wewer, E Engvall. J Clin Invest 1998
152
8

Form and function: the laminin family of heterotrimers.
H Colognato, P D Yurchenco. Dev Dyn 2000
884
8

Expression and function of laminins in the embryonic and mature vasculature.
Rupert Hallmann, Nathalie Horn, Manuel Selg, Olaf Wendler, Friederike Pausch, Lydia M Sorokin. Physiol Rev 2005
335
7

Laminin isoforms in endothelial and perivascular basement membranes.
Lema F Yousif, Jacopo Di Russo, Lydia Sorokin. Cell Adh Migr 2013
121
7

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
7

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.
K J Jones, G Morgan, H Johnston, V Tobias, R A Ouvrier, I Wilkinson, K N North. J Med Genet 2001
103
7

Mutations in the integrin alpha7 gene cause congenital myopathy.
Y K Hayashi, F L Chou, E Engvall, M Ogawa, C Matsuda, S Hirabayashi, K Yokochi, B L Ziober, R H Kramer, S J Kaufman,[...]. Nat Genet 1998
270
7

Fibronectin regulates Wnt7a signaling and satellite cell expansion.
C Florian Bentzinger, Yu Xin Wang, Julia von Maltzahn, Vahab D Soleimani, Hang Yin, Michael A Rudnicki. Cell Stem Cell 2013
187
7

Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy.
Thomas Mehuron, Ajay Kumar, Lina Duarte, Jenny Yamauchi, Anthony Accorsi, Mahasweta Girgenrath. Skelet Muscle 2014
20
25

Laminin functions in tissue morphogenesis.
Jeffrey H Miner, Peter D Yurchenco. Annu Rev Cell Dev Biol 2004
488
7






Functional diversity of laminins.
Anna Domogatskaya, Sergey Rodin, Karl Tryggvason. Annu Rev Cell Dev Biol 2012
184
7

The extracellular matrix protein laminin α2 regulates the maturation and function of the blood-brain barrier.
Michael J Menezes, Freyja K McClenahan, Cindy V Leiton, Azeez Aranmolate, Xiwei Shan, Holly Colognato. J Neurosci 2014
105
7


Losartan, a therapeutic candidate in congenital muscular dystrophy: studies in the dy(2J) /dy(2J) mouse.
Moran Elbaz, Nurit Yanay, Shlomit Aga-Mizrachi, Zivia Brunschwig, Ibaa Kassis, Keren Ettinger, Vivian Barak, Yoram Nevo. Ann Neurol 2012
53
9

Satellite cell of skeletal muscle fibers.
A MAURO. J Biophys Biochem Cytol 1961
7

Extracellular matrix regulation in the muscle satellite cell niche.
Kelsey Thomas, Adam J Engler, Gretchen A Meyer. Connect Tissue Res 2015
84
7

Expression and distribution of laminin alpha1 and alpha2 chains in embryonic and adult mouse tissues: an immunochemical approach.
Takako Sasaki, Richard Giltay, Ulrika Talts, Rupert Timpl, Jan F Talts. Exp Cell Res 2002
85
7

Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies.
Peter D Yurchenco, Karen K McKee, Judith R Reinhard, Markus A Rüegg. Matrix Biol 2018
41
12

Extracellular matrix-driven congenital muscular dystrophies.
Payam Mohassel, A Reghan Foley, Carsten G Bönnemann. Matrix Biol 2018
24
20

Protein composition and biomechanical properties of in vivo-derived basement membranes.
Willi Halfter, Joseph Candiello, Haiyu Hu, Peng Zhang, Emanuel Schreiber, Manimalha Balasubramani. Cell Adh Migr 2013
51
7


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
5



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.