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
Times Cited: 515
Times Cited: 515
Times Cited
Times Co-cited
Similarity
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations.
Fatemeh Geranmayeh, Emma Clement, Lucy H Feng, Caroline Sewry, Judith Pagan, Rachael Mein, Stephen Abbs, Louise Brueton, Anne-Marie Childs, Heinz Jungbluth,[...]. Neuromuscul Disord 2010
Fatemeh Geranmayeh, Emma Clement, Lucy H Feng, Caroline Sewry, Judith Pagan, Rachael Mein, Stephen Abbs, Louise Brueton, Anne-Marie Childs, Heinz Jungbluth,[...]. Neuromuscul Disord 2010
22
Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin).
Valérie Allamand, Pascale Guicheney. Eur J Hum Genet 2002
Valérie Allamand, Pascale Guicheney. Eur J Hum Genet 2002
22
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.
J M Ervasti, K P Campbell. J Cell Biol 1993
J M Ervasti, K P Campbell. J Cell Biol 1993
17
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
K J Jones, G Morgan, H Johnston, V Tobias, R A Ouvrier, I Wilkinson, K N North. J Med Genet 2001
17
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
16
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
Jachinta E Rooney, Jolie R Knapp, Bradley L Hodges, Ryan D Wuebbles, Dean J Burkin. Am J Pathol 2012
23
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
Y Miyagoe, K Hanaoka, I Nonaka, M Hayasaka, Y Nabeshima, K Arahata, Y Nabeshima, S Takeda. FEBS Lett 1997
16
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.
Kinga I Gawlik, Madeleine Durbeej. Skelet Muscle 2011
Kinga I Gawlik, Madeleine Durbeej. Skelet Muscle 2011
20
Congenital muscular dystrophy with merosin deficiency.
F M Tomé, T Evangelista, A Leclerc, Y Sunada, E Manole, B Estournet, A Barois, K P Campbell, M Fardeau. C R Acad Sci III 1994
F M Tomé, T Evangelista, A Leclerc, Y Sunada, E Manole, B Estournet, A Barois, K P Campbell, M Fardeau. C R Acad Sci III 1994
14
Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy.
P H Vachon, H Xu, L Liu, F Loechel, Y Hayashi, K Arahata, J C Reed, U M Wewer, E Engvall. J Clin Invest 1997
P H Vachon, H Xu, L Liu, F Loechel, Y Hayashi, K Arahata, J C Reed, U M Wewer, E Engvall. J Clin Invest 1997
14
LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients.
J Oliveira, R Santos, I Soares-Silva, P Jorge, E Vieira, M E Oliveira, A Moreira, T Coelho, J C Ferreira, M J Fonseca,[...]. Clin Genet 2008
J Oliveira, R Santos, I Soares-Silva, P Jorge, E Vieira, M E Oliveira, A Moreira, T Coelho, J C Ferreira, M J Fonseca,[...]. Clin Genet 2008
38
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
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
13
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
13
Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice.
B L Patton, J H Miner, A Y Chiu, J R Sanes. J Cell Biol 1997
B L Patton, J H Miner, A Y Chiu, J R Sanes. J Cell Biol 1997
13
Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency.
Michael Erb, Sarina Meinen, Patrizia Barzaghi, Lazar T Sumanovski, Isabelle Courdier-Früh, Markus A Rüegg, Thomas Meier. J Pharmacol Exp Ther 2009
Michael Erb, Sarina Meinen, Patrizia Barzaghi, Lazar T Sumanovski, Isabelle Courdier-Früh, Markus A Rüegg, Thomas Meier. J Pharmacol Exp Ther 2009
20
16
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
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
13
Diagnostic approach to the congenital muscular dystrophies.
Carsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, Nicolas Deconinck, Enrico Bertini, Ana Ferreiro, Francesco Muntoni, Caroline Sewry, Christophe Béroud, Katherine D Mathews,[...]. Neuromuscul Disord 2014
Carsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, Nicolas Deconinck, Enrico Bertini, Ana Ferreiro, Francesco Muntoni, Caroline Sewry, Christophe Béroud, Katherine D Mathews,[...]. Neuromuscul Disord 2014
13
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
W Kuang, H Xu, P H Vachon, L Liu, F Loechel, U M Wewer, E Engvall. J Clin Invest 1998
12
Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.
Virginie Carmignac, Martina Svensson, Zandra Körner, Linda Elowsson, Cintia Matsumura, Kinga I Gawlik, Valerie Allamand, Madeleine Durbeej. Hum Mol Genet 2011
Virginie Carmignac, Martina Svensson, Zandra Körner, Linda Elowsson, Cintia Matsumura, Kinga I Gawlik, Valerie Allamand, Madeleine Durbeej. Hum Mol Genet 2011
13
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
K Ehrig, I Leivo, W S Argraves, E Ruoslahti, E Engvall. Proc Natl Acad Sci U S A 1990
12
An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.
J Moll, P Barzaghi, S Lin, G Bezakova, H Lochmüller, E Engvall, U Müller, M A Ruegg. Nature 2001
J Moll, P Barzaghi, S Lin, G Bezakova, H Lochmüller, E Engvall, U Müller, M A Ruegg. Nature 2001
12
Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice.
Kinga Gawlik, Yuko Miyagoe-Suzuki, Peter Ekblom, Shin'ichi Takeda, Madeleine Durbeej. Hum Mol Genet 2004
Kinga Gawlik, Yuko Miyagoe-Suzuki, Peter Ekblom, Shin'ichi Takeda, Madeleine Durbeej. Hum Mol Genet 2004
12
Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene.
H Xu, X R Wu, U M Wewer, E Engvall. Nat Genet 1994
H Xu, X R Wu, U M Wewer, E Engvall. Nat Genet 1994
11
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
Peter D Yurchenco, Karen K McKee, Judith R Reinhard, Markus A Rüegg. Matrix Biol 2018
22
Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins.
J F Talts, Z Andac, W Göhring, A Brancaccio, R Timpl. EMBO J 1999
J F Talts, Z Andac, W Göhring, A Brancaccio, R Timpl. EMBO J 1999
10
Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan.
Renzhi Han, Motoi Kanagawa, Takako Yoshida-Moriguchi, Erik P Rader, Rainer A Ng, Daniel E Michele, David E Muirhead, Stefan Kunz, Steven A Moore, Susan T Iannaccone,[...]. Proc Natl Acad Sci U S A 2009
Renzhi Han, Motoi Kanagawa, Takako Yoshida-Moriguchi, Erik P Rader, Rainer A Ng, Daniel E Michele, David E Muirhead, Stefan Kunz, Steven A Moore, Susan T Iannaccone,[...]. Proc Natl Acad Sci U S A 2009
10
Activation of the lama2 gene in muscle regeneration: abortive regeneration in laminin alpha2-deficiency.
W Kuang, H Xu, J T Vilquin, E Engvall. Lab Invest 1999
W Kuang, H Xu, J T Vilquin, E Engvall. Lab Invest 1999
16
Pathology is alleviated by doxycycline in a laminin-alpha2-null model of congenital muscular dystrophy.
Mahasweta Girgenrath, Mary Lou Beermann, Vivek K Vishnudas, Sachiko Homma, Jeffrey Boone Miller. Ann Neurol 2009
Mahasweta Girgenrath, Mary Lou Beermann, Vivek K Vishnudas, Sachiko Homma, Jeffrey Boone Miller. Ann Neurol 2009
15
Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy.
Mahasweta Girgenrath, Janice A Dominov, Christine A Kostek, Jeffrey Boone Miller. J Clin Invest 2004
Mahasweta Girgenrath, Janice A Dominov, Christine A Kostek, Jeffrey Boone Miller. J Clin Invest 2004
10
Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice.
Virginie Carmignac, Ronan Quéré, Madeleine Durbeej. Hum Mol Genet 2011
Virginie Carmignac, Ronan Quéré, Madeleine Durbeej. Hum Mol Genet 2011
20
Laminin alpha1 chain mediated reduction of laminin alpha2 chain deficient muscular dystrophy involves integrin alpha7beta1 and dystroglycan.
Kinga I Gawlik, Ulrike Mayer, Kristina Blomberg, Arnoud Sonnenberg, Peter Ekblom, Madeleine Durbeej. FEBS Lett 2006
Kinga I Gawlik, Ulrike Mayer, Kristina Blomberg, Arnoud Sonnenberg, Peter Ekblom, Madeleine Durbeej. FEBS Lett 2006
21
The congenital muscular dystrophies in 2004: a century of exciting progress.
Francesco Muntoni, Thomas Voit. Neuromuscul Disord 2004
Francesco Muntoni, Thomas Voit. Neuromuscul Disord 2004
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
Jachinta E Rooney, Praveen B Gurpur, Zipora Yablonka-Reuveni, Dean J Burkin. Am J Pathol 2009
17
Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.
J Philpot, F Cowan, J Pennock, C Sewry, V Dubowitz, G Bydder, F Muntoni. Neuromuscul Disord 1999
J Philpot, F Cowan, J Pennock, C Sewry, V Dubowitz, G Bydder, F Muntoni. Neuromuscul Disord 1999
11
Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.
Tamar E Sztal, Carmen Sonntag, Thomas E Hall, Peter D Currie. Hum Mol Genet 2012
Tamar E Sztal, Carmen Sonntag, Thomas E Hall, Peter D Currie. Hum Mol Genet 2012
26
Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development.
I Leivo, E Engvall. Proc Natl Acad Sci U S A 1988
I Leivo, E Engvall. Proc Natl Acad Sci U S A 1988
10
Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients.
H Xiong, D Tan, S Wang, S Song, H Yang, K Gao, A Liu, H Jiao, B Mao, J Ding,[...]. Clin Genet 2015
H Xiong, D Tan, S Wang, S Song, H Yang, K Gao, A Liu, H Jiao, B Mao, J Ding,[...]. Clin Genet 2015
30
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
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
10
Apoptosis inhibitors and mini-agrin have additive benefits in congenital muscular dystrophy mice.
Sarina Meinen, Shuo Lin, Raphael Thurnherr, Michael Erb, Thomas Meier, Markus A Rüegg. EMBO Mol Med 2011
Sarina Meinen, Shuo Lin, Raphael Thurnherr, Michael Erb, Thomas Meier, Markus A Rüegg. EMBO Mol Med 2011
25
Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy.
M L Mostacciuolo, M Miorin, F Martinello, C Angelini, P Perini, C P Trevisan. Hum Genet 1996
M L Mostacciuolo, M Miorin, F Martinello, C Angelini, P Perini, C P Trevisan. Hum Genet 1996
12
Transgenic overexpression of the α7 integrin reduces muscle pathology and improves viability in the dy(W) mouse model of merosin-deficient congenital muscular dystrophy type 1A.
Jinger A Doe, Ryan D Wuebbles, Erika T Allred, Jachinta E Rooney, Margaret Elorza, Dean J Burkin. J Cell Sci 2011
Jinger A Doe, Ryan D Wuebbles, Erika T Allred, Jachinta E Rooney, Margaret Elorza, Dean J Burkin. J Cell Sci 2011
25
The ever-expanding spectrum of congenital muscular dystrophies.
Eugenio Mercuri, Francesco Muntoni. Ann Neurol 2012
Eugenio Mercuri, Francesco Muntoni. Ann Neurol 2012
14
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
V Nigro, E de Sá Moreira, G Piluso, M Vainzof, A Belsito, L Politano, A A Puca, M R Passos-Bueno, M Zatz. Nat Genet 1996
V Nigro, E de Sá Moreira, G Piluso, M Vainzof, A Belsito, L Politano, A A Puca, M R Passos-Bueno, M Zatz. Nat Genet 1996
9
Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle.
K Matsumura, J M Ervasti, K Ohlendieck, S D Kahl, K P Campbell. Nature 1992
K Matsumura, J M Ervasti, K Ohlendieck, S D Kahl, K P Campbell. Nature 1992
9
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
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
9
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
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
9
Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophies.
B L Hodges, Y K Hayashi, I Nonaka, W Wang, K Arahata, S J Kaufman. J Cell Sci 1997
B L Hodges, Y K Hayashi, I Nonaka, W Wang, K Arahata, S J Kaufman. J Cell Sci 1997
8
Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.
V Straub, J A Rafael, J S Chamberlain, K P Campbell. J Cell Biol 1997
V Straub, J A Rafael, J S Chamberlain, K P Campbell. J Cell Biol 1997
8
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.