432 related articles for article (PubMed ID: 17438294)
1. The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.
Hall TE; Bryson-Richardson RJ; Berger S; Jacoby AS; Cole NJ; Hollway GE; Berger J; Currie PD
Proc Natl Acad Sci U S A; 2007 Apr; 104(17):7092-7. PubMed ID: 17438294
[TBL] [Abstract][Full Text] [Related]
2. Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.
Sztal TE; Sonntag C; Hall TE; Currie PD
Hum Mol Genet; 2012 Nov; 21(21):4718-31. PubMed ID: 22859503
[TBL] [Abstract][Full Text] [Related]
3. A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination.
Patton BL; Wang B; Tarumi YS; Seburn KL; Burgess RW
J Cell Sci; 2008 May; 121(Pt 10):1593-604. PubMed ID: 18430779
[TBL] [Abstract][Full Text] [Related]
4. A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish.
Gupta VA; Kawahara G; Myers JA; Chen AT; Hall TE; Manzini MC; Currie PD; Zhou Y; Zon LI; Kunkel LM; Beggs AH
PLoS One; 2012; 7(8):e43794. PubMed ID: 22952766
[TBL] [Abstract][Full Text] [Related]
5. Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice.
Ringelmann B; Röder C; Hallmann R; Maley M; Davies M; Grounds M; Sorokin L
Exp Cell Res; 1999 Jan; 246(1):165-82. PubMed ID: 9882526
[TBL] [Abstract][Full Text] [Related]
6. Current understanding and treatment of cardiac and skeletal muscle pathology in laminin-α2 chain-deficient congenital muscular dystrophy.
Nguyen Q; Lim KRQ; Yokota T
Appl Clin Genet; 2019; 12():113-130. PubMed ID: 31308722
[TBL] [Abstract][Full Text] [Related]
7. The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment.
Jacoby AS; Busch-Nentwich E; Bryson-Richardson RJ; Hall TE; Berger J; Berger S; Sonntag C; Sachs C; Geisler R; Stemple DL; Currie PD
Development; 2009 Oct; 136(19):3367-76. PubMed ID: 19736328
[TBL] [Abstract][Full Text] [Related]
8. Activation of the lama2 gene in muscle regeneration: abortive regeneration in laminin alpha2-deficiency.
Kuang W; Xu H; Vilquin JT; Engvall E
Lab Invest; 1999 Dec; 79(12):1601-13. PubMed ID: 10616210
[TBL] [Abstract][Full Text] [Related]
9. Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy.
Homma S; Beermann ML; Miller JB
Hum Mol Genet; 2011 Jul; 20(13):2662-72. PubMed ID: 21505075
[TBL] [Abstract][Full Text] [Related]
10. Synaptic plasticity in the dy2J mouse model of laminin alpha2-deficient congenital muscular dystrophy.
Anderson JL; Head SI; Morley JW
Brain Res; 2005 Apr; 1042(1):23-8. PubMed ID: 15823249
[TBL] [Abstract][Full Text] [Related]
11. Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle.
Cohn RD; Mayer U; Saher G; Herrmann R; van der Flier A; Sonnenberg A; Sorokin L; Voit T
J Neurol Sci; 1999 Mar; 163(2):140-52. PubMed ID: 10371075
[TBL] [Abstract][Full Text] [Related]
12. A Low-Cost Pulse Generator for Exacerbating Muscle Fiber Detachment Phenotypes in Zebrafish.
Thomasi ABD; Sonntag C; Pires DF; Zuidema D; Benci A; Currie PD; Wood AJ
Zebrafish; 2018 Aug; 15(4):420-424. PubMed ID: 29381425
[TBL] [Abstract][Full Text] [Related]
13. An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.
Moll J; Barzaghi P; Lin S; Bezakova G; Lochmüller H; Engvall E; Müller U; Ruegg MA
Nature; 2001 Sep; 413(6853):302-7. PubMed ID: 11565031
[TBL] [Abstract][Full Text] [Related]
14. Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubes.
Allamand V; Bidou L; Arakawa M; Floquet C; Shiozuka M; Paturneau-Jouas M; Gartioux C; Butler-Browne GS; Mouly V; Rousset JP; Matsuda R; Ikeda D; Guicheney P
J Gene Med; 2008 Feb; 10(2):217-24. PubMed ID: 18074402
[TBL] [Abstract][Full Text] [Related]
15. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
Taniguchi M; Kurahashi H; Noguchi S; Sese J; Okinaga T; Tsukahara T; Guicheney P; Ozono K; Nishino I; Morishita S; Toda T
Biochem Biophys Res Commun; 2006 Apr; 342(2):489-502. PubMed ID: 16487936
[TBL] [Abstract][Full Text] [Related]
16. Bortezomib partially improves laminin α2 chain-deficient muscular dystrophy.
Körner Z; Fontes-Oliveira CC; Holmberg J; Carmignac V; Durbeej M
Am J Pathol; 2014 May; 184(5):1518-28. PubMed ID: 24631023
[TBL] [Abstract][Full Text] [Related]
17. Knockdown of col22a1 gene in zebrafish induces a muscular dystrophy by disruption of the myotendinous junction.
Charvet B; Guiraud A; Malbouyres M; Zwolanek D; Guillon E; Bretaud S; Monnot C; Schulze J; Bader HL; Allard B; Koch M; Ruggiero F
Development; 2013 Nov; 140(22):4602-13. PubMed ID: 24131632
[TBL] [Abstract][Full Text] [Related]
18. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin).
Allamand V; Guicheney P
Eur J Hum Genet; 2002 Feb; 10(2):91-4. PubMed ID: 11938437
[TBL] [Abstract][Full Text] [Related]
19. Analysing regenerative potential in zebrafish models of congenital muscular dystrophy.
Wood AJ; Currie PD
Int J Biochem Cell Biol; 2014 Nov; 56():30-7. PubMed ID: 25449259
[TBL] [Abstract][Full Text] [Related]
20. Overexpression of mini-agrin in skeletal muscle increases muscle integrity and regenerative capacity in laminin-alpha2-deficient mice.
Bentzinger CF; Barzaghi P; Lin S; Ruegg MA
FASEB J; 2005 Jun; 19(8):934-42. PubMed ID: 15923403
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
