These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
274 related articles for article (PubMed ID: 9710454)
1. Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models. Kuang W; Xu H; Vachon PH; Liu L; Loechel F; Wewer UM; Engvall E J Clin Invest; 1998 Aug; 102(4):844-52. PubMed ID: 9710454 [TBL] [Abstract][Full Text] [Related]
2. Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy. Vachon PH; Xu H; Liu L; Loechel F; Hayashi Y; Arahata K; Reed JC; Wewer UM; Engvall E J Clin Invest; 1997 Oct; 100(7):1870-81. PubMed ID: 9312189 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy. Pasteuning-Vuhman S; Putker K; Tanganyika-de Winter CL; Boertje-van der Meulen JW; van Vliet L; Overzier M; Plomp JJ; Aartsma-Rus A; van Putten M PLoS One; 2018; 13(5):e0197388. PubMed ID: 29763467 [TBL] [Abstract][Full Text] [Related]
8. Merosin (laminin-2) localization in basal lamina of normal skeletal muscle fibers and changes in plasma membrane of merosin-deficient skeletal muscle fibers. Shibuya S; Wakayama Y; Inoue M; Kojima H; Oniki H Med Electron Microsc; 2003 Dec; 36(4):213-20. PubMed ID: 16228654 [TBL] [Abstract][Full Text] [Related]
16. Merosin and congenital muscular dystrophy. Miyagoe-Suzuki Y; Nakagawa M; Takeda S Microsc Res Tech; 2000 Feb 1-15; 48(3-4):181-91. PubMed ID: 10679965 [TBL] [Abstract][Full Text] [Related]
17. 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. Doe JA; Wuebbles RD; Allred ET; Rooney JE; Elorza M; Burkin DJ J Cell Sci; 2011 Jul; 124(Pt 13):2287-97. PubMed ID: 21652631 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. Sunada Y; Bernier SM; Kozak CA; Yamada Y; Campbell KP J Biol Chem; 1994 May; 269(19):13729-32. PubMed ID: 8188645 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]