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.
53 related articles for article (PubMed ID: 7261505)
1. [Methylamino acid residues of proteins in atrophic skeletal muscle (author's transl)]. Inoue R Rinsho Shinkeigaku; 1981 Mar; 21(3):213-7. PubMed ID: 7261505 [No Abstract] [Full Text] [Related]
2. [The amino acid composition of the myosin and actin of the muscles of animals with hereditary myopathies]. Badalian LO; Bondarenko ES; Gusev EI; Lukoianov IuE; Revich GG; Temin PA; Sharets IuD Biull Eksp Biol Med; 1970 Feb; 69(2):112-4. PubMed ID: 5424226 [No Abstract] [Full Text] [Related]
3. [Proceedings: 230. Creatine metabolism in skeletal muscle of dystrophic mouse (author's transl)]. Yasuda T; Tsuji S Nihon Seirigaku Zasshi; 1973; 35(8):479. PubMed ID: 4799842 [No Abstract] [Full Text] [Related]
4. Observation on incorporation of 3H-taurine in mouse skeletal muscle cells by light and electron microscopic radioautography. Terauchi A; Nagata T Cell Mol Biol (Noisy-le-grand); 1993 Jun; 39(4):397-404. PubMed ID: 8329980 [TBL] [Abstract][Full Text] [Related]
6. The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titin. Garvey SM; Rajan C; Lerner AP; Frankel WN; Cox GA Genomics; 2002 Feb; 79(2):146-9. PubMed ID: 11829483 [TBL] [Abstract][Full Text] [Related]
7. Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro. Kramerova I; Kudryashova E; Tidball JG; Spencer MJ Hum Mol Genet; 2004 Jul; 13(13):1373-88. PubMed ID: 15138196 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy model. Torrente Y; Camirand G; Pisati F; Belicchi M; Rossi B; Colombo F; El Fahime M; Caron NJ; Issekutz AC; Constantin G; Tremblay JP; Bresolin N J Cell Biol; 2003 Aug; 162(3):511-20. PubMed ID: 12885758 [TBL] [Abstract][Full Text] [Related]
10. Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Bittner RE; Anderson LV; Burkhardt E; Bashir R; Vafiadaki E; Ivanova S; Raffelsberger T; Maerk I; Höger H; Jung M; Karbasiyan M; Storch M; Lassmann H; Moss JA; Davison K; Harrison R; Bushby KM; Reis A Nat Genet; 1999 Oct; 23(2):141-2. PubMed ID: 10508505 [No Abstract] [Full Text] [Related]
12. Extracts from mdx and normal mouse skeletal muscle contain similar levels of mitogenic activity for myoblasts. Chen G; Bressler BH; Quinn LS Cell Biol Int; 1994 Apr; 18(4):229-35. PubMed ID: 8044140 [TBL] [Abstract][Full Text] [Related]
13. Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles. Vilquin JT; Guérette B; Puymirat J; Yaffe D; Tomé FM; Fardeau M; Fiszman M; Schwartz K; Tremblay JP Gene Ther; 1999 May; 6(5):792-800. PubMed ID: 10505103 [TBL] [Abstract][Full Text] [Related]
14. Induction of dystrophin-associated proteins together with nicotinic acetylcholine receptors by denervation in the absence of dystrophin in skeletal muscles of mdx mice. Mitsui T; Kawai H; Kawajiri M; Kunishige M; Aki K; Saito S Biochem Biophys Res Commun; 1996 Jul; 224(3):802-7. PubMed ID: 8713126 [TBL] [Abstract][Full Text] [Related]
15. Distribution and toxicity of alpha-amino-beta-methylaminopropionic acid. Polsky FI; Nunn PB; Bell EA Fed Proc; 1972; 31(5):1473-5. PubMed ID: 5056173 [No Abstract] [Full Text] [Related]
16. Platelet-derived growth factor and its receptors are related to the progression of human muscular dystrophy: an immunohistochemical study. Zhao Y; Haginoya K; Sun G; Dai H; Onuma A; Iinuma K J Pathol; 2003 Sep; 201(1):149-59. PubMed ID: 12950028 [TBL] [Abstract][Full Text] [Related]
17. [Information exchange on animal models for human diseases (author's transl)]. Jikken Dobutsu; 1975 Apr; 24(2):61-2. PubMed ID: 1171768 [No Abstract] [Full Text] [Related]
18. Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy. Saito F; Blank M; Schröder J; Manya H; Shimizu T; Campbell KP; Endo T; Mizutani M; Kröger S; Matsumura K FEBS Lett; 2005 Apr; 579(11):2359-63. PubMed ID: 15848172 [TBL] [Abstract][Full Text] [Related]
19. Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ). Fukushima K; Nakamura A; Ueda H; Yuasa K; Yoshida K; Takeda S; Ikeda S BMC Musculoskelet Disord; 2007 Jun; 8():54. PubMed ID: 17598883 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]