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4. Duchenne muscular dystrophy progression induced by downhill running is accompanied by increased endomysial fibrosis and oxidative damage DNA in muscle of mdx mice. Lazzarin MC; Dos Santos JF; Quintana HT; Pidone FAM; de Oliveira F J Mol Histol; 2023 Feb; 54(1):41-54. PubMed ID: 36348131 [TBL] [Abstract][Full Text] [Related]
5. Heme Oxygenase-1 Influences Satellite Cells and Progression of Duchenne Muscular Dystrophy in Mice. Pietraszek-Gremplewicz K; Kozakowska M; Bronisz-Budzynska I; Ciesla M; Mucha O; Podkalicka P; Madej M; Glowniak U; Szade K; Stepniewski J; Jez M; Andrysiak K; Bukowska-Strakova K; Kaminska A; Kostera-Pruszczyk A; Jozkowicz A; Loboda A; Dulak J Antioxid Redox Signal; 2018 Jul; 29(2):128-148. PubMed ID: 29669436 [TBL] [Abstract][Full Text] [Related]
6. Increased plasma lipid levels exacerbate muscle pathology in the mdx mouse model of Duchenne muscular dystrophy. Milad N; White Z; Tehrani AY; Sellers S; Rossi FMV; Bernatchez P Skelet Muscle; 2017 Sep; 7(1):19. PubMed ID: 28899419 [TBL] [Abstract][Full Text] [Related]
7. Skeletal muscle fibrosis in the mdx/utrn+/- mouse validates its suitability as a murine model of Duchenne muscular dystrophy. Gutpell KM; Hrinivich WT; Hoffman LM PLoS One; 2015; 10(1):e0117306. PubMed ID: 25607927 [TBL] [Abstract][Full Text] [Related]
8. Phosphodiesterase 4 inhibitor and phosphodiesterase 5 inhibitor combination therapy has antifibrotic and anti-inflammatory effects in mdx mice with Duchenne muscular dystrophy. Nio Y; Tanaka M; Hirozane Y; Muraki Y; Okawara M; Hazama M; Matsuo T FASEB J; 2017 Dec; 31(12):5307-5320. PubMed ID: 28798156 [TBL] [Abstract][Full Text] [Related]
9. Assessing the Use of the sGC Stimulator BAY-747, as a Potential Treatment for Duchenne Muscular Dystrophy. Krishnan SM; Nordlohne J; Dietz L; Vakalopoulos A; Haning P; Hartmann E; Seifert R; Hüser J; Mathar I; Sandner P Int J Mol Sci; 2021 Jul; 22(15):. PubMed ID: 34360780 [TBL] [Abstract][Full Text] [Related]
10. Matrix metalloproteinase-9 inhibition ameliorates pathogenesis and improves skeletal muscle regeneration in muscular dystrophy. Li H; Mittal A; Makonchuk DY; Bhatnagar S; Kumar A Hum Mol Genet; 2009 Jul; 18(14):2584-98. PubMed ID: 19401296 [TBL] [Abstract][Full Text] [Related]
11. Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strains. van Putten M; Kumar D; Hulsker M; Hoogaars WM; Plomp JJ; van Opstal A; van Iterson M; Admiraal P; van Ommen GJ; 't Hoen PA; Aartsma-Rus A Neuromuscul Disord; 2012 May; 22(5):406-17. PubMed ID: 22284942 [TBL] [Abstract][Full Text] [Related]
12. Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin. Rooney JE; Welser JV; Dechert MA; Flintoff-Dye NL; Kaufman SJ; Burkin DJ J Cell Sci; 2006 Jun; 119(Pt 11):2185-95. PubMed ID: 16684813 [TBL] [Abstract][Full Text] [Related]
13. iNOS expression in dystrophinopathies can be reduced by somatic gene transfer of dystrophin or utrophin. Louboutin JP; Rouger K; Tinsley JM; Halldorson J; Wilson JM Mol Med; 2001 May; 7(5):355-64. PubMed ID: 11474581 [TBL] [Abstract][Full Text] [Related]
14. Photobiomodulation therapy protects skeletal muscle and improves muscular function of mdx mice in a dose-dependent manner through modulation of dystrophin. Albuquerque-Pontes GM; Casalechi HL; Tomazoni SS; Serra AJ; Ferreira CSB; Brito RBO; de Melo BL; Vanin AA; Monteiro KKDS; Dellê H; Frigo L; Marcos RL; de Carvalho PTC; Leal-Junior ECP Lasers Med Sci; 2018 May; 33(4):755-764. PubMed ID: 29209866 [TBL] [Abstract][Full Text] [Related]
15. Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis. Cea LA; Puebla C; Cisterna BA; Escamilla R; Vargas AA; Frank M; Martínez-Montero P; Prior C; Molano J; Esteban-Rodríguez I; Pascual I; Gallano P; Lorenzo G; Pian H; Barrio LC; Willecke K; Sáez JC Cell Mol Life Sci; 2016 Jul; 73(13):2583-99. PubMed ID: 26803842 [TBL] [Abstract][Full Text] [Related]
16. Cloning of cDNA encoding a regeneration-associated muscle protease whose expression is attenuated in cell lines derived from Duchenne muscular dystrophy patients. Nakayama Y; Nara N; Kawakita Y; Takeshima Y; Arakawa M; Katoh M; Morita S; Iwatsuki K; Tanaka K; Okamoto S; Kitamura T; Seki N; Matsuda R; Matsuo M; Saito K; Hara T Am J Pathol; 2004 May; 164(5):1773-82. PubMed ID: 15111323 [TBL] [Abstract][Full Text] [Related]
17. Deletion of Galgt2 (B4Galnt2) reduces muscle growth in response to acute injury and increases muscle inflammation and pathology in dystrophin-deficient mice. Xu R; Singhal N; Serinagaoglu Y; Chandrasekharan K; Joshi M; Bauer JA; Janssen PM; Martin PT Am J Pathol; 2015 Oct; 185(10):2668-84. PubMed ID: 26435413 [TBL] [Abstract][Full Text] [Related]
18. Presence of metalloproteinases 2 and 9 and 8-OHdG in the fibrotic process in skeletal muscle of Mdx mice. Souza LB; Maziero C; Lazzarin MC; Quintana HT; Tomé TC; Baptista VIA; de Oliveira F Acta Histochem; 2020 Jan; 122(1):151458. PubMed ID: 31699373 [TBL] [Abstract][Full Text] [Related]
19. Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD. Guiraud S; Edwards B; Squire SE; Moir L; Berg A; Babbs A; Ramadan N; Wood MJ; Davies KE Hum Mol Genet; 2019 Jan; 28(2):307-319. PubMed ID: 30304405 [TBL] [Abstract][Full Text] [Related]
20. Structural and Functional Alterations of Skeletal Muscle Microvasculature in Dystrophin-Deficient mdx Mice. Latroche C; Matot B; Martins-Bach A; Briand D; Chazaud B; Wary C; Carlier PG; Chrétien F; Jouvion G Am J Pathol; 2015 Sep; 185(9):2482-94. PubMed ID: 26193666 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]