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47. Reorganization of inhibitory synapses and increased PSD length of perforated excitatory synapses in hippocampal area CA1 of dystrophin-deficient mdx mice. Miranda R; Sébrié C; Degrouard J; Gillet B; Jaillard D; Laroche S; Vaillend C Cereb Cortex; 2009 Apr; 19(4):876-88. PubMed ID: 18794205 [TBL] [Abstract][Full Text] [Related]
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49. Coisogenic all-plus-one immunization: a model for identifying missing proteins in null-mutant conditions. Antibodies to dystrophin in mdx mouse after transplantation of muscle from normal coisogenic donor. Bittner RE; Streubel B; Shorny S; Schaden G; Voit T; Höger H Neuropediatrics; 1994 Aug; 25(4):176-82. PubMed ID: 7824089 [TBL] [Abstract][Full Text] [Related]
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51. Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulation. Denetclaw WF; Hopf FW; Cox GA; Chamberlain JS; Steinhardt RA Mol Biol Cell; 1994 Oct; 5(10):1159-67. PubMed ID: 7865881 [TBL] [Abstract][Full Text] [Related]
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53. Reduced levels of dystrophin associated proteins in the brains of mice deficient for Dp71. Greenberg DS; Schatz Y; Levy Z; Pizzo P; Yaffe D; Nudel U Hum Mol Genet; 1996 Sep; 5(9):1299-303. PubMed ID: 8872469 [TBL] [Abstract][Full Text] [Related]
54. Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice. Rafael JA; Tinsley JM; Potter AC; Deconinck AE; Davies KE Nat Genet; 1998 May; 19(1):79-82. PubMed ID: 9590295 [TBL] [Abstract][Full Text] [Related]
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57. Is the normal content of sulfhydryl groups attributable to sparing from dystrophic pathology in dystrophin-deficient muscles? Niebrój-Dobosz I; Fidziańska A; Glinka Z; Hausmanowa-Petrusewicz I Folia Neuropathol; 2002; 40(3):143-50. PubMed ID: 12572920 [TBL] [Abstract][Full Text] [Related]
58. mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy. Pillers DA; Weleber RG; Woodward WR; Green DG; Chapman VM; Ray PN Invest Ophthalmol Vis Sci; 1995 Feb; 36(2):462-6. PubMed ID: 7843915 [TBL] [Abstract][Full Text] [Related]
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