Additional file 1: Figure S1. Genotyping. Genotyping of tail DNA from male mdx and female mdx/+ control mice using a primer competition PCR as described in Shin et al. [30]. Arrows denote the typical products used to identify mdx/+Â females and mdx males
Although muscular dystrophies are among the most common human genetic disorders, there are few treat...
Duchenne muscular dystrophy is an X-linked disease characterized by progressive and lethal muscular ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Additional file 5: Figure S5. Normal CNP levels in dystrophin-deficient oligodendrocytes. Western bl...
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy...
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy...
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy...
Duchenne muscular dystrophy (DMD) is a severe, progressive neuromuscular disorder caused by reading ...
Genetic background significantly affects phenotype in multiple mouse models of human diseases, inclu...
Genetic background significantly affects phenotype in multiple mouse models of human diseases, inclu...
Additional file 15: Table S8. (A) Features of large differentially methylated blocks in germ cells. ...
Genetic background significantly affects phenotype in multiple mouse models of human diseases, inclu...
Abstract Background In Duchenne muscular dystrophy (DMD), the loss of the dystrophin component of th...
Duchenne muscular dystrophy (DMD) is a severe muscle-wasting disease generally caused by reading fra...
Duchenne muscular dystrophy (DMD) is a severe, progressive neuromuscular disorder caused by reading ...
Although muscular dystrophies are among the most common human genetic disorders, there are few treat...
Duchenne muscular dystrophy is an X-linked disease characterized by progressive and lethal muscular ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Additional file 5: Figure S5. Normal CNP levels in dystrophin-deficient oligodendrocytes. Western bl...
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy...
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy...
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy...
Duchenne muscular dystrophy (DMD) is a severe, progressive neuromuscular disorder caused by reading ...
Genetic background significantly affects phenotype in multiple mouse models of human diseases, inclu...
Genetic background significantly affects phenotype in multiple mouse models of human diseases, inclu...
Additional file 15: Table S8. (A) Features of large differentially methylated blocks in germ cells. ...
Genetic background significantly affects phenotype in multiple mouse models of human diseases, inclu...
Abstract Background In Duchenne muscular dystrophy (DMD), the loss of the dystrophin component of th...
Duchenne muscular dystrophy (DMD) is a severe muscle-wasting disease generally caused by reading fra...
Duchenne muscular dystrophy (DMD) is a severe, progressive neuromuscular disorder caused by reading ...
Although muscular dystrophies are among the most common human genetic disorders, there are few treat...
Duchenne muscular dystrophy is an X-linked disease characterized by progressive and lethal muscular ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
DOI
Add to ORKG