Additional file 5: Figure S5. Normal CNP levels in dystrophin-deficient oligodendrocytes. Western blot analysis of CNP protein in lysates obtained from differentiating oligodendrocytes at indicated days post-transfection with dystrophin (DMD) or control siRNA. Representative western blots are shown, including those for p115 as a loading control. CNP levels were similar in control and DMD siRNA transfected oligodendrocytes
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceThe intrinsic necrosis of skeletal muscles in animal models of Duchenne muscul...
Abstract Background In Duchenne muscular dystrophy (DMD), the loss of the dystrophin component of th...
Additional file 1: Figure S1. Genotyping. Genotyping of tail DNA from male mdx and female mdx/+ cont...
This study investigates changes with respect to increasing protein levels in dystrophic nerves of tw...
Duchenne muscular dystrophy is an X-linked disease characterized by progressive and lethal muscular ...
This study investigates changes with respect to increasing protein levels in dystrophic nerves of tw...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
Duchenne muscular dystrophy (DMD) is the second most commonly occurring genetically inherited diseas...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
Duchenne muscular dystrophy (DMD) is a common X-linked recessive neuromuscular disease due to altere...
International audienceThe intrinsic necrosis of skeletal muscles in animal models of Duchenne muscul...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceThe intrinsic necrosis of skeletal muscles in animal models of Duchenne muscul...
Abstract Background In Duchenne muscular dystrophy (DMD), the loss of the dystrophin component of th...
Additional file 1: Figure S1. Genotyping. Genotyping of tail DNA from male mdx and female mdx/+ cont...
This study investigates changes with respect to increasing protein levels in dystrophic nerves of tw...
Duchenne muscular dystrophy is an X-linked disease characterized by progressive and lethal muscular ...
This study investigates changes with respect to increasing protein levels in dystrophic nerves of tw...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
International audienceDuchenne muscular dystrophy is an X-linked disease characterized by progressiv...
Duchenne muscular dystrophy (DMD) is the second most commonly occurring genetically inherited diseas...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
Duchenne muscular dystrophy (DMD) is a common X-linked recessive neuromuscular disease due to altere...
International audienceThe intrinsic necrosis of skeletal muscles in animal models of Duchenne muscul...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceMyotonic dystrophy type 1 (DM1) is a trinucleotide repeat expansion disorder t...
International audienceThe intrinsic necrosis of skeletal muscles in animal models of Duchenne muscul...