Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy. [electronic resource]
Producer: 20141028Description: 618-36 p. digitalISSN:- 1460-2083
- Animals
- Diaphragm -- physiopathology
- Dystrophin -- genetics
- Gene Expression Regulation
- Humans
- Intracellular Signaling Peptides and Proteins -- genetics
- LIM Domain Proteins -- genetics
- Mice
- Mice, Inbred mdx
- Mice, Transgenic
- Muscle Contraction
- Muscle Proteins -- genetics
- Muscle, Skeletal -- physiopathology
- Muscular Dystrophy, Duchenne -- genetics
- NFATC Transcription Factors -- genetics
- Promoter Regions, Genetic
- Sarcolemma -- metabolism
- Signal Transduction
- Utrophin -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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