D'Arcy, Colleen E <br/><br/>
Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy.  [electronic resource] 

 -  Human molecular genetics  Feb 2014 
 - 618-36 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddt449  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Diaphragm--physiopathology<br/>Dystrophin--genetics<br/>Gene Expression Regulation<br/>Humans<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>LIM Domain Proteins--genetics<br/>Mice<br/>Mice, Inbred mdx<br/>Mice, Transgenic<br/>Muscle Contraction<br/>Muscle Proteins--genetics<br/>Muscle, Skeletal--physiopathology<br/>Muscular Dystrophy, Duchenne--genetics<br/>NFATC Transcription Factors--genetics<br/>Promoter Regions, Genetic<br/>Sarcolemma--metabolism<br/>Signal Transduction<br/>Utrophin--genetics