Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy.

D'Arcy, Colleen E

Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy. [electronic resource] - Human molecular genetics Feb 2014 - 618-36 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1460-2083

10.1093/hmg/ddt449 doi


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