作者: A A Lev , C C Feener , L M Kunkel , R H Brown
DOI: 10.1016/S0021-9258(18)47660-0
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摘要: A partial cDNA clone for the Duchenne's muscular dystrophy (DMD) locus was used to investigate expression of this in human muscle vitro. Hybridization a 14-kilobase RNA transcript demonstrated both fetal and mature skeletal four lines cells culture. The DMD not detected cultured outside lineage. In cells, gene evident only myotubes before after innervation with mouse spinal cord. Primary cultures myoblasts did show presence prior fusion form myotubes. An vitro model is potentially an excellent system which factors controlling normal how altered muscle.