COMPOSITIONS AND METHODS FOR IDENTIFYING, MODULATING AND MONITORING DRUG TARGETS IN MUSCULAR DISEASE

摘要

The present disclosure relates to customized therapy for disease. The present disclosure also relates to aptamer-based compositions and methods for identifying, modulating and monitoring drug targets in muscular disease (e.g., Duchenne muscular dystrophy).

主权项

1. A method for treating a subject for muscular dystrophy comprising administering, to a subject in need, a therapeutic effective amount of a therapeutic agent selected from GDF-11, RELT, CD55, WFIKKN1, gelsolin, fibroblast activation protein alpha (FAP), protein jagged-1 (JAG1), bone sialoprotein 2 (IBSP), ADAM metallopeptidase domain 9 (ADAM9), cadherin-5 (CDH5), neural cell adhesion molecule L1-like protein (CHL1), osteomodulin (OMD), contactin-5 (CNTN5), and combinations thereof.