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Defining the optimal dose and therapeutic window in spinal muscular atrophy with...
Mechanism of disease and therapeutic rescue of Dok7 congenital myasthenia
Myopathy associated LDB3 mutation causes Z-disc disassembly and protein aggregation...
JAK2-IGF1 axis in osteoclasts regulates postnatal growth in mice
A novel recessive mutation affecting DNAJB6a causes myofibrillar myopathy
Differential physiological role of BIN1 isoforms in skeletal muscle development,...
Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with...
Blocking substance P signaling reduces musculotendinous and dermal fibrosis and...
STIM1 over-activation generates a multi-systemic phenotype affecting skeletal muscle,...