Myofibrillar disruption and RNA-binding protein aggregation in a mouse model of limb-girdle muscular dystrophy 1D

Rocío Bengoechea(Washington University in St. Louis), Conrad C. Weihl(Washington University in St. Louis)
Human Molecular Genetics
September 11, 2015
10.1093/hmg/ddv363
Cited by 47

Related Papers

<i>SQSTM1</i> splice site mutation in distal myopathy with rimmed vacuoles
|Neurology|2015|89
A Knock-In Mouse Model for the R120G Mutation of αB-Crystallin Recapitulates Human Hereditary Myopathy and Cataracts
|PLoS ONE|2011|76
Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy
|bioRxiv (Cold Spring Harbor Laboratory)|2020|18
DNAJB6 Isoform Specific Knockdown: Therapeutic Potential for LGMDD1
|bioRxiv (Cold Spring Harbor Laboratory)|2022|0