Calpains, Cleaved Mini-Dysferlin<sub>C72</sub>, and L-Type Channels Underpin Calcium-Dependent Muscle Membrane Repair
Angela Lek(Muscular Dystrophy Association), Sandra T. Cooper(Children's Medical Research Institute), Frances A. Lemckert(The University of Sydney), Cynthia B. Whitchurch(University of East Anglia), Gregory Redpath(University of Otago), Lynne Turnbull(Vistec Electron Beam (Germany)), Frances J. Evesson(Harvard University), Ann-Katrin Lueders(Children's Hospital at Westmead), Kathryn N. North(The University of Melbourne)
Cited by 135
Related Papers
Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis
|Nature Genetics|2000|1.3k
ACTN3 Genotype Is Associated with Human Elite Athletic Performance
|The American Journal of Human Genetics|2003|917
Improving genetic diagnosis in Mendelian disease with transcriptome sequencing
|Science Translational Medicine|2017|809
A brief history of human disease genetics
|Nature|2020|737
Explosive cell lysis as a mechanism for the biogenesis of bacterial membrane vesicles and biofilms
|Nature Communications|2016|690