Functional KCa1. 1 channels are crucial for regulating the proliferation, migration and differentiation of human primary skeletal myoblasts
RB Tajhya, X Hu, MR Tanner, R Huq, N Kongchan… - Cell death & …, 2016 - nature.com
Myoblasts are mononucleated precursors of myofibers; they persist in mature skeletal
muscles for growth and regeneration post injury. During myotonic dystrophy type 1 (DM1), a …
muscles for growth and regeneration post injury. During myotonic dystrophy type 1 (DM1), a …
Afterdischarges in myotonic dystrophy type 1
L Yang, X Chen, R Wu - Neurological Sciences, 2024 - Springer
Objective Electrodiagnostic testing is an important screening test for myotonic dystrophy type
1 (DM1). Although myotonic discharges are observed on electromyography in cases of DM1 …
1 (DM1). Although myotonic discharges are observed on electromyography in cases of DM1 …
Specific DMPK-promoter targeting by CRISPRi reverses myotonic dystrophy type 1-associated defects in patient muscle cells
Myotonic dystrophy type 1 (DM1) is a neuromuscular disease that originates from an
expansion of CTG microsatellites in the 3′ untranslated region of the DMPK gene, thus …
expansion of CTG microsatellites in the 3′ untranslated region of the DMPK gene, thus …