Functional analysis of the epilepsy gene Pcdh19 using a novel GFP-reporter mouse model
Stefka Mincheva-Tasheva(South Australian Health and Medical Research Institute), Paul Q. Thomas(South Australian Health and Medical Research Institute)
Cited by 0
Related Papers
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation
|Nature Genetics|2007|294
Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice
|Scientific Reports|2016|67
SOX3 promotes generation of committed spermatogonia in postnatal mouse testes
|Scientific Reports|2020|38
Parallel assembly of actin and tropomyosin, but not myosin II, during <i>de novo</i> actin filament formation in live mice
|Journal of Cell Science|2018|20