Restless in the mouse cage-A new genetic model for restless legs syndrome An Editorial Highlight for"Deficiency of Meis1, a transcriptional regulator, in mice and worms:Neurochemical and behavioral characterizations with implications in the restless legs syndrome" on https://doi.org/10.1111/jnc.15177

被引:0
作者
Stegmueller, Judith [1 ,2 ,3 ]
机构
[1] RWTH Univ Hosp, Dept Neurol, Pauwelsstr 30, D-52074 Aachen, Germany
[2] Rhein Westfal TH Aachen, Aachen, Germany
[3] Rhein Westfal TH Aachen, Res Training Grp 2416 MultiSenses MultiScales, Aachen, Germany
关键词
IRON-DEFICIENCY; RISK; EPIDEMIOLOGY; ASSOCIATION; PREVALENCE; FERRITIN; DISEASE; VARIANT; RLS;
D O I
10.1111/jnc.15165
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Restless legs syndrome (RLS) is a movement disorder that is characterized by an uncomfortable sensation in the legs, and the urge to move the legs.Meis1has previously identified as a risk gene for RLS. This Editorial highlights the study by Lyu and colleagues who developed a novel genetic mouse model heterozygous forMeis1expression in neurons of the central nervous system. Using behavioral tests, the authors established hyperactivity of the mice, reminiscent of symptoms found in RLS patients. In addition, the authors took a closer look at the iron, dopaminergic, and cholinergic system of these mice.
引用
收藏
页码:471 / 474
页数:4
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