Huntington's Disease: Nuclear Gatekeepers Under Attack. Neuron 2017 Apr 05;94(1):1-4
Date
04/07/2017Pubmed ID
28384467DOI
10.1016/j.neuron.2017.03.032Scopus ID
2-s2.0-85016944880 (requires institutional sign-in at Scopus site) 9 CitationsAbstract
In this issue of Neuron, Gasset-Rosa et al. (2017) and Grima et al. (2017) describe defects in the nuclear pore complex and impaired nucleocytoplasmic transport in Huntington's disease (HD). The findings suggest that erosion of nuclear gatekeeping function, which is found in normal brain aging, may play an important role in the pathogenesis of multiple neurodegenerative disorders, including HD.
Author List
Veldman MB, Yang XWAuthor
Matthew B. Veldman PhD Assistant Professor in the Cell Biology, Neurobiology and Anatomy department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
AgingBrain
Humans
Huntington Disease
Neurons
Nuclear Proteins