Lv4
450 积分 2024-09-27 加入
The DYT6 dystonia causative protein THAP1 is responsible for proteasome activity via PSMB5 transcriptional regulation
9小时前
待确认
Striatal cell-type–specific molecular signatures reveal potential therapeutic targets in a model of dystonia
9小时前
求助中
Adult‐Onset Dystonia‐Parkinsonism: Do Not Forget SERAC1
9小时前
求助中
Differential Effects of Short-term and Long-term Deep Brain Stimulation on Striatal Neuronal Excitability in a Dystonia Animal Model
9小时前
求助中
Eye movement disorders in genetic dystonia syndromes: a literature overview
9小时前
待确认
Aberrant outputs of glutamatergic neurons in deep cerebellar nuclei mediate dystonic movements
9小时前
已完结
Clinical and Basic Research on Dopa-Responsive Dystonia: Neuropathological and Neurochemical Findings
9小时前
已关闭
Genotype–Phenotype Relations for the Dystonia-Parkinsonism Genes GLB1, SLC6A3, SLC30A10, SLC39A14, and PLA2G6: MDSGene Systematic Review
9小时前
待确认
Loss-of-function mutations in the dystonia gene THAP1 impair proteasome function by inhibiting PSMB5 expression
9小时前
已完结
Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders
9小时前
求助中
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