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核纤层蛋白B1失调在DYT1肌张力障碍中加厚核纤层并破坏14-3-3蛋白的 ...
【编辑推荐】儿童期发病的DYT1肌张力障碍是一种由TOR1A基因ΔE突变导致的严重运动障碍,其致病机制尚不明确。本研究聚焦于维持核结构与功能的关键支架——核纤层,探讨了核纤层蛋白Lamin B1失调在DYT1病理中的作用。利用患者成纤维细胞和人iPSC来源的神经元 ...
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