日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The tau isoform 1N4R confers vulnerability of MAPT knockout human iPSC-derived neurons to amyloid beta and phosphorylated tau-induced neuronal dysfunction

tau 亚型 1N4R 使 MAPT 敲除的人类 iPSC 衍生神经元更容易受到淀粉样蛋白 β 和磷酸化 tau 诱导的神经元功能障碍的影响。

Buchholz, Sarah; Kabbani, Mohamed Aghyad Al; Bell-Simons, Michael; Kluge, Lena; Cagmak, Cagla; Klimek, Jennifer; Haag, Natja; Iohan, Lukas C; Coulon, Audrey; Costa, Marcos R; Kilinc, Devrim; Zempel, Hans

Tau Axonal Sorting and Interaction With Synaptic Plasticity Modulators Is Domain- and Isoform-Dependent in Human iPSC-Derived Neurons

在人类iPSC衍生神经元中,tau蛋白轴突分选及其与突触可塑性调节因子的相互作用取决于其结构域和亚型。

Michael Bell-Simons ,Helen Breuer ,Laura Wunderlich ,Hanin Chmes ,Daniel Adam ,Jennifer Klimek ,Sarah Buchholz ,Hans Zempel

Axodendritic targeting of TAU and MAP2 and microtubule polarization in iPSC-derived versus SH-SY5Y-derived human neurons

iPSC衍生的人类神经元与SH-SY5Y衍生的人类神经元中TAU和MAP2的轴突靶向以及微管极化

Breuer, Helen; Bell-Simons, Michael; Zempel, Hans

Laser-Induced Axotomy of Human iPSC-Derived and Murine Primary Neurons Decreases Somatic Tau and AT8 Tau Phosphorylation: A Single-Cell Approach to Study Effects of Acute Axonal Damage

激光诱导人类 iPSC 衍生和小鼠原代神经元轴突切断可降低躯体 Tau 和 AT8 Tau 磷酸化:一种研究急性轴突损伤影响的单细胞方法

M Bell-Simons, S Buchholz, J Klimek, H Zempel