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

A human electrophysiological signature of Fragile X pathophysiology is shared in V1 of Fmr1(-/y) mice

Fmr1(-/y)小鼠的V1区与人类脆性X染色体综合征的病理生理特征相似。

Kornfeld-Sylla, Sara S; Gelegen, Cigdem; Norris, Jordan E; Chaloner, Francesca A; Lee, Maia; Khela, Michael; Heinrich, Maxwell J; Finnie, Peter S B; Ethridge, Lauren E; Erickson, Craig A; Schmitt, Lauren M; Cooke, Sam F; Wilkinson, Carol L; Bear, Mark F

Cell-intrinsic mechanisms underlying spontaneous activity in the mouse visual cortical slice: implications for fragile X pathophysiology

小鼠视觉皮层切片自发活动的细胞内在机制:对脆性X染色体综合征病理生理学的启示

Heinrich, Maxwell J; Bear, Mark F

FMR1 reduction alters cellular and circuit properties in human cortex

FMR1减少会改变人类大脑皮层的细胞和回路特性

Singh, Aditi; Abbaspoor, Saman; Chung, Leeyup; Heinrich, Maxwell J; Stone, Scellig; Lidov, Hart; Maio, Beatriz; Phuoc-Tran, Tien; Yoon, Jaeyoung; Teng, Jiawen; Martinez-Reyes, Catalina; Hammarlund, Elijah; Xu, Xiguang; Rotenberg, Alexander; Gavornik, Jeff; Ferguson, Brielle; Farrell, Jordan S; Osterweil, Emily K

Non-ionotropic signaling through the NMDA receptor GluN2B carboxy-terminal domain drives dendritic spine plasticity and reverses fragile X phenotypes.

通过 NMDA 受体 GluN2B 羧基末端结构域的非离子型信号传导驱动树突棘可塑性并逆转脆性 X 表型

Barnes Stephanie A, Thomazeau Aurore, Finnie Peter S B, Heinrich Maxwell J, Heynen Arnold J, Komiyama Noburu H, Grant Seth G N, Menniti Frank S, Osterweil Emily K, Bear Mark F