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

A chromosome region linked to neurodevelopmental disorders influences locomotor behavior through sex-specific neural circuits

与神经发育障碍相关的染色体区域通过性别特异性神经回路影响运动行为。

Kim, Jaekyoon; Vanrobaeys, Yann; Rajan, Remya; Davatolhagh, M Felicia; Kelvington, Benjamin; Chatterjee, Snehajyoti; Ferri, Sarah L; Angelakos, Christopher; Mills, Alea A; Fuccillo, Marc V; Blackwell, Kim T; Nickl-Jockschat, Thomas; Abel, Ted

Complement contributes to hyperactive behavior in the 16p11.2 hemideletion mouse model.

补体在 16p11.2 半缺失小鼠模型中导致过度活跃行为

Kelvington Benjamin A, Kim Jaekyoon, Fair Regan, Gaine Marie E, Abel Ted

hnRNPH2 gain-of-function mutations reveal therapeutic strategies and a role for RNA granules in neurodevelopmental disorders

hnRNPH2功能获得性突变揭示了治疗策略以及RNA颗粒在神经发育障碍中的作用

Kelvington, Benjamin A; Abel, Ted

Sterol dysregulation in Smith-Lemli-Opitz syndrome causes astrocyte immune reactivity through microglia crosstalk

Smith-Lemli-Opitz 综合征中的甾醇失调通过小胶质细胞串扰引起星形胶质细胞免疫反应

Bethany A Freel, Benjamin A Kelvington, Sonali Sengupta, Malini Mukherjee, Kevin R Francis