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

Central biogenic amine deficiency with concomitant exploratory behavioral deficits in Dnajc12 knock-out mice.

Dnajc12 基因敲除小鼠出现中枢生物胺缺乏和探索行为缺陷

Deng Isaac Bul, Follett Jordan, Fox Jesse D, Wall Shannon, Farrer Matthew J

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses

RAB32 Ser71Arg 与常染色体显性帕金森病:连锁、关联和功能分析

Gustavsson, Emil K; Follett, Jordan; Trinh, Joanne; Barodia, Sandeep K; Real, Raquel; Liu, Zhiyong; Grant-Peters, Melissa; Fox, Jesse D; Appel-Cresswell, Silke; Stoessl, A Jon; Rajput, Alex; Rajput, Ali H; Auer, Roland; Tilney, Russel; Sturm, Marc; Haack, Tobias B; Lesage, Suzanne; Tesson, Christelle; Brice, Alexis; Vilariño-Güell, Carles; Ryten, Mina; Goldberg, Matthew S; West, Andrew B; Hu, Michele T; Morris, Huw R; Sharma, Manu; Gan-Or, Ziv; Samanci, Bedia; Lis, Pawel; Periñan, Maria Teresa; Amouri, Rim; Ben Sassi, Samia; Hentati, Faycel; Tonelli, Francesca; Alessi, Dario R; Farrer, Matthew J

Characterization of Dnajc12 knockout mice, a model of hypodopaminergia

Dnajc12基因敲除小鼠的特征分析,一种多巴胺能低下模型

Deng, Isaac Bul; Follett, Jordan; Fox, Jesse D; Wall, Shannon; Farrer, Matthew James

A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase

RAB32基因的致病变异会导致常染色体显性遗传帕金森病,并激活LRRK2激酶。

Gustavsson, Emil K; Follett, Jordan; Trinh, Joanne; Barodia, Sandeep K; Real, Raquel; Liu, Zhiyong; Grant-Peters, Melissa; Fox, Jesse D; Appel-Cresswell, Silke; Stoessl, A Jon; Rajput, Alex; Rajput, Ali H; Auer, Roland; Tilney, Russel; Sturm, Marc; Haack, Tobias B; Lesage, Suzanne; Tesson, Christelle; Brice, Alexis; Vilariño-Güell, Carles; Ryten, Mina; Goldberg, Matthew S; West, Andrew B; Hu, Michele T; Morris, Huw R; Sharma, Manu; Gan-Or, Ziv; Samanci, Bedia; Lis, Pawel; Tocino, Teresa; Amouri, Rim; Sassi, Samia Ben; Hentati, Faycel; Tonelli, Francesca; Alessi, Dario R; Farrer, Matthew J