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

Torpor induces reversible tau hyperphosphorylation and accumulation in mice expressing human tau

蛰伏可诱导表达人tau蛋白的小鼠体内tau蛋白可逆性过度磷酸化和积累

de Veij Mestdagh, C F; Witte, M E; Scheper, W; Smit, A B; Henning, R H; van Kesteren, R E

Fractionated brain X-irradiation profoundly reduces hippocampal immature neuron numbers without affecting spontaneous behavior in mice

分次脑部X射线照射可显著减少小鼠海马体中未成熟神经元的数量,但不影响其自发行为。

Kuil, L E; Seigers, R; Loos, M; de Gooijer, M C; Compter, A; Boogerd, W; van Tellingen, O; Smit, A B; Schagen, S B

Dysregulation of synaptic and developmental transcriptomic/proteomic profiles upon depletion of MUNC18-1

MUNC18-1 缺失导致突触和发育转录组/蛋白质组谱失调

Van Berkel, A A; Koopmans, F; Gonzalez-Lozano, M A; Lammertse, H C A; Feringa, F; Bryois, J; Sullivan, P F; Smit, A B; Toonen, R F; Verhage, M

Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions.

缝合突触:将交联质谱技术应用于解析突触蛋白相互作用

Gonzalez-Lozano M A, Koopmans F, Sullivan P F, Protze J, Krause G, Verhage M, Li K W, Liu F, Smit A B

Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

作者更正:通过DNA甲基化和全基因组关联研究(GWAS)鉴定额颞叶痴呆和伴有肌萎缩侧索硬化症的额颞叶痴呆的易感基因和疾病机制

Taskesen, E; Mishra, A; van der Sluis, S; Ferrari, R; Veldink, J H; van Es, M A; Smit, A B; Posthuma, D; Pijnenburg, Y

Temporal profiling of depression vulnerability in a preclinical model of sustained depression

在持续性抑郁症的临床前模型中,抑郁症易感性的时间特征分析

Riga, D; Schmitz, L J M; Hoogendijk, W J G; Smit, A B; Spijker, S

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

通过DNA甲基化和全基因组关联分析(GWAS)鉴定额颞叶痴呆和伴有肌萎缩侧索硬化症的额颞叶痴呆的易感基因和疾病机制

Taskesen, E; Mishra, A; van der Sluis, S; Ferrari, R; Veldink, J H; van Es, M A; Smit, A B; Posthuma, D; Pijnenburg, Y

HCN channels are a novel therapeutic target for cognitive dysfunction in Neurofibromatosis type 1

HCN通道是1型神经纤维瘤病认知功能障碍的一种新型治疗靶点。

Omrani, A; van der Vaart, T; Mientjes, E; van Woerden, G M; Hojjati, M R; Li, K W; Gutmann, D H; Levelt, C N; Smit, A B; Silva, A J; Kushner, S A; Elgersma, Y

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

功能基因组分析发现突触基因组是精神分裂症的风险因素

Lips, E S; Cornelisse, L N; Toonen, R F; Min, J L; Hultman, C M; Holmans, P A; O'Donovan, M C; Purcell, S M; Smit, A B; Verhage, M; Sullivan, P F; Visscher, P M; Posthuma, D

High-throughput phenotyping of avoidance learning in mice discriminates different genotypes and identifies a novel gene

利用高通量表型分析小鼠的回避学习能力,可以区分不同的基因型并鉴定出一个新的基因。

Maroteaux, G; Loos, M; van der Sluis, S; Koopmans, B; Aarts, E; van Gassen, K; Geurts, A; Largaespada, D A; Spruijt, B M; Stiedl, O; Smit, A B; Verhage, M