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

AUTS2 isoforms control neuronal differentiation

AUTS2 亚型控制神经元分化

Galya Monderer-Rothkoff, Nitzan Tal, Marina Risman, Odem Shani, Malka Nissim-Rafinia, Laura Malki-Feldman, Vera Medvedeva, Matthias Groszer, Eran Meshorer, Sagiv Shifman

An Etiological Foxp2 Mutation Impairs Neuronal Gain in Layer VI Cortico-Thalamic Cells through Increased GABA(B)/GIRK Signaling

Foxp2 基因突变通过增强 GABA(B)/GIRK 信号传导损害第六层皮质丘脑细胞的神经元增益

Druart, Mélanie; Groszer, Matthias; Le Magueresse, Corentin

TBR2 coordinates neurogenesis expansion and precise microcircuit organization via Protocadherin 19 in the mammalian cortex

TBR2通过原钙黏蛋白19协调哺乳动物皮层中的神经发生扩张和精确的微回路组织。

Xiaohui Lv ,Si-Qiang Ren ,Xin-Jun Zhang ,Zhongfu Shen ,Tanay Ghosh ,Anjin Xianyu ,Peng Gao ,Zhizhong Li ,Susan Lin ,Yang Yu ,Qiangqiang Zhang ,Matthias Groszer ,Song-Hai Shi

Altered social behavior in mice carrying a cortical Foxp2 deletion

携带皮质 Foxp2 缺失的小鼠的社交行为发生改变

Vera P Medvedeva, Michael A Rieger, Beate Vieth, Cédric Mombereau, Christoph Ziegenhain, Tanay Ghosh, Arnaud Cressant, Wolfgang Enard, Sylvie Granon, Joseph D Dougherty, Matthias Groszer

Thalamic WNT3 Secretion Spatiotemporally Regulates the Neocortical Ribosome Signature and mRNA Translation to Specify Neocortical Cell Subtypes

丘脑 WNT3 分泌在时空上调节新皮质核糖体特征和 mRNA 翻译以指定新皮质细胞亚型

Matthew L Kraushar, Barbara Viljetic, H R Sagara Wijeratne, Kevin Thompson, Xinfu Jiao, Jack W Pike, Vera Medvedeva, Matthias Groszer, Megerditch Kiledjian, Ronald P Hart, Mladen-Roko Rasin

Transcriptome sequencing during mouse brain development identifies long non-coding RNAs functionally involved in neurogenic commitment

小鼠脑发育过程中的转录组测序鉴定出参与神经发生定向的长链非编码RNA。

Aprea, Julieta; Prenninger, Silvia; Dori, Martina; Ghosh, Tanay; Monasor, Laura Sebastian; Wessendorf, Elke; Zocher, Sara; Massalini, Simone; Alexopoulou, Dimitra; Lesche, Mathias; Dahl, Andreas; Groszer, Matthias; Hiller, Michael; Calegari, Federico

An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning

Foxp2 基因突变会导致纹状体活动异常,并改变技能学习过程中的可塑性。

French, C A; Jin, X; Campbell, T G; Gerfen, E; Groszer, M; Fisher, S E; Costa, R M

Genetic disruption of Pten in a novel mouse model of tomaculous neuropathy

在一种新型小鼠眼球神经病变模型中,Pten基因的破坏

Goebbels, Sandra; Oltrogge, Jan H; Wolfer, Susanne; Wieser, Georg L; Nientiedt, Tobias; Pieper, Alexander; Ruhwedel, Torben; Groszer, Matthias; Sereda, Michael W; Nave, Klaus-Armin

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain

Foxp2调控发育中大脑神经突生长相关的基因网络

Vernes, Sonja C; Oliver, Peter L; Spiteri, Elizabeth; Lockstone, Helen E; Puliyadi, Rathi; Taylor, Jennifer M; Ho, Joses; Mombereau, Cedric; Brewer, Ariel; Lowy, Ernesto; Nicod, Jérôme; Groszer, Matthias; Baban, Dilair; Sahgal, Natasha; Cazier, Jean-Baptiste; Ragoussis, Jiannis; Davies, Kay E; Geschwind, Daniel H; Fisher, Simon E

Elevated phosphatidylinositol 3,4,5-trisphosphate in glia triggers cell-autonomous membrane wrapping and myelination

神经胶质细胞中磷脂酰肌醇3,4,5-三磷酸酯水平升高会触发细胞自主的膜包裹和髓鞘形成。

Goebbels, Sandra; Oltrogge, Jan H; Kemper, Robert; Heilmann, Ingo; Bormuth, Ingo; Wolfer, Susanne; Wichert, Sven P; Möbius, Wiebke; Liu, Xin; Lappe-Siefke, Corinna; Rossner, Moritz J; Groszer, Matthias; Suter, Ueli; Frahm, Jens; Boretius, Susann; Nave, Klaus-Armin