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

Conserved sleep disturbances in FOXP1 syndrome originate from developmental dysregulation of peptidergic signaling

FOXP1综合征中保守的睡眠障碍源于肽能信号传导的发育失调。

Coll-Tané, Mireia; Eidhof, Ilse; Han, Jie; Raun, Nicholas; van Renssen, Lara V; Fisher, Simon E; Kayser, Matthew S; Kleefstra, Tjitske; Pillen, Sigrid; Hudac, Caitlin M; Mayneris-Perxachs, Jordi; Klein, Marieke; Koene, Saskia; Castells-Nobau, Anna; Schenck, Annette

Super-enhancer-driven core transcription factor FOXP1 delays endothelial cell senescence via phase separation-mediated SESN3 activation

超级增强子驱动的核心转录因子FOXP1通过相分离介导的SESN3激活延缓内皮细胞衰老。

Lushuang Mao ,Zhao-Fu Liao ,Dong Tang ,Yumin Qiu ,Min Yang ,Yanshang Li ,Yituan Xie ,Weimin Feng ,Ze-Jun Zheng ,Xiao-Meng Liu ,Jing-Ru Ye ,Shui-Hong Lu ,Xin-Bin Tang ,Ming Shi ,Yun-Fei Qu ,Heng Li ,Zhu-Guo Wu ,Shun Xu ,Xinguang Liu ,Junjun Ding ,Jian-Jun Xie ,Jun Tao ,Xing-Dong Xiong

Retraction Notice to: circ-SHKBP1 Regulates the Angiogenesis of U87 Glioma-Exposed Endothelial Cells through miR-544a/FOXP1 and miR-379/FOXP2 Pathways

撤稿声明:circ-SHKBP1 通过 miR-544a/FOXP1 和 miR-379/FOXP2 通路调控 U87 胶质瘤暴露内皮细胞的血管生成

He, Qianru; Zhao, Lini; Liu, Yunhui; Liu, Xiaobai; Zheng, Jian; Yu, Hai; Cai, Heng; Ma, Jun; Liu, Libo; Wang, Ping; Li, Zhen; Xue, Yixue

Luteolin Enhances Endothelial Barrier Function and Attenuates Myocardial Ischemia-Reperfusion Injury via FOXP1-NLRP3 Pathway.

木犀草素通过 FOXP1-NLRP3 通路增强内皮屏障功能并减轻心肌缺血再灌注损伤。

Xie Hanyan, Zhong Xinyi, Li Nan, Zhou Mijia, Zhang Miao, Yang Xiaomin, Wang Hui, Yan Yu, Gao Pengrong, Liu Tianhua, Wang Qiyan, Guo Dongqing

Cortex-Restricted Deletion of Foxp1 Impairs Visual Responses by Disrupting Geniculocortical Connections in a Mouse Model of Autism.

在自闭症小鼠模型中,皮质特异性敲除 Foxp1 会破坏膝状体皮质连接,从而损害视觉反应。

Li Xue, Wang Chao, Tu Xiaomeng, Wang Jieni, Zhang Zihao, Wu Jialu, Tang Qi, Qu Chunsheng, Chen Jie-Guang

Resolving non‑coding splice‑altering variants using an integrative genomic and transcriptomic workflow: application to FOXP1

利用整合基因组学和转录组学工作流程解析非编码剪接改变变异:以FOXP1为例

Planté-Bordeneuve, Pauline; Jourdain, Anne-Sophie; Thuillier, Caroline; Caux, Aurélien; Tessarech, Marine; Meneboo, Jean-Pascal; Ait-Yahya, Emilie; Costantini, Sara; Brunelle, Perrine; Smol, Thomas

Long noncoding RNA FOXP1-DT modulates regulatory T cells in Graves' disease

长链非编码RNA FOXP1-DT在格雷夫斯病中调节调节性T细胞

Xu, Qian; Lu, Chuanbin; Xu, Juan; Zhou, Mengli; Li, Shanshan; Shen, Xianfang; Wang, Shengjun; Liu, Yingzhao; Peng, Huiyong

Intragenic loss-of-function variants in transcription factors MAZ, FOXP1 and SIN3B in colobomatous microphthalmia

眼裂小眼畸形中转录因子 MAZ、FOXP1 和 SIN3B 的基因内功能缺失变异

Seese, Sarah E; Reis, Linda M; Schneider, Adele; Bardakjian, Tanya; Semina, Elena V

Identification of novel FOXP1 variants in four unrelated patients with intellectual disability and speech impairment

在四名互不相关的智力障碍和语言障碍患者中鉴定出新的FOXP1变异体

Xiang, Jingjing; Mao, Jun; Zhang, Qin; Meng, Qingxia

FBXO44 Regulates FOXP1 Degradation Through AURKA-Dependent Phosphorylation to Promote Colorectal Cancer Progression

FBXO44通过AURKA依赖性磷酸化调控FOXP1降解,从而促进结直肠癌进展

Nie, Hongxu; Xu, Hengjie; Yang, Sheng; Tian, Chuanxin; Wang, Tuo; Jin, Chi; Chen, Zhihao; Wang, Xiaowei; Tang, Junwei; Feng, Yifei; Sun, Yueming