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

Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders

编码染色质重塑因子的EP400基因变异会导致伴有神经发育障碍的癫痫。

Luo, Sheng; Wang, Peng-Yu; Zhou, Peng; Zhang, Wen-Jun; Gu, Yu-Jie; Liang, Xiao-Yu; Zhang, Jing-Wen; Luo, Jun-Xia; Zhang, Hong-Wei; Lan, Song; Zhang, Ting-Ting; Yang, Jie-Hua; Sun, Su-Zhen; Guo, Xiang-Yang; Wang, Ju-Li; Deng, Lin-Fan; Xu, Ze-Hai; Jin, Liang; He, Yun-Yan; Ye, Zi-Long; Gu, Wei-Yue; Li, Bing-Mei; Shi, Yi-Wu; Liu, Xiao-Rong; Yan, Hong-Jun; Yi, Yong-Hong; Jiang, Yu-Wu; Mao, Xiao; Li, Wen-Ling; Meng, Heng; Liao, Wei-Ping

[Corrigendum] MCM7 amplification and overexpression promote cell proliferation, colony formation and migration in esophageal squamous cell carcinoma by activating the AKT1/mTOR signaling pathway

【更正】MCM7扩增和过表达通过激活AKT1/mTOR信号通路促进食管鳞状细胞癌细胞的增殖、克隆形成和迁移

Qiu, Yun-Tan; Wang, Wen-Jun; Zhang, Bing; Mei, Li-Li; Shi, Zhi-Zhou

Identification of MACF1 as a causative gene of generalised epilepsy

鉴定MACF1为全身性癫痫的致病基因

Lei, Xiao-Yun; Zhang, Meng-Wen; Sun, Hui; Song, Wang; Liang, Xiao-Yu; Wang, Cui-Shan; Luo, Sheng; Li, Bing-Mei; Liu, Xiao-Rong; Wang, Yao; Tian, Yang; Peng, Qian; Wang, Jie; Meng, Heng; He, Na; Liao, Wei-Ping

Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay

SLC9A6基因的错义变异会导致部分性癫痫,但不会引起神经发育迟缓。

Jiao, Jun-Ping; Zhang, Hong-Wei; Zhou, Xi-Zhong; Tian, Shu-Juan; Gao, Li; Li, Bing-Mei; Luo, Jun-Xia; Wang, Jie; Lan, Song; Li, Bin; Liao, Wei-Ping

Osteonecrosis of the external auditory canal in two patients on denosumab therapy

两名接受地诺单抗治疗的患者出现外耳道骨坏死

Wang, Holly; Yii, Matthew; Teh, Bing Mei; Premaratne, Erosha; Chiang, Cherie

The Prevalence and Risk Factors of Residual Back Pain After Vertebroplasty for Osteoporotic Vertebral Compression Fractures: A Systematic Review and Meta-Analysis

骨质疏松性椎体压缩性骨折椎体成形术后残余背痛的患病率和危险因素:系统评价和荟萃分析

Li, Wenlong; Zhang, Bing; Mei, Chencheng; Li, Hui; Zhu, Ruizheng; Lin, Hao; Wen, Jianmin; Wu, Yang; Ma, Xianzhi

Enhanced interaction between genome-edited mesenchymal stem cells and platelets improves wound healing in mice

基因组编辑的间充质干细胞与血小板之间的增强相互作用可改善小鼠的伤口愈合

De-Yong Li, Yu-Meng Li, Dan-Yi Lv, Tian Deng, Xin Zeng, Lu You, Qiu-Yu Pang, Yi Li, Bing-Mei Zhu

[Retracted] Upregulation of miR‑183‑5p is responsible for the promotion of apoptosis and inhibition of the epithelial‑mesenchymal transition, proliferation, invasion and migration of human endometrial cancer cells by downregulating Ezrin

[已撤稿] miR-183-5p 的上调通过下调 Ezrin 促进人子宫内膜癌细胞凋亡,并抑制其上皮-间质转化、增殖、侵袭和迁移。

Yan, Hua; Sun, Bing-Mei; Zhang, Yu-Ying; Li, Yu-Juan; Huang, Cheng-Xiang; Feng, Fu-Zhong; Li, Cui

Efficacy and safety of Bacteroides fragilis BF839 for pediatric autism spectrum disorder: a randomized clinical trial

脆弱拟杆菌BF839治疗儿童自闭症谱系障碍的疗效和安全性:一项随机临床试验

Lin, Chu-Hui; Zeng, Ting; Lu, Cui-Wei; Li, De-Yang; Liu, Yi-Ying; Li, Bing-Mei; Chen, Sheng-Qiang; Deng, Yu-Hong

NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation

NUS1 变异导致与未折叠蛋白反应激活相关的 Lennox-Gastaut 综合征

Nan-Xiang Shen #, Xiao-Chong Qu #, Jing Yu, Cui-Xia Fan, Fu-Li Min, Ling-Ying Li, Ming-Rui Zhang, Bing-Mei Li, Jie Wang, Na He, Wei-Ping Liao, Yi-Wu Shi, Wen-Bin Li