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

3D-printed magnetic scaffolds promote bone and vessel regeneration through CRYAB/PI3K-AKT and NF-κB pathways identified by proteomics

蛋白质组学研究表明,3D打印磁性支架可通过CRYAB/PI3K-AKT和NF-κB通路促进骨骼和血管再生。

Liu, Jieying; Liu, Fuze; Li, Cairong; Li, Zhengyao; Li, Tianle; Wu, Yuanhao; Wu, Di; Huang, Yue; Chen, Hui; Wang, Hai; Lai, Yuxiao; Wu, Zhihong

Technical Specification for Hemocompatibility Assessment of Human Mesenchymal Stem Cells

人类间充质干细胞血液相容性评估技术规范

Liu, Jialing; Liang, Weiyang; Xia, Wenjie; Wang, Ping; Hao, Jie; Na, Tao; Yan, Sunxing; Zhang, Yu; Li, Ka; Li, Qiyuan; Pan, Guangjin; Wei, Jun; Chen, Qubo; Cao, Jiani; Zhai, Peijun; Fu, Boqiang; Gao, Hengjun; Zhang, Yong; Wang, Lei; Guo, Meimei; Hu, Shijun; Zhu, Lijun; Zhao, Yang; Zhang, Weiqi; Wu, Zhihong; Ping, Yifang; Zhao, Hongling; Niu, Shuaishuai; Zhao, Tongbiao; Ma, Aijin; Xiang, Andy Peng; Chen, Xiaoyong

Addressing the diagnostic gap through deep phenotyping

通过深度表型分析解决诊断差距

Li, John Guozhuang; Xu, Kexin; Xiao, Bin; Li, Jingnan; Zhu, Yi-Cheng; Jin, Hongzhong; Qi, Qingwei; Wang, Lianlei; Zhao, Lina; Wu, Zhihong; Zhao, Sen; Zhang, Terry Jianguo; Wu, Nan

Genetic and embryonic transcriptome analyses reveal the molecular and developmental basis of Mayer-Rokitansky-Küster-Hauser syndrome

遗传和胚胎转录组分析揭示了 Mayer-Rokitansky-Küster-Hauser 综合征的分子和发育基础

Chen, Na; Cheng, Xi; Zhao, Sen; Zhao, Hengqiang; Qin, Chenglu; Zhang, Yaru; Lin, Xijuan; Li, Qing; Wang, Yuan; Kang, Jia; Yu, Jing; Guo, Jianbin; Gao, Qianqian; Duan, Jiali; Niu, Yuchen; Su, Jianzhong; Wu, Zhihong; Zhang, Terry Jianguo; Liu, Wanlu; Liu, Pengfei; Deng, Shan; Wu, Nan; Zhu, Lan

Effects of Pinglu Canal Construction on Camouflage in Two Sesarmid Crab Species

平鲁运河建设对两种沙蟹伪装的影响

Zhai, Binyu; Lai, Fuxi; Lu, Sichen; Deng, Xinglai; Li, Wenjie; Yang, Lin; Deng, Changyin; Wu, Zhihong; Huang, Yiran; Wang, Haitao; Liao, Yuhao; Bu, Rongping

Case Report: Recurrent sinus arrest induced by repeated vomiting

病例报告:反复呕吐引起的复发性鼻窦阻塞

Jiang, Zhongbiao; Zhang, Yudong; Wu, Zhihong; Jiang, Xuan; Hu, Lin; Zhang, Shuang; Chen, Mingxian

Runx2 mutation plays a key role in the development of scoliosis

Runx2基因突变在脊柱侧弯的发生发展中起着关键作用。

Lu, Ke; Wei, Guizheng; Li, Guozhuang; Zhao, Lina; Hsu, Yu-Ching; Qin, Ling; Xiao, Guozhi; Wu, Zhihong; Wang, Huaiyu; Chen, Jianquan; Shen, Jianxiong; Wu, Nan; Chen, Di

Surgical Management of Ventricular Tachycardia Originating From Left Ventricular Diverticulum

左心室憩室源性室性心动过速的外科治疗

Zhou, Zhiang; Nasar, Naqibullah; Zhu, Yixiao; Chen, Heming; Wang, Min; Liao, Xiaobo; Liu, Zhenjiang; Wu, Zhihong; Yuan, Zhaoshun

Harnessing Individual Omics Signatures for Precision Medicine in Alzheimer's Disease

利用个体组学特征进行阿尔茨海默病精准医疗

Leng, Ling; Cao, Ruiyuan; Ma, Jie; Lv, Luye; Li, Wei; Zhu, Yunping; Wu, Zhihong; Wang, Manli; Zhou, Yiwu; Zhong, Wu; Podder, Avijit; Liew, Yi Juin; Pandey, Ravi S; Cary, Gregory A; Carter, Gregory W; Uyar, Asli

Activin A-Activated ALK4 Induces Pathogenic Th17-Involved Endothelial-Mesenchymal Transition in Systemic Lupus Erythematosus-Associated Pulmonary Arterial Hypertension

激活素A激活的ALK4诱导系统性红斑狼疮相关肺动脉高压中致病性Th17细胞参与的内皮-间质转化

Jing, Shuliang; Qian, Junyan; Ying, Hongjie; Mao, Pei; Yao, Mingxin; Wu, Zhihong; Bogaard, Harm J; Wang, Lie; Li, Mengtao; Yang, Jun