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

Processing Laue Microdiffraction Raster Scanning Patterns with Machine Learning Algorithms: A Case Study with a Fatigued Polycrystalline Sample

利用机器学习算法处理劳厄微衍射光栅扫描图：以疲劳多晶样品为例

期刊:Materials
影响因子:3.2
doi:10.3390/ma15041502
Rong, Peng; Zhang, Fengguo; Yang, Qing; Chen, Han; Shi, Qiwei; Zhong, Shengyi; Chen, Zhe; Wang, Haowei
发表日期：2022
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Functional metabolomics reveal the role of AHR/GPR35 mediated kynurenic acid gradient sensing in chemotherapy-induced intestinal damage

功能代谢组学揭示 AHR/GPR35 介导的犬尿氨酸梯度感应在化疗引起的肠道损伤中的作用

期刊:Acta Pharmaceutica Sinica B
影响因子:14.7
doi:10.1016/j.apsb.2020.07.017
Di Wang, Danting Li, Yuxin Zhang, Jie Chen, Ying Zhang, Chuyao Liao, Siyuan Qin, Yuan Tian, Zunjian Zhang, Fengguo Xu
代谢
信号转导
发表日期：2021
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SYP-5 regulates meiotic thermotolerance in Caenorhabditis elegans

SYP-5 调控秀丽隐杆线虫的减数分裂耐热性

期刊:Journal of Molecular Cell Biology
影响因子:5.9
doi:10.1093/jmcb/mjab035
Liu, Yuanyuan; Zhao, Qiuchen; Nie, Hui; Zhang, Fengguo; Fu, Tingting; Zhang, Zhenguo; Qi, Feifei; Wang, Ruoxi; Zhou, Jun; Gao, Jinmin
信号转导
C. elegans
发表日期：2021
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Tryptophan Pathway-Targeted Metabolomics Study on the Mechanism and Intervention of Cisplatin-Induced Acute Kidney Injury in Rats

以色氨酸通路为靶点的代谢组学研究顺铂致大鼠急性肾损伤的机制及干预措施

期刊:Chemical Research in Toxicology
影响因子:3.7
doi:10.1021/acs.chemrestox.1c00110
Bei Tan, Jie Chen, Siyuan Qin, Chuyao Liao, Ying Zhang, Di Wang, Siqi Li, Zunjian Zhang, Pei Zhang, Fengguo Xu
代谢
信号转导
肾损伤
发表日期：2021
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Oleic Acid and Insulin as Key Characteristics of T2D Promote Colorectal Cancer Deterioration in Xenograft Mice Revealed by Functional Metabolomics

功能代谢组学揭示油酸和胰岛素作为 2 型糖尿病的关键特征促进异种移植小鼠结直肠癌恶化

期刊:Frontiers in Oncology
影响因子:3.5
doi:10.3389/fonc.2021.685059
Ying Zhang, Di Wang, Bo Lv, Xiaoying Hou, Qiwei Liu, Chuyao Liao, Ruijie Xu, Yuxin Zhang, Fengguo Xu, Pei Zhang
代谢
糖尿病
肠癌
发表日期：2021
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Multivalent weak interactions between assembly units drive synaptonemal complex formation

组装单元之间的多价弱相互作用驱动突触复合体的形成

期刊:Journal of Cell Biology
影响因子:6.4
doi:10.1083/jcb.201910086
Zhang, Zhenguo; Xie, Songbo; Wang, Ruoxi; Guo, Shuqun; Zhao, Qiuchen; Nie, Hui; Liu, Yuanyuan; Zhang, Fengguo; Chen, Miao; Liu, Libo; Meng, Xiaoqian; Liu, Min; Zhao, Li; Colaiácovo, Monica P; Zhou, Jun; Gao, Jinmin
神经科学
发表日期：2020
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Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families.

在中国家族中发现了与常染色体显性遗传性听力损失相关的 POU4F3 基因的两个新突变

期刊:Journal of Cellular and Molecular Medicine
影响因子:4.2
doi:10.1111/jcmm.15359
Bai Xiaohui, Zhang Fengguo, Xiao Yun, Jin Yu, Zheng Qingyin, Wang Haibo, Xu Lei
发表日期：2020
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Cochlear Implantation in a Patient with a Novel POU3F4 Mutation and Incomplete Partition Type-III Malformation

为一名患有新型 POU3F4 突变和不完全分隔型 III 畸形的患者进行人工耳蜗植入

期刊:Neural Plasticity
影响因子:3.7
doi:10.1155/2020/8829587
Chao, Xiuhua; Xiao, Yun; Zhang, Fengguo; Luo, Jianfen; Wang, Ruijie; Liu, Wenwen; Wang, Haibo; Xu, Lei
发表日期：2020
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Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families

在四个中国家庭中发现了LOXHD1基因的五个新突变，这些突变导致常染色体隐性非综合征性听力损失。

期刊:Biomed Research International
影响因子:2.3
doi:10.1155/2020/1685974
Bai, Xiaohui; Zhang, Chi; Zhang, Fengguo; Xiao, Yun; Jin, Yu; Wang, Haibo; Xu, Lei
LOX
发表日期：2020
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Corrigendum to "Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families"

关于“在四个中国家庭中发现 LOXHD1 基因的五个新突变导致常染色体隐性非综合征性听力损失”的更正

期刊:Biomed Research International
影响因子:2.3
doi:10.1155/2020/9519415
Bai, Xiaohui; Zhang, Chi; Zhang, Fengguo; Xiao, Yun; Jin, Yu; Wang, Haibo; Xu, Lei
LOX
发表日期：2020
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