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

The Potential Application of Exosomes as Therapeutic Agents, Carriers, and Biomarkers in Skin Diseases

外泌体作为皮肤疾病治疗剂、载体和生物标志物的潜在应用

Li, Wenjing; Li, Haiyan; Fan, Liangliang; Zhao, Ronghua; Dong, Fusong; Jia, Xuxia; Yin, Lijia; Yang, Song; Zhao, Daqing; Wang, Jiawen

A Novel LAMA2 Mutation (c.7412G>A) Was Found in a Chinese Patient With Congenital Muscular Dystrophy.

在中国一名先天性肌营养不良症患者中发现了一种新的 LAMA2 突变(c.7412G>A)

Zhao Meifang, Liu Yuxing, Fan Liangliang, Liu Zhaochuan, Deng Yao, Tao Lihong

Bioinformatics analysis of a CLCN5 geneframeshift mutation in a patient with Dent disease

对一名患有Dent病的患者的CLCN5基因移码突变进行生物信息学分析

Zhang, Yingying; Li, Nannan; Fan, Liangliang; Liu, Jishi

Ginseng-derived nanoparticles alleviate inflammatory bowel disease via the TLR4/MAPK and p62/Nrf2/Keap1 pathways

人参纳米颗粒通过TLR4/MAPK和p62/Nrf2/Keap1通路缓解炎症性肠病

Yang, Song; Li, Wenjing; Bai, Xueyuan; Di Nunzio, Giada; Fan, Liangliang; Zhao, Yueming; Ren, Limei; Zhao, Ronghua; Bian, Shuai; Liu, Meichen; Wei, Yuchi; Zhao, Daqing; Wang, Jiawen

Accumulation of neutral lipids in dystrophic neurites surrounding amyloid plaques in Alzheimer's disease.

阿尔茨海默病中淀粉样斑块周围营养不良性神经突中中性脂质的积累

Huang Hao, Sharoar Md Golam, Pathoulas Joseph, Fan Liangliang, He Wanxia, Xiang Rong, Yan Riqiang

Associated factors of osteoporosis in Chinese patients with rheumatoid arthritis: A systematic review and meta-analysis

中国类风湿性关节炎患者骨质疏松症的相关因素:系统评价和荟萃分析

Song, Zhiming; Fan, Liangliang; Wang, Hongyan; Cao, Jun; Wen, Zhifei; Tao, Yanmin; Zhang, Xiangeng

Whole-exome sequencing detected a novel AIFM1 variant in a Han-Chinese family with Cowchock syndrome

全外显子组测序在一个患有考乔克综合征的汉族家族中发现了一个新的AIFM1变异。

Wang, Chenyu; Lin, Zhaojing; Yuan, ZhuangZhuang; Tang, Tieyu; Fan, Liangliang; Liu, Yihui; Wu, Xuan

Novel heterozygous mutation in COL4A4 responsible for Alport syndrome in a Chinese family

中国某家族中发现COL4A4基因的新型杂合突变导致Alport综合征

Du, Ran; Liu, Jishi; Hu, Yiqiao; Peng, Song; Fan, Liangliang; Xiang, Rong; Huang, Hao

Case report: A de novo Non-sense SOX9 mutation (p.Q417*) located in transactivation domain is Responsible for Campomelic Dysplasia

病例报告:位于转录激活结构域的新生无义SOX9突变(p.Q417*)是坎波梅利克发育不良的病因

Qiao, Xingxing; Wu, Liping; Tang, Jianjun; Xiang, Rong; Fan, Liangliang; Huang, Hao; Chen, Yaqin

Baicalin Prevents Myocardial Ischemia/Reperfusion Injury Through Inhibiting ACSL4 Mediated Ferroptosis

黄芩苷通过抑制 ACSL4 介导的铁死亡预防心肌缺血/再灌注损伤

Zhenyu Fan, Liangliang Cai, Shengnan Wang, Jing Wang, Bohua Chen