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

Deciphering the complexity: a case of kidney failure with co-inheritance of COL4A5 and APOE variants

解读复杂性:一例同时遗传COL4A5和APOE变异基因的肾衰竭病例

Zhang, Xiaoyan; Jin, Shi; Dai, Xuantong; Yao, Chenlin; Zhao, Ziyi; Lin, Fujun; Shi, Yiqin

Absent, Small, or Homeotic 2-Like-Mediated H3K4 Methylation and Nephrogenesis.

缺乏、少量或同源异型 2 样介导的 H3K4 甲基化与肾脏发生

Zhao Ziyi, Dai Xuantong, Jiang Gengru, Lin Fujun

Age at disease onset and risk of chronic kidney disease in patients with heterozygous disease-causing variants in COL4A3 and COL4A4

携带 COL4A3 和 COL4A4 杂合致病变异的患者发病年龄与慢性肾脏病风险的关系

Hu, Ningning; Sun, Lei; Dai, Xuantong; Zhao, Ziyi; Zhang, Xi; Rao, Jia; Zhou, Xujie; Fang, Yi; Shi, Yiqin; Jin, Shi; Xu, Xialian; Yu, Jiawei; Bian, Qi; Fan, Ying; Chen, Jia; Yang, Ning; Lin, Lirong; Peng, Zhangzhe; Liu, Guangyi; Zheng, Bixia; Sun, Yu; Zhao, Mingzhu; Sun, Xin; Xu, Hong; Huang, Wenyan; Jiang, Gengru; Lin, Fujun

Coenzyme Q10 supplementation in adult-onset focal segmental glomerulosclerosis caused by the Chinese common pathogenic variant c.737G > A (p.Ser246Asn) in the COQ8B gene

辅酶Q10补充剂可用于治疗由COQ8B基因中常见的中国致病变异c.737G>A (p.Ser246Asn)引起的成人发病局灶节段性肾小球硬化症

Jin, Shi; Shi, Yiqin; Lin, Pan; Liu, Hong; Xu, Xialian; Dai, Xuantong; Jiang, Gengru; Ding, Xiaoqiang; Lin, Fujun

Homozygous FAT1 frameshift mutation linked to glomerulotubular nephropathy with impaired cell adhesion and Rap1 signaling.

纯合 FAT1 移码突变与肾小管肾病相关,伴有细胞粘附和 Rap1 信号传导受损。

Fei Yang, Jin Zhouhui, He Li, Zhang Meng, Jiao Qiong, Liu Qiye, Lin Fujun, Wang Wei, Wang Niansong, Cao Aili, Cheng Dongsheng

A comprehensive immune repertoire signature distinguishes pulmonary infiltration in SARS-CoV-2 Omicron variant infection

全面的免疫谱特征可区分SARS-CoV-2 Omicron变异株感染中的肺部浸润

Li, Xuechuan; Zhu, Hongyi; Xu, Peipei; Zhang, Jie; Wang, Zhe; He, Hui; Shen, Fang; Jiang, Yi; Shen, Lijuan; Xiang, Jing; Yang, Linhua; Yang, Chao; Jiang, Hao; Gao, Ganglong; Jin, Junshuo; Shen, Huojian; Wang, Yinping; Wu, Linshi; Qian, Changlin; Liu, Dejun; Qiu, Weiqing; Li, Qiwei; Chen, Yuanwen; Lin, Fujun; Liu, Yun

A novel CLCN5 frame shift mutation responsible for Dent disease 1: Case report

一种导致 Dent 病 1 型的新型 CLCN5 移码突变:病例报告

Ni, Jiajia; Zhu, Yaju; Lin, Fujun; Guan, Wenbin; Jin, Jing; Li, Yufeng; Guo, Guimei

ACSL4 contributes to sevoflurane-induced ferroptotic neuronal death in SH-SY5Y cells via the 5' AMP-activated protein kinase/mammalian target of rapamycin pathway

ACSL4 通过 5' AMP 活化蛋白激酶/哺乳动物雷帕霉素靶蛋白通路促进七氟醚诱导的 SH-SY5Y 细胞铁凋亡

Lei Cheng, Xiaodan Zhu, Yang Liu, Kai Zhu, Kang Lin, Fujun Li

LncAPC drives Wnt/β-catenin activation and liver TIC self-renewal through EZH2 mediated APC transcriptional inhibition

LncAPC 通过 EZH2 介导的 APC 转录抑制驱动 Wnt/β-catenin 激活和肝脏 TIC 自我更新

Xiaomin Fu, Jizhen Lin, Fujun Qin, Zihe Yang, Yuechao Ding, Yong Zhang, Lu Han, Xiaoyan Zhu, Qinxian Zhang

Clinical and Histological Features of Phospholipase A2 Receptor-Associated and Thrombospondin Type-I Domain-containing 7A-Associated Idiopathic Membranous Nephropathy: A Single Center Retrospective Study from China

中国单中心回顾性研究:磷脂酶A2受体相关及血小板反应蛋白I型结构域7A相关特发性膜性肾病的临床及组织学特征

Zhang, Dan; Zou, Jun; Zhang, Chong; Zhang, Wenzhu; Lin, Fujun; Jiang, Gengru