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

Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutation.

维生素 A 治疗可以恢复由莱伯氏遗传性视神经病变相关的 mtDNA 突变引起的视力障碍

期刊:JCI Insight
影响因子:6.1
doi:10.1172/jci.insight.188962
Ai Cheng, Li Huiying, Wang Chunyan, Ji Yanchun, Wallace Douglas C, Qian Junbin, Zhu Yimin, Guan Min-Xin
神经科学
发表日期：2025
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Leber's hereditary optic neuropathy-associated ND1 3733G>C mutation ameliorates the mitochondrial quality control and cellular homeostasis.

Leber 遗传性视神经病变相关的 ND1 3733G>C 突变可改善线粒体质量控制和细胞稳态

期刊:Journal of Biological Chemistry
影响因子:3.9
doi:10.1016/j.jbc.2025.110464
Yasheng Meiheriayi, Ji Yanchun, He Yunfan, Yi Qiuzi, Zhang Huanhuan, Shan Wenqi, Wang Kai, Zhang Juanjuan, Li Ya, Meng Feilong, Zhang Minglian, Mo Jun Qin, Wei Shihui, Guan Min-Xin
神经科学
细胞生物学
线粒体
发表日期：2025
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Mechanism of adenosine monophosphate-activated protein kinase promoting lower extremity varicose veins development via cytoskeletal dynamics.

腺苷单磷酸活化蛋白激酶通过细胞骨架动力学促进下肢静脉曲张发展的机制

期刊:BMC Cardiovascular Disorders
影响因子:2.3
doi:10.1186/s12872-025-04821-6
Zhang Yongmei, Ju Zhinan, Dai Kanghui, Wan Liqun, Zhou Guangmao, Ji Yanchun, Qiu Jiehua
细胞生物学
发表日期：2025
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Identification of TGFBR1 Gene Variants in Two Chinese Pedigrees with Loeys-Dietz Syndrome

在两个中国Loeys-Dietz综合征家系中鉴定出TGFBR1基因变异

期刊:Revista Brasileira De Cirurgia Cardiovascular
影响因子:1.2
doi:10.21470/1678-9741-2023-0495
Qiu, Jiehua; Chen, Wei; Min, Xixi; Shen, Yang; Zhu, Xianhua; Qiu, Jiacong; Zeng, Xiande; Zeng, Xiong; Ji, Yanchun; Zhou, Weimin
发表日期：2025
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Autoinducer-2 promotes the colonization of Lactobacillus rhamnosus GG to improve the intestinal barrier function in a neonatal mouse model of antibiotic-induced intestinal dysbiosis

自诱导物-2促进鼠李糖乳杆菌GG的定植，从而改善抗生素诱导的新生小鼠肠道菌群失调模型中的肠道屏障功能。

期刊:Journal of Translational Medicine
影响因子:7.5
doi:10.1186/s12967-024-04991-5
Hu, Riqiang; Yang, Ting; Ai, Qing; Shi, Yuan; Ji, Yanchun; Sun, Qian; Tong, Bei; Chen, Jie; Wang, Zhengli
微生物学
肠道菌群
发表日期：2024
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Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family

中国某家族中发现一种新的线粒体tRNACys 5802A>G突变与肥胖相关

期刊:Bioscience Reports
影响因子:4.7
doi:10.1042/BSR20192153
Wang, Jinling; Zhao, Ningning; Mao, Xiaoting; Meng, Feilong; Huang, Ke; Dong, Guanping; Ji, Yanchun; Fu, JunFen
肥胖
代谢
线粒体
发表日期：2020
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Reply to comments on: "Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family"

回复关于“中国某家族中一种新的线粒体tRNACys 5802A>G突变与肥胖相关”的评论

期刊:Bioscience Reports
影响因子:4.7
doi:10.1042/BSR20200131
Wang, Jinling; Zhao, Ningning; Mao, Xiaoting; Meng, Feilong; Huang, Ke; Dong, Guanping; Ji, Yanchun; Fu, JunFen
肥胖
线粒体
代谢
发表日期：2020
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Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families

在三个汉族家族中，莱伯氏遗传性视神经病变与线粒体ND1基因的T3866C突变有关。

期刊:Investigative Ophthalmology & Visual Science
影响因子:4.7
doi:10.1167/iovs.11-9109
Zhou, Xiangtian; Qian, Yaping; Zhang, Juanjuan; Tong, Yi; Jiang, Pingping; Liang, Min; Dai, Xianning; Zhou, Huihui; Zhao, Fuxin; Ji, Yanchun; Mo, Jun Qin; Qu, Jia; Guan, Min-Xin
线粒体
发表日期：2012
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Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

在一个携带ND4 G11778A突变的汉族大家系中，莱伯氏遗传性视神经病变的发生率和外显率都非常高。

期刊:Molecular Genetics and Metabolism
影响因子:3.5
doi:10.1016/j.ymgme.2010.04.013
Zhou, Xiangtian; Zhang, Hongxing; Zhao, Fuxin; Ji, Yanchun; Tong, Yi; Zhang, Juanjuan; Zhang, Yu; Yang, Li; Qian, Yaping; Lu, Fan; Qu, Jia; Guan, Min-Xin
发表日期：2010
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