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

Echocardiographic characteristics of PRKAG2 syndrome: a research using three-dimensional speckle tracking echocardiography compared with sarcomeric hypertrophic cardiomyopathy

PRKAG2综合征的超声心动图特征：一项采用三维斑点追踪超声心动图与肉节肥厚型心肌病比较的研究

期刊:Cardiovascular Ultrasound
影响因子:1.6
doi:10.1186/s12947-022-00284-3
Tang, Lu; Li, Xuejie; Zhou, Nianwei; Jiang, Yingying; Pan, Cuizhen; Shu, Xianhong
心血管
心肌病
发表日期：2022
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The mechanical effects of CRT promoting autophagy via mitochondrial calcium uniporter down-regulation and mitochondrial dynamics alteration.

CRT 的机械效应通过线粒体钙单向转运蛋白下调和线粒体动力学改变促进自噬

期刊:Journal of Cellular and Molecular Medicine
影响因子:4.2
doi:10.1111/jcmm.14227
Yu Ziqing, Gong Xue, Yu Yong, Li Minghui, Liang Yixiu, Qin Shengmei, Fulati Zibire, Zhou Nianwei, Shu Xianhong, Nie Zhenning, Dai Shimo, Chen Xueying, Wang Jingfeng, Chen Ruizhen, Su Yangang, Ge Junbo
免疫/内分泌
线粒体
自噬
发表日期：2019
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A family with Danon disease caused by a splice site mutation in LAMP2 that generates a truncated protein

一个患有达农病（Danon disease）的家族，该病由LAMP2基因剪接位点突变引起，导致产生截短蛋白。

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.561
Zhou, Nianwei; Cui, Jie; Zhao, Weipeng; Jiang, Yingying; Zhu, Wenqing; Tang, Lu; Li, Xuejie; Sun, Minmin; Pan, Cuizhen; Shu, Xianhong
LAMP2
发表日期：2019
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Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance

全外显子组测序揭示线粒体心肌病家系中MT-ND5基因的新突变：患者表现出双心室肥厚、高乳酸血症、肺动脉高压和运动耐量下降。

期刊:Anatolian Journal of Cardiology
影响因子:1.5
doi:10.14744/AnatolJCardiol.2018.53258
Zhou, Nianwei; Tang, Lu; Jiang, Yingying; Qin, Shengmei; Cui, Jie; Wang, Yanan; Zhu, Wenqing; Zhao, Weipeng; Pan, Cuizhen; Shu, Xianhong
肺动脉高压
心血管
线粒体
心肌病
发表日期：2019
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