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

Effects of cognitive behavioral therapy on anxiety and depression in patients with myocardial infarction: a systematic review and meta-analysis

认知行为疗法对心肌梗死患者焦虑和抑郁的影响:系统评价和荟萃分析

Wei, Xin; Fu, Lin; Liu, Huiling; Huang, Zhihong; Lu, Xiaoqian

Correction: Effects of cognitive behavioral therapy on anxiety and depression in patients with myocardial infarction: a systematic review and meta-analysis

更正:认知行为疗法对心肌梗死患者焦虑和抑郁的影响:系统评价和荟萃分析

Wei, Xin; Fu, Lin; Liu, Huiling; Huang, Zhihong; Lu, Xiaoqian

Serum osteopontin as a prognostic biomarker in acute exacerbations of chronic obstructive pulmonary disease

血清骨桥蛋白作为慢性阻塞性肺疾病急性加重的预后生物标志物

Ma, Kai-Shu; Li, Li-Na; Ma, Yi-Cheng; Fan, Ru-Liu; Chen, Gang; Zhao, Hui; Qu, Kai-Xin; Fu, Lin

Analysis of low-density lipoprotein receptor gene mutations in a family with familial hypercholesterolemia

家族性高胆固醇血症一家系低密度脂蛋白受体基因突变分析

Ya-Nan Hu, Min Wu, Hong-Ping Yu, Qiu-Yan Wu, Ying Chen, Jian-Hui Zhang, Dan-Dan Ruan, Yan-Ping Zhang, Jing Zou, Li Zhang, Xin-Fu Lin, Zhu-Ting Fang, Li-Sheng Liao, Fan Lin, Hong Li, Jie-Wei Luo

Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis

Nrf2/HMGB1/TLR4/NF-κB信号通路在狼疮性肾炎中的潜在调控作用

Shi-Jie Li #, Dan-Dan Ruan #, Wei-Zhen Wu #, Min Wu #, Qiu-Yan Wu, Han-Lu Wang, Yuan-Yuan Ji, Yan-Ping Zhang, Xin-Fu Lin, Zhu-Ting Fang, Li-Sheng Liao, Jie-Wei Luo, Mei-Zhu Gao, Jia-Bin Wu0

Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

PHEX 突变 p.Glu145* 和 p.Trp749Arg 在 X 连锁低磷血症性佝偻病家族中通过 FGF23 启动子转录负调控机制发挥作用

Yu-Mian Gan #, Yan-Ping Zhang #, Dan-Dan Ruan #, Jian-Bin Huang #, Yao-Bin Zhu, Xin-Fu Lin, Xiao-Ping Xiao, Qiong Cheng, Zhen-Bo Geng, Li-Sheng Liao, Fa-Qiang Tang, Jie-Wei Luo

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency

一种新的复合杂合变异与遗传性 VII 因子缺乏症家族中的血尿有关

Ya-Nan Hu, Yu-Mian Gan, Yan-Ping Zhang, Dan-Dan Ruan, Yao-Bin Zhu, Xin-Fu Lin, Zhu-Ting Fang, Li-Sheng Liao, Fa-Qiang Tang, Jie-Wei Luo

Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

对一个患有布鲁加达综合征并因SCN5A基因新突变而猝死的家族进行分析

Yao-Bin Zhu,Jian-Hui Zhang,Yuan-Yuan Ji,Ya-Nan Hu,Han-Lu Wang,Dan-Dan Ruan,Xiao-Rong Meng,Xin-Fu Lin,Jie-Wei Luo,Wei Chen

A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1

一个因 PROS1 基因 Leu607Ser 杂合突变导致蛋白质翻译障碍而患有蛋白质 S 缺乏症的血栓形成倾向家族

Yan-Ping Zhang #, Bin Lin #, Yuan-Yuan Ji #, Ya-Nan Hu #, Xin-Fu Lin #, Yi Tang, Jian-Hui Zhang, Shao-Jie Wu, Sen-Lin Cai, Yan-Feng Zhou, Ting Chen, Zhu-Ting Fang, Jie-Wei Luo

Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene

一例遗传性肾小管酸中毒家族致病基因的筛选及功能探讨

Li Chen #, Han-Lu Wang #, Yao-Bin Zhu #, Zhao Jin #, Jian-Bin Huang, Xin-Fu Lin, Jie-Wei Luo, Zhu-Ting Fang