Qiu Shiwei相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

Single Administration of AAV-mAtp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2-Induced Lysosomal Dysfunction in Hair Cells.

单次注射 AAV-mAtp6v1b2 基因疗法可挽救由 Atp6v1b2 诱导的毛细胞溶酶体功能障碍引起的听力和前庭疾病

期刊:Advanced Science

影响因子:14.1

doi:10.1002/advs.202408878

Wei Gege, Qiu Shiwei, Gao Xue, Zheng Lu, Chen Yijin, Ma Ying, Feng Haifeng, Yang Jinyuan, Dong Guojie, Nie Huiyi, Zhao Weihao, Li Xiaoge, Wang Guangqin, Xiong Wei, Dai Pu, Yuan Yongyi

细胞生物学

发表日期：2025

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Novel autosomal dominant syndromic hearing loss caused by COL4A2 -related basement membrane dysfunction of cochlear capillaries and microcirculation disturbance

一种由COL4A2相关基底膜功能障碍引起的耳蜗毛细血管和微循环紊乱导致的新型常染色体显性遗传综合征性听力损失。

期刊:Chinese Medical Journal

影响因子:7.3

doi:10.1097/CM9.0000000000003600

Yang, Jinyuan; Ma, Ying; Gao, Xue; Qiu, Shiwei; Li, Xiaoge; Zhao, Weihao; Chen, Yijin; Dong, Guojie; Lin, Rongfeng; Wei, Gege; Nie, Huiyi; Feng, Haifeng; Gu, Xiaoning; Gao, Bo; Dai, Pu; Yuan, Yongyi

发表日期：2025

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[Corrigendum] MCMV triggers ROS/NLRP3‑associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss

[更正] MCMV 可诱导小鼠内耳和培养的螺旋神经节神经元中 ROS/NLRP3 相关炎症小体的激活，从而导致感音神经性听力损失

期刊:International Journal of Molecular Medicine

影响因子:5.8

doi:10.3892/ijmm.2025.5514

Zhuang, Wei; Wang, Caiji; Shi, Xi; Qiu, Shiwei; Zhang, Shili; Xu, Bing; Chen, Min; Jiang, Wen; Dong, Hongyan; Qiao, Yuehua

免疫/内分泌

发表日期：2025

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Yishen Jiangzhuo decoction attenuates cisplatin‑induced acute kidney injury by inhibiting inflammation, oxidative stress and apoptosis through the TNF signal pathway

益肾降浊汤通过TNF信号通路抑制炎症、氧化应激和细胞凋亡减轻顺铂诱导的急性肾损伤

期刊:Experimental and Therapeutic Medicine

影响因子:2.4

doi:10.3892/etm.2024.12620

Dengyong Zheng, Xinglin Ruan, Qiang Wu, Yuliang Qiu, Shiwei Ruan

细胞生物学

Immunology/Inflammation

发表日期：2024

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A Novel GJB2 compound heterozygous mutation c.257C>G (p.T86R)/c.176del16 (p.G59A fs*18) causes sensorineural hearing loss in a Chinese family

一种新的GJB2复合杂合突变c.257C>G (p.T86R)/c.176del16 (p.G59A fs*18)导致中国某家族出现感音神经性听力损失。

期刊:Journal of Clinical Laboratory Analysis

影响因子:2.9

doi:10.1002/jcla.22444

Shi, Xi; Zhang, Yan; Qiu, Shiwei; Zhuang, Wei; Yuan, Na; Sun, Tiantian; Gao, Jian; Qiao, Yuehua; Liu, Ke

发表日期：2018

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Follicle-stimulating hormone inhibits cervical cancer via NF-κB pathway

促卵泡激素通过NF-κB通路抑制宫颈癌。

期刊:Oncotargets and Therapy

影响因子:2.8

doi:10.2147/OTT.S173339

Shi, Xi; Qiu, Shiwei; Zhuang, Wei; Wang, Caiji; Zhang, Shili; Yuan, Na; Yuan, Fukang; Qiao, Yuehua

免疫/内分泌

发表日期：2018

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Hearing analysis in heterozygous and homozygous klotho gene deficient mice

对杂合子和纯合子klotho基因缺陷小鼠进行听力分析

doi:10.1016/j.joto.2018.04.001

Yuan, Na; Qiu, Shiwei; Wang, Qian; Zhuang, Wei; Li, Guoping; Sun, Tiantian; Yang, Shiming; Qiao, Yuehua; Shi, Xi

发表日期：2018

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Polymorphism of the 86th amino acid in CX26 protein and hereditary deafness

CX26蛋白第86位氨基酸的多态性与遗传性耳聋

doi:10.1016/j.joto.2016.05.004

Shi, Xi; Qiu, Shiwei; Yan, Fendong; Shi, Lizhang; Xuan, Yili; Zhuang, Wei; Bei, Yingli; Yao, Hanli; Yuan, Na; Yang, Shiming; Qiao, Yuehua

发表日期：2016

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Vestibular-evoked myogenic potentials in miniature pigs

小型猪前庭诱发肌源性电位

doi:10.1016/j.joto.2016.05.003

Shi, Xi; Zhang, Yan; Li, Ya; Qiu, Shiwei; Zhang, Shili; Li, Yaohan; Yuan, Na; Qiao, Yuehua; Yang, Shiming

发表日期：2016

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A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family

对中国某家族遗传性耳聋的致病基因GJB2 c.176 del 16突变进行筛查分析

doi:10.1016/j.joto.2016.09.002

Jiang, Hao; Shi, Xi; Qiu, Shiwei; Dong, Yanfen; Qiao, Yuehua; Wei, Dongzhi

发表日期：2016

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