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

Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness

基因疗法与人工耳蜗植入术在恢复先天性耳聋患者的听力功能和言语感知方面的比较

Cheng, Xiaoting; Zhong, Jiake; Zhang, Jiajia; Cui, Chong; Jiang, Luoying; Liu, Yang-Wenyi; Chen, Yuxin; Cao, Qi; Wang, Daqi; Cheng, Guiqing; Zong, Yuxin; Shen, Min; Xu, Chunxin; Lv, Jun; Wang, Hui; Zhang, Longlong; Zhu, Biyun; Tang, Honghai; Wang, Jinghan; Fan, Xintai; Fang, Yanqing; Guo, Luo; Guo, Jiawei; Chen, Liheng; Yin, Yanbo; Wang, Zijing; Han, Lei; Hu, Shaowei; Wang, Shengyi; Qin, Guoyou; Liu, Xuezhong; Sang, Jinqiu; Zeng, Fangang; Wang, Wuqing; Chen, Bing; Chen, Zheng-Yi; Li, Huawei; Shu, Yilai

Effects of Oligomeric Proanthocyanidins on Cadmium-Induced Extracellular Matrix Damage via Inhibiting the ERK1/2 Signaling Pathway in Chicken Chondrocytes

低聚原花青素通过抑制ERK1/2信号通路对镉诱导的鸡软骨细胞外基质损伤的影响

Gu, Jianhong; Liu, Dan; Gong, Anqing; Zhao, Xinrui; Zhou, Jiatao; Wang, Panting; Xia, Han; Song, Ruilong; Ma, Yonggang; Zou, Hui; Memon, Muhammad Azhar; Yuan, Yan; Liu, Xuezhong; Bian, Jianchun; Liu, Zongping; Tong, Xishuai

Treatment of monogenic and digenic dominant genetic hearing loss by CRISPR-Cas9 ribonucleoprotein delivery in vivo.

利用 CRISPR-Cas9 核糖核蛋白在体内递送治疗单基因和双基因显性遗传性听力损失

Tao Yong, Lamas Veronica, Du Wan, Zhu Wenliang, Li Yiran, Whittaker Madelynn N, Zuris John A, Thompson David B, Rameshbabu Arun Prabhu, Shu Yilai, Gao Xue, Hu Johnny H, Pei Charles, Kong Wei-Jia, Liu Xuezhong, Wu Hao, Kleinstiver Benjamin P, Liu David R, Chen Zheng-Yi

Gambogenic acid induces cell death in human osteosarcoma through altering iron metabolism, disturbing the redox balance, and activating the P53 signaling pathway

新木酸通过改变铁代谢、扰乱氧化还原平衡和激活 P53 信号通路诱导人类骨肉瘤细胞死亡

Zilin Liu, Xuezhong Wang, Jianping Li, Xiaoming Yang, Jun Huang, Chuang Ji, Xuyang Li, Lan Li, Jianlin Zhou, Yong Hu

Preimplantation genetic testing for hereditary hearing loss in Chinese population

中国人群遗传性听力损失的植入前基因检测

Bi, Qingling; Huang, Shasha; Wang, Hui; Gao, Xue; Ma, Minyue; Han, Mingyu; Lu, Sijia; Kang, Dongyang; Nourbakhsh, Aida; Yan, Denise; Blanton, Susan; Liu, Xuezhong; Yuan, Yongyi; Yao, Yuanqing; Dai, Pu

Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History

TMPRSS3 (DFNB10/DFNB8) 的基因型-表型相关性及其自然史研究

Nisenbaum, Eric; Yan, Denise; Shearer, A Eliot; de Joya, Evan; Thielhelm, Torin; Russell, Nicole; Staecker, Hinrich; Chen, Zhengyi; Holt, Jeffrey R; Liu, Xuezhong

Responsiveness of the electrically stimulated cochlear nerve in patients with a missense variant in ACTG1: Preliminary Results

ACTG1错义变异患者耳蜗神经电刺激反应性:初步结果

Yuan, Yi; Yan, Denise; Skidmore, Jeffrey; Chapagain, Prem; Liu, Xuezhong; He, Shuman

Review of Genotype-Phenotype Correlations in Usher Syndrome

Usher综合征基因型-表型相关性研究综述

Nisenbaum, Eric; Thielhelm, Torin P; Nourbakhsh, Aida; Yan, Denise; Blanton, Susan H; Shu, Yilai; Koehler, Karl R; El-Amraoui, Aziz; Chen, Zhengyi; Lam, Byron L; Liu, Xuezhong

A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder

TMEM43 无义变异导致连接蛋白相关功能紊乱,并引发常染色体显性遗传性听觉神经病谱系障碍。

Jang, Minwoo Wendy; Oh, Doo-Yi; Yi, Eunyoung; Liu, Xuezhong; Ling, Jie; Kim, Nayoung; Sharma, Kushal; Kim, Tai Young; Lee, Seungmin; Kim, Ah-Reum; Kim, Min Young; Kim, Min-A; Lee, Mingyu; Han, Jin-Hee; Han, Jae Joon; Park, Hye-Rim; Kim, Bong Jik; Lee, Sang-Yeon; Woo, Dong Ho; Oh, Jayoung; Oh, Soo-Jin; Du, Tingting; Koo, Ja-Won; Oh, Seung-Ha; Shin, Hyun-Woo; Seong, Moon-Woo; Lee, Kyu-Yup; Kim, Un-Kyung; Shin, Jung Bum; Sang, Shushan; Cai, Xinzhang; Mei, Lingyun; He, Chufeng; Blanton, Susan H; Chen, Zheng-Yi; Chen, Hongsheng; Liu, Xianlin; Nourbakhsh, Aida; Huang, Zaohua; Kang, Kwon-Woo; Park, Woong-Yang; Feng, Yong; Lee, C Justin; Choi, Byung Yoon

Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy

内耳 Usher 综合征:病因及基因治疗进展

de Joya, Evan M; Colbert, Brett M; Tang, Pei-Ciao; Lam, Byron L; Yang, Jun; Blanton, Susan H; Dykxhoorn, Derek M; Liu, Xuezhong