Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing

by Qing Chang, Wenxue Tang, Yeunjung Kim, Xi Lin
Published 2015-01-01

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing

by Sen Zhang, Hongen Xu, Hongen Xu, Yongan Tian, Danhua Liu, Xinyue Hou, Beiping Zeng, Bei Chen, Huanfei Liu, Ruijun Li, Xiaohua Li, Bin Zuo, Ryan Tang, Wenxue Tang, Wenxue Tang, Wenxue Tang
Published 2021-06-01

Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice.

by Qing Chang, Wenxue Tang, Shoeb Ahmad, Binfei Zhou, Xi Lin
Published 2008-01-01

Localization of Glucose Transporter 10 to Hair Cells’ Cuticular Plate in the Mouse Inner Ear

by Bei Chen, Yunfeng Wang, Manying Geng, Xi Lin, Wenxue Tang
Published 2018-01-01

Myeloid-derived suppressor cells—new and exciting players in lung cancer

by Zhenzhen Yang, Jiacheng Guo, Lanling Weng, Wenxue Tang, Shuiling Jin, Wang Ma
Published 2020-01-01

Roles of HMGB1 in regulating myeloid-derived suppressor cells in the tumor microenvironment

by Shuiling Jin, Zhenzhen Yang, Xin Hao, Wenxue Tang, Wang Ma, Hong Zong
Published 2020-06-01

Assessing Community-Level Livability Using Combined Remote Sensing and Internet-Based Big Geospatial Data

by Likai Zhu, Yuanyuan Guo, Chi Zhang, Jijun Meng, Lei Ju, Yuansuo Zhang, Wenxue Tang
Published 2020-12-01

Perrault syndrome: Clinical report and retrospective analysis

by Zhaoyu Pan, Hongen Xu, Yongan Tian, Danhua Liu, Huanfei Liu, Ruijun Li, Qian Dou, Bin Zuo, Rongqun Zhai, Wenxue Tang, Wei Lu
Published 2020-10-01

Early truncation of the N‐terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype

by Yanfang Mi, Danhua Liu, Beiping Zeng, Yongan Tian, Hui Zhang, Bei Chen, Juanli Zhang, Hong Xue, Wenxue Tang, Yulin Zhao, Hongen Xu
Published 2021-01-01

Auditory Neuropathy Spectrum Disorder (ANSD)—Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families

by Rongqun Zhai, Haifeng Feng, Qingli Li, Wei Lu, Danhua Liu, Yongan Tian, Huanfei Liu, Ruijun Li, Bin Zuo, Wenxue Tang, Hongen Xu, Bei Chen
Published 2020-01-01

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

by Jinying Li, Hongen Xu, Jianfeng Sun, Yongan Tian, Danhua Liu, Yaping Qin, Huanfei Liu, Ruijun Li, Lingling Neng, Xiaohua Deng, Binbin Xue, Changyun Yu, Wenxue Tang
Published 2021-01-01

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients

by Zhaoyu Pan, Hongen Xu, Bei Chen, Yongan Tian, Linlin Zhang, Sen Zhang, Danhua Liu, Huanfei Liu, Ruijun Li, Xinxin Hu, Jingyuan Guan, Wenxue Tang, Wei Lu
Published 2021-02-01

Thymosin alpha-1 blocks the accumulation of myeloid suppressor cells in NSCLC by inhibiting VEGF production

by Zhenzhen Yang, Jiacheng Guo, Kang Cui, Yabing Du, Huan Zhao, Lili Zhu, Lanling Weng, Wenxue Tang, Jiancheng Guo, Tengfei Zhang, Xiaojing Shi, Hong Zong, Shuiling Jin, Wang Ma
Published 2020-11-01

Deoxygedunin, a natural product with potent neurotrophic activity in mice.

by Sung-Wuk Jang, Xia Liu, Chi Bun Chan, Stefan A France, Iqbal Sayeed, Wenxue Tang, Xi Lin, Ge Xiao, Raul Andero, Qiang Chang, Kerry J Ressler, Keqiang Ye
Published 2010-07-01

Involvement of Glutathione Depletion in Selective Cytotoxicity of Oridonin to p53-Mutant Esophageal Squamous Carcinoma Cells

by Yinchao Li, Yinchao Li, Nana Li, Nana Li, Jianxiang Shi, Tanzeel Ahmed, Tanzeel Ahmed, Hongmin Liu, Hongmin Liu, Jiancheng Guo, Wenxue Tang, Yongjun Guo, Qi Zhang, Qi Zhang, Qi Zhang
Published 2020-01-01

Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans

by Xia Xue, Jianxiang Shi, Hongen Xu, Yaping Qin, Zengguang Yang, Shuaisheng Feng, Danhua Liu, Liguo Jian, Linlin Hua, Yaohe Wang, Qi Zhang, Xueyong Huang, Xiaoju Zhang, Xinxin Li, Chunguang Chen, Jiancheng Guo, Wenxue Tang, Jianbo Liu
Published 2021-02-01

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease

by Zhigang Wang, Hongen Xu, Tianchao Xiang, Danhua Liu, Fei Xu, Lixiang Zhao, Yonghua Feng, Linan Xu, Jialu Liu, Ye Fang, Huanfei Liu, Ruijun Li, Xinxin Hu, Jingyuan Guan, Longshan Liu, Guiwen Feng, Qian Shen, Hong Xu, Dmitrij Frishman, Wenxue Tang, Jiancheng Guo, Jia Rao, Wenjun Shang
Published 2021-07-01

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next‐generation sequencing of the SLC26A4 gene

by Yongan Tian, Hongen Xu, Danhua Liu, Juanli Zhang, Zengguang Yang, Sen Zhang, Huanfei Liu, Ruijun Li, Yingtao Tian, Beiping Zeng, Tong Li, Qianyu Lin, Haili Wang, Xiaohua Li, Wei Lu, Ying Shi, Yan Zhang, Hui Zhang, Chang Jiang, Ying Xu, Bei Chen, Jun Liu, Wenxue Tang
Published 2021-08-01

Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma

by Wei Cao, Hayan Lee, Wei Wu, Aubhishek Zaman, Sean McCorkle, Ming Yan, Justin Chen, Qinghe Xing, Nasa Sinnott-Armstrong, Hongen Xu, M. Reza Sailani, Wenxue Tang, Yuanbo Cui, Jia liu, Hongyan Guan, Pengju Lv, Xiaoyan Sun, Lei Sun, Pengli Han, Yanan Lou, Jing Chang, Jinwu Wang, Yuchi Gao, Jiancheng Guo, Gundolf Schenk, Alan Hunter Shain, Fred G. Biddle, Eric Collisson, Michael Snyder, Trever G. Bivona
Published 2020-07-01