Efficient introduction of an isogenic homozygous mutation to induced pluripotent stem cells from a hereditary hearing loss family using CRISPR/Cas9 and single-stranded donor oligon... von Dong, Yunpeng, Peng, Tao, Wu, Weijing, Tan, Donghui, Liu, Xuezhong, Xie, Dinghua

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Vestibular function in children with cochlear implant: Impact and evaluation von Deng, Jianhang, Zhu, Qianchen, Zhang, Kangjia, Xie, Dinghua, Wu, Weijing

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Zebrafish myo7aa affects congenital hearing by regulating Rho-GTPase signaling von Xie, Binling, Liang, Jiaxin, Jiang, Jifan, Zeng, Ting, Liu, Ling, Xie, Dinghua, Zhu, Ganghua, Xiong, Lei, Zhang, Kanjia, Liu, Dong, Gong, Jie, Chen, Xiangding, Lai, Ruosha, Xie, Huaping

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Mutation of the ATP-gated P2X₂ receptor leads to progressive hearing loss and increased susceptibility to noise von Yan, Denise, Zhu, Yan, Walsh, Tom, Xie, Dinghua, Yuan, Huijun, Sirmaci, Asli, Fujikawa, Taro, Wong, Ann Chi Yan, Loh, Tze L., Du, Lilin, Grati, M'hamed, Vlajkovic, Srdjan M., Blanton, Susan, Ryan, Allen F., Chen, Zheng-Yi, Thorne, Peter R., Kachar, Bechara, Tekin, Mustafa, Zhao, Hong-Bo, Housley, Gary D., King, Mary-Claire, Liu, Xue Z.

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Anti-neutrophil cytoplasmic antibody-associated hypertrophic cranial pachymeningitis and otitis media: a review of literature von Peng, Anquan, Yang, Xinming, Wu, Weijing, Xiao, Zian, Xie, Dinghua, Ge, Shenglei

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The Role of EGFR/PI3K/Akt/cyclinD1 Signaling Pathway in Acquired Middle Ear Cholesteatoma von Liu, Wei, Ren, Hongmiao, Ren, Jihao, Yin, Tuanfang, Hu, Bing, Xie, Shumin, Dai, Yinghuan, Wu, Weijing, Xiao, Zian, Yang, Xinming, Xie, Dinghua

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Whole-exome sequencing to decipher the genetic heterogeneity of hearing loss in a Chinese family with deaf by deaf mating von Qing, Jie, Yan, Denise, Zhou, Yuan, Liu, Qiong, Wu, Weijing, Xiao, Zian, Liu, Yuyuan, Liu, Jia, Du, Lilin, Xie, Dinghua, Liu, Xue Zhong

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Intelligence Development of Pre-Lingual Deaf Children with Unilateral Cochlear Implantation von Chen, Mo, PH.D candidate, Wang, Zhaoyan, Master candidate, Zhang, Zhiwen, Master candidate, Li, Xun, Master candidate, Wu, Weijing, PH.D,MD, Xie, Dinghua, PH.D,MD, Xiao, Zi-an, PH.D, MD

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Induced pluripotent stem cells:Landscape for studying and treating hereditary hearing loss von Peng, Tao, Dong, Yunpeng, Zhu, Ganghua, Xie, Dinghua

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（-）-Epigallocatechin-3-gallate protects spiral ganglion neurons against amikacin-induced apoptosis von Qianghe Liu Dinghua Xie Xinming Yang

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Role of Hsp90/Akt pathway in the pathogenesis of gentamicin-induced hearing loss von Lai, Ruosha, Li, Wei, Hu, Peng, Xie, Dinghua, Wen, Jie

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The application of genome editing in studying hearing loss von Zou, Bing, Mittal, Rahul, Grati, M'hamed, Lu, Zhongmin, Shu, Yilai, Tao, Yong, Feng, Youg, Xie, Dinghua, Kong, Weijia, Yang, Shiming, Chen, Zheng-Yi, Liu, Xuezhong

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Subunits of voltage-gated calcium channels in murine spiral ganglion cells von Xie, Dinghua, Hu, Peng, Xiao, Zi'An, Wu, Weijing, Chen, Yong, Xia, Kun

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Cochlear implantation in prelingually deafened patients: Evaluation in hearing, speech ability, and quality of life von Wu, Mengbo, Li, Huan, Li, Shaohong, Wu, Weijing, Xie, Dinghua, Lai, Ruosha

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Activation of the EGFR/Akt/NF-κB/cyclinD1 survival signaling pathway in human cholesteatoma epithelium von Liu, Wei, Yin, Tuanfang, Ren, Jihao, Li, Lihua, Xiao, Zian, Chen, Xing, Xie, Dinghua

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(−)-Epigallocatechin-3-gallate protects cultured spiral ganglion cells from H2O2-induced oxidizing damage von Xie, Dinghua, Liu, Guohui, Zhu, Ganghua, Wu, Weijing, Ge, Shenglei

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Congenital Middle Ear Malformation with Common Deafness Gene Mutation Analysis: A Review of 813 Profound Sensorineural Hearing Loss Child Patients von Dong, Yunpeng, He, Xiangbo, Wu, Weijing, Yang, Shu, Peng, Anquan, Xiao, Zian, Liu, Yuyuan, Gao, Shuichao, Tan, Donghui, Liu, Xue Zhong, Xie, Dinghua

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DAPT mediates atoh1 expression to induce hair cell-like cells von Ren, Hongmiao, Guo, Weiwei, Liu, Wei, Gao, Weiqiang, Xie, Dinghua, Yin, Tuanfang, Yang, Shiming, Ren, Jihao

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Acute Mediastinitis Associated with Foreign Body Erosion from the Hypopharynx and Esophagus von Liu, Jiajia, Zhang, Xiaoli, Xie, Dinghua, Peng, Anquan, Yang, Xinming, Yu, Fenglei, Liu, Deliang

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Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China von Qing, Jie, Zhou, Yuan, Lai, Ruosha, Hu, Peng, Ding, Yan, Wu, Weijing, Xiao, Zian, Ho, Phi T, Liu, Yuyuan, Liu, Jia, Du, Lilin, Yan, Denise, Goldstein, Bradley J, Liu, Xuezhong, Xie, Dinghua

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