Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications
Bian, Panpan, Chai, Jing, Xu, Baicheng
Published in Journal of International Advanced Otology (01.09.2023)
Published in Journal of International Advanced Otology (01.09.2023)
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Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene
Wang, Yanli, Liu, Zengping, Chen, Chi, Li, Yong, Guan, Minxin, Xu, Baicheng, Guo, Yufen
Published in Stem cell research (01.05.2022)
Published in Stem cell research (01.05.2022)
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Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China
Bian, Panpan, Xu, Baicheng, Zhao, Xiaoyun, Zhu, YiMing, Chen, Chi, Chen, XingJian, Liu, Xiaowen, Wang, Yanli, Guo, Yufen
Published in Inquiry (Chicago) (01.10.2022)
Published in Inquiry (Chicago) (01.10.2022)
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A novel intronic variant causing aberrant splicing identified in two deaf Chinese siblings with enlarged vestibular aqueducts
Wang, Suyang, Zhu, Yi‐Ming, Xu, ChenYang, Ding, Wenjuan, Jia, Hui, Bian, Panpan, Xu, Baicheng, Guo, Yufen, Liu, Xiaowen
Published in Molecular genetics & genomic medicine (01.02.2024)
Published in Molecular genetics & genomic medicine (01.02.2024)
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Targeted Next Generation Sequencing Revealed a Novel Homozygous Loss-of-Function Mutation in ILDR1 Gene Causes Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in a Chinese Family
An, Jinxia, Yang, Jie, Wang, Yan, Wang, Yanxia, Xu, Baicheng, Xie, Guangmei, Chai, Sanming, Liu, Xiaoling, Xu, Sijuan, Wen, Xiaoxiao, He, Qing, Liu, Huijun, Li, Chen, Dey, Subrata Kumar, Ni, Yali, Banerjee, Santasree
Published in Frontiers in genetics (05.02.2019)
Published in Frontiers in genetics (05.02.2019)
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Deafness-associated tRNAPhe mutation impaired mitochondrial and cellular integrity
Chen, Xiaowan, Meng, Feilong, Chen, Chao, Li, Shujuan, Chou, Zhiqiang, Xu, Baicheng, Mo, Jun Q., Guo, Yufen, Guan, Min-Xin
Published in The Journal of biological chemistry (01.05.2024)
Published in The Journal of biological chemistry (01.05.2024)
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Research on congenital severe-to-profound sensorineural hearing loss associated with central lucency of the bony island of the lateral semicircular canal
Wang, Qin, Bian, Panpan, Bai, Shengjin, Chen, Chi, Wang, Yanli, Guo, Yufen, Xu, Baicheng
Published in Acta oto-laryngologica (01.02.2023)
Published in Acta oto-laryngologica (01.02.2023)
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The effect of SLC26A4 gene mutations on long-term rehabilitative outcomes in cochlear implant patients
Wang, Qin, Hu, Jian, Bian, Panpan, Chen, Chi, Wang, Yanli, Cheng, Shihong, Guo, Yufen, Xu, Baicheng
Published in Acta oto-laryngologica (01.02.2023)
Published in Acta oto-laryngologica (01.02.2023)
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Surgical management of mucosal contact headache
Li, Yong, Liu, Zengping, Xu, Baicheng, Jia, Hui, Wang, Yanli, Zhu, Yiming, Zhao, Xiaoyun, Guo, Yufen
Published in American journal of otolaryngology (01.03.2022)
Published in American journal of otolaryngology (01.03.2022)
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Analysis between phenotypes and genotypes of inner ear malformation
Wang, Suyang, Ding, Wenjuan, Chen, Chi, Xu, Baicheng, Liu, Xiaowen, Bian, Panpan, Guo, Yufen
Published in Acta oto-laryngologica (04.03.2019)
Published in Acta oto-laryngologica (04.03.2019)
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Deafness-associated tRNA Phe mutation impaired mitochondrial and cellular integrity
Chen, Xiaowan, Meng, Feilong, Chen, Chao, Li, Shujuan, Chou, Zhiqiang, Xu, Baicheng, Mo, Jun Q, Guo, Yufen, Guan, Min-Xin
Published in The Journal of biological chemistry (27.03.2024)
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Published in The Journal of biological chemistry (27.03.2024)
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The screening report of hearing and the common deafness gene in the elderly
Bao, Xiaolin, Wang, Yuan, Xu, Baicheng, Liu, Xiaowen, Guo, Jialiang, Guo, Yufen
Published in Minerva surgery (01.04.2023)
Published in Minerva surgery (01.04.2023)
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