Xianlin Liu - Xiangya Hospital, Central South University

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论文共 13 篇作者统计合作学者相似作者

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A Case of Langerhans Cell Histiocytosis with a Neck Mass As the First Symptom

Yuxin Xie, Xiaoming Kang,Xianlin Liu, Zhigan Wang,Qiancheng Jing

Clinical case reportsno. 4 (2025): e70365-e70365

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Modeling of Auditory Neuropathy Spectrum Disorders Associated with the TEME43 Variant Reveals Impaired Gap Junction Function of Ipsc-Derived Glia-Like Support Cells

Xiaoming Kang,Lu Ma,Jie Wen, Wei Gong,Xianlin Liu, Yihan Hu, Zhili Feng,Qiancheng Jing,Yuexiang Cai, Sijun Li,Xinzhang Cai,Kai Yuan,Yong Feng

FRONTIERS IN MOLECULAR NEUROSCIENCE (2025)

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ABCC1 Deficiency Potentiated Noise-Induced Hearing Loss in Mice by Impairing Cochlear Antioxidant Capacity

Jing Liu,Yijiang Bai,Yong Feng,Xianlin Liu,Bo Pang,Shuai Zhang,Mengzhu Jiang,Anhai Chen,Huping Huang,Yongjia Chen,Jie Ling,Lingyun Mei

Redox biology (2024): 103218-103218

引用3浏览0WOS引用

A Non-Coding Variant in 5' Untranslated Region Drove Up-Regulation of Pseudo-Kinase EPHA10 and Caused Non-Syndromic Hearing Loss in Humans

Sida Huang,Lu Ma,Xuezhong Liu,Chufeng He,Jiada Li,Zhengmao Hu,Lu Jiang,Yalan Liu,Xianlin Liu,Yong Feng,Xinzhang Cai

HUMAN MOLECULAR GENETICS（2023）

引用1浏览0WOS引用

Gene Regulation Analysis of Patient-Derived Ipscs and Its CRISPR-corrected Control Provides a New Tool for Studying Perturbations of ELMOD3 C.512a>g Mutation During the Development of Inherited Hearing Loss

Xianlin Liu,Jie Wen,Xuezhong Liu,Anhai Chen,Sijun Li,Jing Liu,Jie Sun,Wei Gong,Xiaoming Kang,Zhili Feng,Chufeng He,Lingyun Mei,Jie Ling,Yong Feng

PLOS ONE（2023）

引用2浏览0WOS引用

A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family with Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application

Anhai Chen,Jie Ling, Xin Peng,Xianlin Liu,Shuang Mao,Yongjia Chen,Mengyao Qin,Shuai Zhang,Yijiang Bai,Jian Song,Zhili Feng,Lu Ma,Dinghua He,Lingyun Mei,Chufeng He,Yong Feng

CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY（2023）

引用2浏览0WOS引用

Establishment of Two Ipsc Lines from Healthy Donor with Heterozygous Mutation in the SLC26A4 Gene

SiJun Li,Chufeng He, Qi Feng,YiJiang Bai,Xianlin Liu,Jie Ling,Lingyun Mei,XueWen Wu,Yong Feng,Jian Song

Stem Cell Research（2022）

引用3浏览0WOS引用

Establishment of an Ipsc Line (Csuxhi004-A) from a Patient with Waardenburg Syndrome Type I Caused by a PAX3 Splice Mutation

Jie Wen,Chufeng He,Yong Feng,Jian Song,Jing Liu,Xianlin Liu,Lingyun Mei,Jie Ling,Hongsheng Chen,Yalan Liu

Stem Cell Research（2021）

引用7浏览0WOS引用

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