Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency

por Liu, Cheng, Bu, Xingkuan, Wu, Feiyun, Xing, Guangqian
Publicado 2012

Middle ear squamous papilloma: A report of four cases analyzed by HPV and EBV in situ hybridization

por ZHOU, HAN, CHEN, ZHIBIN, ZHANG, WEIMING, XING, GUANGQIAN
Publicado 2014

Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1

por Qian, Xuli, Qin, Luyang, Xing, Guangqian, Cao, Xin
Publicado 2015

A systematic review and meta-analysis of 235delC mutation of GJB2 gene

por Yao, Jun, Lu, Yajie, Wei, Qinjun, Cao, Xin, Xing, Guangqian
Publicado 2012

Inflammatory myofibroblastic tumor of the temporal bone presenting with pulsatile tinnitus: a case report

por Zhou, Xiaoli, Liu, Tingting, Chen, Zhibin, Zhang, Zhihong, Xing, Guangqian
Publicado 2013

Inflammatory Pseudotumor of the Temporal Bone: Three Cases and a Review of the Literature

por Tian, Huiqin, Liu, Tingting, Wang, Cong, Tang, Lijun, Chen, Zhibin, Xing, Guangqian
Publicado 2013

Dynamic expression analysis of armc10, the homologous gene of human GPRASP2, in zebrafish embryos

por Liu, Chunyu, Lin, Changsong, Yao, Jun, Wei, Qinjun, Xing, Guangqian, Cao, Xin
Publicado 2017

Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of China()

por Lu, Yajie, Dai, Dachun, Chen, Zhibin, Cao, Xin, Bu, Xingkuan, Wei, Qinjun, Xing, Guangqian
Publicado 2011

Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China

por Wei, Qinjun, Wang, Shuai, Yao, Jun, Lu, Yajie, Chen, Zhibin, Xing, Guangqian, Cao, Xin
Publicado 2013

A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family

por WEI, QINJUN, LIU, YOUGUO, WANG, SHUAI, LIU, TINGTING, LU, YAJIE, XING, GUANGQIAN, CAO, XIN
Publicado 2014

Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non-syndromic hearing loss

por TAN, MINXING, SHEN, XIAOFEI, YAO, JUN, WEI, QINJUN, LU, YAJIE, CAO, XIN, XING, GUANGQIAN
Publicado 2014

Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss

por Wei, Qinjun, Zhu, Hongmei, Qian, Xuli, Chen, Zhibin, Yao, Jun, Lu, Yajie, Cao, Xin, Xing, Guangqian
Publicado 2014

Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations

por Yao, Jun, Qian, Xuli, Bao, Jingxiao, Wei, Qinjun, Lu, Yajie, Zheng, Heng, Cao, Xin, Xing, Guangqian
Publicado 2015

GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss

por Xing, Guangqian, Yao, Jun, Liu, Chunyu, Wei, Qinjun, Qian, Xuli, Wu, Lingxin, Lu, Yajie, Cao, Xin
Publicado 2017

Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling

por Shi, Hairong, Wang, Hongshun, Zhang, Cheng, Lu, Yajie, Yao, Jun, Chen, Zhibin, Xing, Guangqian, Wei, Qinjun, Cao, Xin
Publicado 2022

Deletion of OSBPL2 in auditory cells increases cholesterol biosynthesis and drives reactive oxygen species production by inhibiting AMPK activity

por Wang, Hongshun, Lin, Changsong, Yao, Jun, Shi, Hairong, Zhang, Cui, Wei, Qinjun, Lu, Yajie, Chen, Zhibin, Xing, Guangqian, Cao, Xin
Publicado 2019

OSBPL2 Is Required for the Binding of COPB1 to ATGL and the Regulation of Lipid Droplet Lipolysis

por Wang, Tianming, Wei, Qinjun, Liang, Lihong, Tang, Xujun, Yao, Jun, Lu, Yajie, Qu, Yuan, Chen, Zhibin, Xing, Guangqian, Cao, Xin
Publicado 2020