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

The association between abnormal microRNA-10b expression and cancer risk: a meta-analysis

por Lu, Yajie, Yao, Jun, Yu, Jiani, Wei, Qinjun, Cao, Xin
Publicado 2014

Metabolic Abnormalities Linked to Auditory Pathways in ApoE-Knockout HEI-OC1 Cells: A Transcription-Metabolism Co-Analysis

por Ma, Lu, Wang, Hongshun, Yao, Jun, Wei, Qinjun, Cao, Xin
Publicado 2022

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

Application of ultrasound in the closed reduction and percutaneous pinning in supracondylar humeral fractures

por Wu, Yang, Lu, Rongbin, Liao, Shijie, Ding, Xiaofei, Su, Wei, Wei, Qinjun
Publicado 2021

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

NPC1 Deficiency Contributes to Autophagy-Dependent Ferritinophagy in HEI-OC1 Auditory Cells

por Liang, Lihong, Wang, Hongshun, Yao, Jun, Wei, Qinjun, Lu, Yajie, Wang, Tianming, Cao, Xin
Publicado 2022

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

Oxysterol-binding protein-like 2 contributes to the developmental progression of preadipocytes by binding to β-catenin

por Wang, Tianming, Zhang, Tianyu, Tang, Youzhi, Wang, Hongshun, Wei, Qinjun, Lu, Yajie, Yao, Jun, Qu, Yuan, Cao, Xin
Publicado 2021

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