Effect of the tumor suppressor gene ING4 on the proliferation of MCF-7 human breast cancer cells

Por WEI, QINJUN, HE, WEI, LU, YAJIE, YAO, JUN, CAO, XIN
Publicado em 2012

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

Por Yao, Jun, Lu, Yajie, Wei, Qinjun, Cao, Xin, Xing, Guangqian
Publicado em 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 no Sci Rep (2014)

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 no Mol Med Rep (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 em 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 em 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 em 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 em 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 no J Transl Med (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 no Sci Rep (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 no J Med Genet (2017)