Repression of miR-142 by p300 and MAPK is required for survival signalling via gp130 during adaptive hypertrophy

by Sharma, Salil, Liu, Jing, Wei, Jianqin, Yuan, Huijun, Zhang, Taifang, Bishopric, Nanette H
Published 2012

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

by Zhu, Yuhua, Huang, Shasha, Kang, Dongyang, Han, Mingyu, Wang, Guojian, Yuan, Yongyi, Su, Yu, Yuan, Huijun, Zhai, Suoqiang, Dai, Pu
Published 2014

Genetic and Phenotypic Heterogeneity in Chinese Patients with Waardenburg Syndrome Type II

by Yang, Shuzhi, Dai, Pu, Liu, Xin, Kang, Dongyang, Zhang, Xin, Yang, Weiyan, Zhou, Chengyong, Yang, Shiming, Yuan, Huijun
Published 2013

MicroRNA-20a Constrains p300-Driven Myocardial Angiogenic Transcription by Direct Targeting of p300

by Shehadeh, Lina A., Sharma, Salil, Pessanha, Mônica, Wei, Jian Qin, Liu, Jing, Yuan, Huijun, Rodrigues, Claudia O., Scherr, Michaela, Tsinoremas, Nicholas F., Bishopric, Nanette H.
Published 2013

Identification of a Novel TECTA Mutation in a Chinese DFNA8/12 Family with Prelingual Progressive Sensorineural Hearing Impairment

by Li, Zhengyue, Guo, Yilian, Lu, Yu, Li, Jianzhong, Jin, Zhanguo, Li, Hongbo, Lu, Yanping, Dai, Pu, Han, Dongyi, Cheng, Jing, Yuan, Huijun
Published 2013

A Novel Missense SNRNP200 Mutation Associated with Autosomal Dominant Retinitis Pigmentosa in a Chinese Family

by Liu, Tiecheng, Jin, Xin, Zhang, Xuemin, Yuan, Huijun, Cheng, Jing, Lee, Janet, Zhang, Baoquan, Zhang, Maonian, Wu, Jing, Wang, Lijuan, Tian, Geng, Wang, Weifeng
Published 2012

Preimplantation Genetic Diagnosis for a Chinese Family with Autosomal Recessive Meckel-Gruber Syndrome Type 3 (MKS3)

by Lu, Yanping, Peng, Hongmei, Jin, Zhanguo, Cheng, Jing, Wang, Shufang, Ma, Minyue, Lu, Yu, Han, Dongyi, Yao, Yuanqing, Li, Yali, Yuan, Huijun
Published 2013

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

by Lu, Yu, Zhou, Xueya, Jin, Zhanguo, Cheng, Jing, Shen, Weidong, Ji, Fei, Liu, Liyang, Zhang, Xuegong, Zhang, Michael, Cao, Ye, Han, Dongyi, Choy, KwongWai, Yuan, Huijun
Published 2014

Application of SNPscan in Genetic Screening for Common Hearing Loss Genes

by Gao, Zixuan, Lu, Yu, Ke, Jia, Li, Tao, Hu, Ping, Song, Yu, Xu, Chiyu, Wang, Jie, Cheng, Jing, Zhang, Lei, Duan, Hong, Yuan, Huijun, Ma, Furong
Published 2016

Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing

by Buniello, Annalisa, Ingham, Neil J, Lewis, Morag A, Huma, Andreea C, Martinez‐Vega, Raquel, Varela‐Nieto, Isabel, Vizcay‐Barrena, Gema, Fleck, Roland A, Houston, Oliver, Bardhan, Tanaya, Johnson, Stuart L, White, Jacqueline K, Yuan, Huijun, Marcotti, Walter, Steel, Karen P
Published 2016

De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

by Yuan, Yongyi, Zhang, Jianguo, Chang, Qing, Zeng, Jin, Xin, Feng, Wang, Jianjun, Zhu, Qingyan, Wu, Jing, Lu, Jingqiao, Guo, Weiwei, Yan, Xukun, Jiang, Hui, Zhou, Binfei, Li, Qi, Gao, Xue, Yuan, Huijun, Yang, Shiming, Han, Dongyi, Mao, Zixu, Chen, Ping, Lin, Xi, Dai, Pu
Published 2014