Preferential Protection of Genetic Fidelity within Open Chromatin by the Mismatch Repair Machinery

Por Sun, Lue, Zhang, Yan, Zhang, Zhuqiang, Zheng, Yong, Du, Lilin, Zhu, Bing
Publicado no J Biol Chem (2016)

Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations

Por King, Peter J., Ouyang, Xiaomei, Du, Lilin, Yan, Denise, Angeli, Simon I., Liu, Xue Zhong
Publicado no Otolaryngol Head Neck Surg (2012)

Mitochondrial DNA Mutation Screening in an Ethnically Diverse Nonsyndromic Deafness Cohort

Por Vivero, Richard J., Ouyang, Xiaomei, Yan, Denise, Du, Lilin, Liu, Wendy, Angeli, Simon I., Liu, Xue Zhong
Publicado em 2012

Audiologic and Genetic Features of the A3243G mtDNA Mutation

Por Vivero, Richard J., Ouyang, Xiaomei, Kim, Yeunjung Grant, Liu, Wendy, Du, Lilin, Yan, Denise, Liu, Xue Zhong
Publicado em 2013

Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating

Por Qing, Jie, Yan, Denise, Zhou, Yuan, Liu, Qiong, Wu, Weijing, Xiao, Zian, Liu, Yuyuan, Liu, Jia, Du, Lilin, Xie, Dinghua, Liu, Xue Zhong
Publicado em 2014

CRL4(Wdr70) regulates H2B monoubiquitination and facilitates Exo1-dependent resection

Por Zeng, Ming, Ren, Laifeng, Mizuno, Ken'Ichi, Nestoras, Konstantinos, Wang, Haibin, Tang, Zizhi, Guo, Liandi, Kong, Daochun, Hu, Qiwen, He, Qun, Du, Lilin, Carr, Antony M., Liu, Cong
Publicado no Nat Commun (2016)

Prevalence of Mutations in GJB2, SLC26A4, and mtDNA in Children with Severe or Profound Sensorineural Hearing Loss in Southwestern China

Por Qing, Jie, Zhou, Yuan, Lai, Ruosha, Hu, Peng, Ding, Yan, Wu, Weijing, Xiao, Zian, Ho, Phi T., Liu, Yuyuan, Liu, Jia, Du, Lilin, Yan, Denise, Goldstein, Bradley J., Liu, Xuezhong, Xie, Dinghua
Publicado no Genet Test Mol Biomarkers (2015)

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

Por Liu, Xue Zhong, Yuan, Yongyi, Yan, Denise, Ding, Emilie Hong, Ouyang, Xiao Mei, Fei, Yu, Tang, Wenxue, Yuan, Huijun, Chang, Qing, Du, LiLin, Zhang, Xin, Wang, Guojian, Ahmad, Shoeb, Kang, Dongyang, Lin, Xi, Dai, Pu
Publicado em 2008

Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise

Por Yan, Denise, Zhu, Yan, Walsh, Tom, Xie, Dinghua, Yuan, Huijun, Sirmaci, Asli, Fujikawa, Taro, Wong, Ann Chi Yan, Loh, Tze L., Du, Lilin, Grati, M’hamed, Vlajkovic, Srdjan M., Blanton, Susan, Ryan, Allen F., Chen, Zheng-Yi, Thorne, Peter R., Kachar, Bechara, Tekin, Mustafa, Zhao, Hong-Bo, Housley, Gary D., King, Mary-Claire, Liu, Xue Z.
Publicado em 2013