Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2 von Liu, Xuezhong, Han, Dongyi, Li, Jianzhong, Han, Bing, Ouyang, Xiaomei, Cheng, Jing, Li, Xu, Jin, Zhanguo, Wang, Youqin, Bitner-Glindzicz, Maria, Kong, Xiangyin, Xu, Heng, Kantardzhieva, Albena, Eavey, Roland D., Seidman, Christine E., Seidman, Jonathan G., Du, Li L., Chen, Zheng-Yi, Dai, Pu, Teng, Maikun, Yan, Denise, Yuan, Huijun

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Antioxidant enzymes, presbycusis, and ethnic variability von Bared, Anthony, Ouyang, Xiaomei, Angeli, Simon, Du, Li Lin, Hoang, Kimberly, Yan, Denise, Liu, Xue Zhong

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Audioprofiles and antioxidant enzyme genotypes in presbycusis von Angeli, Simon I., Bared, Anthony, Ouyang, Xiaomei, Du, Li Lin, Yan, Denise, Zhong Liu, Xue

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Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II von Yan, Denise, Ouyang, Xiaomei, Patterson, D Michael, Du, Li Lin, Jacobson, Samuel G, Liu, Xue-Zhong

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Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies von Su, Meng, Benke, Paul J, Bademci, Guney, Cengiz, Filiz Basak, Ouyang, Xiaomei, Peng, Jinghong, Casas, Carmen E, Tekin, Mustafa, Fan, Yao-Shan

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Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations von Lipan, Michael, Ouyang, Xiaomei, Yan, Denise, Angeli, Simon, Du, Li Lin, Liu, Xue-Zhong

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Audiologic and genetic features of the A3243G mtDNA mutation von Vivero, Richard J, Ouyang, Xiaomei, Kim, Yeunjung Grant, Liu, Wendy, Du, Lilin, Yan, Denise, Liu, Xue Zhong

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Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China von Sun, Yi, Chen, Jing, Sun, Hanjun, Cheng, Jing, Li, Jianzhong, Lu, Yu, Lu, Yanping, Jin, Zhanguo, Zhu, Yuhua, Ouyang, Xiaomei, Yan, Denise, Dai, Pu, Han, Dongyi, Yang, Weiyan, Wang, Rongguang, Liu, Xuezhong, Yuan, Huijun

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Proxy activation of protein ErbB2 by heterologous ligands implies a heterotetrameric mode of receptor tyrosine kinase interaction von Huang, G C, Ouyang, X, Epstein, R J

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the genetic deafness in chinese population von Xuezhong, Liu, Xiaomei, Ouyang, Yan, Denise

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Absence of GJB2 gene mutations, the GJB6 deletion ( GJB6 -D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population von Kabahuma, Rosemary I, Ouyang, Xiaomei, Du, Li Lin, Yan, Denise, Hutchin, Tim, Ramsay, Michele, Penn, Claire, Liu, Xue-Zhong

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Genotype-Phenotype Correlation of MELAS over 3 Generations von Ouyang, Xiaomei, Yan, Denise, Liu, Xue

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Reduced ability of transforming growth factor-alpha to induce EGF receptor heterodimerization and downregulation suggests a mechanism of oncogenic synergy with ErbB2 von GULLIFORD, T. J, GUO CAI HUANG, OUYANG, X, EPSTEIN, R. J

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The duration of phorbol-inducible ErbB2 tyrosine dephosphorylation parallels that of receptor endocytosis rather than threonine-686 phosphorylation : Implications for the physiolog... von XIAOMEI OUYANG, GULLIFORD, T, EPSTEIN, R. J

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Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations von King, Peter J., Ouyang, Xiaomei, Du, Lilin, Yan, Denise, Angeli, Simon I., Liu, Xue Zhong

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Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueduct von Reyes, Samuel, Wang, Guojian, Ouyang, Xiaomei, Han, Bing, Du, Li Lin, Yuan, Hui Jun, Yan, Denise, Dai, Pu, Liu, Xue-Zhong

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Analysis of miR-376 RNA cluster members in the mouse inner ear von Yan, Denise, Xing, Yazhi, Ouyang, Xiaomei, Zhu, Juhong, Chen, Zheng-yi, Lang, Hainan, Liu, Xue Z.

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Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations von King, Peter, Angeli, Simon I., Ouyang, Xiaomei, Liu, Xue-Zhong

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Analysis of mi R ‐376 RNA cluster members in the mouse inner ear von Yan, Denise, Xing, Yazhi, Ouyang, Xiaomei, Zhu, Juhong, Chen, Zheng‐yi, Lang, Hainan, Liu, Xue Z.

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Mutations in the WFS1 gene and low frequency hearing loss von Whitley, Matthew, Garg, Megha, Liu, Xue, Ouyang, Xiaomei

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