Liu XZ - Search Results

1

Whole-exome sequencing to decipher the genetic heterogeneity of hearing loss in a Chinese family with deaf by deaf mating.

Qing J, Yan D, Zhou Y, Liu Q, Wu W, Xiao Z, Liu Y, Liu J, Du L, Xie D, Liu XZ. Qing J, et al. Among authors: liu j, liu y, liu xz, liu q. PLoS One. 2014 Oct 7;9(10):e109178. doi: 10.1371/journal.pone.0109178. eCollection 2014. PLoS One. 2014. PMID: 25289672 Free PMC article.

2

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.

Liu XZ, Ouyang XM, Xia XJ, Zheng J, Pandya A, Li F, Du LL, Welch KO, Petit C, Smith RJ, Webb BT, Yan D, Arnos KS, Corey D, Dallos P, Nance WE, Chen ZY. Liu XZ, et al. Hum Mol Genet. 2003 May 15;12(10):1155-62. doi: 10.1093/hmg/ddg127. Hum Mol Genet. 2003. PMID: 12719379

3

Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians.

Yan D, Park HJ, Ouyang XM, Pandya A, Doi K, Erdenetungalag R, Du LL, Matsushiro N, Nance WE, Griffith AJ, Liu XZ. Yan D, et al. Among authors: liu xz. Hum Genet. 2003 Dec;114(1):44-50. doi: 10.1007/s00439-003-1018-1. Epub 2003 Sep 18. Hum Genet. 2003. PMID: 14505035

4

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.

Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, Li AR, Angeli S, Kaiser M, Newton V, Brown SD, Balkany T, Liu XZ. Ouyang XM, et al. Among authors: liu xz. Hum Genet. 2005 Mar;116(4):292-9. doi: 10.1007/s00439-004-1227-2. Epub 2005 Jan 20. Hum Genet. 2005. PMID: 15660226

5

Refinement of the DFNA41 locus and candidate genes analysis.

Yan D, Ouyang XM, Zhu X, Du LL, Chen ZY, Liu XZ. Yan D, et al. Among authors: liu xz. J Hum Genet. 2005;50(10):516-522. doi: 10.1007/s10038-005-0286-0. Epub 2005 Sep 30. J Hum Genet. 2005. PMID: 16195816

6

The genetic bases for non-syndromic hearing loss among Chinese.

Ouyang XM, Yan D, Yuan HJ, Pu D, Du LL, Han DY, Liu XZ. Ouyang XM, et al. Among authors: liu xz. J Hum Genet. 2009 Mar;54(3):131-40. doi: 10.1038/jhg.2009.4. Epub 2009 Feb 6. J Hum Genet. 2009. PMID: 19197336 Free PMC article. Review.

7

Antioxidant enzymes, presbycusis, and ethnic variability.

Bared A, Ouyang X, Angeli S, Du LL, Hoang K, Yan D, Liu XZ. Bared A, et al. Among authors: liu xz. Otolaryngol Head Neck Surg. 2010 Aug;143(2):263-8. doi: 10.1016/j.otohns.2010.03.024. Otolaryngol Head Neck Surg. 2010. PMID: 20647132 Free PMC article.

8

Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice.

Yan D, Kamiya K, Ouyang XM, Liu XZ. Yan D, et al. Among authors: liu xz. Int J Exp Pathol. 2011 Feb;92(1):66-71. doi: 10.1111/j.1365-2613.2010.00751.x. Epub 2010 Dec 13. Int J Exp Pathol. 2011. PMID: 21156003 Free PMC article.

9

Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populations.

King PJ, Ouyang X, Du L, Yan D, Angeli SI, Liu XZ. King PJ, et al. Among authors: liu xz. Otolaryngol Head Neck Surg. 2012 Nov;147(5):932-6. doi: 10.1177/0194599812453553. Epub 2012 Jul 11. Otolaryngol Head Neck Surg. 2012. PMID: 22785241 Free PMC article.

10

Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.

Vivero RJ, Ouyang X, Yan D, Du L, Liu W, Angeli SI, Liu XZ. Vivero RJ, et al. Among authors: liu xz, liu w. Genet Test Mol Biomarkers. 2012 Sep;16(9):1146-8. doi: 10.1089/gtmb.2011.0365. Epub 2012 Aug 1. Genet Test Mol Biomarkers. 2012. PMID: 22853457 Free PMC article.

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