Liu XZ - Search Results

1

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing.

Li W, Mei L, Chen H, Cai X, Liu Y, Men M, Liu XZ, Yan D, Ling J, Feng Y. Li W, et al. Among authors: liu y, liu xz. Neural Plast. 2019 Feb 27;2019:7143458. doi: 10.1155/2019/7143458. eCollection 2019. Neural Plast. 2019. PMID: 30936914 Free PMC article.

2

An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C).

Yan D, Li F, Hall ML, Sage C, Hu WH, Giallourakis C, Upadhyay G, Ouyang XM, Du LL, Bethea JR, Chen ZY, Yajnik V, Liu XZ. Yan D, et al. Among authors: liu xz. J Mol Biol. 2006 Mar 31;357(3):755-64. doi: 10.1016/j.jmb.2006.01.017. Epub 2006 Jan 23. J Mol Biol. 2006. PMID: 16464467

3

Ageing and hearing loss.

Liu XZ, Yan D. Liu XZ, et al. J Pathol. 2007 Jan;211(2):188-97. doi: 10.1002/path.2102. J Pathol. 2007. PMID: 17200945 Review.

4

Cochlear molecules and hereditary deafness.

Yan D, Liu XZ. Yan D, et al. Among authors: liu xz. Front Biosci. 2008 May 1;13:4972-83. doi: 10.2741/3056. Front Biosci. 2008. PMID: 18508562 Review.

5

Audiological and genetic features of the mtDNA mutations.

Liu XZ, Angeli S, Ouyang XM, Liu W, Ke XM, Liu YH, Liu SX, Du LL, Deng XW, Yuan H, Yan D. Liu XZ, et al. Among authors: liu sx, liu w, liu yh. Acta Otolaryngol. 2008 Jul;128(7):732-8. doi: 10.1080/00016480701719011. Acta Otolaryngol. 2008. PMID: 18568513 Free PMC article.

6

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

Liu XZ, Yuan Y, Yan D, Ding EH, Ouyang XM, Fei Y, Tang W, Yuan H, Chang Q, Du LL, Zhang X, Wang G, Ahmad S, Kang DY, Lin X, Dai P. Liu XZ, et al. Hum Genet. 2009 Feb;125(1):53-62. doi: 10.1007/s00439-008-0602-9. Epub 2008 Dec 3. Hum Genet. 2009. PMID: 19050930 Free PMC article.

7

Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueduct.

Reyes S, Wang G, Ouyang X, Han B, Du LL, Yuan HJ, Yan D, Dai P, Liu XZ. Reyes S, et al. Among authors: liu xz. Otolaryngol Head Neck Surg. 2009 Oct;141(4):502-8. doi: 10.1016/j.otohns.2009.07.004. Otolaryngol Head Neck Surg. 2009. PMID: 19786220 Free PMC article.

8

Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.

Yan D, Ouyang X, Patterson DM, Du LL, Jacobson SG, Liu XZ. Yan D, et al. Among authors: liu xz. J Hum Genet. 2009 Dec;54(12):732-8. doi: 10.1038/jhg.2009.107. Epub 2009 Oct 30. J Hum Genet. 2009. PMID: 19881469 Free PMC article.

9

Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2.

Liu X, Han D, Li J, Han B, Ouyang X, Cheng J, Li X, Jin Z, Wang Y, Bitner-Glindzicz M, Kong X, Xu H, Kantardzhieva A, Eavey RD, Seidman CE, Seidman JG, Du LL, Chen ZY, Dai P, Teng M, Yan D, Yuan H. Liu X, et al. Am J Hum Genet. 2010 Jan;86(1):65-71. doi: 10.1016/j.ajhg.2009.11.015. Am J Hum Genet. 2010. PMID: 20021999 Free PMC article.

10

Modifiers of hearing impairment in humans and mice.

Yan D, Liu XZ. Yan D, et al. Among authors: liu xz. Curr Genomics. 2010 Jun;11(4):269-78. doi: 10.2174/138920210791233054. Curr Genomics. 2010. PMID: 21119891 Free PMC article.

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