Liu XZ - Search Results

1

Current concepts in the pathogenesis and treatment of chronic suppurative otitis media.

Mittal R, Lisi CV, Gerring R, Mittal J, Mathee K, Narasimhan G, Azad RK, Yao Q, Grati M, Yan D, Eshraghi AA, Angeli SI, Telischi FF, Liu XZ. Mittal R, et al. Among authors: liu xz. J Med Microbiol. 2015 Oct;64(10):1103-1116. doi: 10.1099/jmm.0.000155. Epub 2015 Aug 5. J Med Microbiol. 2015. PMID: 26248613 Free PMC article. Review.

2

Mutational spectrum in Usher syndrome type II.

Ouyang XM, Hejtmancik JF, Jacobson SG, Li AR, Du LL, Angeli S, Kaiser M, Balkany T, Liu XZ. Ouyang XM, et al. Among authors: liu xz. Clin Genet. 2004 Apr;65(4):288-93. doi: 10.1046/j.1399-0004.2004.00216.x. Clin Genet. 2004. PMID: 15025721

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

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.

7

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.

8

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.

9

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.

10

Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairment.

Ouyang XM, Yan D, Aslan I, Du LL, Tekin M, Liu XZ. Ouyang XM, et al. Among authors: liu xz. Genet Test Mol Biomarkers. 2011 May;15(5):333-6. doi: 10.1089/gtmb.2010.0085. Epub 2011 Jan 22. Genet Test Mol Biomarkers. 2011. PMID: 21254920 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

858 results

Search Page