Liu X - Search Results

1

A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss.

Niu Z, Yan D, Bressler S, Mei L, Feng Y, Liu X. Niu Z, et al. Among authors: liu x. Int J Pediatr Otorhinolaryngol. 2018 Jan;104:47-50. doi: 10.1016/j.ijporl.2017.10.040. Epub 2017 Nov 2. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29287879

2

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

Yan D, Ke X, Blanton SH, Ouyang XM, Pandya A, Du LL, Nance WE, Liu XZ. Yan D, et al. Among authors: liu xz. J Med Genet. 2006 Feb;43(2):170-4. doi: 10.1136/jmg.2005.034710. Epub 2005 Jun 15. J Med Genet. 2006. PMID: 15958501 Free PMC article.

3

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

4

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.

5

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.

Cheng J, Han DY, Dai P, Sun HJ, Tao R, Sun Q, Yan D, Qin W, Wang HY, Ouyang XM, Yang SZ, Cao JY, Feng GY, Du LL, Zhang YZ, Zhai SQ, Yang WY, Liu XZ, He L, Yuan HJ. Cheng J, et al. Among authors: liu xz. Clin Genet. 2007 Nov;72(5):471-7. doi: 10.1111/j.1399-0004.2007.00889.x. Epub 2007 Sep 14. Clin Genet. 2007. PMID: 17868390

6

Cochlear molecules and hereditary deafness.

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

7

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.

8

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.

9

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.

10

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.

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