DC 05575/DC/NIDCD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2001	1
2002	3
2003	2
2004	1
2005	5
2006	2
2008	2
2009	1
2010	2
2012	1
2025	0

1

Genetics and pathological mechanisms of Usher syndrome.

Yan D, Liu XZ. Yan D, et al. J Hum Genet. 2010 Jun;55(6):327-35. doi: 10.1038/jhg.2010.29. Epub 2010 Apr 9. J Hum Genet. 2010. PMID: 20379205 Free PMC article. Review.

2

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.

3

Etiologic diagnosis of sensorineural hearing loss in adults.

Angeli SI, Yan D, Telischi F, Balkany TJ, Ouyang XM, Du LL, Eshraghi A, Goodwin L, Liu XZ. Angeli SI, et al. Otolaryngol Head Neck Surg. 2005 Jun;132(6):890-5. doi: 10.1016/j.otohns.2005.03.001. Otolaryngol Head Neck Surg. 2005. PMID: 15944560

4

Cochlear implantation in common forms of genetic deafness.

Vivero RJ, Fan K, Angeli S, Balkany TJ, Liu XZ. Vivero RJ, et al. Int J Pediatr Otorhinolaryngol. 2010 Oct;74(10):1107-12. doi: 10.1016/j.ijporl.2010.06.010. Epub 2010 Jul 22. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20655117 Free PMC article. Review.

5

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. 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.

6

Cochlear implantation in individuals with Usher type 1 syndrome.

Liu XZ, Angeli SI, Rajput K, Yan D, Hodges AV, Eshraghi A, Telischi FF, Balkany TJ. Liu XZ, et al. Int J Pediatr Otorhinolaryngol. 2008 Jun;72(6):841-7. doi: 10.1016/j.ijporl.2008.02.013. Epub 2008 Apr 18. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18395802

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. 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

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

9

The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.

Liu XZ, Xia XJ, Ke XM, Ouyang XM, Du LL, Liu YH, Angeli S, Telischi FF, Nance WE, Balkany T, Xu LR. Liu XZ, et al. Hum Genet. 2002 Oct;111(4-5):394-7. doi: 10.1007/s00439-002-0811-6. Epub 2002 Aug 16. Hum Genet. 2002. PMID: 12384781

10

Audiological features of GJB2 (connexin 26) deafness.

Liu XZ, Pandya A, Angeli S, Telischi FF, Arnos KS, Nance WE, Balkany T. Liu XZ, et al. Ear Hear. 2005 Jun;26(3):361-9. doi: 10.1097/00003446-200506000-00011. Ear Hear. 2005. PMID: 15937416

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