Yan D - 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: yan d. 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

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. Among authors: yan d. Hum Mol Genet. 2003 May 15;12(10):1155-62. doi: 10.1093/hmg/ddg127. Hum Mol Genet. 2003. PMID: 12719379

3

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. Clin Genet. 2004 Apr;65(4):288-93. doi: 10.1046/j.1399-0004.2004.00216.x. Clin Genet. 2004. PMID: 15025721

4

Coenzyme Q-10 treatment of patients with a 7445A--->G mitochondrial DNA mutation stops the progression of hearing loss.

Angeli SI, Liu XZ, Yan D, Balkany T, Telischi F. Angeli SI, et al. Among authors: yan d. Acta Otolaryngol. 2005 May;125(5):510-2. doi: 10.1080/00016480510026232. Acta Otolaryngol. 2005. PMID: 16092542

5

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. Among authors: yan d. 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

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

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. Among authors: yan d. 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.

8

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: yan d. 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.

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: yan d. 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. 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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