Yan D - Search Results

1

Molecular Structure and Regulation of P2X Receptors With a Special Emphasis on the Role of P2X2 in the Auditory System.

Mittal R, Chan B, Grati M, Mittal J, Patel K, Debs LH, Patel AP, Yan D, Chapagain P, Liu XZ. Mittal R, et al. Among authors: yan d. J Cell Physiol. 2016 Aug;231(8):1656-70. doi: 10.1002/jcp.25274. Epub 2015 Dec 30. J Cell Physiol. 2016. PMID: 26627116 Review.

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

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.

Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, Li AR, Angeli S, Kaiser M, Newton V, Brown SD, Balkany T, Liu XZ. Ouyang XM, et al. Among authors: yan d. Hum Genet. 2005 Mar;116(4):292-9. doi: 10.1007/s00439-004-1227-2. Epub 2005 Jan 20. Hum Genet. 2005. PMID: 15660226

5

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. Among authors: yan d. 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

6

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

7

Refinement of the DFNA41 locus and candidate genes analysis.

Yan D, Ouyang XM, Zhu X, Du LL, Chen ZY, Liu XZ. Yan D, et al. J Hum Genet. 2005;50(10):516-522. doi: 10.1007/s10038-005-0286-0. Epub 2005 Sep 30. J Hum Genet. 2005. PMID: 16195816

8

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

9

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.

10

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.

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

4,648 results

Search Page