Yan D - Search Results

1

Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2-associated schwannomas reveals differences in efficacy and drug resistance development.

Fuse MA, Dinh CT, Vitte J, Kirkpatrick J, Mindos T, Plati SK, Young JI, Huang J, Carlstedt A, Franco MC, Brnjos K, Nagamoto J, Petrilli AM, Copik AJ, Soulakova JN, Bracho O, Yan D, Mittal R, Shen R, Telischi FF, Morrison H, Giovannini M, Liu XZ, Chang LS, Fernandez-Valle C. Fuse MA, et al. Among authors: yan d. Neuro Oncol. 2019 Mar 18;21(4):486-497. doi: 10.1093/neuonc/noz002. Neuro Oncol. 2019. PMID: 30615146 Free PMC article.

2

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

3

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

4

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.

5

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.

6

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.

7

Modifiers of hearing impairment in humans and mice.

Yan D, Liu XZ. Yan D, et al. Curr Genomics. 2010 Jun;11(4):269-78. doi: 10.2174/138920210791233054. Curr Genomics. 2010. PMID: 21119891 Free PMC article.

8

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: yan d. 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.

9

Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations.

Lipan M, Ouyang X, Yan D, Angeli S, Du LL, Liu XZ. Lipan M, et al. Among authors: yan d. Laryngoscope. 2011 Apr;121(4):811-4. doi: 10.1002/lary.21422. Epub 2011 Feb 1. Laryngoscope. 2011. PMID: 21287563 Free PMC article.

10

In vitro interaction of Pseudomonas aeruginosa with human middle ear epithelial cells.

Mittal R, Grati M, Gerring R, Blackwelder P, Yan D, Li JD, Liu XZ. Mittal R, et al. Among authors: yan d. PLoS One. 2014 Mar 14;9(3):e91885. doi: 10.1371/journal.pone.0091885. eCollection 2014. PLoS One. 2014. PMID: 24632826 Free PMC article.

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