PubMed for id: 453237

Year	Number of Results
2004	2
2005	1
2009	1
2010	1
2011	1
2012	1
2013	3
2014	1
2015	1
2016	1
2020	1
2024	0

1

Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafish.

Shen X, Liu F, Wang Y, Wang H, Ma J, Xia W, Zhang J, Jiang N, Sun S, Wang X, Ma D. Shen X, et al. Int J Dev Biol. 2015;59(4-6):195-203. doi: 10.1387/ijdb.140200md. Int J Dev Biol. 2015. PMID: 26505252 Free article.

2

Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.

Kwon TJ, Cho HJ, Kim UK, Lee E, Oh SK, Bok J, Bae YC, Yi JK, Lee JW, Ryoo ZY, Lee SH, Lee KY, Kim HY. Kwon TJ, et al. Hum Mol Genet. 2014 Mar 15;23(6):1591-601. doi: 10.1093/hmg/ddt549. Epub 2013 Nov 3. Hum Mol Genet. 2014. PMID: 24191262

3

Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.

Ahmed ZM, Yousaf R, Lee BC, Khan SN, Lee S, Lee K, Husnain T, Rehman AU, Bonneux S, Ansar M, Ahmad W, Leal SM, Gladyshev VN, Belyantseva IA, Van Camp G, Riazuddin S, Friedman TB, Riazuddin S. Ahmed ZM, et al. Am J Hum Genet. 2011 Jan 7;88(1):19-29. doi: 10.1016/j.ajhg.2010.11.010. Epub 2010 Dec 23. Am J Hum Genet. 2011. PMID: 21185009 Free PMC article.

4

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

Waryah AM, Rehman A, Ahmed ZM, Bashir ZH, Khan SY, Zafar AU, Riazuddin S, Friedman TB, Riazuddin S. Waryah AM, et al. Clin Genet. 2009 Sep;76(3):270-5. doi: 10.1111/j.1399-0004.2009.01209.x. Epub 2009 Jul 23. Clin Genet. 2009. PMID: 19650862

5

[Analysis of MYO15A variation in children with DFNB3].

Ren SM, Wu QH, Jiao ZH, Chen YB, Chen C, Kong XD, Qin ZB. Ren SM, et al. Zhonghua Er Ke Za Zhi. 2020 Oct 2;58(10):818-823. doi: 10.3760/cma.j.cn112140-20200220-00115. Zhonghua Er Ke Za Zhi. 2020. PMID: 32987461 Chinese.

6

Slc26a4 expression prevents fluctuation of hearing in a mouse model of large vestibular aqueduct syndrome.

Nishio A, Ito T, Cheng H, Fitzgerald TS, Wangemann P, Griffith AJ. Nishio A, et al. Neuroscience. 2016 Aug 4;329:74-82. doi: 10.1016/j.neuroscience.2016.04.042. Epub 2016 May 4. Neuroscience. 2016. PMID: 27155149 Free PMC article.

7

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.

Riahi Z, Hammami H, Ouragini H, Messai H, Zainine R, Bouyacoub Y, Romdhane L, Essaid D, Kefi R, Rhimi M, Bedoui M, Dhaouadi A, Feldmann D, Jonard L, Besbes G, Abdelhak S. Riahi Z, et al. Gene. 2013 Aug 1;525(1):1-4. doi: 10.1016/j.gene.2013.04.078. Epub 2013 May 13. Gene. 2013. PMID: 23680645

8

Significance of unilateral enlarged vestibular aqueduct.

Greinwald J, DeAlarcon A, Cohen A, Uwiera T, Zhang K, Benton C, Halstead M, Meinzen-Derr J. Greinwald J, et al. Laryngoscope. 2013 Jun;123(6):1537-46. doi: 10.1002/lary.23889. Epub 2013 Feb 9. Laryngoscope. 2013. PMID: 23401162

9

USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.

Jaworek TJ, Bhatti R, Latief N, Khan SN, Riazuddin S, Ahmed ZM. Jaworek TJ, et al. J Hum Genet. 2012 Oct;57(10):633-7. doi: 10.1038/jhg.2012.79. Epub 2012 Jun 21. J Hum Genet. 2012. PMID: 22718019 Free PMC article.

10

GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.

Xiao ZA, Xie DH. Xiao ZA, et al. Chin Med J (Engl). 2004 Dec;117(12):1797-801. Chin Med J (Engl). 2004. PMID: 15603707

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