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Items: 17

1.

Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.

Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H, Guan MX.

J Med Genet. 2011 Oct;48(10):682-90. doi: 10.1136/jmedgenet-2011-100219.

PMID:
21931169
2.

[Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].

YANG AF, ZHENG J, LV JX, GUAN MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):165-71. doi: 10.3760/cma.j.issn.1003-9406.2011.02.010. Review. Chinese.

PMID:
21462128
3.

Mitochondrial deafness.

Kokotas H, Petersen MB, Willems PJ.

Clin Genet. 2007 May;71(5):379-91. Review.

PMID:
17489842
4.

The role of mitochondrial DNA mutations in hearing loss.

Ding Y, Leng J, Fan F, Xia B, Xu P.

Biochem Genet. 2013 Aug;51(7-8):588-602. doi: 10.1007/s10528-013-9589-6. Epub 2013 Apr 21. Review.

PMID:
23605717
5.

[Modification factors associated with maternally inherited non-syndromic hearing loss].

Hong WJ, Zheng BJ, Qian JF, Wu H, Jin H, Zhu YT.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Jun 7;52(6):472-477. doi: 10.3760/cma.j.issn.1673-0860.2017.06.017. Review. Chinese.

PMID:
28635225
6.

The genetic bases for non-syndromic hearing loss among Chinese.

Ouyang XM, Yan D, Yuan HJ, Pu D, Du LL, Han DY, Liu XZ.

J Hum Genet. 2009 Mar;54(3):131-40. doi: 10.1038/jhg.2009.4. Epub 2009 Feb 6. Review.

7.
8.

c-Ret-mediated hearing losses.

Ohgami N, Tamura H, Ohgami K, Iida M, Yajima I, Kumasaka MY, Goto Y, Sone M, Nakashima T, Kato M.

Int J Clin Exp Pathol. 2012;5(1):23-8. Epub 2012 Jan 1. Review.

9.

Nuclear factors: roles related to mitochondrial deafness.

Luo LF, Hou CC, Yang WX.

Gene. 2013 May 15;520(2):79-89. doi: 10.1016/j.gene.2013.03.041. Epub 2013 Mar 17. Review.

PMID:
23510774
10.

An overview of hereditary hearing loss.

Bayazit YA, Yilmaz M.

ORL J Otorhinolaryngol Relat Spec. 2006;68(2):57-63. Epub 2006 Jan 20. Review.

11.

Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapy.

Liu XZ, Xie D, Yuan HJ, de Brouwer AP, Christodoulou J, Yan D.

Int J Audiol. 2013 Jan;52(1):23-8. doi: 10.3109/14992027.2012.736032. Epub 2012 Nov 28. Review.

12.

Non-syndromic hearing loss gene identification: A brief history and glimpse into the future.

Vona B, Nanda I, Hofrichter MA, Shehata-Dieler W, Haaf T.

Mol Cell Probes. 2015 Oct;29(5):260-70. doi: 10.1016/j.mcp.2015.03.008. Epub 2015 Apr 3. Review.

13.

Next-generation sequencing in genetic hearing loss.

Yan D, Tekin M, Blanton SH, Liu XZ.

Genet Test Mol Biomarkers. 2013 Aug;17(8):581-7. doi: 10.1089/gtmb.2012.0464. Epub 2013 Jun 5. Review.

14.

High-throughput sequencing to decipher the genetic heterogeneity of deafness.

Brownstein Z, Bhonker Y, Avraham KB.

Genome Biol. 2012 May 29;13(5):245. doi: 10.1186/gb-2012-13-5-245. Review.

15.

Inheritance patterns of progressive hearing loss in laboratory strains of mice.

Noben-Trauth K, Johnson KR.

Brain Res. 2009 Jun 24;1277:42-51. doi: 10.1016/j.brainres.2009.02.012. Epub 2009 Feb 21. Review.

16.
17.

Republished: Genetic investigations in childhood deafness.

Parker M, Bitner-Glindzicz M.

Postgrad Med J. 2015 Jul;91(1077):395-402. doi: 10.1136/postgradmedj-2014-306099rep. Review.

PMID:
26187953

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