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Items: 1 to 20 of 42

1.

Predictive Value of GJB2 Mutation Status for Hearing Outcomes of Pediatric Cochlear Implantation.

Abdurehim Y, Lehmann A, Zeitouni AG.

Otolaryngol Head Neck Surg. 2017 Jul;157(1):16-24. doi: 10.1177/0194599817697054. Epub 2017 Mar 21. Review.

PMID:
28322114
2.

Advances in genetic hearing loss: CIB2 gene.

Jacoszek A, Pollak A, Płoski R, Ołdak M.

Eur Arch Otorhinolaryngol. 2017 Apr;274(4):1791-1795. doi: 10.1007/s00405-016-4330-9. Epub 2016 Oct 22. Review.

3.

The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.

Yan D, Kannan-Sundhari A, Vishwanath S, Qing J, Mittal R, Kameswaran M, Liu XZ.

Genet Test Mol Biomarkers. 2015 Sep;19(9):512-27. doi: 10.1089/gtmb.2015.0023. Epub 2015 Jul 17. Review.

4.

The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review.

Zhu YM, Li Y, Wang YL, Bian PP, Xu BC, Liu XW, Chen XJ, Liu F, Guo YF, Wang QJ.

Acta Otolaryngol. 2015 Sep;135(9):914-8. doi: 10.3109/00016489.2015.1035796. Epub 2015 Apr 20. Review.

PMID:
25891447
5.

Whole-exome sequencing and its impact in hereditary hearing loss.

Atik T, Bademci G, Diaz-Horta O, Blanton SH, Tekin M.

Genet Res (Camb). 2015 Mar 31;97:e4. doi: 10.1017/S001667231500004X. Review.

6.

Tight junction, selective permeability, and related diseases.

Krug SM, Schulzke JD, Fromm M.

Semin Cell Dev Biol. 2014 Dec;36:166-76. doi: 10.1016/j.semcdb.2014.09.002. Epub 2014 Sep 16. Review.

PMID:
25220018
7.

[Hereditary hearing loss: Part 2: Syndromic forms of hearing loss].

Burke WF, Lenarz T, Maier H.

HNO. 2014 Oct;62(10):759-69; quiz 770. doi: 10.1007/s00106-014-2901-x. Review. German.

PMID:
25217188
8.

[Hearing loss associated with GJB2 gene mutation].

Cui Q, Huang L.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Oct;27(19):1099-102. Review. Chinese.

PMID:
24417175
9.

Genetics of dizziness: cerebellar and vestibular disorders.

Requena T, Espinosa-Sanchez JM, Lopez-Escamez JA.

Curr Opin Neurol. 2014 Feb;27(1):98-104. doi: 10.1097/WCO.0000000000000053. Review.

PMID:
24275721
10.

Functional proteomics, human genetics and cancer biology of GIPC family members.

Katoh M.

Exp Mol Med. 2013 Jun 7;45:e26. doi: 10.1038/emm.2013.49. Review.

11.

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
12.

Genetics: advances in genetic testing for deafness.

Shearer AE, Smith RJ.

Curr Opin Pediatr. 2012 Dec;24(6):679-86. doi: 10.1097/MOP.0b013e3283588f5e. Review.

13.

Autosomal recessive nonsyndromic deafness genes: a review.

Duman D, Tekin M.

Front Biosci (Landmark Ed). 2012 Jun 1;17:2213-36. Review.

14.

Genetic disorders of the vestibular system.

Eppsteiner RW, Smith RJ.

Curr Opin Otolaryngol Head Neck Surg. 2011 Oct;19(5):397-402. doi: 10.1097/MOO.0b013e32834a9852. Review.

15.

Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.

Bazazzadegan N, Sheffield AM, Sobhani M, Kahrizi K, Meyer NC, Van Camp G, Hilgert N, Abedini SS, Habibi F, Daneshi A, Nishimura C, Avenarius MR, Farhadi M, Smith RJ, Najmabadi H.

Am J Med Genet A. 2011 May;155A(5):1202-11. doi: 10.1002/ajmg.a.33209. Epub 2011 Apr 11. Review.

16.
17.

Connexin-26 mutations in deafness and skin disease.

Lee JR, White TW.

Expert Rev Mol Med. 2009 Nov 19;11:e35. doi: 10.1017/S1462399409001276. Review.

PMID:
19939300
18.

MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness.

Friedman LM, Avraham KB.

Mamm Genome. 2009 Sep-Oct;20(9-10):581-603. doi: 10.1007/s00335-009-9230-5. Epub 2009 Oct 30. Review.

PMID:
19876605
19.

Function and expression pattern of nonsyndromic deafness genes.

Hilgert N, Smith RJ, Van Camp G.

Curr Mol Med. 2009 Jun;9(5):546-64. Review.

20.

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.

Bindu LH, Reddy PP.

Int J Audiol. 2008 Nov;47(11):702-7. doi: 10.1080/14992020802215862. Review.

PMID:
19031229

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