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Results: 9

Related Articles by Review for PubMed (Select 12719379)

1.

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.

Hum Mol Genet. 2003 May 15;12(10):1155-62.

2.

Pathogenetics of the human SLC26 transporters.

Dawson PA, Markovich D.

Curr Med Chem. 2005;12(4):385-96. Review.

PMID:
15720248
3.

Overview of the SLC26 family and associated diseases.

Kere J.

Novartis Found Symp. 2006;273:2-11; discussion 11-8, 261-4. Review.

PMID:
17120758
4.

Prestin, a new type of motor protein.

Dallos P, Fakler B.

Nat Rev Mol Cell Biol. 2002 Feb;3(2):104-11. Review.

PMID:
11836512
5.

[Genetic type of progressive hearing loss].

Martini A.

Acta Otorhinolaryngol Ital. 1998 Aug;18(4 Suppl 59):21-7. Review. Italian.

PMID:
10205929
6.

The genetics of deafness.

Nance WE.

Ment Retard Dev Disabil Res Rev. 2003;9(2):109-19. Review.

PMID:
12784229
7.

Hereditary hearing loss: from human mutation to mechanism.

Lenz DR, Avraham KB.

Hear Res. 2011 Nov;281(1-2):3-10. doi: 10.1016/j.heares.2011.05.021. Epub 2011 Jun 6. Review.

PMID:
21664957
8.

Prestin at year 14: progress and prospect.

He DZ, Lovas S, Ai Y, Li Y, Beisel KW.

Hear Res. 2014 May;311:25-35. doi: 10.1016/j.heares.2013.12.002. Epub 2013 Dec 17. Review.

9.

[Prestin].

Chen W, Yang SM.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 May;42(5):394-6. Review. Chinese. No abstract available.

PMID:
17629019
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