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Results: 17

1.

Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness.

Lentz JJ, Jodelka FM, Hinrich AJ, McCaffrey KE, Farris HE, Spalitta MJ, Bazan NG, Duelli DM, Rigo F, Hastings ML.

Nat Med. 2013 Mar;19(3):345-50. doi: 10.1038/nm.3106. Epub 2013 Feb 4.

PMID:
23380860
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.

Reiners J, Nagel-Wolfrum K, Jürgens K, Märker T, Wolfrum U.

Exp Eye Res. 2006 Jul;83(1):97-119. Epub 2006 Mar 20. Review.

PMID:
16545802
[PubMed - indexed for MEDLINE]
3.

Usher protein functions in hair cells and photoreceptors.

Cosgrove D, Zallocchi M.

Int J Biochem Cell Biol. 2014 Jan;46:80-9. doi: 10.1016/j.biocel.2013.11.001. Epub 2013 Nov 12. Review.

PMID:
24239741
[PubMed - indexed for MEDLINE]
4.

Auditory and vestibular hair cell stereocilia: relationship between functionality and inner ear disease.

Ciuman RR.

J Laryngol Otol. 2011 Oct;125(10):991-1003. doi: 10.1017/S0022215111001459. Epub 2011 Jul 21. Review.

PMID:
21774850
[PubMed - indexed for MEDLINE]
5.

Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells.

El-Amraoui A, Petit C.

J Cell Sci. 2005 Oct 15;118(Pt 20):4593-603. Review.

PMID:
16219682
[PubMed - indexed for MEDLINE]
Free Article
6.

Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches.

Bonnet C, El-Amraoui A.

Curr Opin Neurol. 2012 Feb;25(1):42-9. doi: 10.1097/WCO.0b013e32834ef8b2. Review.

PMID:
22185901
[PubMed - indexed for MEDLINE]
7.

How the genetics of deafness illuminates auditory physiology.

Richardson GP, de Monvel JB, Petit C.

Annu Rev Physiol. 2011;73:311-34. doi: 10.1146/annurev-physiol-012110-142228. Review.

PMID:
21073336
[PubMed - indexed for MEDLINE]
8.

Unravelling the genetics of deafness.

Steel KP, Mburu P, Gibson F, Walsh J, Varela A, Brown K, Self T, Mahony M, Fleming J, Pearce A, Harvey D, Cable J, Brown SD.

Ann Otol Rhinol Laryngol Suppl. 1997 May;168:59-62. Review.

PMID:
9153119
[PubMed - indexed for MEDLINE]
9.

Mouse models for human hereditary deafness.

Leibovici M, Safieddine S, Petit C.

Curr Top Dev Biol. 2008;84:385-429. doi: 10.1016/S0070-2153(08)00608-X. Review.

PMID:
19186249
[PubMed - indexed for MEDLINE]
10.

The usher syndromes.

Keats BJ, Corey DP.

Am J Med Genet. 1999 Sep 24;89(3):158-66. Review.

PMID:
10704190
[PubMed - indexed for MEDLINE]
11.

Cochlear development: hair cells don their wigs and get wired.

Whitlon DS.

Curr Opin Otolaryngol Head Neck Surg. 2004 Oct;12(5):449-54. Review.

PMID:
15377960
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
19601806
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Auditory and vestibular mouse mutants: models for human deafness.

Ahituv N, Avraham KB.

J Basic Clin Physiol Pharmacol. 2000;11(3):181-91. Review.

PMID:
11041382
[PubMed - indexed for MEDLINE]
14.
15.

Therapy strategies for Usher syndrome Type 1C in the retina.

Nagel-Wolfrum K, Baasov T, Wolfrum U.

Adv Exp Med Biol. 2014;801:741-7. doi: 10.1007/978-1-4614-3209-8_93. Review.

PMID:
24664766
[PubMed - indexed for MEDLINE]
16.

Advantages of a mouse model for human hearing impairment.

Kikkawa Y, Seki Y, Okumura K, Ohshiba Y, Miyasaka Y, Suzuki S, Ozaki M, Matsuoka K, Noguchi Y, Yonekawa H.

Exp Anim. 2012;61(2):85-98. Review.

PMID:
22531723
[PubMed - indexed for MEDLINE]
Free Article
17.

Gene therapy for deafness.

Kohrman DC, Raphael Y.

Gene Ther. 2013 Dec;20(12):1119-23. doi: 10.1038/gt.2013.39. Epub 2013 Jul 18. Review.

PMID:
23864018
[PubMed - indexed for MEDLINE]
Free PMC Article

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