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Results: 1 to 20 of 100

1.

The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.

Johnson KR, Zheng QY, Weston MD, Ptacek LJ, Noben-Trauth K.

Genomics. 2005 May;85(5):582-90.

PMID:
15820310
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Auditory deficits associated with the frings mgr1 (mass1) mutation in mice.

Klein BD, Fu YH, Ptacek LJ, White HS.

Dev Neurosci. 2005;27(5):321-32.

PMID:
16137990
[PubMed - indexed for MEDLINE]
3.

Ahl2, a second locus affecting age-related hearing loss in mice.

Johnson KR, Zheng QY.

Genomics. 2002 Nov;80(5):461-4.

PMID:
12408962
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice.

Miyasaka Y, Suzuki S, Ohshiba Y, Watanabe K, Sagara Y, Yasuda SP, Matsuoka K, Shitara H, Yonekawa H, Kominami R, Kikkawa Y.

Exp Anim. 2013;62(4):333-46.

PMID:
24172198
[PubMed - indexed for MEDLINE]
Free Article
5.
6.

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B, Steel KP, Noben-Trauth K.

Nat Genet. 2001 Jan;27(1):103-7.

PMID:
11138008
[PubMed - indexed for MEDLINE]
7.

Auditory development in progressive motor neuronopathy mouse mutants.

Volkenstein S, Brors D, Hansen S, Berend A, Mlynski R, Aletsee C, Dazert S.

Neurosci Lett. 2009 Nov 6;465(1):45-9. doi: 10.1016/j.neulet.2009.09.006. Epub 2009 Sep 6.

PMID:
19735697
[PubMed - indexed for MEDLINE]
8.

Progressive degeneration of stereocilia in cochlear hair cells in hearing-impaired kuru2 mice.

Watanabe M, Akiyama N, Hasegawa N, Manome Y.

In Vivo. 2005 Jul-Aug;19(4):675-81.

PMID:
15999533
[PubMed - indexed for MEDLINE]
Free Article
9.

A new Atp2b2 deafwaddler allele, dfw(i5), interacts strongly with Cdh23 and other auditory modifiers.

Watson CJ, Tempel BL.

Hear Res. 2013 Oct;304:41-8. doi: 10.1016/j.heares.2013.06.003. Epub 2013 Jun 18.

PMID:
23792079
[PubMed - indexed for MEDLINE]
10.

A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) mice.

Liu S, Li S, Zhu H, Cheng S, Zheng QY.

Gene. 2012 May 15;499(2):309-17. doi: 10.1016/j.gene.2012.01.084. Epub 2012 Feb 4.

PMID:
22326520
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Separate and combined effects of Sod1 and Cdh23 mutations on age-related hearing loss and cochlear pathology in C57BL/6J mice.

Johnson KR, Yu H, Ding D, Jiang H, Gagnon LH, Salvi RJ.

Hear Res. 2010 Sep 1;268(1-2):85-92. doi: 10.1016/j.heares.2010.05.002. Epub 2010 May 12.

PMID:
20470874
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice.

Kane KL, Longo-Guess CM, Gagnon LH, Ding D, Salvi RJ, Johnson KR.

Hear Res. 2012 Jan;283(1-2):80-8. doi: 10.1016/j.heares.2011.11.007. Epub 2011 Nov 22.

PMID:
22138310
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Deficiency of Vlgr1 resulted in deafness and susceptibility to audiogenic seizures while the degree of hearing impairment was not correlated with seizure severity in C57BL/6- and 129-backcrossed lines of Vlgr1 knockout mice.

Yagi H, Noguchi Y, Kitamura K, Sato M.

Neurosci Lett. 2009 Sep 18;461(2):190-5. doi: 10.1016/j.neulet.2009.06.012. Epub 2009 Jun 17.

PMID:
19539720
[PubMed - indexed for MEDLINE]
14.

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.

Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC.

Hum Mol Genet. 2002 Aug 1;11(16):1887-98.

PMID:
12140191
[PubMed - indexed for MEDLINE]
Free Article
15.

A comparison of vestibular and auditory phenotypes in inbred mouse strains.

Jones SM, Jones TA, Johnson KR, Yu H, Erway LC, Zheng QY.

Brain Res. 2006 May 26;1091(1):40-6. Epub 2006 Feb 24.

PMID:
16499890
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Strain background effects and genetic modifiers of hearing in mice.

Johnson KR, Zheng QY, Noben-Trauth K.

Brain Res. 2006 May 26;1091(1):79-88. Epub 2006 Mar 31. Review.

PMID:
16579977
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources.

Parker LL, Gao J, Zuo J.

Brain Res. 2006 May 26;1091(1):235-42. Epub 2006 Apr 21.

PMID:
16630581
[PubMed - indexed for MEDLINE]
18.

Hearing loss in athyroid pax8 knockout mice and effects of thyroxine substitution.

Christ S, Biebel UW, Hoidis S, Friedrichsen S, Bauer K, Smolders JW.

Audiol Neurootol. 2004 Mar-Apr;9(2):88-106.

PMID:
14981357
[PubMed - indexed for MEDLINE]
19.

The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.

McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG, Birch DG, Legan PK, White PC, Walsh EJ, Richardson GP.

J Neurosci. 2006 Jun 14;26(24):6543-53.

PMID:
16775142
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice.

Johnson KR, Longo-Guess C, Gagnon LH, Yu H, Zheng QY.

Genomics. 2008 Oct;92(4):219-25. doi: 10.1016/j.ygeno.2008.06.007. Epub 2008 Aug 15.

PMID:
18662770
[PubMed - indexed for MEDLINE]
Free PMC Article

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