179 related articles for article (PubMed ID: 26936824)
1. Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23.
Miyasaka Y; Shitara H; Suzuki S; Yoshimoto S; Seki Y; Ohshiba Y; Okumura K; Taya C; Tokano H; Kitamura K; Takada T; Hibino H; Shiroishi T; Kominami R; Yonekawa H; Kikkawa Y
Hum Mol Genet; 2016 May; 25(10):2045-2059. PubMed ID: 26936824
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 24172198
[TBL] [Abstract][Full Text] [Related]
3. Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.
Zheng QY; Scarborough JD; Zheng Y; Yu H; Choi D; Gillespie PG
Hum Mol Genet; 2012 Jun; 21(11):2588-98. PubMed ID: 22381527
[TBL] [Abstract][Full Text] [Related]
4. Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice.
Holme RH; Steel KP
Hear Res; 2002 Jul; 169(1-2):13-23. PubMed ID: 12121736
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 23792079
[TBL] [Abstract][Full Text] [Related]
6. Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation.
Holme RH; Steel KP
J Assoc Res Otolaryngol; 2004 Mar; 5(1):66-79. PubMed ID: 14648237
[TBL] [Abstract][Full Text] [Related]
7. Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice.
Kikkawa Y; Shitara H; Wakana S; Kohara Y; Takada T; Okamoto M; Taya C; Kamiya K; Yoshikawa Y; Tokano H; Kitamura K; Shimizu K; Wakabayashi Y; Shiroishi T; Kominami R; Yonekawa H
Hum Mol Genet; 2003 Mar; 12(5):453-61. PubMed ID: 12588793
[TBL] [Abstract][Full Text] [Related]
8. Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment.
Schrauwen I; Chakchouk I; Acharya A; Liaqat K; Irfanullah ; ; Nickerson DA; Bamshad MJ; Shah K; Ahmad W; Leal SM
BMC Med Genet; 2018 Jul; 19(1):122. PubMed ID: 30029624
[TBL] [Abstract][Full Text] [Related]
9. Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).
Di Palma F; Pellegrino R; Noben-Trauth K
Gene; 2001 Dec; 281(1-2):31-41. PubMed ID: 11750125
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 11138008
[TBL] [Abstract][Full Text] [Related]
11. Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.
Kwon TJ; Cho HJ; Kim UK; Lee E; Oh SK; Bok J; Bae YC; Yi JK; Lee JW; Ryoo ZY; Lee SH; Lee KY; Kim HY
Hum Mol Genet; 2014 Mar; 23(6):1591-601. PubMed ID: 24191262
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 22138310
[TBL] [Abstract][Full Text] [Related]
13. 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; 499(2):309-17. PubMed ID: 22326520
[TBL] [Abstract][Full Text] [Related]
14. An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.
Manji SS; Miller KA; Williams LH; Andreasen L; Siboe M; Rose E; Bahlo M; Kuiper M; Dahl HH
Am J Pathol; 2011 Aug; 179(2):903-14. PubMed ID: 21689626
[TBL] [Abstract][Full Text] [Related]
15. Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice.
Wilson SM; Householder DB; Coppola V; Tessarollo L; Fritzsch B; Lee EC; Goss D; Carlson GA; Copeland NG; Jenkins NA
Genomics; 2001 Jun; 74(2):228-33. PubMed ID: 11386759
[TBL] [Abstract][Full Text] [Related]
16. A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs.
Han F; Yu H; Tian C; Chen HE; Benedict-Alderfer C; Zheng Y; Wang Q; Han X; Zheng QY
Pharmacogenomics J; 2012 Feb; 12(1):30-44. PubMed ID: 20644563
[TBL] [Abstract][Full Text] [Related]
17. Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.
Zheng QY; Yan D; Ouyang XM; Du LL; Yu H; Chang B; Johnson KR; Liu XZ
Hum Mol Genet; 2005 Jan; 14(1):103-11. PubMed ID: 15537665
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family.
de Brouwer AP; Pennings RJ; Roeters M; Van Hauwe P; Astuto LM; Hoefsloot LH; Huygen PL; van den Helm B; Deutman AF; Bork JM; Kimberling WJ; Cremers FP; Cremers CW; Kremer H
Hum Genet; 2003 Feb; 112(2):156-63. PubMed ID: 12522556
[TBL] [Abstract][Full Text] [Related]
19. Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9.
Verdoodt D; van Wijk E; Broekman S; Venselaar H; Aben F; Sels L; De Backer E; Gommeren H; Szewczyk K; Van Camp G; Ponsaerts P; Van Rompaey V; de Vrieze E
Hear Res; 2024 Feb; 442():108947. PubMed ID: 38218018
[TBL] [Abstract][Full Text] [Related]
20. Sustained cadherin 23 expression in young and adult cochlea of normal and hearing-impaired mice.
Rzadzinska AK; Derr A; Kachar B; Noben-Trauth K
Hear Res; 2005 Oct; 208(1-2):114-21. PubMed ID: 16005171
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]