228 related articles for article (PubMed ID: 21689626)
1. 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]
2. 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]
3. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
Schultz JM; Bhatti R; Madeo AC; Turriff A; Muskett JA; Zalewski CK; King KA; Ahmed ZM; Riazuddin S; Ahmad N; Hussain Z; Qasim M; Kahn SN; Meltzer MR; Liu XZ; Munisamy M; Ghosh M; Rehm HL; Tsilou ET; Griffith AJ; Zein WM; Brewer CC; Riazuddin S; Friedman TB
J Med Genet; 2011 Nov; 48(11):767-75. PubMed ID: 21940737
[TBL] [Abstract][Full Text] [Related]
4. A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells.
Schwander M; Xiong W; Tokita J; Lelli A; Elledge HM; Kazmierczak P; Sczaniecka A; Kolatkar A; Wiltshire T; Kuhn P; Holt JR; Kachar B; Tarantino L; Müller U
Proc Natl Acad Sci U S A; 2009 Mar; 106(13):5252-7. PubMed ID: 19270079
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Identification of Novel
Ramzan K; Al-Numair NS; Al-Ageel S; Elbaik L; Sakati N; Al-Hazzaa SAF; Al-Owain M; Imtiaz F
Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33316915
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
Bork JM; Peters LM; Riazuddin S; Bernstein SL; Ahmed ZM; Ness SL; Polomeno R; Ramesh A; Schloss M; Srisailpathy CR; Wayne S; Bellman S; Desmukh D; Ahmed Z; Khan SN; Kaloustian VM; Li XC; Lalwani A; Riazuddin S; Bitner-Glindzicz M; Nance WE; Liu XZ; Wistow G; Smith RJ; Griffith AJ; Wilcox ER; Friedman TB; Morell RJ
Am J Hum Genet; 2001 Jan; 68(1):26-37. PubMed ID: 11090341
[TBL] [Abstract][Full Text] [Related]
9. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Bolz H; von Brederlow B; Ramírez A; Bryda EC; Kutsche K; Nothwang HG; Seeliger M; del C-Salcedó Cabrera M; Vila MC; Molina OP; Gal A; Kubisch C
Nat Genet; 2001 Jan; 27(1):108-12. PubMed ID: 11138009
[TBL] [Abstract][Full Text] [Related]
10. CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
Astuto LM; Bork JM; Weston MD; Askew JW; Fields RR; Orten DJ; Ohliger SJ; Riazuddin S; Morell RJ; Khan S; Riazuddin S; Kremer H; van Hauwe P; Moller CG; Cremers CW; Ayuso C; Heckenlively JR; Rohrschneider K; Spandau U; Greenberg J; Ramesar R; Reardon W; Bitoun P; Millan J; Legge R; Friedman TB; Kimberling WJ
Am J Hum Genet; 2002 Aug; 71(2):262-75. PubMed ID: 12075507
[TBL] [Abstract][Full Text] [Related]
11. Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12).
Pennings RJ; Topsakal V; Astuto L; de Brouwer AP; Wagenaar M; Huygen PL; Kimberling WJ; Deutman AF; Kremer H; Cremers CW
Otol Neurotol; 2004 Sep; 25(5):699-706. PubMed ID: 15353998
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Phenotypic differences in the inner ears of CBA/CaJ and C57BL/6J mice carrying missense and single base pair deletion mutations in the Cdh23 gene.
Zhao T; Ma P; Zhao F; Zheng T; Yan B; Zhang Q; Yuan J; Hu B; Yang Y; Hu J; Geng R; Hu BH; Sun T; Zheng QY; Li B
J Neurosci Res; 2021 Oct; 99(10):2743-2758. PubMed ID: 34133797
[TBL] [Abstract][Full Text] [Related]
14. Sector Retinitis Pigmentosa Associated With Novel Compound Heterozygous Mutations of CDH23.
Branson SV; McClintic JI; Stamper TH; Haldeman-Englert CR; John VJ
Ophthalmic Surg Lasers Imaging Retina; 2016 Feb; 47(2):183-6. PubMed ID: 26878454
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.
Wagatsuma M; Kitoh R; Suzuki H; Fukuoka H; Takumi Y; Usami S
Clin Genet; 2007 Oct; 72(4):339-44. PubMed ID: 17850630
[TBL] [Abstract][Full Text] [Related]
17. Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D.
von Brederlow B; Bolz H; Janecke A; La O Cabrera A; Rudolph G; Lorenz B; Schwinger E; Gal A
Hum Mutat; 2002 Mar; 19(3):268-73. PubMed ID: 11857743
[TBL] [Abstract][Full Text] [Related]
18. Usher syndrome type 1 due to missense mutations on both CDH23 alleles: investigation of mRNA splicing.
Becirovic E; Ebermann I; Nagy D; Zrenner E; Seeliger MW; Bolz HJ
Hum Mutat; 2008 Mar; 29(3):452. PubMed ID: 18273900
[TBL] [Abstract][Full Text] [Related]
19. Recombinant protein of the first two ectodomains of cadherin 23 from erl mice shows impairment in Ca
Zhao M; Li P; Xie Y; Liu X; Cheng L; Liu T; Kong L; Wang O; Han F
Protein Expr Purif; 2018 Jul; 147():55-60. PubMed ID: 29486248
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]