These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Characterization of a new allele of Ames waltzer generated by ENU mutagenesis. Washington JL; Pitts D; Wright CG; Erway LC; Davis RR; Alagramam K Hear Res; 2005 Apr; 202(1-2):161-9. PubMed ID: 15811708 [TBL] [Abstract][Full Text] [Related]
7. Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development. Pawlowski KS; Kikkawa YS; Wright CG; Alagramam KN J Assoc Res Otolaryngol; 2006 Jun; 7(2):83-94. PubMed ID: 16408167 [TBL] [Abstract][Full Text] [Related]
8. A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15. Hampton LL; Wright CG; Alagramam KN; Battey JF; Noben-Trauth K Hear Res; 2003 Jun; 180(1-2):67-75. PubMed ID: 12782354 [TBL] [Abstract][Full Text] [Related]
9. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene. Alagramam KN; Murcia CL; Kwon HY; Pawlowski KS; Wright CG; Woychik RP Nat Genet; 2001 Jan; 27(1):99-102. PubMed ID: 11138007 [TBL] [Abstract][Full Text] [Related]
10. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA). Pang JJ; Chang B; Hawes NL; Hurd RE; Davisson MT; Li J; Noorwez SM; Malhotra R; McDowell JH; Kaushal S; Hauswirth WW; Nusinowitz S; Thompson DA; Heckenlively JR Mol Vis; 2005 Feb; 11():152-62. PubMed ID: 15765048 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D. Lagziel A; Overlack N; Bernstein SL; Morell RJ; Wolfrum U; Friedman TB Mol Vis; 2009 Sep; 15():1843-57. PubMed ID: 19756182 [TBL] [Abstract][Full Text] [Related]
13. Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F. Alagramam KN; Stahl JS; Jones SM; Pawlowski KS; Wright CG J Assoc Res Otolaryngol; 2005 Jun; 6(2):106-18. PubMed ID: 15952048 [TBL] [Abstract][Full Text] [Related]
14. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Ahmed ZM; Riazuddin S; Bernstein SL; Ahmed Z; Khan S; Griffith AJ; Morell RJ; Friedman TB; Riazuddin S; Wilcox ER Am J Hum Genet; 2001 Jul; 69(1):25-34. PubMed ID: 11398101 [TBL] [Abstract][Full Text] [Related]
15. Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development. Lagziel A; Ahmed ZM; Schultz JM; Morell RJ; Belyantseva IA; Friedman TB Dev Biol; 2005 Apr; 280(2):295-306. PubMed ID: 15882574 [TBL] [Abstract][Full Text] [Related]
16. The Usher gene cadherin 23 is expressed in the zebrafish brain and a subset of retinal amacrine cells. Glover G; Mueller KP; Söllner C; Neuhauss SC; Nicolson T Mol Vis; 2012; 18():2309-22. PubMed ID: 22977299 [TBL] [Abstract][Full Text] [Related]
17. Characterization of the Kyoto circling (KCI) rat carrying a spontaneous nonsense mutation in the protocadherin 15 (Pcdh15) gene. Naoi K; Kuramoto T; Kuwamura Y; Gohma H; Kuwamura M; Serikawa T Exp Anim; 2009 Jan; 58(1):1-10. PubMed ID: 19151506 [TBL] [Abstract][Full Text] [Related]
18. Retinal cadherins and the retinal cadherinopathies: Current concepts and future directions. Yusuf IH; Garrett AM; MacLaren RE; Charbel Issa P Prog Retin Eye Res; 2022 Sep; 90():101038. PubMed ID: 35066146 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse model. Sahu B; Chavali VR; Alapati A; Suk J; Bartsch DU; Jablonski MM; Ayyagari R Mol Vis; 2015; 21():273-84. PubMed ID: 25814825 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]