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Interactions in the network of Usher syndrome type 1 proteins.
Adato A, Michel V, Kikkawa Y, Reiners J, Alagramam KN, Weil D, Yonekawa H, Wolfrum U, El-Amraoui A, Petit C. Adato A, et al. Among authors: kikkawa y. Hum Mol Genet. 2005 Feb 1;14(3):347-56. doi: 10.1093/hmg/ddi031. Epub 2004 Dec 8. Hum Mol Genet. 2005. PMID: 15590703
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. Kikkawa Y, et al. Hum Mol Genet. 2003 Mar 1;12(5):453-61. doi: 10.1093/hmg/ddg042. Hum Mol Genet. 2003. PMID: 12588793
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. Miyasaka Y, et al. Among authors: kikkawa y. Hum Mol Genet. 2016 May 15;25(10):2045-2059. doi: 10.1093/hmg/ddw078. Epub 2016 Mar 2. Hum Mol Genet. 2016. PMID: 26936824
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. Kikkawa Y, et al. Exp Anim. 2012;61(2):85-98. doi: 10.1538/expanim.61.85. Exp Anim. 2012. PMID: 22531723 Free article. Review.
Protein 4.1 expression in the developing hair cells of the mouse inner ear.
Okumura K, Mochizuki E, Yokohama M, Yamakawa H, Shitara H, Mburu P, Yonekawa H, Brown SD, Kikkawa Y. Okumura K, et al. Among authors: kikkawa y. Brain Res. 2010 Jan 11;1307:53-62. doi: 10.1016/j.brainres.2009.10.039. Epub 2009 Oct 22. Brain Res. 2010. PMID: 19853587
539 results