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Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse.
Mochizuki E, Okumura K, Ishikawa M, Yoshimoto S, Yamaguchi J, Seki Y, Wada K, Yokohama M, Ushiki T, Tokano H, Ishii R, Shitara H, Taya C, Kitamura K, Yonekawa H, Kikkawa Y. Mochizuki E, et al. Among authors: seki y. Exp Anim. 2010;59(1):57-71. doi: 10.1538/expanim.59.57. Exp Anim. 2010. PMID: 20224170 Free article.
A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct mice.
Wada K, Maeda YY, Watanabe K, Oshio T, Ueda T, Takahashi G, Yokohama M, Saito J, Seki Y, Takahama S, Ishii R, Shitara H, Taya C, Yonekawa H, Kikkawa Y. Wada K, et al. Among authors: seki y. Mamm Genome. 2011 Dec;22(11-12):693-702. doi: 10.1007/s00335-011-9358-y. Epub 2011 Oct 15. Mamm Genome. 2011. PMID: 22002806
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. Among authors: seki y. Exp Anim. 2012;61(2):85-98. doi: 10.1538/expanim.61.85. Exp Anim. 2012. PMID: 22531723 Free article. Review.
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: seki 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
A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cells.
Seki Y, Miyasaka Y, Suzuki S, Wada K, Yasuda SP, Matsuoka K, Ohshiba Y, Endo K, Ishii R, Shitara H, Kitajiri SI, Nakagata N, Takebayashi H, Kikkawa Y. Seki Y, et al. PLoS One. 2017 Aug 23;12(8):e0183477. doi: 10.1371/journal.pone.0183477. eCollection 2017. PLoS One. 2017. PMID: 28832620 Free PMC article.
Pde6brd1 mutation modifies cataractogenesis in Foxe3rct mice.
Wada K, Saito J, Yamaguchi M, Seki Y, Furugori M, Takahashi G, Nishito Y, Matsuda H, Shitara H, Kikkawa Y. Wada K, et al. Among authors: seki y. Biochem Biophys Res Commun. 2018 Jan 29;496(1):231-237. doi: 10.1016/j.bbrc.2018.01.031. Epub 2018 Jan 6. Biochem Biophys Res Commun. 2018. PMID: 29317205
1,098 results