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543 results

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Page 1
Polymorphic mutations in mouse mitochondrial DNA regulate a tumor phenotype.
Takibuchi G, Imanishi H, Morimoto M, Ishikawa K, Nakada K, Toyama-Sorimachi N, Kikkawa Y, Takenaga K, Hayashi J. Takibuchi G, et al. Among authors: kikkawa y. Mitochondrion. 2013 Nov;13(6):881-7. doi: 10.1016/j.mito.2013.07.117. Epub 2013 Aug 6. Mitochondrion. 2013. PMID: 23932994
A 5-bp insertion in Mip causes recessive congenital cataract in KFRS4/Kyo rats.
Watanabe K, Wada K, Ohashi T, Okubo S, Takekuma K, Hashizume R, Hayashi J, Serikawa T, Kuramoto T, Kikkawa Y. Watanabe K, et al. Among authors: kikkawa y. PLoS One. 2012;7(11):e50737. doi: 10.1371/journal.pone.0050737. Epub 2012 Nov 30. PLoS One. 2012. PMID: 23226368 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: kikkawa 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
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: kikkawa y. Exp Anim. 2010;59(1):57-71. doi: 10.1538/expanim.59.57. Exp Anim. 2010. PMID: 20224170 Free article.
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
543 results