Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

542 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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.
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
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
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. Among authors: kikkawa y. 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: 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
542 results