Minowa O - Search Results

1

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

Iizuka T, Kamiya K, Gotoh S, Sugitani Y, Suzuki M, Noda T, Minowa O, Ikeda K. Iizuka T, et al. Among authors: minowa o. Hum Mol Genet. 2015 Jul 1;24(13):3651-61. doi: 10.1093/hmg/ddv109. Epub 2015 Mar 23. Hum Mol Genet. 2015. PMID: 25801282

2

Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness.

Kidokoro Y, Karasawa K, Minowa O, Sugitani Y, Noda T, Ikeda K, Kamiya K. Kidokoro Y, et al. Among authors: minowa o. PLoS One. 2014 Sep 26;9(9):e108216. doi: 10.1371/journal.pone.0108216. eCollection 2014. PLoS One. 2014. PMID: 25259580 Free PMC article.

3

In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca²⁺ Transients via a Gap Junction Characteristic of Developing Cochlea.

Fukunaga I, Fujimoto A, Hatakeyama K, Aoki T, Nishikawa A, Noda T, Minowa O, Kurebayashi N, Ikeda K, Kamiya K. Fukunaga I, et al. Among authors: minowa o. Stem Cell Reports. 2016 Dec 13;7(6):1023-1036. doi: 10.1016/j.stemcr.2016.10.005. Epub 2016 Nov 10. Stem Cell Reports. 2016. PMID: 27840044 Free PMC article.

4

Corrigendum: Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

Iizuka T, Kamiya K, Gotoh S, Sugitani Y, Suzuki M, Noda T, Minowa O, Ikeda K. Iizuka T, et al. Among authors: minowa o. Hum Mol Genet. 2019 Jul 15;28(14):2458. doi: 10.1093/hmg/ddz041. Hum Mol Genet. 2019. PMID: 30816417 No abstract available.

5

Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice.

Anzai T, Fukunaga I, Hatakeyama K, Fujimoto A, Kobayashi K, Nishikawa A, Aoki T, Noda T, Minowa O, Ikeda K, Kamiya K. Anzai T, et al. Among authors: minowa o. PLoS One. 2015 Oct 22;10(10):e0141258. doi: 10.1371/journal.pone.0141258. eCollection 2015. PLoS One. 2015. PMID: 26492081 Free PMC article.

6

Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses.

Xia AP, Kikuchi T, Minowa O, Katori Y, Oshima T, Noda T, Ikeda K. Xia AP, et al. Among authors: minowa o. Hear Res. 2002 Apr;166(1-2):150-8. doi: 10.1016/s0378-5955(02)00309-x. Hear Res. 2002. PMID: 12062767

7

Assembly of the cochlear gap junction macromolecular complex requires connexin 26.

Kamiya K, Yum SW, Kurebayashi N, Muraki M, Ogawa K, Karasawa K, Miwa A, Guo X, Gotoh S, Sugitani Y, Yamanaka H, Ito-Kawashima S, Iizuka T, Sakurai T, Noda T, Minowa O, Ikeda K. Kamiya K, et al. Among authors: minowa o. J Clin Invest. 2014 Apr;124(4):1598-607. doi: 10.1172/JCI67621. Epub 2014 Mar 3. J Clin Invest. 2014. PMID: 24590285 Free PMC article.

8

Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

Minowa O, Ikeda K, Sugitani Y, Oshima T, Nakai S, Katori Y, Suzuki M, Furukawa M, Kawase T, Zheng Y, Ogura M, Asada Y, Watanabe K, Yamanaka H, Gotoh S, Nishi-Takeshima M, Sugimoto T, Kikuchi T, Takasaka T, Noda T. Minowa O, et al. Science. 1999 Aug 27;285(5432):1408-11. doi: 10.1126/science.285.5432.1408. Science. 1999. PMID: 10464101

9

A series of maturity onset diabetes of the young, type 2 (MODY2) mouse models generated by a large-scale ENU mutagenesis program.

Inoue M, Sakuraba Y, Motegi H, Kubota N, Toki H, Matsui J, Toyoda Y, Miwa I, Terauchi Y, Kadowaki T, Shigeyama Y, Kasuga M, Adachi T, Fujimoto N, Matsumoto R, Tsuchihashi K, Kagami T, Inoue A, Kaneda H, Ishijima J, Masuya H, Suzuki T, Wakana S, Gondo Y, Minowa O, Shiroishi T, Noda T. Inoue M, et al. Among authors: minowa o. Hum Mol Genet. 2004 Jun 1;13(11):1147-57. doi: 10.1093/hmg/ddh133. Epub 2004 Apr 21. Hum Mol Genet. 2004. PMID: 15102714

10

Brn-1 and Brn-2 share crucial roles in the production and positioning of mouse neocortical neurons.

Sugitani Y, Nakai S, Minowa O, Nishi M, Jishage K, Kawano H, Mori K, Ogawa M, Noda T. Sugitani Y, et al. Among authors: minowa o. Genes Dev. 2002 Jul 15;16(14):1760-5. doi: 10.1101/gad.978002. Genes Dev. 2002. PMID: 12130536 Free PMC article.

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