Minowa O - Search Results

1

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

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

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

4

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

5

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.

6

Crucial roles of Brn1 in distal tubule formation and function in mouse kidney.

Nakai S, Sugitani Y, Sato H, Ito S, Miura Y, Ogawa M, Nishi M, Jishage K, Minowa O, Noda T. Nakai S, et al. Among authors: minowa o. Development. 2003 Oct;130(19):4751-9. doi: 10.1242/dev.00666. Development. 2003. PMID: 12925600

7

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.

8

A germ-line Tsc1 mutation causes tumor development and embryonic lethality that are similar, but not identical to, those caused by Tsc2 mutation in mice.

Kobayashi T, Minowa O, Sugitani Y, Takai S, Mitani H, Kobayashi E, Noda T, Hino O. Kobayashi T, et al. Among authors: minowa o. Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8762-7. doi: 10.1073/pnas.151033798. Epub 2001 Jul 3. Proc Natl Acad Sci U S A. 2001. PMID: 11438694 Free PMC article.

9

BMP type II receptor is required for gastrulation and early development of mouse embryos.

Beppu H, Kawabata M, Hamamoto T, Chytil A, Minowa O, Noda T, Miyazono K. Beppu H, et al. Among authors: minowa o. Dev Biol. 2000 May 1;221(1):249-58. doi: 10.1006/dbio.2000.9670. Dev Biol. 2000. PMID: 10772805 Free article.

10

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.

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