Nishio A - Search Results

1

Slc26a4 expression prevents fluctuation of hearing in a mouse model of large vestibular aqueduct syndrome.

Nishio A, Ito T, Cheng H, Fitzgerald TS, Wangemann P, Griffith AJ. Nishio A, et al. Neuroscience. 2016 Aug 4;329:74-82. doi: 10.1016/j.neuroscience.2016.04.042. Epub 2016 May 4. Neuroscience. 2016. PMID: 27155149 Free PMC article.

2

Progressive irreversible hearing loss is caused by stria vascularis degeneration in an Slc26a4-insufficient mouse model of large vestibular aqueduct syndrome.

Ito T, Nishio A, Wangemann P, Griffith AJ. Ito T, et al. Among authors: nishio a. Neuroscience. 2015 Dec 3;310:188-97. doi: 10.1016/j.neuroscience.2015.09.016. Epub 2015 Sep 9. Neuroscience. 2015. PMID: 26363152 Free PMC article.

3

ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells.

Morozko EL, Nishio A, Ingham NJ, Chandra R, Fitzgerald T, Martelletti E, Borck G, Wilson E, Riordan GP, Wangemann P, Forge A, Steel KP, Liddle RA, Friedman TB, Belyantseva IA. Morozko EL, et al. Among authors: nishio a. Hum Mol Genet. 2015 Feb 1;24(3):609-24. doi: 10.1093/hmg/ddu474. Epub 2014 Sep 12. Hum Mol Genet. 2015. PMID: 25217574 Free PMC article.

4

Audiovestibular findings in a branchio-oto syndrome patient with a SIX1 mutation.

Noguchi Y, Ito T, Nishio A, Honda K, Kitamura K. Noguchi Y, et al. Among authors: nishio a. Acta Otolaryngol. 2011 Apr;131(4):413-8. doi: 10.3109/00016489.2010.543146. Epub 2011 Jan 24. Acta Otolaryngol. 2011. PMID: 21254961

5

Audiovestibular findings in patients with Vogt-Koyanagi-Harada disease.

Noguchi Y, Nishio A, Takase H, Miyanaga M, Takahashi H, Mochizuki M, Kitamura K. Noguchi Y, et al. Among authors: nishio a. Acta Otolaryngol. 2014 Apr;134(4):339-44. doi: 10.3109/00016489.2013.868604. Acta Otolaryngol. 2014. PMID: 24628333

6

Longitudinal study of 29 patients with Meniere's disease with follow-up of 10 years or more (In commemoration of Professor Emeritus Isamu Watanabe).

Sumi T, Watanabe I, Tsunoda A, Nishio A, Komatsuzaki A, Kitamura K. Sumi T, et al. Among authors: nishio a. Acta Otolaryngol. 2012 Jan;132(1):10-5. doi: 10.3109/00016489.2011.627570. Epub 2011 Nov 6. Acta Otolaryngol. 2012. PMID: 22054051

7

A DFNA5 mutation identified in Japanese families with autosomal dominant hereditary hearing loss.

Nishio A, Noguchi Y, Sato T, Naruse TK, Kimura A, Takagi A, Kitamura K. Nishio A, et al. Ann Hum Genet. 2014 Mar;78(2):83-91. doi: 10.1111/ahg.12053. Epub 2014 Feb 10. Ann Hum Genet. 2014. PMID: 24506266

8

Ex vivo visualization of the mouse otoconial layer compared with micro-computed tomography.

Honda K, Noguchi Y, Kawashima Y, Takahashi M, Nishio A, Kitamura K. Honda K, et al. Among authors: nishio a. Otol Neurotol. 2015 Feb;36(2):311-7. doi: 10.1097/MAO.0000000000000376. Otol Neurotol. 2015. PMID: 24892370

9

Two Novel Diphenolic Metabolites from the Inedible Mushroom Thelephora palmata.

Nishio A, Mikami H, Imagawa H, Hashimoto T, Tanaka M, Ito T, Iuchia M, Iseki K, Noji M, Umevama A. Nishio A, et al. Nat Prod Commun. 2016 Aug;11(8):1147-1149. Nat Prod Commun. 2016. PMID: 30725577

10

[The expression of oncogene fms in human chorionic tissue].

Hoshina M, Nishio A, Bo M, Boime I, Mochizuki M. Hoshina M, et al. Among authors: nishio a. Nihon Sanka Fujinka Gakkai Zasshi. 1985 Dec;37(12):2791-8. Nihon Sanka Fujinka Gakkai Zasshi. 1985. PMID: 2418137 Japanese.

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