Kamiya K - Search Results

1

Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation.

Fukunaga I, Shiga T, Chen C, Oe Y, Danzaki K, Ohta S, Matsuoka R, Anzai T, Hibiya-Motegi R, Tajima S, Ikeda K, Akamatsu W, Kamiya K. Fukunaga I, et al. Among authors: kamiya k. Stem Cell Res. 2020 Mar;43:101674. doi: 10.1016/j.scr.2019.101674. Epub 2019 Dec 4. Stem Cell Res. 2020. PMID: 31926383 Free article.

2

Cochlear outer hair cells in a dominant-negative connexin26 mutant mouse preserve non-linear capacitance in spite of impaired distortion product otoacoustic emission.

Minekawa A, Abe T, Inoshita A, Iizuka T, Kakehata S, Narui Y, Koike T, Kamiya K, Okamura HO, Shinkawa H, Ikeda K. Minekawa A, et al. Among authors: kamiya k. Neuroscience. 2009 Dec 15;164(3):1312-9. doi: 10.1016/j.neuroscience.2009.08.043. Epub 2009 Aug 25. Neuroscience. 2009. PMID: 19712724

3

Vestibular function of patients with profound deafness related to GJB2 mutation.

Kasai M, Hayashi C, Iizuka T, Inoshita A, Kamiya K, Okada H, Nakajima Y, Kaga K, Ikeda K. Kasai M, et al. Among authors: kamiya k. Acta Otolaryngol. 2010 Sep;130(9):990-5. doi: 10.3109/00016481003596508. Acta Otolaryngol. 2010. PMID: 20377502

4

Prevalence of GJB2 causing recessive profound non-syndromic deafness in Japanese children.

Hayashi C, Funayama M, Li Y, Kamiya K, Kawano A, Suzuki M, Hattori N, Ikeda K. Hayashi C, et al. Among authors: kamiya k. Int J Pediatr Otorhinolaryngol. 2011 Feb;75(2):211-4. doi: 10.1016/j.ijporl.2010.11.001. Epub 2010 Nov 26. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21112098

5

[Inner ear cell therapy for hereditary deafness with multipotent stem cells].

Kamiya K, Ikeda K. Kamiya K, et al. Nihon Rinsho. 2011 Dec;69(12):2215-9. Nihon Rinsho. 2011. PMID: 22242322 Japanese.

6

Gene transfer targeting mouse vestibule using adenovirus and adeno-associated virus vectors.

Okada H, Iizuka T, Mochizuki H, Nihira T, Kamiya K, Inoshita A, Kasagi H, Kasai M, Ikeda K. Okada H, et al. Among authors: kamiya k. Otol Neurotol. 2012 Jun;33(4):655-9. doi: 10.1097/MAO.0b013e31825368d1. Otol Neurotol. 2012. PMID: 22525215

7

[Cell therapy for hereditary hearing loss with stem cell homing factors].

Kamiya K. Kamiya K. Nihon Yakurigaku Zasshi. 2013 Apr;141(4):191-4. doi: 10.1254/fpj.141.191. Nihon Yakurigaku Zasshi. 2013. PMID: 23575423 Review. Japanese. No abstract available.

8

Multiplex analyses of cytokine and chemokine release from the cultured fibroblast of nasal polyps: the effect of IL-17A.

Homma H, Kamiya K, Kusunoki T, Ikeda K. Homma H, et al. Among authors: kamiya k. Acta Otolaryngol. 2013 Oct;133(10):1065-72. doi: 10.3109/00016489.2013.796091. Acta Otolaryngol. 2013. PMID: 24032570

9

Treatment with 17-allylamino-17-demethoxygeldanamycin ameliorated symptoms of Bartter syndrome type IV caused by mutated Bsnd in mice.

Nomura N, Kamiya K, Ikeda K, Yui N, Chiga M, Sohara E, Rai T, Sakaki S, Uchida S. Nomura N, et al. Among authors: kamiya k. Biochem Biophys Res Commun. 2013 Nov 22;441(3):544-9. doi: 10.1016/j.bbrc.2013.10.129. Epub 2013 Nov 1. Biochem Biophys Res Commun. 2013. PMID: 24189473

10

Dominant negative connexin26 mutation R75W causing severe hearing loss influences normal programmed cell death in postnatal organ of Corti.

Inoshita A, Karasawa K, Funakubo M, Miwa A, Ikeda K, Kamiya K. Inoshita A, et al. Among authors: kamiya k. BMC Genet. 2014 Jan 3;15:1. doi: 10.1186/1471-2156-15-1. BMC Genet. 2014. PMID: 24387126 Free PMC article.

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