Kamiya K - Search Results

1

Enhanced expression of C/EBP homologous protein (CHOP) precedes degeneration of fibrocytes in the lateral wall after acute cochlear mitochondrial dysfunction induced by 3-nitropropionic acid.

Fujinami Y, Mutai H, Kamiya K, Mizutari K, Fujii M, Matsunaga T. Fujinami Y, et al. Among authors: kamiya k. Neurochem Int. 2010 Feb;56(3):487-94. doi: 10.1016/j.neuint.2009.12.008. Epub 2009 Dec 21. Neurochem Int. 2010. PMID: 20026213

2

A novel animal model of acute cochlear mitochondrial dysfunction.

Hoya N, Okamoto Y, Kamiya K, Fujii M, Matsunaga T. Hoya N, et al. Among authors: kamiya k. Neuroreport. 2004 Jul 19;15(10):1597-600. doi: 10.1097/01.wnr.0000133226.94662.80. Neuroreport. 2004. PMID: 15232290

3

Permanent threshold shift caused by acute cochlear mitochondrial dysfunction is primarily mediated by degeneration of the lateral wall of the cochlea.

Okamoto Y, Hoya N, Kamiya K, Fujii M, Ogawa K, Matsunaga T. Okamoto Y, et al. Among authors: kamiya k. Audiol Neurootol. 2005 Jul-Aug;10(4):220-33. doi: 10.1159/000084843. Epub 2005 Mar 3. Audiol Neurootol. 2005. PMID: 15809501

4

Mesenchymal stem cell transplantation accelerates hearing recovery through the repair of injured cochlear fibrocytes.

Kamiya K, Fujinami Y, Hoya N, Okamoto Y, Kouike H, Komatsuzaki R, Kusano R, Nakagawa S, Satoh H, Fujii M, Matsunaga T. Kamiya K, et al. Am J Pathol. 2007 Jul;171(1):214-26. doi: 10.2353/ajpath.2007.060948. Am J Pathol. 2007. PMID: 17591967 Free PMC article.

5

Caspase inhibitor facilitates recovery of hearing by protecting the cochlear lateral wall from acute cochlear mitochondrial dysfunction.

Mizutari K, Matsunaga T, Kamiya K, Fujinami Y, Fujii M, Ogawa K. Mizutari K, et al. Among authors: kamiya k. J Neurosci Res. 2008 Jan;86(1):215-22. doi: 10.1002/jnr.21470. J Neurosci Res. 2008. PMID: 17722114

6

Decreased expression of connexin-30 and aberrant expression of connexin-26 in human head and neck cancer.

Ozawa H, Matsunaga T, Kamiya K, Tokumaru Y, Fujii M, Tomita T, Ogawa K. Ozawa H, et al. Among authors: kamiya k. Anticancer Res. 2007 Jul-Aug;27(4B):2189-95. Anticancer Res. 2007. PMID: 17695503 Free article.

7

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

8

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.

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

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

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