Oshima A - Search Results

1

Light Chain 3 associates with a Sos1 guanine nucleotide exchange factor: its significance in the Sos1-mediated Rac1 signaling leading to membrane ruffling.

Furuta S, Miura K, Copeland T, Shang WH, Oshima A, Kamata T. Furuta S, et al. Among authors: oshima a. Oncogene. 2002 Oct 10;21(46):7060-6. doi: 10.1038/sj.onc.1205790. Oncogene. 2002. PMID: 12370828

2

micro-Crystallin as an intracellular 3,5,3'-triiodothyronine holder in vivo.

Suzuki S, Suzuki N, Mori J, Oshima A, Usami S, Hashizume K. Suzuki S, et al. Among authors: oshima a. Mol Endocrinol. 2007 Apr;21(4):885-94. doi: 10.1210/me.2006-0403. Epub 2007 Jan 30. Mol Endocrinol. 2007. PMID: 17264173

3

The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochlea.

Usami S, Takumi Y, Suzuki N, Oguchi T, Oshima A, Suzuki H, Kitoh R, Abe S, Sasaki A, Matsubara A. Usami S, et al. Among authors: oshima a. Neuroscience. 2008 Jun 12;154(1):22-8. doi: 10.1016/j.neuroscience.2008.03.018. Epub 2008 Mar 19. Neuroscience. 2008. PMID: 18448257

4

Immunocytochemical localization of ubiquitin A-52 protein in the mouse inner ear.

Kitoh R, Oshima A, Suzuki N, Hashimoto S, Takumi Y, Usami S. Kitoh R, et al. Among authors: oshima a. Neuroreport. 2007 Jun 11;18(9):869-73. doi: 10.1097/WNR.0b013e32813ef147. Neuroreport. 2007. PMID: 17515792

5

Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.

Oguchi T, Ohtsuka A, Hashimoto S, Oshima A, Abe S, Kobayashi Y, Nagai K, Matsunaga T, Iwasaki S, Nakagawa T, Usami SI. Oguchi T, et al. Among authors: oshima a. J Hum Genet. 2005;50(2):76-83. doi: 10.1007/s10038-004-0223-7. Epub 2005 Feb 8. J Hum Genet. 2005. PMID: 15700112

6

CRYM mutations cause deafness through thyroid hormone binding properties in the fibrocytes of the cochlea.

Oshima A, Suzuki S, Takumi Y, Hashizume K, Abe S, Usami S. Oshima A, et al. J Med Genet. 2006 Jun;43(6):e25. doi: 10.1136/jmg.2005.034397. J Med Genet. 2006. PMID: 16740909 Free PMC article.

7

Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations.

Suzuki H, Oshima A, Tsukamoto K, Abe S, Kumakawa K, Nagai K, Satoh H, Kanda Y, Iwasaki S, Usami S. Suzuki H, et al. Among authors: oshima a. Acta Otolaryngol. 2007 Dec;127(12):1292-7. doi: 10.1080/00016480701258739. Acta Otolaryngol. 2007. PMID: 17851929

8

Hybrid carcinoma of the parotid gland: report of a case (epithelial-myoepithelial carcinoma and salivary duct carcinoma) and review of the literature.

Kainuma K, Oshima A, Suzuki H, Fukushima M, Shimojo H, Usami S. Kainuma K, et al. Among authors: oshima a. Acta Otolaryngol. 2010;130(1):185-9. doi: 10.3109/00016480902930458. Acta Otolaryngol. 2010. PMID: 19449226 Review.

9

Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I.

Jaijo T, Oshima A, Aller E, Carney C, Usami S, Millán JM, Kimberling WJ. Jaijo T, et al. Among authors: oshima a. Mol Vis. 2012;18:1719-26. Epub 2012 Jun 23. Mol Vis. 2012. PMID: 22815625 Free PMC article.

10

Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I.

Oshima A, Jaijo T, Aller E, Millan JM, Carney C, Usami S, Moller C, Kimberling WJ. Oshima A, et al. Hum Mutat. 2008 Jun;29(6):E37-46. doi: 10.1002/humu.20761. Hum Mutat. 2008. PMID: 18429043 Free PMC article.

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