Hosono K - Search Results

1

Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN.

Mizobuchi K, Hayashi T, Oishi N, Kubota D, Kameya S, Higasa K, Futami T, Kondo H, Hosono K, Kurata K, Hotta Y, Yoshitake K, Iwata T, Matsuura T, Nakano T. Mizobuchi K, et al. Among authors: hosono k. J Clin Med. 2021 May 24;10(11):2265. doi: 10.3390/jcm10112265. J Clin Med. 2021. PMID: 34073704 Free PMC article.

2

Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1.

Nakanishi H, Ohtsubo M, Iwasaki S, Hotta Y, Takizawa Y, Hosono K, Mizuta K, Mineta H, Minoshima S. Nakanishi H, et al. Among authors: hosono k. J Hum Genet. 2010 Dec;55(12):796-800. doi: 10.1038/jhg.2010.115. Epub 2010 Sep 16. J Hum Genet. 2010. PMID: 20844544

3

Case of Japanese patient with x-linked ocular albinism associated with GPR143 gene mutation.

Ohtsubo M, Sato M, Hikoya A, Hosono K, Minoshima S, Hotta Y. Ohtsubo M, et al. Among authors: hosono k. Jpn J Ophthalmol. 2010 Nov;54(6):624-6. doi: 10.1007/s10384-010-0872-3. Jpn J Ophthalmol. 2010. PMID: 21274678 No abstract available.

4

Case of Japanese patient with x-linked ocular albinism associated with GPR143 gene mutation.

Ohtsubo M, Sato M, Hikoya A, Hosono K, Minoshima S, Hotta Y. Ohtsubo M, et al. Among authors: hosono k. Jpn J Ophthalmol. 2010 Nov;54(6):624-6. Jpn J Ophthalmol. 2010. PMID: 21348135 No abstract available.

5

Clinical features of a Japanese case with Bothnia dystrophy.

Nojima K, Hosono K, Zhao Y, Toshiba T, Hikoya A, Asai T, Kato M, Kondo M, Minoshima S, Hotta Y. Nojima K, et al. Among authors: hosono k. Ophthalmic Genet. 2012 Jun;33(2):83-8. doi: 10.3109/13816810.2011.634877. Epub 2011 Dec 15. Ophthalmic Genet. 2012. PMID: 22171637

6

Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population.

Hosono K, Ishigami C, Takahashi M, Park DH, Hirami Y, Nakanishi H, Ueno S, Yokoi T, Hikoya A, Fujita T, Zhao Y, Nishina S, Shin JP, Kim IT, Yamamoto S, Azuma N, Terasaki H, Sato M, Kondo M, Minoshima S, Hotta Y. Hosono K, et al. PLoS One. 2012;7(2):e31036. doi: 10.1371/journal.pone.0031036. Epub 2012 Feb 17. PLoS One. 2012. PMID: 22363543 Free PMC article.

7

Clinical phenotype in ten unrelated Japanese patients with mutations in the EYS gene.

Suto K, Hosono K, Takahashi M, Hirami Y, Arai Y, Nagase Y, Ueno S, Terasaki H, Minoshima S, Kondo M, Hotta Y. Suto K, et al. Among authors: hosono k. Ophthalmic Genet. 2014 Mar;35(1):25-34. doi: 10.3109/13816810.2013.768673. Epub 2013 Feb 20. Ophthalmic Genet. 2014. PMID: 23421333

8

Interaction between optineurin and the bZIP transcription factor NRL.

Wang C, Hosono K, Ohtsubo M, Ohishi K, Gao J, Nakanishi N, Hikoya A, Sato M, Hotta Y, Minoshima S. Wang C, et al. Among authors: hosono k. Cell Biol Int. 2014 Jan;38(1):16-25. doi: 10.1002/cbin.10174. Epub 2013 Sep 12. Cell Biol Int. 2014. PMID: 23956131

9

Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital Amaurosis.

Hosono K, Harada Y, Kurata K, Hikoya A, Sato M, Minoshima S, Hotta Y. Hosono K, et al. J Ophthalmol. 2015;2015:693468. doi: 10.1155/2015/693468. Epub 2015 May 13. J Ophthalmol. 2015. PMID: 26097748 Free PMC article.

10

Genotype-phenotype correlation of PAX6 gene mutations in aniridia.

Yokoi T, Nishina S, Fukami M, Ogata T, Hosono K, Hotta Y, Azuma N. Yokoi T, et al. Among authors: hosono k. Hum Genome Var. 2016 Feb 11;3:15052. doi: 10.1038/hgv.2015.52. eCollection 2016. Hum Genome Var. 2016. PMID: 27081561 Free PMC article.

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