Murakami A - Search Results

1

Variants in optineurin gene and their association with tumor necrosis factor-alpha polymorphisms in Japanese patients with glaucoma.

Funayama T, Ishikawa K, Ohtake Y, Tanino T, Kurosaka D, Kimura I, Suzuki K, Ideta H, Nakamoto K, Yasuda N, Fujimaki T, Murakami A, Asaoka R, Hotta Y, Tanihara H, Kanamoto T, Mishima H, Fukuchi T, Abe H, Iwata T, Shimada N, Kudoh J, Shimizu N, Mashima Y. Funayama T, et al. Among authors: murakami a. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4359-67. doi: 10.1167/iovs.03-1403. Invest Ophthalmol Vis Sci. 2004. PMID: 15557444

2

Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa.

Fujiki K, Hotta Y, Murakami A, Yoshii M, Hayakawa M, Ichikawa T, Takeda M, Akeo K, Okisaka S, Kanai A. Fujiki K, et al. Among authors: murakami a. Jpn J Hum Genet. 1995 Sep;40(3):271-7. doi: 10.1007/BF01876186. Jpn J Hum Genet. 1995. PMID: 8527802

3

REP-1 gene mutations in Japanese patients with choroideremia.

Fujiki K, Hotta Y, Hayakawa M, Saito A, Mashima Y, Mori M, Yoshii M, Murakami A, Matsumoto M, Hayasaka S, Tagami N, Isashiki Y, Ohba N, Kanai A. Fujiki K, et al. Among authors: murakami a. Graefes Arch Clin Exp Ophthalmol. 1999 Sep;237(9):735-40. doi: 10.1007/s004170050305. Graefes Arch Clin Exp Ophthalmol. 1999. PMID: 10447648

4

Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese with Meesmann's corneal dystrophy.

Takahashi K, Takahashi K, Murakami A, Okisaka S, Kimura T, Kanai A. Takahashi K, et al. Among authors: murakami a. Jpn J Ophthalmol. 2002 Nov-Dec;46(6):673-4. doi: 10.1016/s0021-5155(02)00563-4. Jpn J Ophthalmol. 2002. PMID: 12543196

5

Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity.

Iida-Hasegawa N, Furuhata A, Hayatsu H, Murakami A, Fujiki K, Nakayasu K, Kanai A. Iida-Hasegawa N, et al. Among authors: murakami a. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3272-7. doi: 10.1167/iovs.02-0910. Invest Ophthalmol Vis Sci. 2003. PMID: 12882769

6

Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.

Ha NT, Chau HM, Cung le X, Thanh TK, Fujiki K, Murakami A, Hiratsuka Y, Kanai A. Ha NT, et al. Among authors: murakami a. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3310-6. doi: 10.1167/iovs.03-0031. Invest Ophthalmol Vis Sci. 2003. PMID: 12882775

7

Analysis of COL8A2 gene mutation in Japanese patients with Fuchs' endothelial dystrophy and posterior polymorphous dystrophy.

Kobayashi A, Fujiki K, Murakami A, Kato T, Chen LZ, Onoe H, Nakayasu K, Sakurai M, Takahashi M, Sugiyama K, Kanai A. Kobayashi A, et al. Among authors: murakami a. Jpn J Ophthalmol. 2004 May-Jun;48(3):195-8. doi: 10.1007/s10384-003-0063-6. Jpn J Ophthalmol. 2004. PMID: 15175909

8

Mutations in the membrane component, chromosome 1, surface marker 1 (M1S1) gene in gelatinous drop-like corneal dystrophy.

Murakami A, Kimura S, Fujiki K, Fujimaki T, Kanai A. Murakami A, et al. Jpn J Ophthalmol. 2004 Jul-Aug;48(4):317-20. doi: 10.1007/s10384-003-0064-5. Jpn J Ophthalmol. 2004. PMID: 15295654

9

Truncation and mutagenesis analysis of the human X-arrestin gene promoter.

Fujimaki T, Huang ZY, Kitagawa H, Sakuma H, Murakami A, Kanai A, McLaren MJ, Inana G. Fujimaki T, et al. Among authors: murakami a. Gene. 2004 Sep 15;339:139-47. doi: 10.1016/j.gene.2004.06.032. Gene. 2004. PMID: 15363854

10

Association between glaucoma and gene polymorphism of endothelin type A receptor.

Ishikawa K, Funayama T, Ohtake Y, Kimura I, Ideta H, Nakamoto K, Yasuda N, Fukuchi T, Fujimaki T, Murakami A, Asaoka R, Hotta Y, Kanamoto T, Tanihara H, Miyaki K, Mashima Y. Ishikawa K, et al. Among authors: murakami a. Mol Vis. 2005 Jun 23;11:431-7. Mol Vis. 2005. PMID: 15988412 Free article.

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