Fujimaki T - 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: fujimaki t. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4359-67. doi: 10.1167/iovs.03-1403. Invest Ophthalmol Vis Sci. 2004. PMID: 15557444

2

Plus/minus screening of rabbit corneal endothelial cDNA library.

Hotta Y, Kitagawa H, Fujiki K, Fujimaki T, Ohnuki H, Sakuma H, Iwata F, Watanabe M, Nakayasu K, Kanai A. Hotta Y, et al. Among authors: fujimaki t. Jpn J Ophthalmol. 1997 Nov-Dec;41(6):370-5. doi: 10.1016/s0021-5155(97)00086-5. Jpn J Ophthalmol. 1997. PMID: 9509303

3

Analysis of peripherin/RDS gene for Japanese retinal dystrophies.

Fujiki K, Hotta Y, Hayakawa M, Fujimaki T, Takeda M, Isashiki Y, Ohba N, Kanai A. Fujiki K, et al. Among authors: fujimaki t. Jpn J Ophthalmol. 1998 May-Jun;42(3):186-92. doi: 10.1016/s0021-5155(97)00133-0. Jpn J Ophthalmol. 1998. PMID: 9690896

4

Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene.

Hotta Y, Fujiki K, Hayakawa M, Ohta T, Fujimaki T, Tamaki K, Yokoyama T, Kanai A, Hirakata A, Hida T, Nishina S, Azuma N. Hotta Y, et al. Among authors: fujimaki t. Hum Genet. 1998 Aug;103(2):142-4. doi: 10.1007/pl00008705. Hum Genet. 1998. PMID: 9760195

5

Arg124Cys mutation of the betaig-h3 bene in a Japanese family with lattice corneal dystrophy type I.

Hotta Y, Fujiki K, Ono K, Fujimaki T, Nakayasu K, Yamaguchi T, Kanai A. Hotta Y, et al. Among authors: fujimaki t. Jpn J Ophthalmol. 1998 Nov-Dec;42(6):450-5. doi: 10.1016/s0021-5155(98)00050-1. Jpn J Ophthalmol. 1998. PMID: 9886734

6

Large-scale sequencing of the rabbit corneal endothelial cDNA library.

Fujimaki T, Hotta Y, Sakuma H, Fujiki K, Kanai A. Fujimaki T, et al. Cornea. 1999 Jan;18(1):109-14. doi: 10.1097/00003226-199901000-00017. Cornea. 1999. PMID: 9894946

7

Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.

Matsumoto M, Hayasaka S, Kadoi C, Hotta Y, Fujiki K, Fujimaki T, Takeda M, Ishida N, Endo S, Kanai A. Matsumoto M, et al. Among authors: fujimaki t. Ophthalmic Genet. 1999 Sep;20(3):153-60. doi: 10.1076/opge.20.3.153.2281. Ophthalmic Genet. 1999. PMID: 10520236

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. Among authors: fujimaki t. 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. Gene. 2004 Sep 15;339:139-47. doi: 10.1016/j.gene.2004.06.032. Gene. 2004. PMID: 15363854

10

Novel MYOC gene mutation, Phe369Leu, in Japanese patients with primary open-angle glaucoma detected by denaturing high-performance liquid chromatography.

Ishikawa K, Funayama T, Ohtake Y, Tanino T, Kurosaka D, Suzuki K, Ideta H, Fujimaki T, Tanihara H, Asaoka R, Naoi N, Yasuda N, Iwata T, Mashima Y. Ishikawa K, et al. Among authors: fujimaki t. J Glaucoma. 2004 Dec;13(6):466-71. doi: 10.1097/0.ijg.0000138204.6d. J Glaucoma. 2004. PMID: 15534471

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

302 results

Search Page