Nakayasu K - Search Results

1

A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities.

Fujiki K, Hotta Y, Nakayasu K, Yokoyama T, Takano T, Yamaguchi T, Kanai A. Fujiki K, et al. Among authors: nakayasu k. Hum Genet. 1998 Sep;103(3):286-9. doi: 10.1007/s004390050818. Hum Genet. 1998. PMID: 9799082

2

Homozygotic patient with betaig-h3 gene mutation in granular dystrophy.

Fujiki K, Hotta Y, Nakayasu K, Kanai A. Fujiki K, et al. Among authors: nakayasu k. Cornea. 1998 May;17(3):288-92. Cornea. 1998. PMID: 9603385

3

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: nakayasu k. Jpn J Ophthalmol. 1998 Nov-Dec;42(6):450-5. doi: 10.1016/s0021-5155(98)00050-1. Jpn J Ophthalmol. 1998. PMID: 9886734

4

Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type I.

Endo S, Nguyen TH, Fujiki K, Hotta Y, Nakayasu K, Yamaguchi T, Ishida N, Kanai A. Endo S, et al. Among authors: nakayasu k. Am J Ophthalmol. 1999 Jul;128(1):104-6. doi: 10.1016/s0002-9394(99)00053-7. Am J Ophthalmol. 1999. PMID: 10482106

5

Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy: the P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophy.

Ha NT, Fujiki K, Hotta Y, Nakayasu K, Kanai A. Ha NT, et al. Among authors: nakayasu k. Am J Ophthalmol. 2000 Jul;130(1):119-20. doi: 10.1016/s0002-9394(00)00596-1. Am J Ophthalmol. 2000. PMID: 11004271

6

Six different mutations of TGFBI (betaig-h3, keratoepithelin) gene found in Japanese corneal dystrophies.

Fujiki K, Hotta Y, Nakayasu K, Yamaguchi T, Kato T, Uesugi Y, Ha NT, Endo S, Ishida N, Lu WN, Kanai A. Fujiki K, et al. Among authors: nakayasu k. Cornea. 2000 Nov;19(6):842-5. doi: 10.1097/00003226-200011000-00015. Cornea. 2000. PMID: 11095060 Clinical Trial.

7

Corneal dystrophies in Japan.

Fujiki K, Nakayasu K, Kanai A. Fujiki K, et al. Among authors: nakayasu k. J Hum Genet. 2001;46(8):431-5. doi: 10.1007/s100380170041. J Hum Genet. 2001. PMID: 11501939 Review.

8

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: nakayasu k. Jpn J Ophthalmol. 1997 Nov-Dec;41(6):370-5. doi: 10.1016/s0021-5155(97)00086-5. Jpn J Ophthalmol. 1997. PMID: 9509303

9

Visual impairment and REP-1 gene mutations in Japanese choroideremia patients.

Hayakawa M, Fujiki K, Hotta Y, Ito R, Ohki J, Ono J, Saito A, Nakayasu K, Kanai A, Ishidoh K, Kominami E, Yoshida K, Kim KC, Ohashi H. Hayakawa M, et al. Among authors: nakayasu k. Ophthalmic Genet. 1999 Jun;20(2):107-15. doi: 10.1076/opge.20.2.107.2285. Ophthalmic Genet. 1999. PMID: 10420196

10

Corneal wound healing: Immunohistological features of extracellular matrix following penetrating keratoplasty in rabbits.

Kato T, Nakayasu K, Kanai A. Kato T, et al. Among authors: nakayasu k. Jpn J Ophthalmol. 2000 Jul-Aug;44(4):334-41. doi: 10.1016/s0021-5155(00)00168-4. Jpn J Ophthalmol. 2000. PMID: 10974287

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