Detalhe da pesquisa
1.
Evaluation of Pigment Distribution and Depth Analysis Methods for Decorative Soft Contact Lenses.
Eye Contact Lens
; 44 Suppl 2: S105-S112, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28953599
2.
A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy.
Jpn J Ophthalmol
; 52(3): 224-226, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18661274
3.
A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.
Am J Ophthalmol
; 144(3): 473-5, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17765440
4.
Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I.
Jpn J Ophthalmol
; 49(2): 84-8, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-15838722
5.
[Analysis of gene mutation in Chinese patients with Reis-Bücklers corneal dystrophy].
Zhonghua Yan Ke Za Zhi
; 41(3): 239-42, 2005 Mar.
Artigo
em Zh
| MEDLINE | ID: mdl-15840366
6.
Truncation and mutagenesis analysis of the human X-arrestin gene promoter.
Gene
; 339: 139-47, 2004 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15363854
7.
Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity.
Invest Ophthalmol Vis Sci
; 44(8): 3272-7, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12882769
8.
Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.
Invest Ophthalmol Vis Sci
; 44(8): 3310-6, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12882775
9.
Long-term follow-up for bullous keratopathy after sato-type anterior-posterior corneal refractive surgery.
Am J Ophthalmol
; 136(6): 1154-5, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14644229
10.
Transthyretin Ser-44 mutation in a case with vitreous amyloidosis.
Am J Ophthalmol
; 133(2): 272-3, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11812437
11.
Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy.
Am J Ophthalmol
; 137(3): 567-9, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15013888
12.
A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy.
Am J Ophthalmol
; 135(3): 390-3, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12614764
13.
Identification of novel mutations of the CHST6 gene in Vietnamese families affected with macular corneal dystrophy in two generations.
Cornea
; 22(6): 508-11, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12883341
14.
Smad7 suppresses the inhibitory effect of TGF-beta2 on corneal endothelial cell proliferation and accelerates corneal endothelial wound closure in vitro.
Cornea
; 22(2): 153-9, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12605052
15.
Microarray analysis identified differentially expressed genes in keratocytes from keratoconus patients.
Curr Eye Res
; 28(6): 373-9, 2004 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15512944
16.
Molecular cloning of ELOVL4 gene from cynomolgus monkey (Macaca fascicularis).
Exp Anim
; 52(2): 129-35, 2003 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-12806887
17.
Endogenous substance P in corneal epithelial cells and keratocytes.
Jpn J Ophthalmol
; 46(6): 616-20, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12543186
18.
Mutations in the membrane component, chromosome 1, surface marker 1 (M1S1) gene in gelatinous drop-like corneal dystrophy.
Jpn J Ophthalmol
; 48(4): 317-20, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15295654
19.
Transferrin-polyethylenimine conjugate, FuGENE6 and TransIT-LT as nonviral vectors for gene transfer to the corneal endothelium.
Jpn J Ophthalmol
; 46(2): 140-6, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12062218
20.
High level of Fc epsilon receptor I-bindable immunoglobulin E in the tear fluid and increased immunoglobulin E-saturated cells in the giant papillae of vernal keratoconjunctivitis patients.
Jpn J Ophthalmol
; 46(4): 357-63, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12225812