about
A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore ChineseRanibizumab for the treatment of degenerative ocular conditions.Analysis of fundus shape in highly myopic eyes by using curvature maps constructed from optical coherence tomographyAssociation between Insulin-Like Growth Factor 1 Gene rs12423791 or rs6214 Polymorphisms and High Myopia: A Meta-AnalysisAssociation of paired box 6 with high myopia in Japanese.Evaluation of MMP2 as a candidate gene for high myopia.Insulin-like growth factor 1 is not associated with high myopia in a large Japanese cohort.Common variant in myocilin gene is associated with high myopia in isolated population of Korcula Island, Croatia.High susceptibility to experimental myopia in a mouse model with a retinal on pathway defectRole of the dopaminergic system in the development of myopia in children and adolescents.Association of Body Length with Ocular Parameters in Mice.Association of ZNF644, GRM6, and CTNND2 genes with high myopia in the Han Chinese population: Jiangsu Eye Study.Assessment of BicC family RNA binding protein 1 and Ras protein specific guanine nucleotide releasing factor 1 as candidate genes for high myopia: A case-control study.Influence of high myopia on outcomes of trabeculectomy with mitomycin C in patients with primary open-angle glaucoma.TGIF1 is a potential candidate gene for high myopia in ethnic Kashmiri population.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
A genetic perspective on myopia.
@ast
A genetic perspective on myopia.
@en
type
label
A genetic perspective on myopia.
@ast
A genetic perspective on myopia.
@en
prefLabel
A genetic perspective on myopia.
@ast
A genetic perspective on myopia.
@en
P2093
P1476
A genetic perspective on myopia
@en
P2093
P2888
P304
P356
10.1007/S00018-004-4353-Z
P577
2005-04-01T00:00:00Z