Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese
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Novel Insights into the Role of Long Noncoding RNA in Ocular DiseasesAn Updated Review on the Genetics of Primary Open Angle GlaucomaRegulation of intraocular pressure by soluble and membrane guanylate cyclases and their role in glaucomaPrecise long non-coding RNA modulation in visual maintenance and impairmentOcular expression and distribution of products of the POAG-associated chromosome 9p21 gene regionAn approach to predict the risk of glaucoma development by integrating different attribute data.Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population.Identification and characterization of variants and a novel 4 bp deletion in the regulatory region of SIX6, a risk factor for primary open-angle glaucoma.MTHFR C677T predisposes to POAG but not to PACG in a North Indian population: a case control study.Genome-wide association studies: applications and insights gained in Ophthalmology.Common variants on chromosome 9p21 are associated with normal tension glaucoma.Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative.Exome array analysis identifies CAV1/CAV2 as a susceptibility locus for intraocular pressure.The genetics of POAG in black South Africans: a candidate gene association study.Association of MYOC and APOE promoter polymorphisms and primary open-angle glaucoma: a meta-analysis.Extracting Primary Open-Angle Glaucoma from Electronic Medical Records for Genetic Association StudiesA common variant near TGFBR3 is associated with primary open angle glaucoma.Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent.Molecular biomarkers in glaucomaCDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States.Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry.Gene expression profile in human trabecular meshwork from patients with primary open-angle glaucoma.Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis).Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma.Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.Chromosome 9p21 primary open-angle glaucoma susceptibility locus: a review.Genetics of primary open angle glaucoma.The Role of Long Noncoding RNAs in Neurodegenerative Diseases.Genetic risk factors for glaucoma and exfoliation syndrome identified by genome-wide association studies.Efficient and reliable establishment of lymphoblastoid cell lines by Epstein-Barr virus transformation from a limited amount of peripheral blood.Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study.Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old age.HEDD: Human Enhancer Disease Database.Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7.DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma.Primary Open-Angle Glaucoma Genetics in African Americans.Genetic variation of superoxide dismutases in patients with primary open-angle glaucoma.Clinical and genetic characterization of a large primary open angle glaucoma pedigree.Analysis of the 9p21.3 sequence associated with coronary artery disease reveals a tendency for duplication in a CAD patient.Mice Homozygous for a Deletion in the Glaucoma Susceptibility Locus INK4 Show Increased Vulnerability of Retinal Ganglion Cells to Elevated Intraocular Pressure.
P2860
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P2860
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese
description
2012 nî lūn-bûn
@nan
2012 թուականին հրատարակուած գիտական յօդուած
@hyw
2012 թվականին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@ast
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@en
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@nl
type
label
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@ast
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@en
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@nl
prefLabel
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@ast
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@en
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@nl
P2093
P2860
P3181
P1433
P1476
Common variants in CDKN2B-AS1 ...... ssociation studies in Japanese
@en
P2093
Hiroko Adachi
Kazuhiko Mori
Kei Tashiro
Kojiro Imai
Masaaki Kageyama
Masahiro Fuwa
Masakazu Nakano
Morio Ueno
Natsue Omi
Shigeru Kinoshita
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0033389
P407
P577
2012-01-01T00:00:00Z