Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.
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CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMDInterpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiersStructural effects of fibulin 5 missense mutations associated with age-related macular degeneration and cutis laxaAge-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNACigarette smoking strongly modifies the association of LOC387715 and age-related macular degenerationVariation near complement factor I is associated with risk of advanced AMDGenetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degenerationGenome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)Therapeutic targets in age-related macular diseaseA longitudinal follow-up study of saffron supplementation in early age-related macular degeneration: sustained benefits to central retinal functionExpression of recombinant protein encoded by LOC387715 in Escherichia coliThe LOC387715 polymorphism and age-related macular degeneration: replication in three case-control samplesCFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degenerationA variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degenerationA global reference for human genetic variationAMD and the alternative complement pathway: genetics and functional implicationsGenetics of immunological and inflammatory components in age-related macular degenerationThe proteomics of drusenAdvances in the genomics of common eye diseasesMitochondrial variation and the risk of age-related macular degeneration across diverse populationsA common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degenerationSystemic complement activation in age-related macular degenerationAn imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control studyGenetic determinants of age-related macular degeneration in diverse populations from the PAGE studyGenetic determinants of human health span and life span: progress and new opportunitiesUsing genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degenerationOverexpression of HTRA1 leads to ultrastructural changes in the elastic layer of Bruch's membrane via cleavage of extracellular matrix componentsThe ERCC6 gene and age-related macular degenerationGenetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysisHeritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypesSeven new loci associated with age-related macular degeneration.Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3Genotype imputationGenetic mapping in human diseaseAssociation of ARMS2/LOC387715 A69S, CFH Y402H, and CFH I62V polymorphisms with retinal angiomatous proliferation compared with typical age-related macular degeneration: a meta-analysis.Genetic variations strongly influence phenotypic outcome in the mouse retina.Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiologyEfficient study designs for test of genetic association using sibship data and unrelated cases and controls.LOC387715/HTRA1 gene polymorphisms and susceptibility to age-related macular degeneration: A HuGE review and meta-analysis
P2860
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P2860
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.
description
2005 nî lūn-bûn
@nan
2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
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
name
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@ast
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@en
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@nl
type
label
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@ast
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@en
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@nl
prefLabel
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@ast
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@en
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@nl
P2093
P2860
P50
P356
P1476
Hypothetical LOC387715 is a se ...... ment factor H to disease risk.
@en
P2093
Andrea Rivera
Bernhard H F Weber
Claudia N Keilhauer
Sheila A Fisher
P2860
P304
P356
10.1093/HMG/DDI353
P577
2005-09-20T00:00:00Z