Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
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Current perspectives on the immunopathogenesis of systemic sclerosisExpression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic VariationGenetics of systemic sclerosis: recent advancesGenetics, Epigenetics, and Genomics of Systemic SclerosisRecent advances in the genetics of systemic sclerosis: toward biological and clinical significanceIdentification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.An IRF5 Decoy Peptide Reduces Myocardial Inflammation and Fibrosis and Improves Endothelial Cell Function in Tight-Skin MiceExpression of Notch signaling components in cutaneous foreign body and sarcoidal granulomas and fusing macrophages.Premature Ovarian Failure - An Unusual Manifestation of Systemic SclerosisSystemic lupus erythematosus diagnostics in the 'omics' eraAssociation of the HLA-DRB1 with scleroderma in Chinese population.Analysis of the association between CD40 and CD40 ligand polymorphisms and systemic sclerosis.The transcription factors IRF8 and PU.1 negatively regulate plasma cell differentiation.Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibilityClinical and autoimmune profile of scleroderma patients from Western India.Genetics of scleroderma: implications for personalized medicine?The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis.Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.Possible single-nucleotide polymorphism loci associated with systemic sclerosis susceptibility: a genetic association study in a Chinese Han population.Potential role of the lectin pathway of complement in the pathogenesis and disease manifestations of systemic sclerosis: a case-control and cohort study.Systems level analysis of systemic sclerosis shows a network of immune and profibrotic pathways connected with genetic polymorphisms.Genetic association of CD247 (CD3ζ) with SLE in a large-scale multiethnic study.PTPN22: the archetypal non-HLA autoimmunity gene.Multilevel-analysis identify a cis-expression quantitative trait locus associated with risk of renal cell carcinomaIdentification of NF-κB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis.A candidate gene study reveals association between a variant of the Peroxisome Proliferator-Activated Receptor Gamma (PPAR-γ) gene and systemic sclerosisHLA Class I and II Blocks Are Associated to Susceptibility, Clinical Subtypes and Autoantibodies in Mexican Systemic Sclerosis (SSc) Patients.Pathogenesis of Systemic Sclerosis.A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populationsIdentification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-upCD1a+ survivin+ dendritic cell infiltration in dermal lesions of systemic sclerosisHLA Immune Function Genes in Autism.Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyGenetic susceptibility loci of idiopathic interstitial pneumonia do not represent risk for systemic sclerosis: a case control study in Caucasian patientsTwo Genetic Variations in the IRF8 region are associated with Behçet's disease in Han Chinese.Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.Identification of an Association of TNFAIP3 Polymorphisms With Matrix Metalloproteinase Expression in Fibroblasts in an Integrative Study of Systemic Sclerosis-Associated Genetic and Environmental FactorsGenetic Susceptibility to Interstitial Lung Disease Associated with Systemic Sclerosis.KCNA5 gene is not confirmed as a systemic sclerosis-related pulmonary arterial hypertension genetic susceptibility factorThe genetics of scleroderma: looking into the postgenomic era
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P2860
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Identification of novel geneti ...... nome-wide association strategy
@ast
Identification of novel geneti ...... nome-wide association strategy
@en
type
label
Identification of novel geneti ...... nome-wide association strategy
@ast
Identification of novel geneti ...... nome-wide association strategy
@en
prefLabel
Identification of novel geneti ...... nome-wide association strategy
@ast
Identification of novel geneti ...... nome-wide association strategy
@en
P2093
P2860
P50
P3181
P1433
P1476
Identification of novel geneti ...... nome-wide association strategy
@en
P2093
Alexander Kreuter
Alexandre E Voskuyl
Annemie J Schuerwegh
Annet Italiaander
Annette T Lee
Benedicte A Lie
Blanca Rueda
Bobby P C Koeleman
Carmen Fonseca
Carmen P Simeon
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1002178
P50
P5008
P577
2011-07-14T00:00:00Z