Unraveling the genetic component of systemic sclerosis (Q37973287)

26 August 2017

Unraveling the genetic component of systemic sclerosis (English)

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26 August 2017

José Ezequiel Martín

1

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Lara Bossini-Castillo

object named as

Lara Bossini-Castillo

series ordinal

2

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Javier Martin

object named as

Javier Martín

series ordinal

3

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publication date

5 January 2012

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26 August 2017

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26 August 2017

131

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26 August 2017

1023-1037

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26 August 2017

7

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https://scigraph.springernature.com/pub.10.1007/s00439-011-1137-z

26 August 2017

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cites work

Intracellular localization of the P21rho proteins

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Genome structural variation discovery and genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Increased prevalence of systemic sclerosis in a Native American tribe in Oklahoma. Association with an Amerindian HLA haplotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Familial occurrence frequencies and relative risks for systemic sclerosis (scleroderma) in three United States cohorts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Major histocompatibility complex (MHC) class II alleles, haplotypes and epitopes which confer susceptibility or protection in systemic sclerosis: analyses in 1300 Caucasian, African-American and Hispanic cases and 1000 controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Systemic sclerosis and lupus: points in an interferon-mediated continuum

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Associated autoimmune diseases in systemic sclerosis define a subset of patients with milder disease: results from 2 large cohorts of European Caucasian patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Statistical analysis strategies for association studies involving rare variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Epigenetics and autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Macrophage migration inhibitory factor: a regulator of innate immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Molecular mechanisms for the assembly of the T cell receptor-CD3 complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Novel identification of the IRF7 region as an anticentromere autoantibody propensity locus in systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Conditional meta-analysis stratifying on detailed HLA genotypes identifies a novel type 1 diabetes locus around TCF19 in the MHC

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Detecting gene-gene interactions that underlie human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association study of ITGAM, ITGAX, and CD58 autoimmune risk loci in systemic sclerosis: results from 2 large European Caucasian cohorts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

C8orf13-BLK is a genetic risk locus for systemic sclerosis and has additive effects with BANK1: results from a large french cohort and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Genome-wide genetic marker discovery and genotyping using next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Recent findings on genetics of systemic autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Specific expression of a tyrosine kinase gene, blk, in B lymphoid cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Analysis of systemic sclerosis in twins reveals low concordance for disease and high concordance for the presence of antinuclear antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Endothelin axis polymorphisms in patients with scleroderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Human genetic variation and its contribution to complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Class II HLA associations with autoantibodies in scleroderma: a highly significant role for HLA-DP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

21 January 2018

OX40 (CD134) and OX40L.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of the PTPN22 R620W polymorphism with anti-topoisomerase I- and anticentromere antibody-positive systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Polymorphisms in TBX21 and STAT4 increase the risk of systemic sclerosis: evidence of possible gene-gene interaction and alterations in Th1/Th2 cytokines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Replication of the BANK1 genetic association with systemic lupus erythematosus in a European-derived population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Type I interferons: crucial participants in disease amplification in autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Genomics, health care, and society

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Polyautoimmunity and familial autoimmunity in systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

The current state of biomarkers in systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Future directions in genetic for autoimmune diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of a functional polymorphism in the IRF5 region with systemic sclerosis in a Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

NOS2 polymorphisms associated with the susceptibility to pulmonary arterial hypertension with systemic sclerosis: contribution to the transcriptional activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

HLA class II genes associated with anticentromere antibody in Japanese patients with systemic sclerosis (scleroderma).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Unexpected role for the B cell-specific Src family kinase B lymphoid kinase in the development of IL-17-producing γδ T cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Abnormal DNA methylation in CD4+ T cells from patients with systemic lupus erythematosus, systemic sclerosis, and dermatomyositis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Structure, function, and regulation of STAT proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association between a stromal cell-derived factor 1 (SDF-1/CXCL12) gene polymorphism and microvascular disease in systemic sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of a functional polymorphism in the matrix metalloproteinase-12 promoter region with systemic sclerosis in an Italian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A genetic variation located in the promoter region of the UPAR (CD87) gene is associated with the vascular complications of systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Prevalence, incidence, survival, and disease characteristics of systemic sclerosis in a large US population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Systemic sclerosis: environmental factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Epigenetic instability of cytokine and transcription factor gene loci underlies plasticity of the T helper 17 cell lineage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

HLA class II and autoimmunity: epitope selection vs differential expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Role of protein tyrosine phosphatases in T cell activation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Physiological and pathological roles for microRNAs in the immune system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Study of functional variants of theBANK1gene in rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Study of the common genetic background for rheumatoid arthritis and systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Jaks, STATs, cytokine signal transduction, and immunoregulation: are we there yet?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of SEEK1 and psoriatic arthritis in two distinct Canadian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Epigenome-wide association studies for common human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Targeted therapy for systemic sclerosis: how close are we?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Geoepidemiology of systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Common variants at CD40 and other loci confer risk of rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Ethnicity and race and systemic sclerosis: how it affects susceptibility, severity, antibody genetics, and clinical manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Genetic and hormonal factors in female-biased autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

BANK1 functional variants are associated with susceptibility to diffuse systemic sclerosis in Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Essential role of Src-family protein tyrosine kinases in NF-kappaB activation during B cell development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of HLA class II genes with systemic sclerosis in Spanish patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

The ubiquitin modifying enzyme A20 restricts B cell survival and prevents autoimmunity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Gene--environment-wide association studies: emerging approaches

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Mimicry of pre-B cell receptor signaling by activation of the tyrosine kinase Blk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Skewed X-chromosome inactivation in scleroderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

The ubiquitin-editing enzyme A20 (TNFAIP3) is a central regulator of immunopathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Sex differences in autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Positional identification of TNFSF4, encoding OX40 ligand, as a gene that influences atherosclerosis susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Signaling by IL-12 and IL-23 and the immunoregulatory roles of STAT4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of hypoxia-inducible factor 1A (HIF1A) gene polymorphisms with systemic sclerosis in a French European Caucasian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

BANK regulates BCR-induced calcium mobilization by promoting tyrosine phosphorylation of IP(3) receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Copy number variation in human health, disease, and evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

HLA-DPB1 and DPB2 are genetic loci for systemic sclerosis: a genome-wide association study in Koreans with replication in North Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Confirmation of association of the macrophage migration inhibitory factor gene with systemic sclerosis in a large European population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Associations between vitamin D receptor polymorphisms and susceptibility to rheumatoid arthritis and systemic lupus erythematosus: a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

A nonsynonymous functional variant in integrin-αM (encoded by ITGAM) is associated with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association between theIRF5rs2004640 functional polymorphism and systemic sclerosis: A new perspective for pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

STAT4is a genetic risk factor for systemic sclerosis having additive effects withIRF5on disease susceptibility and related pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

BANK1is a genetic risk factor for diffuse cutaneous systemic sclerosis and has additive effects withIRF5andSTAT4

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Phenotype-Haplotype Correlation of IRF5 in Systemic Sclerosis: Role of 2 Haplotypes in Disease Severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Independent replication establishes the CD247 gene as a genetic systemic sclerosis susceptibility factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of a KCNA5 gene polymorphism with systemic sclerosis-associated pulmonary arterial hypertension in the European Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

-Chain phosphorylation of the human leukocyte CD11b/CD18 (Mac-1) integrin is pivotal for integrin activation to bind ICAMs and leukocyte extravasation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1137-Z

Association of human leukocyte antigen class II genes with autoantibody profiles, but not with disease susceptibility in Japanese patients with systemic sclerosis

21 January 2018

1 reference

12 December 2020

HLA associations in three mutually exclusive autoantibody subgroups in UK systemic sclerosis patients

1 reference

12 December 2020

X chromosome monosomy in primary and overlapping autoimmune diseases

1 reference

12 December 2020

Evaluation of genetic association between an ITGAM non-synonymous SNP (rs1143679) and multiple autoimmune diseases

1 reference

12 December 2020

Association between enhanced type I collagen expression and epigenetic repression of the FLI1 gene in scleroderma fibroblasts

1 reference

12 December 2020

Association of STAT4 polymorphism with systemic sclerosis in a Japanese population

1 reference

12 December 2020

Association of polymorphisms in the IL1B and IL2 genes with susceptibility and severity of systemic sclerosis

1 reference

12 December 2020

Association of the STAT4 gene with increased susceptibility for some immune-mediated diseases

1 reference

12 December 2020

Clinical, immunologic, and genetic features of familial systemic sclerosis

1 reference

12 December 2020

Interleukin-1 gene complex polymorphisms in systemic sclerosis patients with severe restrictive lung physiology

1 reference

12 December 2020

Scleroderma (systemic sclerosis): classification, subsets and pathogenesis

1 reference

12 December 2020

The β-fibrinogen -455 G>A gene polymorphism is associated with peripheral vascular injury in systemic sclerosis patients

1 reference

12 December 2020

A rare polymorphism in the gene for Toll-like receptor 2 is associated with systemic sclerosis phenotype and increases the production of inflammatory mediators

1 reference

12 December 2020

Anti-centromere antibodies (ACA) in systemic sclerosis patients and their relatives: a serological and HLA study

1 reference

12 December 2020

The autoimmune disease-associated IL2RA locus is involved in the clinical manifestations of systemic sclerosis

1 reference

12 December 2020

Macrophage migration inhibitory factor promoter polymorphisms and the clinical expression of scleroderma

1 reference

12 December 2020

The association between the PTPN22 C1858T polymorphism and systemic sclerosis: a meta-analysis

1 reference

12 December 2020

Macrophage migration inhibitory factor, MIF alleles, and the genetics of inflammatory disorders: Incorporating disease outcome into the definition of phenotype

1 reference

12 December 2020

Coexistence of systemic sclerosis with other autoimmune diseases

1 reference

12 December 2020

Inactivation of the transcription factor STAT-4 prevents inflammation-driven fibrosis in animal models of systemic sclerosis

1 reference

12 December 2020

Association of the FAM167A-BLK region with systemic sclerosis

1 reference

12 December 2020

Molecular cloning, characterization, and chromosomal localization of a human lymphoid tyrosine kinase related to murine Blk.

1 reference

12 December 2020

Lack of association of the PTPN22 gene polymorphism R620W with systemic sclerosis.

1 reference

12 December 2020

MHC class II associations with autoantibody and T cell immune responses to the scleroderma autoantigen topoisomerase I

1 reference

12 December 2020

10.1007/S00439-011-1137-Z

Identifiers

DOI

1 reference

release_w6ldsfxegvbgrm7i6b6rfpe3lq

26 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/w6ldsfxegvbgrm7i6b6rfpe3lq

24 November 2022

mapped directly with Wikidata item

PubMed ID

22218928

1 reference

PubMed ID

22218928