Pages that link to "Q57613023"
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The following pages link to Association between theIRF5rs2004640 functional polymorphism and systemic sclerosis: A new perspective for pulmonary fibrosis (Q57613023):
Displaying 50 items.
- Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis (Q21144954) (← links)
- Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus (Q24630434) (← links)
- Genetics of systemic sclerosis: recent advances (Q26796362) (← links)
- Genetics, Epigenetics, and Genomics of Systemic Sclerosis (Q26799577) (← links)
- Interferons in Sjögren's Syndrome: Genes, Mechanisms, and Effects (Q26865427) (← links)
- Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy (Q29417020) (← links)
- Proteome-wide analysis and CXCL4 as a biomarker in systemic sclerosis (Q33693955) (← links)
- Autoimmune diseases and autoantibodies in the first degree relatives of patients with systemic sclerosis (Q33886453) (← links)
- Systemic sclerosis and lupus: points in an interferon-mediated continuum (Q33889629) (← links)
- Systemic sclerosis-associated pulmonary arterial hypertension (Q33950086) (← links)
- Association of interleukin 23 receptor polymorphisms with anti-topoisomerase-I positivity and pulmonary hypertension in systemic sclerosis (Q33955502) (← links)
- 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 (Q34046875) (← links)
- Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis (Q34081935) (← links)
- Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis (Q34087671) (← links)
- A functionally relevant IRF5 haplotype is associated with reduced risk to Wegener's granulomatosis (Q34091008) (← links)
- Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome. (Q34139580) (← links)
- Predictors of interstitial lung disease in early systemic sclerosis: a prospective longitudinal study of the GENISOS cohort (Q34346178) (← links)
- Recent findings on genetics of systemic autoimmune diseases (Q34384322) (← links)
- Genetics of scleroderma: implications for personalized medicine? (Q34545752) (← links)
- The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis. (Q34571170) (← links)
- Systems level analysis of systemic sclerosis shows a network of immune and profibrotic pathways connected with genetic polymorphisms. (Q34888501) (← links)
- The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population (Q34935466) (← links)
- Two functional variants of IRF5 influence the development of macular edema in patients with non-anterior uveitis (Q35014872) (← links)
- Towards systemic sclerosis and away from primary biliary cirrhosis: the case of PTPN22. (Q35309080) (← links)
- Primary biliary cirrhosis associated with systemic sclerosis: diagnostic and clinical challenges. (Q35609106) (← links)
- Genetics of Interstitial Lung Disease: Vol de Nuit (Night Flight). (Q35649228) (← links)
- Pathogenesis of Systemic Sclerosis (Q35693212) (← links)
- KCNA5 gene polymorphism associate with idiopathic atrial fibrillation (Q35959078) (← links)
- Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up (Q36012302) (← links)
- IRF5 polymorphism predicts prognosis in patients with systemic sclerosis (Q36032649) (← links)
- A multicenter study confirms CD226 gene association with systemic sclerosis-related pulmonary fibrosis (Q36245847) (← links)
- Multifaceted contribution of the TLR4-activated IRF5 transcription factor in systemic sclerosis (Q36371453) (← links)
- The pulmonary fibrosis-associated MUC5B promoter polymorphism does not influence the development of interstitial pneumonia in systemic sclerosis (Q36447402) (← links)
- Identification of an Association of TNFAIP3 Polymorphisms With Matrix Metalloproteinase Expression in Fibroblasts in an Integrative Study of Systemic Sclerosis-Associated Genetic and Environmental Factors (Q36619876) (← links)
- Genetic Susceptibility to Interstitial Lung Disease Associated with Systemic Sclerosis (Q36685226) (← links)
- Phenotype and function of B cells and dendritic cells from interferon regulatory factor 5-deficient mice with and without a mutation in DOCK2. (Q36780004) (← links)
- The genetics of scleroderma: looking into the postgenomic era (Q36918205) (← links)
- The role of type 1 interferon in systemic sclerosis (Q37150404) (← links)
- Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis (Q37441841) (← links)
- Understanding fibrosis in systemic sclerosis: shifting paradigms, emerging opportunities (Q37638268) (← links)
- Type I interferons: crucial participants in disease amplification in autoimmunity (Q37666513) (← links)
- Fibrosis in systemic sclerosis: Emerging concepts and implications for targeted therapy (Q37721063) (← links)
- Pulmonary Manifestations of Scleroderma and Mixed Connective Tissue Disease (Q37778578) (← links)
- Deciphering the genetic background of systemic sclerosis (Q37905783) (← links)
- Novel insights on the role of the innate immune system in systemic sclerosis. (Q37905792) (← links)
- Unraveling the genetic component of systemic sclerosis (Q37973287) (← links)
- Update on etiopathogenesis of systemic sclerosis (Q38183300) (← links)
- Epigenetics, the holy grail in the pathogenesis of systemic sclerosis (Q38205150) (← links)
- Personalized medicine in systemic sclerosis: facts and promises (Q38206152) (← links)
- Molecular and cellular basis of scleroderma (Q38230276) (← links)