33 results on '"Skelton, Andrew J."'
Search Results
2. Lymphocyte DNA methylation mediates genetic risk at shared immune-mediated disease loci
3. Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials
4. DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
5. Erratum to “Predicting drug-free remission in rheumatoid arthritis: A prospective interventional cohort study” [J. Autoimmun. 105 (December 2019) 102298]
6. CD4+ and B Lymphocyte Expression Quantitative Traits at Rheumatoid Arthritis Risk Loci in Patients With Untreated Early Arthritis: Implications for Causal Gene Identification
7. Prioritization of PLEC and GRINA as Osteoarthritis Risk Genes Through the Identification and Characterization of Novel Methylation Quantitative Trait Loci
8. Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials
9. Regulation of microRNA‐221, ‐222, ‐21 and ‐27 in articular cartilage subjected to abnormal compressive forces
10. Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
11. microRNA-seq of cartilage reveals an overabundance of miR-140-3p which contains functional isomiRs
12. O11 Lymphocyte DNA methylation mediates genetic risk at RA risk loci that are shared with other immune mediated diseases
13. microRNA-seq of cartilage reveals an over-abundance of miR-140-3p which contains functional isomiRs
14. Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2
15. Predicting drug-free remission in rheumatoid arthritis: A prospective interventional cohort study
16. Expression of STAT3-regulated genes in circulating CD4+ T cells discriminates rheumatoid arthritis independently of clinical parameters in early arthritis
17. CD4+ and B lymphocyte expression quantitative traits at rheumatoid arthritis risk loci in untreated early arthritis: implications for causal gene identification
18. IL-6 Mediated Transcriptional Programming of Naïve CD4+ T Cells in Early Rheumatoid Arthritis Drives Dysregulated Effector Function
19. Prioritization ofPLECandGRINAas Osteoarthritis Risk Genes Through the Identification and Characterization of Novel Methylation Quantitative Trait Loci
20. DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions
21. Expression of STAT3-regulated genes in circulating CD4+ T cells discriminates rheumatoid arthritis independently of clinical parameters in early arthritis
22. Regulation of microRNA‐221, ‐222, ‐21 and ‐27 in articular cartilage subjected to abnormal compressive forces.
23. Functional Characterization of the Osteoarthritis Genetic Risk Residing at ALDH1A2 Identifies rs12915901 as a Key Target Variant
24. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)
25. The first international workshop on the epigenetics of osteoarthritis
26. Leptin and Pro-Inflammatory Stimuli Synergistically Upregulate MMP-1 and MMP-3 Secretion in Human Gingival Fibroblasts
27. Expression analysis of the osteoarthritis genetic susceptibility locus mapping to an intron of the MCF2L gene and marked by the polymorphism rs11842874
28. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in (A20).
29. The long non-coding RNA ROCR contributes to SOX9 expression and chondrogenic differentiation of human mesenchymal stem cells.
30. Human IFNAR2 deficiency: Lessons for antiviral immunity
31. The first international workshop on the epigenetics of osteoarthritis.
32. Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials.
33. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20).
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