Pages that link to "Q28300110"
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The following pages link to Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with type 1 diabetes (Q28300110):
Displaying 50 items.
- Genetic Variations of PTPN2 and PTPN22: Role in the Pathogenesis of Type 1 Diabetes and Crohn's Disease (Q26770562) (← links)
- Genetics of type 1 diabetes (Q26866502) (← links)
- Protein tyrosine phosphatase PTPN22 in human autoimmunity (Q28242744) (← links)
- Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant (Q28280659) (← links)
- PTPN22 1858C>T (R620W) functional polymorphism and human longevity (Q28299415) (← links)
- High basal activity of the PTPN22 gain-of-function variant blunts leukocyte responsiveness negatively affecting IL-10 production in ANCA vasculitis (Q28387176) (← links)
- PTPN22 R620W polymorphism and ANCA disease risk in white populations: a metaanalysis (Q28387197) (← links)
- The R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1. (Q30160168) (← links)
- rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype (Q30437392) (← links)
- Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population (Q33294087) (← links)
- The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes (Q33307633) (← links)
- In silico screening for PTPN22 inhibitors: active hits from an inactive phosphatase conformation (Q33403794) (← links)
- Prediction and pathogenesis in type 1 diabetes. (Q33818896) (← links)
- Genetic evidence that the differential expression of the ligand-independent isoform of CTLA-4 is the molecular basis of the Idd5.1 type 1 diabetes region in nonobese diabetic mice. (Q33854444) (← links)
- Lymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases (Q33895460) (← links)
- Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases (Q34019296) (← links)
- PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis (Q34114509) (← links)
- Improving power of genome-wide association studies with weighted false discovery rate control and prioritized subset analysis (Q34229909) (← links)
- Genes and Sjögren's syndrome (Q34363380) (← links)
- The association between the PTPN22 1858C>T variant and type 1 diabetes depends on HLA risk and GAD65 autoantibodies (Q34607188) (← links)
- Targeting the PTPome in human disease (Q36379394) (← links)
- Functional single nucleotide polymorphism-based association studies (Q36539672) (← links)
- The genetics of systemic lupus erythematosus: understanding how SNPs confer disease susceptibility (Q36590524) (← links)
- Unraveling the genetics of systemic lupus erythematosus (Q36614958) (← links)
- Joint genetic susceptibility to type 1 diabetes and autoimmune thyroiditis: from epidemiology to mechanisms. (Q36973929) (← links)
- Analysis of maternal-offspring HLA compatibility, parent-of-origin and non-inherited maternal effects for the classical HLA loci in type 1 diabetes (Q37083987) (← links)
- Novel biomarkers in type 1 diabetes (Q37088197) (← links)
- Genetic Association of PTPN22 Polymorphisms with Autoimmune Hepatitis and Primary Biliary Cholangitis in Japan (Q37089325) (← links)
- General and Specific Genetic Polymorphism of Cytokines-Related Gene in AITD. (Q37590849) (← links)
- Role of the C1858T polymorphism of protein tyrosine phosphatase non-receptor type 22 (PTPN22) in children and adolescents with type 1 diabetes (Q38904874) (← links)
- PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus (Q40265320) (← links)
- Association of PTPN22 Gene Polymorphisms with Susceptibility to Juvenile Idiopathic Arthritis in Iranian Population (Q40509418) (← links)
- PTPN22 and islet-specific autoimmunity: What have the mouse models taught us? (Q40998229) (← links)
- HLA-DR, HLA-DQB1 and PTPN22 gene polymorphism: association with age at onset for autoimmune diabetes (Q41895902) (← links)
- Allele and haplotype frequency distribution in PTPN22 gene across variable ethnic groups: Implications for genetic association studies for autoimmune diseases (Q43157779) (← links)
- The impact of CTLA4 and PTPN22 genes polymorphisms on long-term renal allograft function and transplant outcomes (Q43646920) (← links)
- Genetic epidemiology of type 1 diabetes (Q43695619) (← links)
- Finnish case-control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis (Q44449408) (← links)
- Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects (Q45129416) (← links)
- A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo (Q46599062) (← links)
- Protein tyrosine phosphatase gene PTPN22 polymorphism in psoriasis: lack of evidence for association (Q46648221) (← links)
- PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases (Q46703705) (← links)
- The association of PTPN22 with rheumatoid arthritis and juvenile idiopathic arthritis (Q46897903) (← links)
- Sex-specific association of the human PTPN22 1858T-allele with type 1 diabetes. (Q46900842) (← links)
- PTPN22 1858C > T polymorphism and susceptibility to systemic lupus erythematosus: a meta-analysis update (Q47839399) (← links)
- PTPN22 and CTLA-4 gene polymorphisms in resected thymomas and thymus for myasthenia gravis (Q47896311) (← links)
- PTPN22 gene polymorphism (C1858T) is associated with susceptibility to type 1 diabetes: a meta-analysis of 19,495 cases and 25,341 controls (Q51271075) (← links)
- The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population. (Q51807268) (← links)
- Meta-analysis of the family-based association between the PTPN22 C1858T polymorphism and type 1 diabetes. (Q53107526) (← links)
- Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele. (Q54572337) (← links)