Pages that link to "Q45138861"
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The following pages link to A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families (Q45138861):
Displaying 50 items.
- Rheumatoid arthritis seropositive for the rheumatoid factor is linked to the protein tyrosine phosphatase nonreceptor 22-620W allele (Q24812738) (← links)
- Genetics of type 1 diabetes (Q26866502) (← links)
- Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population (Q28248685) (← links)
- PTPN22 1858C>T (R620W) functional polymorphism and human longevity (Q28299415) (← 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)
- Prediction and pathogenesis in type 1 diabetes. (Q33818896) (← links)
- Autoimmune diseases and autoantibodies in the first degree relatives of patients with systemic sclerosis (Q33886453) (← links)
- Lymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases (Q33895460) (← links)
- Association of interleukin 23 receptor polymorphisms with anti-topoisomerase-I positivity and pulmonary hypertension in systemic sclerosis (Q33955502) (← links)
- Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease (Q33996046) (← links)
- Tyrosine phosphatase PTPN22: multifunctional regulator of immune signaling, development, and disease. (Q34039427) (← links)
- Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis (Q34081935) (← links)
- PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis (Q34114509) (← links)
- Genes and Sjögren's syndrome (Q34363380) (← links)
- An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4( ) T cells (Q34682216) (← links)
- Paths to understanding the genetic basis of autoimmune disease (Q36148396) (← 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)
- Important genetic checkpoints for insulin resistance in salt-sensitive (S) Dahl rats (Q36761492) (← links)
- Genes mediating environment interactions in type 1 diabetes (Q36816687) (← links)
- The non-obese diabetic mouse sequence, annotation and variation resource: an aid for investigating type 1 diabetes (Q36889364) (← links)
- Joint genetic susceptibility to type 1 diabetes and autoimmune thyroiditis: from epidemiology to mechanisms. (Q36973929) (← links)
- From markers to molecular mechanisms: type 1 diabetes in the post-GWAS era. (Q37088194) (← links)
- Novel biomarkers in type 1 diabetes (Q37088197) (← links)
- Type 1 diabetes and autoimmune thyroiditis: the genetic connection (Q37312563) (← links)
- General and Specific Genetic Polymorphism of Cytokines-Related Gene in AITD. (Q37590849) (← links)
- Association of the PTPN22 gene ( 1858C/T, −1123G/C) polymorphisms with type 1 diabetes mellitus: A systematic review and meta-analysis (Q38008795) (← links)
- Update on etiopathogenesis of systemic sclerosis (Q38183300) (← links)
- PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus (Q40265320) (← links)
- Allele and haplotype frequency distribution in PTPN22 gene across variable ethnic groups: Implications for genetic association studies for autoimmune diseases (Q43157779) (← links)
- Association of PTPN22 rs2476601 and EGFR rs17337023 Gene polymorphisms and rheumatoid arthritis in Zahedan, Southeast Iran. (Q43654959) (← 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)
- High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33. (Q44922542) (← links)
- Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases (Q46368513) (← links)
- Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset (Q46534885) (← 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)
- A case-control study of tyrosine phosphatase (PTPN22) confirms the lack of association with Crohn's disease (Q46704913) (← links)
- Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease (Q46732649) (← links)
- The association of PTPN22 with rheumatoid arthritis and juvenile idiopathic arthritis (Q46897903) (← links)
- Genetic determinants of Type 1 diabetes: immune response genes (Q56806352) (← links)
- Lymphoid tyrosine phosphatase (LYP/PTPN22) Arg620Trp variant regulates insulin autoimmunity and progression to type 1 diabetes (Q56902091) (← links)
- Single-nucleotide polymorphisms in the IL2RA gene are associated with age at diagnosis in late-onset Finnish type 1 diabetes subjects (Q57303224) (← links)
- Familial aggregation and linkage analysis of autoantibody traits in pedigrees multiplex for systemic lupus erythematosus (Q57329898) (← links)
- Genetic Risk Scores for Type 1 Diabetes Prediction and Diagnosis (Q57924676) (← links)
- Functional variants in SUMO4, TAB2 and NFκB and the risk of type 1 diabetes (Q58006371) (← links)