Pages that link to "Q28289699"
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The following pages link to Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus (Q28289699):
Displayed 50 items.
- Structure, inhibitor, and regulatory mechanism of Lyp, a lymphoid-specific tyrosine phosphatase implicated in autoimmune diseases (Q24302097) (← links)
- Identification of a variant form of tyrosine phosphatase LYP (Q24305267) (← links)
- Substrate specificity of lymphoid-specific tyrosine phosphatase (Lyp) and identification of Src kinase-associated protein of 55 kDa homolog (SKAP-HOM) as a Lyp substrate (Q24309015) (← links)
- PTPN22 gene regulates natural killer cell proliferation during in vitro expansion (Q24316976) (← links)
- Reduced CD4+T cell activation in children with type 1 diabetes carrying the PTPN22/Lyp 620Trp variant (Q24317388) (← links)
- Cutting edge: the PTPN22 allelic variant associated with autoimmunity impairs B cell signaling (Q24318432) (← links)
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Q24550675) (← links)
- Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes (Q24651119) (← links)
- Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes (Q24652324) (← links)
- The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the future (Q24673258) (← links)
- Rheumatoid arthritis seropositive for the rheumatoid factor is linked to the protein tyrosine phosphatase nonreceptor 22-620W allele (Q24812738) (← links)
- Polymorphism discovery and association analyses of the interferon genes in type 1 diabetes (Q25256966) (← links)
- Small molecule tools for functional interrogation of protein tyrosine phosphatases (Q26852276) (← links)
- Genetics of type 1 diabetes (Q26866502) (← links)
- Insights into type 1 diabetes from the autoimmune polyendocrine syndromes (Q27006792) (← links)
- Rethinking mechanisms of autoimmune pathogenesis (Q27024290) (← links)
- Interferon Alpha Treatment and Thyroid Dysfunction (Q27483686) (← links)
- A Potent and Selective Small-Molecule Inhibitor for the Lymphoid-Specific Tyrosine Phosphatase (LYP), a Target Associated with Autoimmune Diseases (Q27678355) (← links)
- Recent advances in the genetics of autoimmune disease (Q28238782) (← links)
- Protein tyrosine phosphatase PTPN22 in human autoimmunity (Q28242744) (← links)
- Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population (Q28248685) (← links)
- Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant (Q28280659) (← links)
- Protein tyrosine phosphatases and the immune response (Q28300971) (← 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)
- Novel associations for hypothyroidism include known autoimmune risk loci (Q28730714) (← links)
- A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci (Q28943424) (← links)
- Protein tyrosine phosphatases: from genes, to function, to disease (Q29614826) (← links)
- Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes (Q30300266) (← links)
- Distinct functional and conformational states of the human lymphoid tyrosine phosphatase catalytic domain can be targeted by choice of the inhibitor chemotype (Q30406901) (← links)
- Seven newly identified loci for autoimmune thyroid disease (Q30424090) (← links)
- rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype (Q30437392) (← links)
- Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts. (Q30992731) (← links)
- Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases (Q33235613) (← links)
- Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetes (Q33240464) (← 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)
- Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue (Q33403872) (← links)
- PTPN22 -1123G > C polymorphism is associated with susceptibility to primary immune thrombocytopenia in Chinese population (Q33404016) (← links)
- Idd9.1 locus controls the suppressive activity of FoxP3+CD4+CD25+ regulatory T-cells (Q33556598) (← links)
- Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families. (Q33606764) (← links)
- Lymphoid tyrosine phosphatase R620W variant and inflammatory bowel disease in Tunisia (Q33612241) (← links)
- Interferon induced thyroiditis (Q33636049) (← links)
- Prediction and pathogenesis in type 1 diabetes. (Q33818896) (← links)
- Genetic epidemiology of diabetes (Q33831947) (← links)
- The PTPN22 C1858T gene variant is associated with proinsulin in new-onset type 1 diabetes (Q33853306) (← 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)
- Covalent inhibition of the lymphoid tyrosine phosphatase (Q33897108) (← links)
- Thyrotropin receptor-associated diseases: from adenomata to Graves disease (Q33905841) (← links)