Pages that link to "Q58006357"
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The following pages link to A Haplotype-Based Analysis of the PTPN22 Locus in Type 1 Diabetes (Q58006357):
Displaying 28 items.
- Cutting edge: the PTPN22 allelic variant associated with autoimmunity impairs B cell signaling (Q24318432) (← links)
- A functional framework for interpretation of genetic associations in T1D (Q27001083) (← links)
- Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes (Q30277972) (← links)
- rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype (Q30437392) (← links)
- Tyrosine phosphatase PTPN22: multifunctional regulator of immune signaling, development, and disease. (Q34039427) (← links)
- Association between PTPN22 C1858T polymorphism and alopecia areata risk (Q36335826) (← links)
- Important genetic checkpoints for insulin resistance in salt-sensitive (S) Dahl rats (Q36761492) (← links)
- Progress and challenges for treating Type 1 diabetes (Q36995389) (← links)
- PTPN22: its role in SLE and autoimmunity (Q37030634) (← links)
- Genetic developments in autoimmune thyroid disease: an evolutionary process (Q37032887) (← links)
- Protein tyrosine phosphatases and type 1 diabetes: genetic and functional implications of PTPN2 and PTPN22 (Q37088189) (← links)
- IFIH1 polymorphisms are significantly associated with type 1 diabetes and IFIH1 gene expression in peripheral blood mononuclear cells (Q37089982) (← links)
- Genetic and Molecular Basis of QTL of Diabetes in Mouse: Genes and Polymorphisms (Q37200819) (← links)
- Power of genetic association studies in the presence of linkage disequilibrium and allelic heterogeneity. (Q37453605) (← links)
- The PTPN22 C1858T (R620W) functional polymorphism in kidney transplantation (Q39448357) (← links)
- Association of PTPN22 Single Nucleotide Polymorphisms with Celiac Disease (Q40222230) (← links)
- PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus (Q40265320) (← links)
- Disease-specific biases in alternative splicing and tissue-specific dysregulation revealed by multitissue profiling of lymphocyte gene expression in type 1 diabetes (Q45069924) (← links)
- Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease (Q46732649) (← links)
- Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy (Q46819653) (← links)
- PTPN22 polymorphism presumably plays a role in the genetic background of chronic spontaneous autoreactive urticaria (Q48425448) (← 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)
- Common variants in the TCF7L2 gene help to differentiate autoimmune from non-autoimmune diabetes in young (15-34 years) but not in middle-aged (40-59 years) diabetic patients (Q51439650) (← links)
- Pedigree-Defined Haplotypes and Their Applications to Genetic Studies. (Q52735702) (← links)
- Meta-analysis of the family-based association between the PTPN22 C1858T polymorphism and type 1 diabetes. (Q53107526) (← links)
- Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy. (Q53543182) (← links)
- Tag SNP screening of the PDCD1 gene for association with Graves' disease. (Q53554417) (← links)
- Susceptibility influence of a PTPN22 haplotype with thyroid autoimmunity in Koreans (Q82436903) (← links)