Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis. - Wikidata - wikimedia - TriplyDB

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.

http://www.wikidata.org/entity/Q38367681

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Genetics of systemic sclerosis: recent advances Genetics, Epigenetics, and Genomics of Systemic Sclerosis Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue.Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis.Coherent somatic mutation in autoimmune disease.Genetics of scleroderma: implications for personalized medicine?Systems level analysis of systemic sclerosis shows a network of immune and profibrotic pathways connected with genetic polymorphisms.PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes.PTPN22: the archetypal non-HLA autoimmunity gene.Pathogenesis of Systemic Sclerosis.Reduced incidence of Crohn's disease in systemic sclerosis: a nationwide population study.Genetic Susceptibility to Interstitial Lung Disease Associated with Systemic Sclerosis.Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis.The genetics of scleroderma: looking into the postgenomic era Independent replication and meta analysis of association studies establish TNFSF4 as a susceptibility gene preferentially associated with the subset of anticentromere-positive patients with systemic sclerosis Deciphering the genetic background of systemic sclerosis.Capturing the heterogeneity in systemic sclerosis with genome-wide expression profiling.Genetics of systemic sclerosis: an update.Unraveling the genetic component of systemic sclerosis.Making sense of therapeutics using antisense technology.Genetic Susceptibility to ANCA-Associated Vasculitis: State of the Art.Genetics of systemic sclerosis.Unfolding the pathogenesis of scleroderma through genomics and epigenomics.The PTPN22 R263Q polymorphism confers protection against systemic lupus erythematosus and rheumatoid arthritis, while PTPN22 R620W confers susceptibility to Graves' disease in a Mexican population.Protein Tyrosine Phosphatases in Systemic Sclerosis: Potential Pathogenic Players and Therapeutic Targets.Association of PTPN22 Single Nucleotide Polymorphisms with Celiac Disease.PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus.Systemic Sclerosis is a Complex Disease Associated Mainly with Immune Regulatory and Inflammatory Genes.The association between the PTPN22 C1858T polymorphism and systemic sclerosis: a meta-analysis.Current immunogenetic predisposition to tuberculosis in the Moroccan population.Common genes in autoimmune diseases: a link between immune-mediated diseases Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto's thyroiditis

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Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.

http://www.wikidata.org/entity/Q38367681

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2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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2010年學術文章

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2010年學術文章

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name

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.

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type

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Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.

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Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.

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ARD.2010.130138

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Annals of the Rheumatic Diseases

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Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.

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P2860

Identification of substrates of human protein-tyrosine phosphatase PTPN22

Reduced CD4+T cell activation in children with type 1 diabetes carrying the PTPN22/Lyp 620Trp variant

Interleukin-2 receptor signaling: at the interface between tolerance and immunity

Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

Measuring inconsistency in meta-analyses

Recent advances in the genetics of autoimmune disease

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

Association of the PTPN22 R620W polymorphism with anti-topoisomerase I- and anticentromere antibody-positive systemic sclerosis

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