PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis - Wikidata - wikimedia - TriplyDB

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis

http://www.wikidata.org/entity/Q34114509

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Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?Structure, inhibitor, and regulatory mechanism of Lyp, a lymphoid-specific tyrosine phosphatase implicated in autoimmune diseases Identification of a variant form of tyrosine phosphatase LYP 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 Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4 A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes Small molecule tools for functional interrogation of protein tyrosine phosphatases A Potent and Selective Small-Molecule Inhibitor for the Lymphoid-Specific Tyrosine Phosphatase (LYP), a Target Associated with Autoimmune Diseases Recent advances in the genetics of autoimmune disease Protein tyrosine phosphatase PTPN22 in human autoimmunity Telomere structure and maintenance gene variants and risk of five cancer types A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis.Application of sequential haplotype scan methods to case-control data.Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits Comparing strategies for evaluation of candidate genes in case-control studies using family data Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population.Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1.Application of bivariate mixed counting process models to genetic analysis of rheumatoid arthritis severity.Modeling of PTPN22 and HLA-DRB1 susceptibility to rheumatoid arthritis Evaluating gene x gene and gene x smoking interaction in rheumatoid arthritis using candidate genes in GAW15.Case-control association analysis of rheumatoid arthritis with candidate genes using related cases.Modeling the effect of PTPN22 in rheumatoid arthritis.Exploring epistasis in candidate genes for rheumatoid arthritis.Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis.A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2.Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis method Association of KCNB1 to rheumatoid arthritis via interaction with HLA-DRB1.Data for Genetic Analysis Workshop 16 Problem 1, association analysis of rheumatoid arthritis data Elastic-net regularization approaches for genome-wide association studies of rheumatoid arthritis.Application of seventeen two-locus models in genome-wide association studies by two-stage strategy A combinatorial approach for detecting gene-gene interaction using multiple traits of Genetic Analysis Workshop 16 rheumatoid arthritis data.Assessment of genotype imputation methods Combining least absolute shrinkage and selection operator (LASSO) and principal-components analysis for detection of gene-gene interactions in genome-wide association studies.Single versus multiple imputation for genotypic data.Incorporating biological knowledge in the search for gene x gene interaction in genome-wide association studies.PCA-based bootstrap confidence interval tests for gene-disease association involving multiple SNPs The PTPN22 locus and rheumatoid arthritis: no evidence for an effect on risk independent of Arg620Trp.Lymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases.Covalent inhibition of the lymphoid tyrosine phosphatase.Gene- or region-based association study via kernel principal component analysis.

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P2860

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis

http://www.wikidata.org/entity/Q34114509

description

2005 nî lūn-bûn

@nan

2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի օգոստոսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@ast

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@en

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@nl

type

label

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@ast

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@en

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@nl

prefLabel

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@ast

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

@en

PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

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American Journal of Human Genetics

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PTPN22 genetic variation: evid ...... ated with rheumatoid arthritis

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Anand P Chokkalingam

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Ann B Begovich

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Daniel L Kastner

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Diane U Leong

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Ellen Beasley

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Glenys Thomson

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Kristin G Ardlie

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Lindsey A Criswell

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P2860

Cloning and characterization of a lymphoid-specific, inducible human protein tyrosine phosphatase, Lyp

Commitment to the B-lymphoid lineage depends on the transcription factor Pax5

Association of inhibitory tyrosine protein kinase p50csk with protein tyrosine phosphatase PEP in T cells and other hemopoietic cells

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.

SNPAnalyzer: a web-based integrated workbench for single-nucleotide polymorphism analysis

A New Statistical Method for Haplotype Reconstruction from Population Data

The structure of haplotype blocks in the human genome

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Association of a putative regulatory polymorphism in the PD-1 gene with susceptibility to type 1 diabetes

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

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567-581

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10.1086/468189

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4

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77

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Steven J. Schrodi

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2005-08-10T00:00:00Z

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7587457

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16175503

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