نتایج جستجو برای: ptpn22

تعداد نتایج: 605  

2009
Zhong-Yin Zhang Andrew Funk Jane H. Buckner Adrian F. Arechiga Tania Habib Yantao He Xian Zhang

2016
Wen-Hua Wei John Bowes Darren Plant Sebastien Viatte Annie Yarwood Jonathan Massey Jane Worthington Stephen Eyre

Genotypic variability based genome-wide association studies (vGWASs) can identify potentially interacting loci without prior knowledge of the interacting factors. We report a two-stage approach to make vGWAS applicable to diseases: firstly using a mixed model approach to partition dichotomous phenotypes into additive risk and non-additive environmental residuals on the liability scale and secon...

2010
Vasanth Konda Mohan Nalini Ganesan Rajasekhar Gopalakrishnan Vasanthi Pallinti Vettriselvi Venkatesan

Journal: :American journal of human genetics 2007
Henrik Kallberg Leonid Padyukov Robert M Plenge Johan Ronnelid Peter K Gregersen Annette H M van der Helm-van Mil Rene E M Toes Tom W Huizinga Lars Klareskog Lars Alfredsson

Gene-gene and gene-environment interactions are key features in the development of rheumatoid arthritis (RA) and other complex diseases. The aim of this study was to use and compare three different definitions of interaction between the two major genetic risk factors of RA--the HLA-DRB1 shared epitope (SE) alleles and the PTPN22 R620W allele--in three large case-control studies: the Swedish Epi...

Journal: :BMC Proceedings 2007
Karen Curtin Jathine Wong Kristina Allen-Brady Nicola J Camp

PedGenie beta version 2.1 is a unique, flexible, and easily implemented analysis software tool that is enhanced significantly by incorporation of meta-statistics to allow valid combined analysis of multiple studies, including mixtures of family-based and independent resources, in the detection of genetic association with common disease. Genetic Analysis Workshop 15 Problem 2 data, provided by t...

Journal: :Journal of Immunology 2023

Abstract The tyrosine phosphatase PTPN22 encodes the enzyme Lyp (PEP in mice) all immune cells. 5–10% of North American population expresses autoimmunity risk allele 1858C>T (rs2476601) causing amino acid substitution R620W (R619W mice). This mutation alters lymphocyte activation, toll-like receptor signaling, and cytokine production. Ptpn22 knockout (PEP-null) alternative allele-express...

Journal: :Nature Reviews Rheumatology 2014

2018
Robert C. Sharp Shazia A. Beg Saleh A. Naser

A shared genetic pre-disposition, chronic inflammation, and treatment with similar biologics between Rheumatoid arthritis (RA) and Crohn's disease (CD) have intrigued us to investigate whether the two disorders share trigger association or possible causation. We hypothesized earlier that Single Nucleotide Polymorphisms (SNPs) in the negative regulators Protein Tyrosine Phosphatase Non-receptor ...

Journal: :Arthritis Research & Therapy 2009
Klaus Stark Jozef Rovenský Stanislava Blažičková Hans Grosse-Wilde Stanislav Ferencik Christian Hengstenberg Rainer H Straub

INTRODUCTION Both genetic and environmental factors contribute to rheumatoid arthritis (RA), a common and complex autoimmune disease. As well as the major susceptibility gene HLA-DRB1, recent genome-wide and candidate-gene studies reported additional evidence for association of single nucleotide polymorphism (SNP) markers in the PTPN22, STAT4, OLIG3/TNFAIP3 and TRAF1/C5 loci with RA. This study...

2010
Ann W Morgan James I Robinson Philip G Conaghan Stephen G Martin Elizabeth MA Hensor Michael D Morgan Lori Steiner Henry A Erlich Hock-Chye Gooi Anne Barton Jane Worthington Paul Emery

INTRODUCTION This study investigated five confirmed rheumatoid arthritis (RA) susceptibility genes/loci (HLA-DRB1, PTPN22, STAT4, OLIG3/TNFAIP3 and TRAF1/C5) for association with susceptibility and severity in an inception cohort. METHODS The magnitude of association for each genotype was assessed in 1,046 RA subjects from the Yorkshire Early RA cohort and in 5,968 healthy UK controls. Additi...

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