Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis
Open Access
- 14 December 2005
- journal article
- research article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 14 (3) , 317-321
- https://doi.org/10.1038/sj.ejhg.5201548
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Analysis of Families in the Multiple Autoimmune Disease Genetics Consortium (MADGC) Collection: the PTPN22 620W Allele Associates with Multiple Autoimmune PhenotypesAmerican Journal of Human Genetics, 2005
- Multiple sclerosisImmunological Reviews, 2005
- The R620W Polymorphism of the Protein Tyrosine Phosphatase PTPN22 Is Not Associated with Multiple SclerosisAmerican Journal of Human Genetics, 2005
- 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 LocusDiabetes, 2004
- Genetic Association of the R620W Polymorphism of Protein Tyrosine Phosphatase PTPN22 with Human SLEAmerican Journal of Human Genetics, 2004
- A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid ArthritisAmerican Journal of Human Genetics, 2004
- A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetesNature Genetics, 2004
- PEST Domain-Enriched Tyrosine Phosphatase (PEP) Regulation of Effector/Memory T CellsScience, 2004
- Inflammatory Bowel Disease: Autoimmune or Immune‐mediated Pathogenesis?Clinical and Developmental Immunology, 2000
- Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: Evidence for epistasis between 1p and IBD1Proceedings of the National Academy of Sciences, 1998