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A common functional variant of endoplasmic reticulum aminopeptidase 2 (ERAP2) that reduces major histocompatibility complex class I expression is not associated with ankylosing spondylitis.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
A common functional variant of endoplasmic reticulum aminopeptidase 2 (ERAP2) that reduces major histocompatibility complex class I expression is not associated with ankylosing spondylitis.
- Published in:
- Rheumatology, 2011, v. 50, n. 9, p. 1720, doi. 10.1093/rheumatology/ker199
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- Publication type:
- Article
Association between the interleukin 23 receptor and ankylosing spondylitis is confirmed by a new UK case-control study and meta-analysis of published series.
- Published in:
- Rheumatology, 2009, v. 48, n. 4, p. 386, doi. 10.1093/rheumatology/ken501
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- Publication type:
- Article
Investigating the genetic association between ERAP1 and ankylosing spondylitis.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 21, p. 4204, doi. 10.1093/hmg/ddp371
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- Publication type:
- Article
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.
- Published in:
- Nature Genetics, 2011, v. 43, n. 8, p. 761, doi. 10.1038/ng.873
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- Publication type:
- Article
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.
- Published in:
- Nature Genetics, 2010, v. 42, n. 2, p. 123, doi. 10.1038/ng.513
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- Publication type:
- Article
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 271, doi. 10.1038/15452
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- Publication type:
- Article
A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations.
- Published in:
- Human Mutation, 1999, v. 13, n. 2, p. 154, doi. 10.1002/(SICI)1098-1004(1999)13:2<154::AID-HUMU8>3.0.CO;2-E
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- Publication type:
- Article
The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population.
- Published in:
- British Journal of Haematology, 1998, v. 101, n. 2, p. 369, doi. 10.1046/j.1365-2141.1998.00736.x
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- Publication type:
- Article
A rapid non-invasive method for the detection of the haemochromatosis C282Y mutation.
- Published in:
- British Journal of Haematology, 1997, v. 99, n. 2, p. 460, doi. 10.1046/j.1365-2141.1997.4193224.x
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- Publication type:
- Article
Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 17, p. 2241, doi. 10.1093/hmg/ddg225
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- Publication type:
- Article
New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 10, p. 1869
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- Publication type:
- Article