Associated Papers
NOD/RIPK2 signalling pathway contributes to osteoarthritis susceptibility.
Jurynec MJ et al.
Annals of the Rheumatic Diseases, 2022
Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes.
Vidmar L et al.
Scientific Reports, 2019
31235738 (PubMed )
Supplement: 41598_2019_45598_MOESM2_ESM.xlsx › Sheet1
A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.
Jurynec MJ et al.
Human Molecular Genetics, 2018
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