No abstract available
MeSH terms
-
Genetic Predisposition to Disease
-
Humans
-
NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism
-
Phosphorylation
-
Polymorphism, Single Nucleotide
-
Protein Tyrosine Phosphatase, Non-Receptor Type 22 / genetics
-
Protein Tyrosine Phosphatases*
-
Signal Transduction
-
Tyrosine / metabolism
Substances
-
NLR Family, Pyrin Domain-Containing 3 Protein
-
Protein Tyrosine Phosphatases
-
Tyrosine
-
Protein Tyrosine Phosphatase, Non-Receptor Type 22
-
PTPN22 protein, human