Add to ORKGThe N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancreatitis bu
Context Mutations in cystic fibrosis transmembrane conductance regulator (CFTR), in cationic trypsin...
The SPINK1 protein is a potent antiprotease that can inactivate any intrapancreatic trypsin activity...
The complex interactions between recurrent trypsin-mediated pancreatic injury, alcohol-associated pa...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
International audienceA diverse range of loss-of-function variants in the SPINK1 gene (encoding panc...
Background SPINK1 p.N34S gene variation is one of the endogenous factors which seem to be associated...
Abstract Background The role of mutations in the serine protease inhibitor Kazal type 1 (SPINK1) gen...
inhibitor mutations in hereditary and non-hereditary chronic pancreatitis. Gut 2004;53:723–28
Fibrocalculous pancreatic diabetes (FCPD) is a secondary cause of diabetes due to chronic pancreatit...
OBJECTIVE The pathogenesis of chronic pancreatitis (CP) is poorly understood. Genetic studies revea...
Background and aims: Mutations in the cationic trypsinogen (protease, serine, 1 (trypsin 1); PRSS1) ...
Background The aim was to describe genetic, clinical and morphological features in a large, multicen...
Chronic pancreatitis (CP) is a continuing or relapsing inflammatory disease of the pancreas. In appr...
The aim of this study was to determine whether mutations in SPINK1/PRSS1 genes are associated with b...
Context Mutations in cystic fibrosis transmembrane conductance regulator (CFTR), in cationic trypsin...
The SPINK1 protein is a potent antiprotease that can inactivate any intrapancreatic trypsin activity...
The complex interactions between recurrent trypsin-mediated pancreatic injury, alcohol-associated pa...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
International audienceA diverse range of loss-of-function variants in the SPINK1 gene (encoding panc...
Background SPINK1 p.N34S gene variation is one of the endogenous factors which seem to be associated...
Abstract Background The role of mutations in the serine protease inhibitor Kazal type 1 (SPINK1) gen...
inhibitor mutations in hereditary and non-hereditary chronic pancreatitis. Gut 2004;53:723–28
Fibrocalculous pancreatic diabetes (FCPD) is a secondary cause of diabetes due to chronic pancreatit...
OBJECTIVE The pathogenesis of chronic pancreatitis (CP) is poorly understood. Genetic studies revea...
Background and aims: Mutations in the cationic trypsinogen (protease, serine, 1 (trypsin 1); PRSS1) ...
Background The aim was to describe genetic, clinical and morphological features in a large, multicen...
Chronic pancreatitis (CP) is a continuing or relapsing inflammatory disease of the pancreas. In appr...
The aim of this study was to determine whether mutations in SPINK1/PRSS1 genes are associated with b...
Context Mutations in cystic fibrosis transmembrane conductance regulator (CFTR), in cationic trypsin...
The SPINK1 protein is a potent antiprotease that can inactivate any intrapancreatic trypsin activity...
The complex interactions between recurrent trypsin-mediated pancreatic injury, alcohol-associated pa...