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pancreatitis
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PRSS1
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene
Gene conversion-like missense mutations in the human cationic trypsinogen gene and insights into the molecular evolution of the human trypsinogen family.
Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutations.
SPINK1
Three-dimensional structure of the complexes between bovine chymotrypsinogen A and two recombinant variants of human pancreatic secretory trypsin inhibitor (Kazal-type)
Interactions of pancreatic secretory trypsin inhibitor in small intestinal juice: its hydrolysis and protection by intraluminal factors
PRSS2
The origin of trypsin: evidence for multiple gene duplications in trypsins
CTRC
Molecular cloning and expression of human caldecrin
CFTR
Cystic fibrosis transmembrane conductance regulator and the etiology and pathogenesis of cystic fibrosis
Molecular biology of cystic fibrosis
The molecular basis for disease variability in cystic fibrosis
CFTR: domains, structure, and function
Differential function of the two nucleotide binding domains on cystic fibrosis transmembrane conductance regulator
Unique presentations and chronic complications in adult cystic fibrosis: do they teach us anything about CFTR?
Cystic fibrosis and CFTR
Cancer Gene Census
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Definition
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Neuroactive ligand-receptor interaction
Homo sapiens (human)
2 genes
Clinical Trials
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