Loss of function TRPV6 variants are associated with chronic pancreatitis in nonalcoholic early-onset Polish and German patients
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology,Endocrinology, Diabetes and Metabolism
Reference26 articles.
1. Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene;Whitcomb;Nat Genet,1996
2. Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis;Witt;Nat Genet,2000
3. Chymotrypsin C (CTRC) variants that diminish activity or secretion are associated with chronic pancreatitis;Rosendahl;Nat Genet,2008
4. Chymotrypsinogen C genetic variants, including c.180TT, are strongly associated with chronic pancreatitis in pediatric patients;Grabarczyk;J Pediatr Gastroenterol Nutr,2017
5. Genetic risk in chronic pancreatitis:The trypsin-dependent pathway;Hegyi;Dig Dis Sci,2017
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1. TRPV6 Channel Is Involved in Pancreatic Ductal Adenocarcinoma Aggressiveness and Resistance to Chemotherapeutics;Cancers;2023-12-08
2. A case of early-onset idiopathic chronic pancreatitis associated with a loss-of-function TRPV6 p.R483Q variant successfully treated by pancreatic duct stenting;Clinical Journal of Gastroenterology;2023-04-29
3. Genetic determinants of pancreatitis: relevance in severe hypertriglyceridemia;Current Opinion in Lipidology;2023-02-01
4. A novel frameshift mutation in TRPV6 is associated with hereditary pancreatitis;Frontiers in Genetics;2023-01-09
5. The Coexistence of TRPV6 Variants With Other Pancreatitis-Associated Genes Affects Pediatric-Onset Pancreatitis;Journal of Pediatric Gastroenterology & Nutrition;2023-01-04
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