Autosomal Dominant Hereditary Pancreatitis

 
National Institutes of Health

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Topic mentions per year

2000-2017
01220002017

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Review
2017
Review
2017
PURPOSE OF REVIEW Genetic risk in chronic pancreatitis is partly due to mutations that cause misfolding of digestive enzymes and… (More)
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2012
2012
Mutations in human cationic trypsinogen (PRSS1) cause autosomal dominant hereditary pancreatitis. Increased intrapancreatic… (More)
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2012
2012
Background: Hereditary pancreatitis is caused by mutations in human cationic trypsinogen. Chymotrypsin C is a proteolytic… (More)
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2009
2009
We investigated the biochemical properties and cellular expression of the c.346C>T (p.R116C) human cationic trypsinogen (PRSS1… (More)
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2007
2007
Variants of the SPINK1 gene encoding pancreatic secretory trypsin inhibitor have been described in association with chronic… (More)
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2006
2006
BACKGROUND The cationic trypsinogen (PRSS1) R122H mutation causes autosomal dominant hereditary pancreatitis (HP) with multiple… (More)
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2000
2000
BACKGROUND A distinct type of pancreatitis associated with diabetes, termed fibrocalculous pancreatic diabetes (FCPD), has been… (More)
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