rs111033564
|
|
|
0.710 |
GeneticVariation |
BEFREE |
We detected p.R122H, p.R122C, p.N29I, and p.E79K mutation in 34% (14/41), 27% (11/41), 12% (5/41), and 7% (3/41) of HP patients, respectively.
|
27179762 |
2017 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
|
15776435 |
2005 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
To challenge this notion, here we describe the unique properties of the E79K cationic trypsinogen mutation (c.235G>A), which was identified in three European families affected by sporadic or familial pancreatitis cases.
|
14695529 |
2004 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.
|
11788572 |
2002 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
|
11866271 |
2002 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
10930381 |
2000 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitis.
|
11073545 |
2000 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.
|
10204851 |
1999 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis.
|
10381903 |
1999 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Mutations of the cationic trypsinogen in hereditary pancreatitis.
|
9633818 |
1998 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.
|
9322498 |
1997 |
rs111033564
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
|
8841182 |
1996 |