rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
|
15776435 |
2005 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
|
15776435 |
2005 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).
|
14695529 |
2004 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).
|
14695529 |
2004 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Hereditary pancreatitis (HP) is usually caused by mutations in the cationic trypsinogen (PRSS1) gene, especially R122H or N29I.
|
11788572 |
2002 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
|
11866271 |
2002 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
The mutation R122H of the cationic trypsinogen was found in 21 index patients, N291 in six index patients, and A16V and D22G in one index patient, all from HP families.
|
11866271 |
2002 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Hereditary pancreatitis (HP) is usually caused by mutations in the cationic trypsinogen (PRSS1) gene, especially R122H or N29I.
|
11788572 |
2002 |
rs111033566
|
|
|
0.900 |
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 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
10930381 |
2000 |
rs267606982
|
|
|
0.900 |
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 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
10930381 |
2000 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.
|
10204851 |
1999 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis.
|
10381903 |
1999 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis.
|
10381903 |
1999 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.
|
10204851 |
1999 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Mutations of the cationic trypsinogen in hereditary pancreatitis.
|
9633818 |
1998 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Mutations of the cationic trypsinogen in hereditary pancreatitis.
|
9633818 |
1998 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.
|
9322498 |
1997 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.
|
9322498 |
1997 |
rs111033566
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
|
8841182 |
1996 |
rs267606982
|
|
|
0.900 |
GeneticVariation |
UNIPROT |
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
|
8841182 |
1996 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
|
15776435 |
2005 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).
|
14695529 |
2004 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
The mutation R122H of the cationic trypsinogen was found in 21 index patients, N291 in six index patients, and A16V and D22G in one index patient, all from HP families.
|
11866271 |
2002 |