"Loss of function" mutations in the cationic trypsinogen gene (PRSS1) may act as a protective factor against pancreatitis (Q44452899)

3 December 2017

"Loss of function" mutations in the cationic trypsinogen gene (PRSS1) may act as a protective factor against pancreatitis (English)

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3 December 2017

Jian-Min Chen

1

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3 December 2017

Cedric Le Maréchal

2

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3 December 2017

Danièle Lucas

3

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3 December 2017

Odile Raguénès

4

1 reference

3 December 2017

Claude Férec

5

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3 December 2017

1 May 2003

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Molecular Genetics and Metabolism

3 December 2017

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3 December 2017

79

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3 December 2017

67-70

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3 December 2017

1

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Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene

3 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Mutations of the cystic fibrosis gene in patients with chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Determination of the relative contribution of three genes-the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene-to the etiology of idiopathic chronic pancreat

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Hereditary pancreatitis: new insights into acute and chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

The pathobiochemistry of hereditary pancreatitis: studies on recombinant human cationic trypsinogen.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

A clinically based classification system for alcoholic chronic pancreatitis: summary of an international workshop on chronic pancreatitis.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Mutation in the SPINK1 trypsin inhibitor gene, alcohol use, and chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Idiopathic vs hereditary pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Identification of a novel pancreatitis-associated missense mutation, R116C, in the human cationic trypsinogen gene (PRSS1)

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

Wanted: a consensus nomenclature for cationic trypsinogen mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

The complete 685-kilobase DNA sequence of the human beta T cell receptor locus

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900050-7

7 January 2021

10.1016/S1096-7192(03)00050-7

Identifiers

DOI

1 reference

3 December 2017

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