(Q35011363)

5 August 2017

A Thai family with hereditary pancreatitis and increased cancer risk due to a mutation in PRSS1 gene (English)

1 reference

5 August 2017

Theeraphong Pho-Iam

1

1 reference

5 August 2017

Wanna Thongnoppakhun

series ordinal

2

1 reference

5 August 2017

Pa-Thai Yenchitsomanus

series ordinal

3

1 reference

5 August 2017

Chanin Limwongse

series ordinal

4

1 reference

5 August 2017

language of work or name

English

0 references

publication date

1 March 2005

1 reference

World Journal of Gastroenterology

5 August 2017

1 reference

5 August 2017

11

1 reference

5 August 2017

11

1 reference

5 August 2017

1634-1638

1 reference

Pedigree of a family with hereditary chronic relapsing pancreatitis

5 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

The amino-acid mutational spectrum of human genetic disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

8 July 2018

Hereditary pancreatitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatography

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Gain-of-function mutations associated with hereditary pancreatitis enhance autoactivation of human cationic trypsinogen

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Hereditary pancreatitis: new insights into acute and chronic pancreatitis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Lack of R117H mutation in the cationic trypsinogen gene in patients with tropical pancreatitis from Bangladesh

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Hereditary pancreatitis. Historical perspectives.

8 July 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V11.I11.1634

R116C mutation of cationic trypsinogen in a Turkish family with recurrent pancreatitis illustrates genetic microheterogeneity of hereditary pancreatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V11.I11.1634

Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V11.I11.1634

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V11.I11.1634

Understanding human disease mutations through the use of interspecific genetic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V11.I11.1634

RISK FACTORS FOR CANCER IN HEREDITARY PANCREATITIS

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V11.I11.1634

Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305944

Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation

25 October 2018

1 reference

12 December 2020

[Cationic trypsinogen gene mutation in patients with chronic idiopathic pancreatitis]

1 reference

12 December 2020

The hereditary pancreatitis gene maps to long arm of chromosome 7

1 reference

12 December 2020

Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis

1 reference

12 December 2020

Hereditary pancreatitis: new insights, new directions

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation analysis of the cationic trypsinogen gene in patients with pancreatic cancer

1 reference

12 December 2020

Identifiers

DOI

10.3748/WJG.V11.I11.1634

1 reference

5 August 2017

1 reference

5 August 2017

1 reference