(Q24795679)

English

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

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scholarly article

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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 (English)

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high-performance liquid chromatography

1 reference

based on heuristic

inferred from title

author name string

C Le Maréchal

1

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J M Chen

2

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I Quéré

3

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O Raguénès

4

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C Férec

5

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J Auroux

6

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language of work or name

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publication date

2001

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2

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19

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1

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https://scigraph.springernature.com/pub.10.1186/1471-2156-2-19

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-2156-2-19

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

7 April 2017

'Touchdown' PCR to circumvent spurious priming during gene amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

7 April 2017

A new polymorphism for the RI22H mutation in hereditary pancreatitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

28 September 2017

Denaturing high-performance liquid chromatography: A review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

28 September 2017

Molecular basis of hereditary pancreatitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

28 November 2018

Wanted: a consensus nomenclature for cationic trypsinogen mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

28 November 2018

Nomenclature of trypsinogen mutations in hereditary pancreatitis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=60523

28 November 2018

Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC

1 reference

https://pubmed.ncbi.nlm.nih.gov/11734061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of single-nucleotide polymorphisms with the WAVE DNA fragment analysis system

1 reference

https://pubmed.ncbi.nlm.nih.gov/11734061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of specific BRCA1 and BRCA2 variants by DHPLC

1 reference

https://pubmed.ncbi.nlm.nih.gov/11734061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counselling

1 reference

https://pubmed.ncbi.nlm.nih.gov/11734061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2156-2-19

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Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-2156-2-19

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