Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis

scientific article

Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1136/GUT.44.2.259
P932PMC publication ID1727382
P698PubMed publication ID9895387
P5875ResearchGate publication ID13394514

P2093author name stringYokoyama K
Yamamoto M
Watanabe S
Ogawa M
Morita M
Ishida H
Makino I
Nishimori I
Onishi S
Fujikawa-Adachi K
Kamakura M
P2860cites workHereditary pancreatitis is caused by a mutation in the cationic trypsinogen geneQ24311652
Pedigree of a family with hereditary chronic relapsing pancreatitisQ28244501
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitisQ28250483
Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study GroupQ28307042
Cloning, characterization and nucleotide sequences of two cDNAs encoding human pancreatic trypsinogensQ34162138
The complete 685-kilobase DNA sequence of the human beta T cell receptor locusQ34382665
Two forms of hereditary chronic pancreatitis.Q39431705
Diagnostic Criteria for Chronic Pancreatitis by the Japan Pancreas SocietyQ41522049
Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7q.Q45101857
An exceptional genealogy for hereditary chronic pancreatitisQ71214968
The hereditary pancreatitis gene maps to long arm of chromosome 7Q71625105
A gene for hereditary pancreatitis maps to chromosome 7q35Q71884887
Hereditary pancreatitisQ72115269
Hereditary pancreatitisQ72485640
P433issue2
P407language of work or nameEnglishQ1860
P304page(s)259-263
P577publication date1999-02-01
P1433published inGutQ5621669
P1476titleMutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis
P478volume44

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cites work (P2860)
Q28345956A new polymorphism for the RI22H mutation in hereditary pancreatitis
Q35596502Absence of PRSS1 mutations and association of SPINK1 trypsin inhibitor mutations in hereditary and non-hereditary chronic pancreatitis
Q43004117Association of a new cationic trypsinogen gene mutation (V39A) with chronic pancreatitis in an Italian family.
Q34619449Chronic pancreatitis: Asia-Pacific consensus report
Q28250117Clinical and genetic characteristics of hereditary pancreatitis in Europe
Q77385500Clinical characterization of patients with hereditary pancreatitis and mutations in the cationic trypsinogen gene
Q43581652Comparative in vitro studies on native and recombinant human cationic trypsins. Cathepsin B is a possible pathological activator of trypsinogen in pancreatitis.
Q37172601Comprehensive screening for PRSS1, SPINK1, CFTR, CTRC and CLDN2 gene mutations in Chinese paediatric patients with idiopathic chronic pancreatitis: a cohort study
Q42753462Evaluation of the cationic trypsinogen gene for potential mutations in miniature schnauzers with pancreatitis.
Q35363207Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins
Q36674778Genetic background of pancreatitis
Q35083728Genetic factors in pancreatitis
Q33953444Genetic predispositions to acute and chronic pancreatitis
Q34199888Genetic testing in acute and chronic pancreatitis
Q34034840Genetics of chronic pancreatitis
Q21203019Hereditary chronic pancreatitis
Q35036958Hereditary pancreatitis
Q33992750Hereditary pancreatitis and mutations of the cationic trypsinogen gene
Q41694955Hereditary pancreatitis-associated mutation asn(21) --> ile stabilizes rat trypsinogen in vitro
Q33724434Hereditary pancreatitis. Gene defects and their implications
Q24670166Hereditary pancreatitis: new insights into acute and chronic pancreatitis
Q41734787Human cationic trypsinogen. Role of Asn-21 in zymogen activation and implications in hereditary pancreatitis
Q36713082Is genetic analysis helpful for diagnosing chronic pancreatitis in its early stage?
Q24658116Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitis
Q78001776Mutations of the cationic trypsinogen gene in patients with chronic pancreatitis
Q50238364Nationwide survey of hereditary pancreatitis in Japan
Q34137364PRSS1 and SPINK1 mutations in idiopathic chronic and recurrent acute pancreatitis
Q43161315Relationship of strain-dependent susceptibility to experimentally induced acute pancreatitis with regulation of Prss1 and Spink3 expression
Q38010175Role of Intrapancreatic SPINK1/Spink3 Expression in the Development of Pancreatitis
Q41708880Targeted next-generation sequencing effectively analyzed the cystic fibrosis transmembrane conductance regulator gene in pancreatitis
Q36626791The role of trypsin, trypsin inhibitor, and trypsin receptor in the onset and aggravation of pancreatitis

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