rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
2000-8-22
|
pubmed:abstractText |
Mutations of the cationic trypsinogen have been described in hereditary pancreatitis. We report a new trypsinogen mutation in the activation peptide of the proenzyme in a family with chronic pancreatitis.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0016-5085
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
119
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
461-5
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:10930381-Adult,
pubmed-meshheading:10930381-Cations,
pubmed-meshheading:10930381-Chronic Disease,
pubmed-meshheading:10930381-DNA Mutational Analysis,
pubmed-meshheading:10930381-Enzyme Activation,
pubmed-meshheading:10930381-Family Health,
pubmed-meshheading:10930381-Female,
pubmed-meshheading:10930381-Gene Expression,
pubmed-meshheading:10930381-Humans,
pubmed-meshheading:10930381-Hydrogen-Ion Concentration,
pubmed-meshheading:10930381-Male,
pubmed-meshheading:10930381-Mutation, Missense,
pubmed-meshheading:10930381-Oligopeptides,
pubmed-meshheading:10930381-Pancreatitis,
pubmed-meshheading:10930381-Pedigree,
pubmed-meshheading:10930381-Trypsin,
pubmed-meshheading:10930381-Trypsinogen
|
pubmed:year |
2000
|
pubmed:articleTitle |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
pubmed:affiliation |
Medizinische Klinik II, Universität Leipzig, Leipzig, Germany.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|