Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2003-12-3
pubmed:abstractText
Myocardial infarction (MI) is a complex multifactorial and polygenic disorder that is thought to result from interaction between genetic make-up and various environmental factors. We previously identified a missense mutation, methionine (ATG) to isoleucine (ATC) at nucleotide 1023 (M341I), in exon 3 of the human natriuretic peptide receptor A type (hNPRA) gene. This mutation is associated with increased risk for essential hypertension (EH). The purpose of this study was to investigate association between MI and the M341I mutation in the hNPRA gene.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1234-1010
pubmed:author
pubmed:issnType
Print
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
CR505-10
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:14646971-Aged, pubmed-meshheading:14646971-Alleles, pubmed-meshheading:14646971-Base Sequence, pubmed-meshheading:14646971-Case-Control Studies, pubmed-meshheading:14646971-DNA Primers, pubmed-meshheading:14646971-Exons, pubmed-meshheading:14646971-Female, pubmed-meshheading:14646971-Gene Frequency, pubmed-meshheading:14646971-Genetic Markers, pubmed-meshheading:14646971-Guanylate Cyclase, pubmed-meshheading:14646971-Humans, pubmed-meshheading:14646971-Japan, pubmed-meshheading:14646971-Male, pubmed-meshheading:14646971-Middle Aged, pubmed-meshheading:14646971-Mutation, Missense, pubmed-meshheading:14646971-Myocardial Infarction, pubmed-meshheading:14646971-Polymorphism, Restriction Fragment Length, pubmed-meshheading:14646971-Receptors, Atrial Natriuretic Factor, pubmed-meshheading:14646971-Risk Factors
pubmed:year
2003
pubmed:articleTitle
Missense mutation of exon 3 in the type A human natriuretic peptide receptor gene is associated with myocardial infarction.
pubmed:affiliation
2nd Department of Internal Medicine, Nihon Medical University, Itabashi-ku, Tokyo, Japan. tnakayama@med.nihon-u.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't