Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2008-9-18
pubmed:abstractText
The purpose of this study was to identify rare APOA5 variants in 130 severe hypertriglyceridemic patients by sequencing, and to test their functionality, since no patient recall was possible.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1524-4636
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
28
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1866-71
pubmed:meshHeading
pubmed-meshheading:18635818-Adult, pubmed-meshheading:18635818-Apolipoproteins A, pubmed-meshheading:18635818-DNA Mutational Analysis, pubmed-meshheading:18635818-Europe, pubmed-meshheading:18635818-Female, pubmed-meshheading:18635818-Heterozygote, pubmed-meshheading:18635818-Homozygote, pubmed-meshheading:18635818-Humans, pubmed-meshheading:18635818-Hydrolysis, pubmed-meshheading:18635818-Hypertriglyceridemia, pubmed-meshheading:18635818-Lipoprotein Lipase, pubmed-meshheading:18635818-Lipoproteins, VLDL, pubmed-meshheading:18635818-Male, pubmed-meshheading:18635818-Models, Molecular, pubmed-meshheading:18635818-Mutation, Missense, pubmed-meshheading:18635818-Phenotype, pubmed-meshheading:18635818-Pregnancy, pubmed-meshheading:18635818-Pregnancy Complications, pubmed-meshheading:18635818-Protein Binding, pubmed-meshheading:18635818-Protein Conformation, pubmed-meshheading:18635818-Receptors, LDL, pubmed-meshheading:18635818-Recombinant Proteins, pubmed-meshheading:18635818-Severity of Illness Index, pubmed-meshheading:18635818-Structure-Activity Relationship, pubmed-meshheading:18635818-Surface Plasmon Resonance, pubmed-meshheading:18635818-Triglycerides
pubmed:year
2008
pubmed:articleTitle
Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding.
pubmed:affiliation
Department of Medicine, Division of Cardiovascular Genetics, UCL, London, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Multicenter Study