Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic variation in the amino-terminal part of apolipoprotein B: studies in hyperlipidemic patients.

Atherosclerosis - 1 Jun 1998

Ilmonen M, Knudsen P, Taskinen M R, Tikkanen M J

Abstract excerpt

Hypertriglyceridemia is a heterogeneous lipid disorder often running in families. Variation in the apolipoprotein B (apo B) gene has been associated with serum triglyceride levels. Recently, a role of the amino-terminal end of apo B in binding with lipoprotein lipase (LPL) has been suggested. We...

Topics

Adult
Apolipoproteins B
Codon
Female
Genetic Variation
Humans
Hyperlipidemias
Male
Middle Aged
Polymorphism, Genetic

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9690921
DOI: 10.1016/s0021-9150(98)00038-0

Genes

LPL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9690921-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variation in the amino-terminal part of apolipoprotein B: studies in hyperlipidemic patients.PMID 9690921Read ↗

Screening of the 3' two-thirds of the coding area of the apo B gene in Finnish hypercholesterolemic patients report of six new genetic variants.Semantic proximity Read ↗

Major apolipoprotein B-100 mutations in lipoprotein metabolism and atherosclerosis.Semantic proximity Read ↗

Screening for mutations in the exon 26 of the apolipoprotein B gene in hypercholesterolemic Finnish families by the single-strand conformation polymorphism method.Semantic proximity Read ↗

Denaturing gradient gel electrophoretic analysis of codons 3456-3553 of the apolipoprotein-B gene in 106 type 11a hyperlipoproteinaemic individuals.Semantic proximity Read ↗

Apolipoprotein E1 Baden (Arg(180)-->Cys). A new apolipoprotein E variant associated with hypertriglyceridemia.Semantic proximity Read ↗

Screening for mutations of the apolipoprotein B gene causing hypocholesterolemia.Semantic proximity Read ↗

Hyperlipidaemia associated with genetic variation in the apolipoprotein B gene.Semantic proximity Read ↗

The Asn-291-->Ser and Ser-477-->Stop mutations of the lipoprotein lipase gene and their significance for lipid metabolism in patients with hypertriglyceridaemia.Semantic proximity Read ↗

Two new immunogenetic polymorphisms of the apoB gene and their effect on serum lipid levels and responses to changes in dietary fat intake.Semantic proximity Read ↗

DNA polymorphism studies. Approaches to elucidating multifactorial ischaemic heart disease: the apo B gene as an example.Semantic proximity Read ↗

A truncated species of apolipoprotein B, B-83, associated with hypobetalipoproteinemia.Semantic proximity Read ↗

Patients with apoE3 deficiency (E2/2, E3/2, and E4/2) who manifest with hyperlipidemia have increased frequency of an Asn 291-->Ser mutation in the human LPL gene.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.