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

Electrophoretic screening for human apolipoprotein C-II variants: repeated identification of apolipoprotein C-II(K19T).

Journal of molecular medicine (Berlin, Germany) - 1 Jul 1995

Wiebusch H, Nofer J R, von Eckardstein A, Funke H, Wahrburg U, Martin H, Köhler E, Assmann G

Abstract excerpt

Screening for apolipoprotein (apo) C-II variants in the plasma of 400 students, 600 patients of a cardiological rehabilitation center, and 1200 patients of an outpatient lipid clinic by isoelectric focusing and subsequent anti-apo C-II immunoblotting led to the identification of four individuals...

Topics

Adult
Amino Acid Sequence
Apolipoprotein C-II
Apolipoproteins C
Base Sequence
Genetic Variation
Heterozygote
Humans
Hypercholesterolemia
Hypertriglyceridemia
Isoelectric Focusing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Male

Middle Aged

Molecular Sequence Data

Source

Identifiers

PMID: 8520970
DOI: 10.1007/BF00192889

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8520970-2026-08-30.1. 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

Electrophoretic screening for human apolipoprotein C-II variants: repeated identification of apolipoprotein C-II(K19T).PMID 8520970Read ↗

An apolipoprotein CII mutation, CIILys19----Thr' identified in patients with hyperlipidemia.Semantic proximity Read ↗

Studies on an apolipoprotein C-II variant occurring in Caucasians.Semantic proximity Read ↗

A novel apolipoprotein C-III variant, apoC-III(Gln38-->Lys), associated with moderate hypertriglyceridemia in a large kindred of Mexican origin.Semantic proximity Read ↗

Apolipoprotein C-III(Lys58----Glu). Identification of an apolipoprotein C-III variant in a family with hyperalphalipoproteinemia.Semantic proximity Read ↗

Molecular basis of type III hyperlipoproteinemia in Germany.Semantic proximity Read ↗

Electrophoretic screening for genetic variation in apolipoprotein C-III: identification of a novel apoC-III variant, apoC-III(Asp45-->Asn), in a Turkish patient.Semantic proximity Read ↗

Identification of a new apolipoprotein E variant (E2 Arg142-->Leu) in type III hyperlipidemia.Semantic proximity Read ↗

Hypervariable polymorphism in the APOC3 gene.Semantic proximity Read ↗

Rare apolipoprotein E variant identified in a patient with type III hyperlipidaemia.Semantic proximity Read ↗

Apolipoprotein A-IV polymorphism in the Hungarian population: gene frequencies, effect on lipid levels, and sequence of two new variants.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 ↗

Molecular cloning and characteristics of a new apolipoprotein C-II mutant identified in three unrelated individuals with hypercholesterolemia and hypertriglyceridemia.Semantic proximity Read ↗

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