Article
High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoform.
Journal of lipid research - 1 Jun 1994
Ma Y, Ooi T C, Liu M S, Zhang H, McPherson R, Edwards A L, Forsythe I J, Frohlich J, Brunzell J D, Hayden M R
Abstract excerpt
Partial deficiency in lipolysis usually results in only mild disturbances of lipid levels. However, when this is associated with impairment of the uptake of remnant particles and increased production of triglyceride-rich lipoproteins stimulated by environmental factors such as during normal pregn...
Topics
- Adult
- Apolipoprotein E2
- Apolipoproteins E
- Base Sequence
- Cell Line
- Chylomicrons
- DNA
- Female
- Gene Expression
- Genotype
- Humans
- Hypertriglyceridemia
- Lipoprotein Lipase
- Molecular Sequence Data
