Hypertriglyceridemia characterized by low-density lipoprotein phenotype and lipoprotein lipase gene mutation

Clinical Chemistry and Laboratory Medicine

Volumn 38, Issue 12, 2000, Pages 1263-1270

  Li, J ^a   Kondo, A ^a   Maekawa, M ^a   Kanamori, M ^a   Kanno, T ^a  

^a HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Dense low density lipoprotein; High density lipoprotein cholesterol (HDL C); Lipoprotein lipase (LPL); Small; Triglyceride (TG)

Indexed keywords

HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LIPOPROTEIN LIPASE; LOW DENSITY LIPOPROTEIN; LOW DENSITY LIPOPROTEIN CHOLESTEROL; TRIACYLGLYCEROL;

ADULT; ARTICLE; CONTROLLED STUDY; FEMALE; FREQUENCY ANALYSIS; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPERTRIGLYCERIDEMIA; LIPOPROTEIN BLOOD LEVEL; MAJOR CLINICAL STUDY; MALE; PARTICLE SIZE; PHENOTYPE; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; SERUM; TRIACYLGLYCEROL BLOOD LEVEL;

EID: 0034500469     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/cclm.2000.199     Document Type: Article

References (34)

1. Flotation rates, molecular weights and hydrated densities of the low-density lipoproteins
2. The characterization of a discrete series of low density lipoproteins in the disease, hyper-pre-β-lipoproteinemia
3. Low-density lipoprotein subclass patterns and risk of myocardial infraction
4. Atherogenic lipoprotein phenotype: A proposed genetic marker for coronary heart disease risk
5. Small, dense low-density lipoprotein particles as a predictor of the risk of ischemic heart disease in men
6. LDL particle size distribution: Results from the Framingham offspring study
7. Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency
8. Identification of multiple subclasses of plasma low density lipoproteins in normal humans
9. Identifying the predominant peak diameter of high-density and low-density lipoproteins by electrophoresis
10. Aggregation of low density lipoproteins with unilamellar phosphatidylcholine vesicles
11. Serum lipoprotein lipase in healthy subjects: Effects of gender and age, and relationships to lipid parameters
12. Heterogeneous mutation in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency
13. Structure and polymorphism map of human lipoprotein lipase gene
14. Analysis of genetic mutations in human lactate dehydrogenase-A(M) deficiency using DNA conformation polymorphism in combination with polyacrylamide gradient gel and silver staining
15. A sensitive non-radioactive PCR-RFLP analysis for detecting point mutations at 12th codon of oncogene C-Ha-ras in DNAs of gastric cancer
16. Designed diagnostic restriction fragment length polymorphisms for the detection of point mutations in ras oncogenes
17. Novel nonsense mutation in exon 1 and a transition in intron 3 of the lipoprotein lipase gene
18. Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: Identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene
19. The application of end user computing (EUC) for detection of lipoprotein lipase gene abnormality
20. Role of plasma triglyceride in the regulation of plasma low density lipoprotein (LDL) subfractions: Relative contribution of small, dense LDL to coronary heart disease risk
21. Influence of mild to moderately elevated triglycerides on low density lipoprotein subfraction concentration and composition in healthy men with low high density lipoprotein cholesterol levels
22. Plasma cholesteryl ester transfer protein
23. Detection of two species of low density lipoprotein particles in cholesteryl este transfer protein deficiency
24. Lipoprotein heterogeneity and apolipoprotein B metabolism
25. Influence of plasma cholesteryl ester transfer activity on the LDL and HDL distribution profiles in normolipidemic subjects
26. Combined effects of lipid transfers and lipolysis on gradient gel patterns of human plasma LDL
27. Preferential cholesteryl ester acceptors among triglyceride-rich lipoproteins during alimentary lipemia in normolipidemic subjects
28. Structure, function and role of lipoprotein lipase in lipoprotein metabolism
29. High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: Possible association with apolipoprotein E2 isoform
30. 44-Ter) in Japanese, and association with dyslipoproteinemia
31. DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population
32. Lipoprotein lipase gene polymorphisms: Associations with myocardial infraction and lipoprotein levels, the ECTIM study
33. 447 stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic males
34. Lipoprotein lipase with a defect in lipid interface recognition in a case with type I hyperlipidemia