| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00208282 |
| P698 | PubMed publication ID | 8076943 |
| P2093 | author name string | A Palotie | |
| M J Tikkanen | |||
| T Sane | |||
| K Kontula | |||
| T Heliö | |||
| P2860 | cites work | Apolipoprotein B signal peptide insertion/deletion polymorphism is associated with Ag epitopes and involved in the determination of serum triglyceride levels | Q67671160 |
| Variation at the apo AI/CIII/AIV gene complex is associated with elevated plasma levels of apo CIII | Q67993295 | ||
| DNA polymorphism haplotypes of the human lipoprotein lipase gene: possible association with high density lipoprotein levels | Q68298872 | ||
| Very low density lipoprotein triglyceride metabolism in relatives of hypertriglyceridemic probands. Evidence for genetic control of triglyceride removal | Q68359943 | ||
| Hypertriglyceridemia as a result of human apo CIII gene expression in transgenic mice | Q68473712 | ||
| [Enzymatic determination of total cholesterol in serum (author's transl)] | Q68825859 | ||
| Detection and characterization of the heterozygote state for lipoprotein lipase deficiency | Q69608002 | ||
| Common DNA polymorphism within coding sequence of apolipoprotein B gene associated with altered lipid levels | Q69882249 | ||
| Apolipoprotein B-gene DNA polymorphisms associated with myocardial infarction | Q70155040 | ||
| DNA polymorphisms of apolipoprotein A-I/C-III and insulin genes in familial hypertriglyceridemia and coronary heart disease | Q70358364 | ||
| Integrated regulation of very low density lipoprotein triglyceride and apolipoprotein-B kinetics in man: Normolipemic subjects, familial hypertriglyceridemia and familial combined hyperlipidemia | Q70883514 | ||
| Quantitation of human apolipoprotein C-III and its subspecie by radioimmunoassay and analytical isoelectric focusing: abnormal plasma triglyceride-rich lipoprotein apolipoprotein C-III subspecie concentrations in hypertriglyceridemia | Q70947086 | ||
| Regulation of the hepatic uptake of triglyceride-rich lipoproteins in the rat. Opposing effects of homologous apolipoprotein E and individual C apoproteins | Q71302410 | ||
| Does familial hypertriglyceridemia predispose to NIDDM? | Q72752892 | ||
| Rabbit very low density lipoprotein receptor: a low density lipoprotein receptor-like protein with distinct ligand specificity | Q24293268 | ||
| Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
| Strategies for multilocus linkage analysis in humans | Q27860521 | ||
| Linkage of human apolipoproteins A-I and C-III genes | Q28265457 | ||
| Genetic and developmental regulation of the lipoprotein lipase gene: loci both distal and proximal to the lipoprotein lipase structural gene control enzyme expression | Q28593108 | ||
| Inhibition of lipoprotein lipase by an apoprotein of human very low density lipoprotein | Q28626203 | ||
| THE DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUM | Q29391553 | ||
| Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region | Q33828902 | ||
| Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants | Q35013854 | ||
| Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100 | Q35198304 | ||
| The molecular and cell biology of apolipoprotein-B. | Q38669547 | ||
| Enzymes involved in triglyceride hydrolysis | Q39700056 | ||
| Hereditary diseases in Finland; rare flora in rare soul | Q39932270 | ||
| Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric origin | Q40348644 | ||
| RFLP for the human apolipoprotein B gene: V;XbaI. | Q40471895 | ||
| Dinucleotide repeat polymorphisms at the D11S419 and CD3D loci | Q40518355 | ||
| Lack of association between the apolipoprotein B gene 3' hypervariable region alleles and coronary artery disease in Finnish patients with angiographically documented coronary artery disease | Q42142276 | ||
| Myocardial infarction in the familial forms of hypertriglyceridemia | Q43433663 | ||
| Concept of VNTR alleles: Comparison of apolipoprotein B 3′ hypervariable region genotyping results obtained by three methods | Q44364901 | ||
| Human lipoprotein lipase complementary DNA sequence | Q48347640 | ||
| DNA polymorphisms at the lipoprotein lipase gene: associations in normal and hypertriglyceridaemic subjects. | Q51619176 | ||
| Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hypelipidaemic individuals | Q57840193 | ||
| Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24 | Q59054538 | ||
| DNA POLYMORPHISM ADJACENT TO HUMAN APOPROTEIN A-1 GENE: RELATION TO HYPERTRIGLYCERIDAEMIA | Q63044134 | ||
| P433 | issue | 3 | |
| P921 | main subject | hypertriglyceridemia | Q1467339 |
| familial hypertriglyceridemia | Q5432941 | ||
| P304 | page(s) | 271-278 | |
| P577 | publication date | 1994-09-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | No evidence for linkage between familial hypertriglyceridemia and apolipoprotein B, apolipoprotein C-III or lipoprotein lipase genes | |
| P478 | volume | 94 |
| Q37364446 | Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes |
| Q77452737 | Genetics of lipoprotein disorders |
| Q28118749 | Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia |
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