| P2093 | author name string | J. Shepherd | |
| | C. J. Packard | |
| | J. J. Series | |
| | D. Gaffney | |
| P2860 | cites work | Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100 | Q24316428 |
| | Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 |
| | "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum | Q27860612 |
| | A receptor-mediated pathway for cholesterol homeostasis | Q29616158 |
| | Molecular cloning of human apolipoprotein B cDNA. | Q30406574 |
| | Catabolic rate of low density lipoprotein is influenced by variation in the apolipoprotein B gene | Q34561616 |
| | A three codon insertion/deletion polymorphism in the signal peptide region of the human apolipoprotein B (APOB) gene directly typed by the polymerase chain reaction | Q35229040 |
| | Genetic variation in serum low density lipoproteins and lipid levels in man | Q35988301 |
| | RFLPs for the human apolipoprotein B gene: HincII and PvuII. | Q40418556 |
| | The Xba1 polymorphism of the apolipoprotein B gene influences the degradation of low density lipoprotein in vitro | Q41325745 |
| | Apolipoprotein B amino acid 3611 substitution from arginine to glutamine creates the Ag (h/i) epitope: the polymorphism is not associated with differences in serum cholesterol and apolipoprotein B levels. | Q41921142 |
| | Identification of the base substitution responsible for the Ag(x/y) polymorphism of apolipoprotein B-100. | Q43596653 |
| | Contribution to the Inheritance of the Ag Groups A Population Genetic Study | Q46544070 |
| | Analysis of the human apolipoprotein B gene; complete structure of the B-74 region | Q48371745 |
| | Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hypelipidaemic individuals | Q57840193 |
| | The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene ?a useful marker for human chromosome 2 | Q61561060 |
| | Apolipoprotein E polymorphism and atherosclerosis | Q68126635 |
| | Detection by denaturing gradient gel electrophoresis of a new polymorphism in the apolipoprotein B gene | Q68163310 |
| | Lack of correlation between the apolipoprotein B XbaI polymorphism and blood lipid levels in a Swedish population | Q69369357 |
| | XbaI restriction fragment length polymorphism of apolipoprotein B in Swedish myocardial infarction patients | Q69375236 |
| | Common DNA polymorphism within coding sequence of apolipoprotein B gene associated with altered lipid levels | Q69882249 |
| | Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease | Q69928029 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | hypercholesterolemia | Q762713 |
| | restriction fragment length polymorphism | Q857299 |
| | gene frequency | Q71131180 |
| P304 | page(s) | 89-98 | |
| P577 | publication date | 1993-04-01 | |
| | 1993-04-16 | |
| P1433 | published in | Clinica Chimica Acta | Q5133740 |
| P1476 | title | Frequency of the XbaI, EcoRI, PvuII and MspI polymorphisms of the apolipoprotein B gene in relation to hypercholesterolaemia in the general population | |
| P478 | volume | 215 | |