APOB, apolipoprotein B, 338

N. diseases: 339; N. variants: 122
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease HPO
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Apolipoprotein B gene polymorphisms, lipoproteins and coronary atherosclerosis: a study of young myocardial infarction survivors and healthy population-based individuals. 1352974 1992
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease BEFREE Lipid parameters and apolipoprotein B RFLP studies: comparison of normal and coronary heart disease groups as defined by angiography. 1362695 1992
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Studies comparing patients and controls, however, did not confirm previous studies suggesting that the multi-allelic variation at the 3'VNTR region of the apolipoprotein B gene was associated with coronary artery disease. 1418918 1992
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE We have investigated the frequency of Hind III DNA polymorphism of the human apolipoprotein B gene in a Canadian Caucasian population with coronary artery disease, as documented by angiography, and a healthy control population. 1477972 1992
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE We have examined DNA polymorphisms associated with the apolipoprotein B gene in 95 Sri Lankan males with ischaemic heart disease and 95 matched controls. 1674237 1991
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE 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. 1732399 1992
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Three polymorphic sites of the apolipoprotein B gene - the insertion/deletion signal peptide, XbaI and EcoRI sites - were examined in a sample of 107 healthy men and in 46 men with evidence of coronary heart disease selected from a large population survey of South Asians aged 40-69 in London, U.K. 1789809 1991
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Association of DNA polymorphism at the apolipoprotein B gene locus with coronary heart disease and serum very low density lipoprotein levels. 1967524 1990
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Hypervariability in a minisatellite 3' of the apolipoprotein B gene in patients with coronary heart disease compared with normal controls. 2351870 1990
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease BEFREE Apolipoprotein B allotypes MB19(1) and MB19(2) in subjects with coronary artery disease and hypercholesterolemia. 2434069 1987
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE This suggests that variation at the ApoB locus may be involved independently in the determination of serum lipid levels and in the development of ischaemic heart disease. 2452042 1988
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Together these results suggest that inherited variations of the apolipoprotein-B gene, probably in the form of charged aminoacid substitutions, influence circulating cholesterol concentration, and that these and other functional variants of the apolipoprotein-B gene affect susceptibility to coronary heart disease and obesity. 2904569 1989
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Immunologically defined alleles of the pig apolipoprotein B (ApoB) locus (apoB) are correlated with different blood cholesterol levels and predisposition towards premature coronary heart disease. 2905687 1988
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Coronary heart disease risk correlates directly with plasma concentrations of lipoprotein(a) (Lp(a)), a low-density lipoprotein-like particle distinguished by the presence of the glycoprotein apolipoprotein(a) (apo(a)), which is bound to apolipoprotein B-100 (apoB-100) by disulfide bridges. 2976021 1988
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Levels of apolipoprotein B, the protein component of low-density lipoproteins, correlate with the risk of coronary heart disease. 3024002 1986
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease BEFREE Apolipoprotein B and apolipoprotein AI as predictors of coronary artery disease. 3141025 1988
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Restriction fragment length polymorphisms of apolipoprotein B gene in Chinese population with coronary heart disease. 7533671 1995
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Associations of genotypes at the apolipoprotein AI-CIII-AIV, apolipoprotein B and lipoprotein lipase gene loci with coronary atherosclerosis and high density lipoprotein subclasses. 7834891 1994
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Polymorphisms of apolipoprotein B gene in relation to coronary heart disease in Chinese Han nationality. 7910546 1994
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease BEFREE Low density lipoprotein cholesterol/apolipoprotein B-100 ratio: interaction of family history of premature atherosclerotic coronary artery disease with race and gender in 7 to 11 year olds. 7936858 1994
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE The presence of mutant apo B-100 in low-density lipoproteins (LDL) markedly reduces their affinity for the LDL receptor, leading to hypercholesterolaemia and increased proneness to coronary artery disease. 8141833 1993
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 AlteredExpression disease BEFREE Apolipoprotein B levels were strongly associated with coronary artery disease in four of five prospective studies but were more predictive of coronary artery disease than were total cholesterol levels in only two of the four studies. 8185133 1994
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE By direct comparison of the Lp(a) and apoB plasma concentrations in 28 affected and 31 unaffected members of seven families carrying the FH trait and without history of coronary artery disease, we reached the conclusion that LDL receptor activity is not a major determinant of the Lp(a) plasma levels in these subjects. 8187228 1994
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease BEFREE An elevated plasma level of apolipoprotein B (apoB), the major protein of low density lipoproteins, is a risk factor for coronary artery disease. 8349099 1993