Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Levels of apolipoprotein B, the protein component of low-density lipoproteins, correlate with the risk of coronary heart disease.
|
3024002 |
1986 |
Coronary Artery Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Apolipoprotein B allotypes MB19(1) and MB19(2) in subjects with coronary artery disease and hypercholesterolemia.
|
2434069 |
1987 |
Coronary Artery Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Apolipoprotein B and apolipoprotein AI as predictors of coronary artery disease.
|
3141025 |
1988 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
A high-resolution method was used to study the allele frequencies of a hypervariable minisatellite region close to the apolipoprotein B gene in 110 patients with severe coronary disease and in 117 normal controls.
|
2351870 |
1990 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We examined the possible association between the apoB 3'VNTR alleles and CAD in 387 Finnish subjects.
|
1732399 |
1992 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Lipid parameters and apolipoprotein B RFLP studies: comparison of normal and coronary heart disease groups as defined by angiography.
|
1362695 |
1992 |
Coronary Artery Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
The strong association of hypertriglyceridemic hyperapoB with CAD reflected the multiplicative effect of increased low-density lipoprotein apolipoprotein B and endogenous hypertriglyceridemia, and was independent of the effects of age, sex, diabetes mellitus, systemic hypertension, body mass index and cigarette smoking.
|
8447257 |
1993 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms of apolipoprotein B gene in relation to coronary heart disease in Chinese Han nationality.
|
7910546 |
1994 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
In young children, a low LDL-C/ApoB ratio and high ApoB levels were associated with a positive family history of CAD only in the white girls, suggesting that this group is at increased risk of genetically mediated CAD.
|
7936858 |
1994 |
Coronary Artery Disease
|
0.100 |
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 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Association of polymorphisms of the apolipoprotein B gene with coronary heart disease in Han Chinese.
|
8546754 |
1995 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
To determine whether the APOE association may be a risk factor for coronary disease as well, we examined two APOB gene restriction sites that have previously been found to be associated with coronary artery disease, especially myocardial infarctions.
|
8530010 |
1995 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Using the CE technique, the apoB VNTR loci from some individuals in genotyping were examined towards precise DNA diagnosis for coronary heart disease.
|
8529610 |
1995 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In familial defective apo B-100 (FDB), a mutation in apo B-100 at residue 3500 markedly reduces its affinity for LDL-R, often causing accumulation of defective LDL particles, and an increased proneness to coronary artery disease (CAD).
|
8579620 |
1995 |
Coronary Artery Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Quantitative sib-pair linkage analysis indicates that apo(a) is the major gene controlling Lp(a) levels in this CAD population (P = .001; 99 sib pairs), whereas the apoB gene demonstrated no significant quantitative linkage effect.
|
7825589 |
1995 |