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 |
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 |
Coronary Arteriosclerosis
|
0.200 |
Biomarker
|
disease |
BEFREE |
The aim of this study was to detect mutations in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in patients of Southeast Asian origin with clinically diagnosed familial hypercholesterolemia (FH) and to relate these findings with the observed lower incidence of coronary heart disease in this part of the world.
|
11005141 |
2000 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms of the apolipoprotein B 3' variable number of tandem repeats region associated with coronary artery disease in Taiwanese.
|
9585673 |
1998 |
Coronary Arteriosclerosis
|
0.200 |
Biomarker
|
disease |
BEFREE |
Individuals identified at metabolic risk should undergo 10-year global risk assessment for ASCVD or coronary heart disease to determine targets of therapy for reduction of apolipoprotein B-containing lipoproteins.
|
31365087 |
2019 |
Coronary Arteriosclerosis
|
0.200 |
Biomarker
|
disease |
HPO |
|
|
|
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms in the apolipoprotein B (apoB) gene have been reported to be associated with coronary heart disease (CHD).
|
26537298 |
2015 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Genetic variations of the apolipoprotein B gene in Turkish patients with coronary artery disease.
|
16316917 |
2006 |
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 |
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 |
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 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Genetic variation of the apolipoprotein B gene in Korean patients with coronary artery disease.
|
9339897 |
1997 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms of apolipoprotein B gene in relation to coronary heart disease in Chinese Han nationality.
|
7910546 |
1994 |
Coronary Arteriosclerosis
|
0.200 |
Biomarker
|
disease |
BEFREE |
Apolipoprotein B correlates with intra-plaque necrotic core volume in stable coronary artery disease.
|
30779793 |
2019 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Elevated plasma levels of apolipoprotein B (apoB)-containing lipoproteins constitute a major risk factor for the development of coronary heart disease.
|
8533758 |
1995 |
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 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
5' ins/del and 3' VNTR polymorphisms in the apolipoprotein B gene in relation to lipids and coronary artery disease.
|
18254714 |
2008 |
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 |
Coronary Arteriosclerosis
|
0.200 |
Biomarker
|
disease |
BEFREE |
Serum triglyceride, high-density lipoprotein cholesterol, apolipoprotein B, and coronary heart disease in a Chinese population undergoing coronary angiography.
|
28506386 |
2017 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Angiotensin-converting enzyme and apolipoprotein B polymorphisms in coronary artery disease.
|
10781757 |
2000 |
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 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Integrated role of two apoliprotein E polymorphisms on apolipoprotein B levels and coronary artery disease in a biethnic population.
|
20715976 |
2010 |
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 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease.
|
30939045 |
2019 |
Coronary Arteriosclerosis
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol levels that is associated with mutations in the genes LDLR (encoding low-density lipoprotein receptor) or APOB (encoding apolipoprotein B).
|
12730697 |
2003 |