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 GeneticVariation disease BEFREE Association of polymorphisms of the apolipoprotein B gene with coronary heart disease in Han Chinese. 8546754 1995
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 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 Interaction between SREBP-1a and APOB polymorphisms influences total and low-density lipoprotein cholesterol levels in patients with coronary artery disease. 12752570 2003
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Lipoprotein(a) and the Apolipoprotein B/A1 Ratio Independently Associate With Surgery for Aortic Stenosis Only in Patients With Concomitant Coronary Artery Disease. 29246959 2017
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 The plasma level of apolipoprotein B (apoB) is among the strongest risk factors for coronary artery disease. 24201112 2013
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Evolution of the apolipoprotein B gene and coronary artery disease: a study in low and high risk Asians. 10738520 1999
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease BEFREE Association between apolipoprotein B EcoRI polymorphisms and coronary heart disease : A meta-analysis. 27637205 2016
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
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 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
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Mutations in the apolipoprotein B-100 gene (APOB) can result in a phenotype that is clinically indistinguishable from familial hypercholesterolemia, and mutations in this gene have also been shown to be associated with coronary heart disease. 15321838 2004
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Since the apoB plasma level was not only associated with the apoB SP Ins/Del gene variation but also to the extent of coronary artery disease (P <0.0001), individuals with an InsIns genotype and without CAD had the lowest and subjects with a DelDel genotype and triple vessel disease the highest apoB plasma levels (P <0.0001). 9863550 1998
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 Single effects of apolipoprotein B, (a), and E polymorphisms and interaction between plasminogen activator inhibitor-1 and apolipoprotein(a) genotypes and the risk of coronary artery disease in Czech male caucasians. 10720441 2000
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 Biomarker disease BEFREE Postprandial triglycerides, TG-rich lipoprotein triglycerides, retinyl palmitate and apolipoprotein B48 to B100 ratio were measured before (following a 12-hour fasting period) and after a fat-tolerance test meal in a middle-aged, biracial subcohort without CVD (coronary heart disease (CHD) or stroke) from the community-based Atherosclerosis Risk in Communities (ARIC) Study in 1990-1993. 28191321 2017
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Apolipoprotein B gene 3'VNTR polymorphism: association with plasma lipids and coronary heart disease in Han Chinese. 17032131 2006
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE The XbaI, EcoRI and the signal peptide insertion/deletion (I/D) polymorphic sites of APOB gene, the CfoI polymorphic site of apolipoprotein E gene (APOE), and the insertion/deletion polymorphism of angiotensin I-converting enzyme (ACE) gene were studied using polymerase chain reaction (PCR) in 55 postmenopausal women with coronary artery disease (CAD) and in 119 control women of equivalent age. 9298741 1997
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 Association between the Xba I polymorphism of APOB gene and plasma lipid level in Mexican patients with coronary artery disease. 22507620 2012
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.200 GeneticVariation disease BEFREE Effect of SORT1, APOB and APOE polymorphisms on LDL-C and coronary heart disease in Pakistani subjects and their comparison with Northwick Park Heart Study II. 27112212 2016
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 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 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 The X-X-/E+E+ genotype of the XbaI/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample. 12640502 2003