56 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 26612772 | Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B. | 2016 Jan 15 | 2 |
2 | 24495993 | The role of dietary fat on the association between dietary amino acids and serum lipid profile in European adolescents participating in the HELENA Study. | 2014 Apr | 1 |
3 | 21617182 | Glycation of LDL by methylglyoxal increases arterial atherogenicity: a possible contributor to increased risk of cardiovascular disease in diabetes. | 2011 Jul | 1 |
4 | 20068133 | Increased glycation and oxidative damage to apolipoprotein B100 of LDL cholesterol in patients with type 2 diabetes and effect of metformin. | 2010 Apr | 1 |
5 | 20173184 | Apo B100 similarities to viral proteins suggest basis for LDL-DNA binding and transfection capacity. | 2010 Jul | 2 |
6 | 20067119 | [Polymorphism in beta2 adrenergic receptor gene in Chinese population with obesity]. | 2009 Nov | 3 |
7 | 18247304 | [Analysis of beta2-adrenergic receptor gene (beta2AR) Arg16Gly polymorphism in patients with endogenous hypertriglyceridemia in Chinese population]. | 2008 Feb | 8 |
8 | 18258526 | Absence of apolipoprotein B-3500 mutation in Turkish patients with coronary and cerebrovascular atherosclerosis. | 2008 Feb | 3 |
9 | 16147996 | Decrease in pH strongly enhances binding of native, proteolyzed, lipolyzed, and oxidized low density lipoprotein particles to human aortic proteoglycans. | 2005 Nov 11 | 1 |
10 | 12551903 | A novel nontruncating APOB gene mutation, R463W, causes familial hypobetalipoproteinemia. | 2003 Apr 11 | 1 |
11 | 12890816 | Measurement of 5-hydroxy-2-aminovaleric acid as a specific marker of metal catalysed oxidation of proline and arginine residues of low density lipoprotein apolipoprotein B-100 in human atherosclerotic lesions. | 2003 Aug | 2 |
12 | 12919321 | Glycation and glycoxidation of low-density lipoproteins by glucose and low-molecular mass aldehydes. Formation of modified and oxidized particles. | 2003 Sep | 1 |
13 | 12669678 | Interaction between a common variant of the cholesteryl ester transfer protein gene and the apolipoprotein E polymorphism: effects on plasma lipids and lipoproteins in a cohort of 7-year-old children. | 2002 Dec | 2 |
14 | 11226433 | Different susceptibility to oxidation of proline and arginine residues of apolipoprotein B-100 among subspecies of low density lipoproteins. | 2001 Feb 23 | 2 |
15 | 11238294 | Compound heterozygous familial hypercholesterolemia and familial defective apolipoprotein B-100 produce exaggerated hypercholesterolemia. | 2001 Mar | 1 |
16 | 11242979 | [Screening for mutations in apolipoprotein B genes in a group of patients with hyperlipoproteinemia]. | 2001 Jan 19 | 1 |
17 | 11331277 | Binding of low density lipoproteins to lipoprotein lipase is dependent on lipids but not on apolipoprotein B. | 2001 Jul 20 | 1 |
18 | 10772915 | Measurement of 5-hydroxy-2-aminovaleric acid as a specific marker of iron-mediated oxidation of proline and arginine side-chain residues of low-density lipoprotein apolipoprotein B-100. | 2000 Apr 21 | 1 |
19 | 10090484 | Mutation analysis in 46 German families with familial hypercholesterolemia: identification of 8 new mutations. Mutations in brief no. 226. Online. | 1999 | 1 |
20 | 9521691 | Lysine and arginine residues in the N-terminal 18% of apolipoprotein B are critical for its binding to microsomal triglyceride transfer protein. | 1998 Mar 17 | 4 |
21 | 9065418 | The proteoglycan decorin links low density lipoproteins with collagen type I. | 1997 Mar 21 | 1 |
22 | 9108789 | Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries. | 1997 Apr | 2 |
23 | 9409221 | Interaction of very-low-density, intermediate-density, and low-density lipoproteins with human arterial wall proteoglycans. | 1997 Nov | 1 |
24 | 9520124 | Analysis of the mechanism of lipoprotein(a) assembly. | 1997 Nov | 1 |
25 | 8767448 | Detection of the apolipoprotein B-100 arg(3500) > gl mutation in familial defective apoB-100 by temperature-gradient gel electrophoresis. | 1996 Jun | 2 |
26 | 8843188 | A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: genetic and metabolic studies. | 1996 Oct | 2 |
27 | 7627691 | Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia. | 1995 Aug | 4 |
28 | 7627718 | Apolipoprotein B and E basic amino acid clusters influence low-density lipoprotein association with lipoprotein lipase anchored to the subendothelial matrix. | 1995 Aug | 1 |
29 | 7670940 | Two new immunogenetic polymorphisms of the apoB gene and their effect on serum lipid levels and responses to changes in dietary fat intake. | 1995 Sep | 1 |
30 | 7833952 | Screening for mutations in the exon 26 of the apolipoprotein B gene in hypercholesterolemic Finnish families by the single-strand conformation polymorphism method. | 1994 | 4 |
31 | 7969202 | Application of PCR site-directed mutagenesis for a rapid and accurate detection of mutation 3500 (Arg-->Gln) of human apolipoprotein B-100. | 1994 Jun | 1 |
32 | 8001287 | Detection of familial defective apolipoprotein B-100 among patients clinically diagnosed with heterozygous familial hypercholesterolemia in maritime Canada. | 1994 Aug | 3 |
33 | 8215738 | Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia. | 1993 Oct 25 | 2 |
34 | 8371062 | A unique haplotype of the apolipoprotein B-100 allele associated with familial defective apolipoprotein B-100 in a Chinese man discovered during a study of the prevalence of this disorder. | 1993 Jul | 1 |
35 | 8509718 | Independent mutation of arginine(3500)-->glutamine associated with familial defective apolipoprotein B-100. | 1993 May | 3 |
36 | 1453124 | Occurrence of species of low-density lipoprotein with defective clearance in patients with primary moderate hypercholesterolaemia. | 1992 Nov | 1 |
37 | 1600334 | Familial defective apolipoprotein B-100: a common cause of primary hypercholesterolemia. | 1992 Jan | 1 |
38 | 1619387 | Apolipoprotein B gene mutations affecting cholesterol levels. | 1992 Jun | 3 |
39 | 1632851 | Familial defective apolipoprotein B100: clinical characteristics of 54 cases. | 1992 Feb | 1 |
40 | 1680583 | Using mutagenic polymerase chain reaction primers to detect carriers of familial defective apolipoprotein B-100. | 1991 Oct | 2 |
41 | 1793440 | Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemia. | 1991 Aug | 4 |
42 | 1816326 | Modification of copper-catalyzed oxidation of low density lipoprotein by proteoglycans and glycosaminoglycans. | 1991 Dec | 1 |
43 | 1892487 | Familial defective apolipoprotein B-100: haplotype analysis of the arginine(3500)----glutamine mutation. | 1991 Jun | 1 |
44 | 1993649 | 13C NMR evidence that substitution of glutamine for arginine 3500 in familial defective apolipoprotein B-100 disrupts the conformation of the receptor-binding domain. | 1991 Feb 15 | 1 |
45 | 2018799 | Modifications of low-density lipoprotein induced by arterial proteoglycans and chondroitin-6-sulfate. | 1991 Apr 15 | 1 |
46 | 2067318 | Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100. | 1991 May 3 | 2 |
47 | 2169933 | Measurement of (C13)arginine incorporation into apolipoprotein B-100 in very low density lipoproteins and low density lipoproteins in normal subjects using (13C)sodium bicarbonate infusion and isotope ratio mass spectrometry. | 1990 Aug | 1 |
48 | 2226525 | Molecular basis of the association of arterial proteoglycans with low density lipoproteins: its effect on the structure of the lipoprotein particle. | 1990 Aug | 1 |
49 | 2310429 | Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases. | 1990 Jan | 1 |
50 | 21043983 | Detection of a Protein in Human Platelet Membranes which Binds Low-density Lipoproteins. | 1990 | 1 |