Arginine

apolipoprotein B ; Homo sapiens







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