Results 1 to 10 of about 77,676 (146)
Structure of apolipoprotein B-100 in low density lipoproteins [PDF]
There is general consensus that amphipathic α-helices and β sheets represent the major lipid-associating motifs of apolipoprotein (apo)B-100. In this review, we examine the existing experimental and computational evidence for the pentapartite domain ...
Jere P. Segrest +3 more
doaj +3 more sources
Mini-Review: Immunogenic epitopes in apolipoprotein B-100 for atheroprotective immunization [PDF]
Here, we provide a concise overview of recent developments in the identification of immunogenic epitopes in human apolipoprotein B-100 for immunization against atherosclerotic cardiovascular disease.
Norbert Gerdes +3 more
doaj +2 more sources
High prevalence of familial defective apolipoprotein B-100 in Switzerland.
Familial defective apolipoprotein B-100 (FDB) is caused by a single G-to-A substitution at nucleotide 10,708 leading to an arginine to glutamine change at amino acid 3,500 of the apolipoprotein B-100 and thus, a reduced binding of the apolipoprotein B to
A R Miserez +3 more
doaj +4 more sources
Rapid Diagnosis of Familial Defective Apolipoprotein B-100 [PDF]
A method is described for the rapid, economic and non-radioactive examination of DNA samples from hypercholesterolaemic patients for familial defective apolipoprotein B-100, using a modified polymerase chain reaction (PCR) protocol and restriction enzyme isoform genotyping.
Geisel, J. +3 more
openaire +3 more sources
Lipoprotein [a] (Lp[a]) contains equimolar amounts of apoB-100 and apolipoprotein [a] (apo[a]). Both proteins are amenable to degradation in vivo by mechanisms yet to be clearly defined.
Celina Edelstein +3 more
doaj +1 more source
Familial defective apolipoprotein B-100 is a genetic disorder of apolipoprotein B-100 that causes moderate to severe hypercholesterolemia. A single amino acid mutation in apolipoprotein B diminishes the ability of low density lipoproteins to bind to the ...
TL Innerarity +9 more
doaj +1 more source
Apolipoprotein[a] (apo[a]) is a large disulfide linked glycoprotein synthesized by hepatocytes. We have examined the role of disulfide bond formation in the processing of apo[a] using human and rat hepatoma cells expressing apo[a] isoforms containing ...
Fatiha Nassir +2 more
doaj +1 more source
Human Placenta Secretes Apolipoprotein B-100-containing Lipoproteins [PDF]
Supply of lipids from the mother is essential for fetal growth and development. In mice, disruption of yolk sac cell secretion of apolipoprotein (apo) B-containing lipoproteins results in embryonic lethality. In humans, the yolk sac is vestigial. Nutritional functions are instead established very early during pregnancy in the placenta.
Munk-Madsen, Eva +4 more
openaire +3 more sources
PPARα deficiency increases secretion and serum levels of apolipoprotein B-containing lipoproteins
This study investigates the importance of peroxisome proliferator activated receptor α (PPARα) for serum apolipoprotein B (apoB) levels and hepatic secretion of apoB-containing lipoproteins.
Daniel Lindén +3 more
doaj +1 more source
Degradation of human apolipoprotein B‐100 by apolipoprotein(a)
Human plasma low density lipoproteine (LDL) contain a very high molecular weight protein termed apoB‐100 (M r = 550,000). In many samples of LDL, minor components designated as apoB‐74 (M r = 407,000) and apoB‐26 (M r = 145,000) are present. It has been shown that they can arise as a result of proteolytic degradation of apoB‐100.
Chulkova, T.M., Tertov, V.V.
openaire +2 more sources

