Zobrazeno 1 - 10
of 12
pro vyhledávání: '"K. S. Arnold"'
Publikováno v:
Journal of Lipid Research, Vol 35, Iss 8, Pp 1469-1476 (1994)
Familial defective apolipoprotein B-100 (FDB) is a genetic disorder apparently caused by a single amino acid substitution (Arg3500–>Gln) that disrupts the binding of low density lipoproteins (LDL) to the LDL receptor. The plasma of FDB heterozygote
Externí odkaz:
https://doaj.org/article/b80692fa64d2496c8a5b1a82a01aefe9
Publikováno v:
Journal of Lipid Research, Vol 28, Iss 12, Pp 1410-1423 (1987)
Apolipoprotein (apo) B-100, the protein constituent of low density lipoproteins (LDL), is the determinant responsible for LDL binding to the apoB,E(LDL) receptor on cells. The current study was designed to identify the region(s) of apoB-100 that inte
Externí odkaz:
https://doaj.org/article/87c96d93b6d6489493836c1589be0789
Publikováno v:
Scopus-Elsevier
Familial defective apoB-100 is a genetic mutation that is characterized by abnormal low density lipoprotein (LDL) and moderate hypercholesterolemia. Heterozygotes for this disorder possess two populations of LDL. One has normal receptor binding, and
Akademický článek
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Publikováno v:
The Journal of biological chemistry. 274(49)
Apolipoprotein (apo) B mRNA editing is the deamination of C(6666) to uridine, which changes the codon at position 2153 from a genomically encoded glutamine (CAA) to an in-frame stop codon (UAA). The apoB mRNA-editing enzyme complex recognizes the edi
Publikováno v:
Journal of lipid research. 39(6)
Both apolipoprotein (apo) E2 and apoE-Leiden (tandem repeat of amino acids 121-127) are associated with type III hyperlipoproteinemia and bind defectively to low density lipoprotein receptors. Removing the carboxyl terminus of both variants (residues
Publikováno v:
The Journal of biological chemistry. 272(41)
The low density lipoprotein (LDL) receptor plays a key role in cholesterol homeostasis, mediating cellular uptake of lipoprotein particles by high affinity binding to its ligands, apolipoprotein (apo) B-100 and apoE. The ligand-binding domain of the
Publikováno v:
The Journal of biological chemistry. 266(5)
Familial defective apoB-100 is a genetic mutation that is characterized by abnormal low density lipoprotein (LDL) and moderate hypercholesterolemia. Heterozygotes for this disorder possess two populations of LDL. One has normal receptor binding, and
Publikováno v:
Australian Veterinary Journal. 60:148-148
Publikováno v:
Arteriosclerosis: An Official Journal of the American Heart Association, Inc.. 9:501-510
Watanabe Heritable Hyperlipidemic (WHHL) rabbits are an important animal model used to study the effects of defective low density lipoprotein (LDL) receptors on lipoprotein metabolism. In the present study, the receptor-mediated catabolism of apolipo