1986
DOI: 10.1016/s0021-9258(18)69248-8
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The complete cDNA and amino acid sequence of human apolipoprotein B-100.

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1989
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Cited by 207 publications
(31 citation statements)
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“…Moreover, ApoB derived peptides have been already used in vaccine preparations to treat atherosclerosis [23]. Here, we applied our in silico analysis method to a human ApoB isoform [26,27] and identified a novel ''cryptic" HDP (region 887-922). To the best of our knowledge, this ApoB region has never been analysed before, since all the previously identified biologically active ApoB peptides are far from the high scoring region identified in the present work [22,23].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Moreover, ApoB derived peptides have been already used in vaccine preparations to treat atherosclerosis [23]. Here, we applied our in silico analysis method to a human ApoB isoform [26,27] and identified a novel ''cryptic" HDP (region 887-922). To the best of our knowledge, this ApoB region has never been analysed before, since all the previously identified biologically active ApoB peptides are far from the high scoring region identified in the present work [22,23].…”
Section: Discussionmentioning
confidence: 99%
“…On the basis of the interesting results obtained in the case of human ApoE, we applied our in silico analysis method to a human Apolipoprotein B (ApoB) isoform [26,27]. In Fig.…”
Section: Introductionmentioning
confidence: 99%
“…One such therapeutic approach is to block or reduce binding of ApoB to HSPGs in the subendothelial spaces. ApoB exists in two isoforms on lipoprotein particles, ApoB-48 and ApoB-100, both of which are encoded by the same gene and play a crucial role in lipid homeostasis [221]. ApoB-100 is a very large protein containing 4536 amino acids [222].…”
Section: Remnant Particles and Their Role In Atherosclerosismentioning
confidence: 99%
“…ApoB aids in the assembly, secretion, transport, and cellular uptake of lipoproteins. In mammals, ApoB is expressed in the liver and small intestine in two different isoforms, ApoB100 and ApoB48, which represent the full-length and N-terminal 48% portion of the full-length protein, respectively (Chen et al, 1988;Chen et al, 1987;Chen et al, 1986;Hussain et al, 2005;Hussain et al, 1996;Powell et al, 1987). Not surprisingly, there is a direct correlation between circulating ApoB and CAD: Higher levels cause CAD, whereas lower levels are associated with normal homeostasis or, if severely limited, with hypobetalipoproteinemia, which presents as delayed development, hepatomegaly, steatorrhea, and cytolysis (Jang et al, 2020;Welty, 2020).…”
Section: Introductionmentioning
confidence: 99%