"Apolipoproteins E" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A class of protein components which can be found in several lipoproteins including HIGH-DENSITY LIPOPROTEINS; VERY-LOW-DENSITY LIPOPROTEINS; and CHYLOMICRONS. Synthesized in most organs, Apo E is important in the global transport of lipids and cholesterol throughout the body. Apo E is also a ligand for LDL receptors (RECEPTORS, LDL) that mediates the binding, internalization, and catabolism of lipoprotein particles in cells. There are several allelic isoforms (such as E2, E3, and E4). Deficiency or defects in Apo E are causes of HYPERLIPOPROTEINEMIA TYPE III.
Descriptor ID |
D001057
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MeSH Number(s) |
D10.532.091.500 D12.776.070.400.500 D12.776.521.120.500
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Apolipoproteins E".
Below are MeSH descriptors whose meaning is more specific than "Apolipoproteins E".
This graph shows the total number of publications written about "Apolipoproteins E" by people in this website by year, and whether "Apolipoproteins E" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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1994 | 0 | 1 | 1 |
1995 | 3 | 0 | 3 |
1996 | 3 | 0 | 3 |
1997 | 2 | 1 | 3 |
1998 | 2 | 0 | 2 |
1999 | 1 | 1 | 2 |
2000 | 1 | 0 | 1 |
2001 | 1 | 0 | 1 |
2002 | 2 | 0 | 2 |
2003 | 3 | 1 | 4 |
2004 | 3 | 0 | 3 |
2006 | 1 | 1 | 2 |
2008 | 1 | 1 | 2 |
2011 | 1 | 1 | 2 |
2014 | 1 | 0 | 1 |
2015 | 0 | 1 | 1 |
2018 | 1 | 1 | 2 |
2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Apolipoproteins E" by people in Profiles.
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Comparative analysis of arterial compliance in mice genetically null for cathepsins K, L, or S. J Biomech. 2022 10; 143:111266.
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Alzheimer's Disease Markers in Aged ApoE-PON1 Deficient Mice. J Alzheimers Dis. 2019; 67(4):1353-1365.
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Acute Loss of Apolipoprotein E Triggers an Autoimmune Response That Accelerates Atherosclerosis. Arterioscler Thromb Vasc Biol. 2018 08; 38(8):e145-e158.
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Defective cholesterol metabolism in haematopoietic stem cells promotes monocyte-driven atherosclerosis in rheumatoid arthritis. Eur Heart J. 2018 06 14; 39(23):2158-2167.
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PDGFRß signalling regulates local inflammation and synergizes with hypercholesterolaemia to promote atherosclerosis. Nat Commun. 2015 Jul 17; 6:7770.
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Influence of domain stability on the properties of human apolipoprotein E3 and E4 and mouse apolipoprotein E. Biochemistry. 2014 Jun 24; 53(24):4025-33.
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Recurrent lobar intracerebral hemorrhage in Tangier disease. J Stroke Cerebrovasc Dis. 2012 Nov; 21(8):909.e5-6.
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Deficiency of a transcriptional regulator, inhibitor of differentiation 3, induces glomerulonephritis in apolipoprotein E-deficient mice: a model linking hyperlipidemia and renal disease. Am J Pathol. 2011 Aug; 179(2):651-60.
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Role of the N- and C-terminal domains in binding of apolipoprotein E isoforms to heparan sulfate and dermatan sulfate: a surface plasmon resonance study. Biochemistry. 2008 Jun 24; 47(25):6702-10.
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P-selectin glycoprotein ligand-1 is highly expressed on Ly-6Chi monocytes and a major determinant for Ly-6Chi monocyte recruitment to sites of atherosclerosis in mice. Circulation. 2008 Jun 24; 117(25):3227-37.