"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,
click here.
Year | Major Topic | Minor Topic | Total |
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1993 | 1 | 0 | 1 |
1994 | 2 | 0 | 2 |
1995 | 1 | 0 | 1 |
1996 | 4 | 1 | 5 |
1997 | 4 | 1 | 5 |
1998 | 3 | 2 | 5 |
1999 | 2 | 1 | 3 |
2000 | 4 | 2 | 6 |
2001 | 2 | 2 | 4 |
2002 | 2 | 1 | 3 |
2003 | 2 | 1 | 3 |
2004 | 2 | 2 | 4 |
2005 | 1 | 2 | 3 |
2006 | 2 | 0 | 2 |
2007 | 0 | 1 | 1 |
2008 | 1 | 3 | 4 |
2009 | 1 | 1 | 2 |
2010 | 3 | 1 | 4 |
2011 | 1 | 1 | 2 |
2012 | 3 | 0 | 3 |
2013 | 2 | 1 | 3 |
2014 | 1 | 4 | 5 |
2015 | 3 | 1 | 4 |
2016 | 2 | 0 | 2 |
2018 | 1 | 4 | 5 |
2021 | 0 | 1 | 1 |
2022 | 1 | 0 | 1 |
2023 | 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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ApoE isoform- and microbiota-dependent progression of neurodegeneration in a mouse model of tauopathy. Science. 2023 01 13; 379(6628):eadd1236.
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Single-cell RNA sequencing reveals time- and sex-specific responses of mouse spinal cord microglia to peripheral nerve injury and links ApoE to chronic pain. Nat Commun. 2022 02 11; 13(1):843.
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Absence of coding somatic single nucleotide variants within well-known candidate genes in late-onset sporadic Alzheimer's Disease based on the analysis of multi-omics data. Neurobiol Aging. 2021 12; 108:207-209.
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Apoprotein E and Reverse Cholesterol Transport. Int J Mol Sci. 2018 Nov 06; 19(11).
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Diet, Microbes, and Murine Atherosclerosis. Arterioscler Thromb Vasc Biol. 2018 10; 38(10):2269-2271.
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Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathol. 2018 12; 136(6):857-872.
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Severe hypoglycaemia, mild cognitive impairment, dementia and brain volumes in older adults with type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) cohort study. Diabetologia. 2018 09; 61(9):1956-1965.
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Computer-aided diagnosis with radiogenomics: analysis of the relationship between genotype and morphological changes of the brain magnetic resonance images. Radiol Phys Technol. 2018 Sep; 11(3):265-273.
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Do the Apoe-/- and Ldlr-/- Mice Yield the Same Insight on Atherogenesis? Arterioscler Thromb Vasc Biol. 2016 09; 36(9):1734-41.
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ApoE knockout and knockin mice: the history of their contribution to the understanding of atherogenesis. J Lipid Res. 2016 05; 57(5):758-66.