"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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1995 | 2 | 0 | 2 |
1996 | 3 | 1 | 4 |
1999 | 1 | 2 | 3 |
2000 | 5 | 2 | 7 |
2001 | 4 | 3 | 7 |
2002 | 5 | 2 | 7 |
2003 | 3 | 0 | 3 |
2004 | 4 | 2 | 6 |
2005 | 9 | 1 | 10 |
2006 | 2 | 3 | 5 |
2007 | 1 | 1 | 2 |
2008 | 1 | 4 | 5 |
2009 | 3 | 8 | 11 |
2010 | 3 | 4 | 7 |
2011 | 2 | 5 | 7 |
2012 | 2 | 5 | 7 |
2013 | 4 | 10 | 14 |
2014 | 0 | 7 | 7 |
2015 | 1 | 5 | 6 |
2016 | 0 | 5 | 5 |
2017 | 1 | 5 | 6 |
2018 | 2 | 2 | 4 |
2020 | 0 | 1 | 1 |
2021 | 1 | 4 | 5 |
2022 | 0 | 1 | 1 |
2023 | 0 | 4 | 4 |
2024 | 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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Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Project. Alzheimers Dement. 2024 Dec; 20(12):8470-8483.
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Impact of Apolipoprotein E Genotype on Neurocognitive Function in Patients With Brain Metastases: An Analysis of NRG Oncology's RTOG 0614. Int J Radiat Oncol Biol Phys. 2024 Jul 01; 119(3):846-857.
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Advanced photon counting CT imaging pipeline for cardiac phenotyping of apolipoprotein E mouse models. PLoS One. 2023; 18(10):e0291733.
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Large-scale whole exome sequencing studies identify two genes,CTSL and APOE, associated with lung cancer. PLoS Genet. 2023 09; 19(9):e1010902.
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Behavioral and biologic characteristics of cancer-related cognitive impairment biotypes. Brain Imaging Behav. 2023 Jun; 17(3):320-328.
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Mitochondria-targeted esculetin mitigates atherosclerosis in the setting of aging via the modulation of SIRT1-mediated vascular cell senescence and mitochondrial function in Apoe-/- mice. Atherosclerosis. 2022 09; 356:28-40.
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Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease. JAMA Neurol. 2022 07 01; 79(7):652-663.
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Adipocyte-Derived Serum Amyloid A Promotes Angiotensin II-Induced Abdominal Aortic Aneurysms in Obese C57BL/6J Mice. Arterioscler Thromb Vasc Biol. 2022 05; 42(5):632-643.
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Apolipoprotein E Polymorphism, Cardiac Remodeling, and Heart Failure in the ARIC Study. J Card Fail. 2022 07; 28(7):1128-1136.
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Apolipoprotein E Proteinopathy Is a Major Dementia-Associated Pathologic Biomarker in Individuals with or without the APOE Epsilon 4 Allele. Am J Pathol. 2022 03; 192(3):564-578.