"Membrane Microdomains" 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.
Detergent-insoluble CELL MEMBRANE components. They are enriched in SPHINGOLIPIDS and CHOLESTEROL and clustered with glycosyl-phosphatidylinositol (GPI)-anchored proteins.
Descriptor ID |
D021962
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MeSH Number(s) |
A11.284.149.165.570
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Concept/Terms |
Membrane Microdomains- Membrane Microdomains
- Membrane Microdomain
- Microdomain, Membrane
- Microdomains, Membrane
- Sphingolipid-Cholesterol Rafts
- Sphingolipid Cholesterol Rafts
- Sphingolipid-Cholesterol Raft
- Sphingolipid Microdomains
- Microdomain, Sphingolipid
- Microdomains, Sphingolipid
- Sphingolipid Microdomain
- Lipid Rafts, Cell Membrane
|
Below are MeSH descriptors whose meaning is more general than "Membrane Microdomains".
Below are MeSH descriptors whose meaning is more specific than "Membrane Microdomains".
This graph shows the total number of publications written about "Membrane Microdomains" by people in this website by year, and whether "Membrane Microdomains" 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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2002 | 1 | 1 | 2 |
2003 | 1 | 3 | 4 |
2004 | 1 | 3 | 4 |
2005 | 1 | 1 | 2 |
2006 | 1 | 0 | 1 |
2007 | 3 | 3 | 6 |
2008 | 3 | 1 | 4 |
2009 | 3 | 2 | 5 |
2010 | 3 | 2 | 5 |
2011 | 1 | 1 | 2 |
2012 | 5 | 4 | 9 |
2013 | 2 | 1 | 3 |
2015 | 0 | 1 | 1 |
2016 | 2 | 3 | 5 |
2017 | 0 | 1 | 1 |
2018 | 1 | 2 | 3 |
2020 | 1 | 0 | 1 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Membrane Microdomains" by people in Profiles.
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AIBP regulates TRPV1 activation in chemotherapy-induced peripheral neuropathy by controlling lipid raft dynamics and proximity to TLR4 in dorsal root ganglion neurons. Pain. 2023 06 01; 164(6):e274-e285.
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Caveolin and lipid domains-close companions in managing cellular pathways. Cancer Metastasis Rev. 2020 06; 39(2):341-342.
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Bile acids target proteolipid nano-assemblies of EGFR and phosphatidic acid in the plasma membrane for stimulation of MAPK signaling. PLoS One. 2018; 13(8):e0198983.
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The tumour suppressor OPCML promotes AXL inactivation by the phosphatase PTPRG in ovarian cancer. EMBO Rep. 2018 08; 19(8).
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Cell entry of a host-targeting protein of oomycetes requires gp96. Nat Commun. 2018 06 14; 9(1):2347.
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Endothelial NLRP3 inflammasome activation and arterial neointima formation associated with acid sphingomyelinase during hypercholesterolemia. Redox Biol. 2017 10; 13:336-344.
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The Glycosylphosphatidylinositol-Anchored Variable Region of Llama Heavy Chain-Only Antibody JM4 Efficiently Blocks both Cell-Free and T Cell-T Cell Transmission of Human Immunodeficiency Virus Type 1. J Virol. 2016 Dec 01; 90(23):10642-10659.
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Effects of membrane properties on the binding activities of the HN and HC heavy-chain domains of botulinum neurotoxin A. Biochim Biophys Acta. 2016 12; 1864(12):1678-1685.
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Occupancy of human EPCR by protein C induces ?-arrestin-2 biased PAR1 signaling by both APC and thrombin. Blood. 2016 10 06; 128(14):1884-1893.
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Motility and stem cell properties induced by the epithelial-mesenchymal transition require destabilization of lipid rafts. Oncotarget. 2016 Aug 09; 7(32):51553-51568.