Phosphatidylethanolamines
"Phosphatidylethanolamines" 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.
Derivatives of phosphatidic acids in which the phosphoric acid is bound in ester linkage to an ethanolamine moiety. Complete hydrolysis yields 1 mole of glycerol, phosphoric acid and ethanolamine and 2 moles of fatty acids.
| Descriptor ID |
D010714
|
| MeSH Number(s) |
D10.570.755.375.760.400.840
|
| Concept/Terms |
Phosphatidylethanolamines- Phosphatidylethanolamines
- Ethanolamineglycerophospholipids
- Cephalins
- Ethanolamine Phosphoglycerides
- Phosphoglycerides, Ethanolamine
|
Below are MeSH descriptors whose meaning is more general than "Phosphatidylethanolamines".
Below are MeSH descriptors whose meaning is more specific than "Phosphatidylethanolamines".
This graph shows the total number of publications written about "Phosphatidylethanolamines" by people in this website by year, and whether "Phosphatidylethanolamines" 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 |
|---|
| 1994 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 2 | 2 |
| 2008 | 1 | 1 | 2 |
| 2012 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Phosphatidylethanolamines" by people in Profiles.
-
Covarrubias G, Moon TJ, Loutrianakis G, Sims HM, Umapathy MP, Lorkowski ME, Bielecki PA, Wiese ML, Atukorale PU, Karathanasis E. Comparison of the uptake of untargeted and targeted immunostimulatory nanoparticles by immune cells in the microenvironment of metastatic breast cancer. J Mater Chem B. 2022 01 05; 10(2):224-235.
-
Yao H, Sun L, Li J, Zhou X, Li R, Shao R, Zhang Y, Li L. A Novel Therapeutic siRNA Nanoparticle Designed for Dual-Targeting CD44 and Gli1 of Gastric Cancer Stem Cells. Int J Nanomedicine. 2020; 15:7013-7034.
-
Garle AL, Budhlall BM. PEG Bottle Brush Copolymers as Antimicrobial Mimics: Role of Entropic Templating in Membrane Lysis. Langmuir. 2019 03 05; 35(9):3372-3382.
-
Samdani GK, McClements DJ, Decker EA. Impact of Phospholipids and Tocopherols on the Oxidative Stability of Soybean Oil-in-Water Emulsions. J Agric Food Chem. 2018 Apr 18; 66(15):3939-3948.
-
Cui L, McClements DJ, Decker EA. Impact of phosphatidylethanolamine on the antioxidant activity of a-tocopherol and trolox in bulk oil. J Agric Food Chem. 2015 Apr 01; 63(12):3288-94.
-
Cook PL, Vanderhill JL, Cook AE, Van Norstrand DW, Gordon MT, Harper PE. Light scattering measurement and Avrami analysis of the lamellar to inverse hexagonal phase transition kinetics of the lipid DEPE. Chem Phys Lipids. 2012 Apr; 165(3):270-6.
-
Yuan C, Chen M, Covey DF, Johnston LJ, Treistman SN. Cholesterol tuning of BK ethanol response is enantioselective, and is a function of accompanying lipids. PLoS One. 2011; 6(11):e27572.
-
Yang L, Gordon VD, Trinkle DR, Schmidt NW, Davis MA, DeVries C, Som A, Cronan JE, Tew GN, Wong GC. Mechanism of a prototypical synthetic membrane-active antimicrobial: Efficient hole-punching via interaction with negative intrinsic curvature lipids. Proc Natl Acad Sci U S A. 2008 Dec 30; 105(52):20595-600.
-
Fleming E, Maharaj NP, Chen JL, Nelson RB, Elmore DE. Effect of lipid composition on buforin II structure and membrane entry. Proteins. 2008 Nov 01; 73(2):480-91.
-
Yang L, Gordon VD, Mishra A, Som A, Purdy KR, Davis MA, Tew GN, Wong GC. Synthetic antimicrobial oligomers induce a composition-dependent topological transition in membranes. J Am Chem Soc. 2007 Oct 10; 129(40):12141-7.