"G(M3) Ganglioside" 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 ganglioside present in abnormally large amounts in the brain and liver due to a deficient biosynthetic enzyme, G(M3):UDP-N-acetylgalactosaminyltransferase. Deficiency of this enzyme prevents the formation of G(M2) ganglioside from G(M3) ganglioside and is the cause of an anabolic sphingolipidosis.
| Descriptor ID |
D005679
|
| MeSH Number(s) |
D09.400.410.420.025.475.510 D10.390.470.025.475.510 D10.570.877.360.025.475.510
|
| Concept/Terms |
G(M3) Ganglioside- G(M3) Ganglioside
- Sialyl Lactosylceramide
- Lactosylceramide, Sialyl
- Ganglioside GM3
- GM3, Ganglioside
- Hematoside
- Sialyllactosylceramide
- II3NeuAcLacCer
|
Below are MeSH descriptors whose meaning is more general than "G(M3) Ganglioside".
Below are MeSH descriptors whose meaning is more specific than "G(M3) Ganglioside".
This graph shows the total number of publications written about "G(M3) Ganglioside" by people in this website by year, and whether "G(M3) Ganglioside" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "G(M3) Ganglioside" by people in Profiles.
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Targeting glycosphingolipid metabolism as a potential therapeutic approach for treating disease in female MRL/lpr lupus mice. PLoS One. 2020; 15(3):e0230499.
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A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation. Hum Mol Genet. 2014 Jan 15; 23(2):418-33.
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Characterization of two gangliosides of the paragloboside series from chicken skeletal muscle. Biochim Biophys Acta. 1980 Dec 05; 620(3):454-61.
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Serum gangliosides in cerebral astrocytoma. Ann Neurol. 1980 Nov; 8(5):534-8.