"Hexosamines" 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.
No definition found.
| Descriptor ID |
D006595
|
| MeSH Number(s) |
D09.067.342
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hexosamines".
Below are MeSH descriptors whose meaning is more specific than "Hexosamines".
This graph shows the total number of publications written about "Hexosamines" by people in this website by year, and whether "Hexosamines" 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 |
|---|
| 2019 | 0 | 1 | 1 |
| 2020 | 1 | 1 | 2 |
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Below are the most recent publications written about "Hexosamines" by people in Profiles.
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The hexosamine biosynthesis pathway is a targetable liability in KRAS/LKB1 mutant lung cancer. Nat Metab. 2020 12; 2(12):1401-1412.
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Excess Protein O-GlcNAcylation Links Metabolic Derangements to Right Ventricular Dysfunction in Pulmonary Arterial Hypertension. Int J Mol Sci. 2020 Oct 01; 21(19).
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O-GlcNAcylation Enhances Double-Strand Break Repair, Promotes Cancer Cell Proliferation, and Prevents Therapy-Induced Senescence in Irradiated Tumors. Mol Cancer Res. 2019 06; 17(6):1338-1350.
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Multiple enzymatic activities of the murein hydrolase from staphylococcal phage phi11. Identification of a D-alanyl-glycine endopeptidase activity. J Biol Chem. 1999 May 28; 274(22):15847-56.
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Probucol normalizes cholesteryl ester transfer in IDDM. Diabetes Care. 1995 Oct; 18(10):1341-6.
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Purification and characterization of an incompletely glycosylated form of human chorionic gonadotropin from human placenta. Endocrinology. 1988 Aug; 123(2):795-803.
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Preparation of carcinoembryonic antigen (CEA) containing significantly increased amounts of galactose and galactosamine. Prep Biochem. 1975; 5(4):359-74.
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Excess lipofuscin accumulation in constitutional hepatic dysfunction (Gilbert's syndrome). Light and electron microscopic observations. Arch Pathol. 1971 Jan; 91(1):41-7.