N-Acetylgalactosaminyltransferases
"N-Acetylgalactosaminyltransferases" 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.
Enzymes that catalyze the transfer of N-acetylgalactosamine from a nucleoside diphosphate N-acetylgalactosamine to an acceptor molecule which is frequently another carbohydrate. EC 2.4.1.-.
Descriptor ID |
D017350
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MeSH Number(s) |
D08.811.913.400.100.200
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Concept/Terms |
N-Acetylgalactosaminyltransferases- N-Acetylgalactosaminyltransferases
- N Acetylgalactosaminyltransferases
- N-Acetylgalactosamine Transferases
- N Acetylgalactosamine Transferases
- Transferases, N-Acetylgalactosamine
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Below are MeSH descriptors whose meaning is more general than "N-Acetylgalactosaminyltransferases".
Below are MeSH descriptors whose meaning is more specific than "N-Acetylgalactosaminyltransferases".
This graph shows the total number of publications written about "N-Acetylgalactosaminyltransferases" by people in this website by year, and whether "N-Acetylgalactosaminyltransferases" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2004 | 2 | 0 | 2 |
2005 | 1 | 1 | 2 |
2006 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2015 | 0 | 1 | 1 |
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Below are the most recent publications written about "N-Acetylgalactosaminyltransferases" by people in Profiles.
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Yoshikawa M, Go S, Suzuki S, Suzuki A, Katori Y, Morlet T, Gottlieb SM, Fujiwara M, Iwasaki K, Strauss KA, Inokuchi J. Ganglioside GM3 is essential for the structural integrity and function of cochlear hair cells. Hum Mol Genet. 2015 May 15; 24(10):2796-807.
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Chefetz I, Kohno K, Izumi H, Uitto J, Richard G, Sprecher E. GALNT3, a gene associated with hyperphosphatemic familial tumoral calcinosis, is transcriptionally regulated by extracellular phosphate and modulates matrix metalloproteinase activity. Biochim Biophys Acta. 2009 Jan; 1792(1):61-7.
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Uliana AS, Giraudo CG, Maccioni HJ. Cytoplasmic tails of SialT2 and GalNAcT impose their respective proximal and distal Golgi localization. Traffic. 2006 May; 7(5):604-12.
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Chefetz I, Heller R, Galli-Tsinopoulou A, Richard G, Wollnik B, Indelman M, Koerber F, Topaz O, Bergman R, Sprecher E, Schoenau E. A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification. Hum Genet. 2005 Nov; 118(2):261-6.
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Topaz O, Bergman R, Mandel U, Maor G, Goldberg R, Richard G, Sprecher E. Absence of intraepidermal glycosyltransferase ppGalNac-T3 expression in familial tumoral calcinosis. Am J Dermatopathol. 2005 Jun; 27(3):211-5.
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Frishberg Y, Topaz O, Bergman R, Behar D, Fisher D, Gordon D, Richard G, Sprecher E. Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders. J Mol Med (Berl). 2005 Jan; 83(1):33-8.
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Topaz O, Shurman DL, Bergman R, Indelman M, Ratajczak P, Mizrachi M, Khamaysi Z, Behar D, Petronius D, Friedman V, Zelikovic I, Raimer S, Metzker A, Richard G, Sprecher E. Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis. Nat Genet. 2004 Jun; 36(6):579-81.