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Considering the linear structure of the LARGE modification, its incorporation of GlcA, and the fact that it is synthesized by a polymerizing enzyme that possesses dual glycosyltransferase activities, this novel polysaccharide may fit into the category of GAGs.
Its main sources are cartilage and the vessel wall where it is synthesized by chondrocytes and vascular smooth muscle cells (VSMCs), respectively [ 8, 10, 11].
It is synthesized by bacteria of the species Gluconacetobacter.
The hardware extracts the rule base once it is synthesized by the software.
It is synthesized by the Hummer's method and has oxygenated groups on the surface of the molecule.
It is synthesized by reacting guar gum with sodium monochlorate in the presence of sodium hydroxide [10, 11, 12, 13].
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It was synthesized by attaching the selectin-binding peptide.
It was synthesized by the authors of TID2008 to test metric performance for artificial images.
It was synthesized by wet precipitation method using Ca(NO3 2 · 4 H2O, Na2CO3, and Na3PO4 · 12 H2O as the initial components.
And, it was synthesized by Diels Alder reaction of dicyclopentadiene monomer and sorbic acid from blueberry as renewable resources.
This new dianhydride contains flexible phenoxy side chain and a twist biphenyl moiety and it was synthesized by the nitration of an N-methyl protected 3,3′,4,4′-biphenyltetracarboxylic 3,3′,4,4′-biphenyltetracarboxylicic nucleophilic substitution with phenoxidianhydride
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