Search results

''[[hypomethylating agent]]'' ([[Azacitidine]], [[Decitabine]]) | group3 = [[Crosslinking of DNA]]<BR>([[cell-cycle nonspecific antineoplastic agents|CCNS]])

...rization with multifunctional (3 or more) [[crosslinker]] or by subsequent crosslinking of a linear or branched polymer. They form insoluble materials which swell ...er such as [[glycerin]], [[trimethylol propane]]. Introduction of covalent crosslinking improves in creep, increase in recovery temperature and recovery window.<re

...ple is the reaction with silane to improve its dispersion in polyethylene. Crosslinking or bridging of the –OH groups changes the structure into a network while ...of polymers generate radicals and/or ions that often lead to cleavage and crosslinking. Oxidation also occurs, complicating the situation, since exposure to light

...are on opposite sides of an [[Interface (chemistry)|interface]]. Unlike [[crosslinking]], crossbridging does not join two [[polymer|polymer chains]] to form a sin

...ith multifuctional (tri or higher functional) crosslinker or by subsequent crosslinking of a linear or branched polymer. They form insoluble materials which swell ...trimethylol propane. According to Buckley et al., introduction of covalent crosslinking improves in creep, increase in recovery temperature and recovery window. <r

...r uses include its conversion to specialty [[azo dye]]s and [[crosslinking agent]]s. ...of near-ultraviolet radiation killing of mammalian cells by the sunscreen agent para-aminobenzoic acid