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1 e may be similar to that described for human sorbitol dehydrogenase.
2 orted in the human sperm fibrous sheath, and sorbitol dehydrogenase.
3 novirus infection was marked by elevation of sorbitol dehydrogenase, a marker for hepatocyte necrosis
5 acological inhibition of aldose reductase or sorbitol dehydrogenase blocked JAK2 and STAT5 activation
6 rbitol, D-glucose and L-lactate with using D-sorbitol dehydrogenase, D-glucose dehydrogenase and L-la
7 c from metallothionein (MT) to zinc-depleted sorbitol dehydrogenase (EC 1.1.1.14) in vitro has been u
8 mined the kinetic parameters of mannitol and sorbitol dehydrogenases encoded in the yeast genome, sho
10 hances the transfer of zinc to zinc-depleted sorbitol dehydrogenase, increases the rate of thiol-disu
11 and pharmacology efforts to provide a potent sorbitol dehydrogenase inhibitor (SDI) as a tool to prob
15 ibed to be a potential negative regulator of sorbitol dehydrogenase (SDH) in hippocampal cells, we ex
16 disclosed hypothesis centered on the role of sorbitol dehydrogenase (SDH) in the second step of the p
18 itol (3-FS) and that incubation of dog liver sorbitol dehydrogenase (SDH) with 3-FS results in the fo
19 is a better zinc donor toward zinc-depleted sorbitol dehydrogenase than is the isolated alpha-domain
21 led and found to be a selective inhibitor of sorbitol dehydrogenase, with excellent pharmacodynamic/p
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