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1 orted in the human sperm fibrous sheath, and sorbitol dehydrogenase.
2 e may be similar to that described for human sorbitol dehydrogenase.
3 levels, and inhibiting the expression of the sorbitol dehydrogenase-1 SODH-1, a crucial sugar metabol
4 novirus infection was marked by elevation of sorbitol dehydrogenase, a marker for hepatocyte necrosis
5                                              Sorbitol dehydrogenase activity was reduced in silenced
6 acological inhibition of aldose reductase or sorbitol dehydrogenase blocked JAK2 and STAT5 activation
7 rbitol, D-glucose and L-lactate with using D-sorbitol dehydrogenase, D-glucose dehydrogenase and L-la
8 c from metallothionein (MT) to zinc-depleted sorbitol dehydrogenase (EC 1.1.1.14) in vitro has been u
9 mined the kinetic parameters of mannitol and sorbitol dehydrogenases encoded in the yeast genome, sho
10 -fetoprotein, arginase-1, osteopontin (OPN), sorbitol dehydrogenase, fatty acid binding protein, cadh
11    Here we report biallelic mutations in the sorbitol dehydrogenase gene (SORD) as the most frequent
12         The presence of aldose reductase and sorbitol dehydrogenase in these cells was examined by no
13 hances the transfer of zinc to zinc-depleted sorbitol dehydrogenase, increases the rate of thiol-disu
14 and pharmacology efforts to provide a potent sorbitol dehydrogenase inhibitor (SDI) as a tool to prob
15       Optimization of a previously disclosed sorbitol dehydrogenase inhibitor (SDI, II) for potency a
16                       We report here a novel sorbitol dehydrogenase inhibitor, 16, that shows very hi
17                   A 1:1 molar ratio of MT to sorbitol dehydrogenase is required for full reactivation
18 ntion of DR have been elusive because of low sorbitol dehydrogenase levels in the retina and inadequa
19 ss-of-function changes in the encoded enzyme sorbitol dehydrogenase result in abnormally high sorbito
20 ibed to be a potential negative regulator of sorbitol dehydrogenase (SDH) in hippocampal cells, we ex
21 disclosed hypothesis centered on the role of sorbitol dehydrogenase (SDH) in the second step of the p
22                                              Sorbitol dehydrogenase (SDH) is a polyol pathway enzyme
23 itol (3-FS) and that incubation of dog liver sorbitol dehydrogenase (SDH) with 3-FS results in the fo
24  Biallelic loss-of-function mutations in the sorbitol dehydrogenase (SORD) gene cause the most common
25 ythritol: alcohol dehydrogenase 1 (ADH1) and sorbitol dehydrogenase (SORD).
26  is a better zinc donor toward zinc-depleted sorbitol dehydrogenase than is the isolated alpha-domain
27                                              Sorbitol dehydrogenase was below the detectable limit in
28                       By choosing a suitable sorbitol dehydrogenase, we designed yeast strains in whi
29 genase-1C, fructose-bisphosphate aldolase-B, sorbitol dehydrogenase with elevated type 2 diabetes ris
30 led and found to be a selective inhibitor of sorbitol dehydrogenase, with excellent pharmacodynamic/p