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1          It differs in brain accumulation of galactitol.
2 and has been associated with accumulation of galactitol.
3 ductase activity, and levels of sorbitol and galactitol.
4 orted reactivity for sorbitol, mannitol, and galactitol.
5  exposed for 4 hours to D-galactose (2 muM), galactitol (11 muM) and galactose 1-phosphate (0.1 mM),
6 coli in vitro, but in vivo administration of galactitol-a nutrient that supports the growth of only E
7              In addition, both galactose and galactitol accumulated in tissues of GK-deficient mice.
8 material (AE-CWI-CR) gave 90% of 2,3,6-Me(3)-galactitol acetate.
9 alactosemia rapidly accumulate intracellular galactitol, an experimental manipulation that permitted
10                                 Postprandial galactitol and galactonate after lactose overload appear
11                                              Galactitol and galactonate are 2 products of hepatic gal
12 etic lactase nonpersistence (accuracy 0.92), galactitol and galactonate being more discriminative tha
13  observed for galactose, and its metabolites galactitol and galactonate, in serum and urine.
14 e effect of D-galactose and its metabolites, galactitol and galactose 1-phosphate, on oocyte quality
15 tion of these genes resulted in no growth on galactitol and in reduced growth on D-galactose.
16 and urinary excretion of lactose, galactose, galactitol, and galactonate in 14 healthy men who had co
17 l, sorbitol, erythritol, adonitol, arabitol, galactitol, and xylitol revealed that diols containing t
18                              Two examples of galactitol containing bridging silyl groups are analyzed
19                                              Galactitol content in BLECs exceeded five times that fou
20 lms, 2 and 5% w/w of glycerol, d-glucitol, d-galactitol, d-mannitol, and d-limonene were incorporated
21                             d-glucitol and d-galactitol decreased the microhardness and Young's Modul
22 cond, heterologous xylose reductase (XR) and galactitol dehydrogenase (GDH) are introduced into the D
23 vels in vivo and correlate them with urinary galactitol excretion.
24 ith galactosemia who exhibit massive urinary galactitol excretion.
25 rase system components ManX and PtsH and the galactitol fermentation enzyme GatY.
26  the corresponding 2-deoxy-2-N-acetylamino-D-galactitol (GalNAc-ol) form.
27 other galactose metabolites (galactonate and galactitol) has also been studied.
28  novel catabolic pathways for d-altritol and galactitol in Agrobacterium tumefaciens C58.
29            The pathway intermediates include galactitol, L-xylo-3-hexulose, and d-sorbitol.
30 s demonstrate that a markedly elevated brain galactitol level may be present only in newborn infants
31 years) and control subjects to measure brain galactitol levels in vivo and correlate them with urinar
32                      Erythrocyte and retinal galactitol levels were decreased by 91% and 95%, respect
33 l, erythritol, rhamnose, arabitol, sorbitol, galactitol, mannitol, arabinose, glucose, galactose, lac
34  medium suggested by Dixon plot that neither galactitol nor galactose interacted with the extracellul
35 of HLECs and BLECs to a range of 10 to 40 mM galactitol or 10 to 40 mM galactose plus sorbinil-supple
36 ns regulating trypotophan production and the galactitol phosphotransferase system (including dihydrox
37                      Sorbitol, mannitol, and galactitol were converted via 1,6-tritylation, perbenzyl
38 ell as erythrocyte and retinal galactose and galactitol, were measured in rats in each group.
39 t predisposed to inhibition by intracellular galactitol when the sugar alcohol is present in sufficie
40 ected individual had mildly elevated urinary galactitol, which has been linked to cataract developmen
41 ngenital cataracts due to an accumulation of galactitol within the lens.