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2 meras generated from 5-lipoxygenase(-/-) and leukotriene A(4) (LTA(4)) hydrolase(-/-) mice, we demons
3 nes is the conversion of arachidonic acid to leukotriene A(4) (LTA(4)) in two successive reactions ca
4 ntitate the major product in the reaction of leukotriene A(4) (LTA(4)) with deoxyguanosine (dGuo).
5 iene biosynthesis, the addition of exogenous leukotriene A(4) (LTA(4); the precursor of LTB(4)) to re
6 such as the prostaglandin endoperoxides and leukotriene A(4) epoxide of mammalian biology and the al
11 peripheral blood neutrophils contained both leukotriene A(4) hydrolase and 5-lipoxygenase exclusivel
12 results demonstrate for the first time that leukotriene A(4) hydrolase can be accumulated in the nuc
15 ipoxygenase, the subcellular distribution of leukotriene A(4) hydrolase is cell-specific and dynamic,
19 emistry and immunofluorescence revealed that leukotriene A(4) hydrolase, like 5-lipoxygenase, was mos
20 ible mutant maps to the lta4h locus encoding leukotriene A(4) hydrolase, which catalyzes the final st
23 step transformation of arachidonic acid into leukotriene A(4), leading to the synthesis of various le
25 ls and augmented transcellular conversion of leukotrienes, a disturbance in platelet-leukocyte intera
26 ominent among such signals are the cysteinyl leukotrienes, a family of potent proinflammatory lipid m
27 on of an arachidonic acid hydroperoxide to a leukotriene A (LTA) type epoxide by specific lipoxygenas
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