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1 lost after pretreatment of the extract with PAF acetylhydrolase.
2 e rate of degradation, which is catalyzed by PAF acetylhydrolase.
3 are hydrolyzed and inactivated by the enzyme PAF acetylhydrolase.
4 positive cells now contained an abundance of PAF acetylhydrolase.
5 line-treated animals contained no detectable PAF acetylhydrolase.
6 s proinflammatory actions are antagonized by PAF acetylhydrolase.
7 activating factor (PAF) and is also known as PAF acetylhydrolase.
8 thological actions, and it is inactivated by PAF acetylhydrolase.
9 is hydrolyzed and inactivated by the enzyme PAF-acetylhydrolase.
11 bunits of type I platelet-activating factor (PAF) acetylhydrolase, a phospholipase A(2) with selectiv
18 bunit of a brain platelet-activating factor (PAF) acetylhydrolase, an enzyme that inactivates PAF by
20 ms at determining whether SsE(M28) is also a PAF acetylhydrolase and participates in innate immune ev
23 is association defines the physical state of PAF acetylhydrolase, confers a long half-life, and is a
27 Plasma samples from subjects deficient in PAF acetylhydrolase do not release F2-isoprostanes from
29 ccumulated in oxLDL with a recombinant human PAF acetylhydrolase eliminated the inhibitory effects of
33 e tissues examined, the greatest increase in PAF acetylhydrolase expression was observed in lung foll
34 n Kupffer cells were established in culture, PAF-acetylhydrolase expression became constitutively act
36 Human plasma platelet-activating factor (PAF) acetylhydrolase functions by reducing PAF levels as
37 aining the 5' genomic sequence of the plasma PAF acetylhydrolase gene and further characterized the p
38 a donor with an inactivating mutation in the PAF acetylhydrolase gene did not hydrolyze oxidized phos
42 found that both the intracellular and plasma PAF acetylhydrolases have high affinity for esterified F
43 t PAFAH1B2, but not its family member plasma PAF acetylhydrolase, hydrolyzed aspirin, and PAF competi
45 lotting did not reveal detectable amounts of PAF acetylhydrolase in PON1 preparations, although very
48 H1B2 or PAFAH1B3, and the competitive type I PAF acetylhydrolase inhibitor NaF reduced erythrocyte hy
52 ciency of plasma platelet-activating factor (PAF) acetylhydrolase is an autosomal recessive syndrome
54 poprotein (apo) B100 in the formation of the PAF acetylhydrolase-LDL complex, we tested the ability o
55 an important mechanism for elevating plasma PAF-acetylhydrolase levels and an important component in
57 1 preparations, although very low amounts of PAF acetylhydrolase might still account for PON1 phospho
58 exposure with the production of plasma-type PAF acetylhydrolase mRNA and protein expression specific
63 demonstrated very low levels of plasma-type PAF-acetylhydrolase mRNA transcripts in the livers of sa
66 tain barely detectable levels of plasma-type PAF-acetylhydrolase mRNA, when Kupffer cells were establ
69 evolved to target PAF by characterizing the PAF acetylhydrolase (PAF-AH) activity and substrate spec
74 e plasma form of platelet-activating factor (PAF) acetylhydrolase (PAF-AH), also known as lipoprotein
78 se (PAF-CPT), and its main catabolic enzyme (PAF acetylhydrolase; PAF-AH), on U937 cells, in cell fre
79 from reduced turnover due to lower levels of PAF acetylhydrolase (PAFAH), the enzyme that catabolizes
80 riming was restored by HDL or HDL-associated PAF acetylhydrolase (PAFAH), which mediates inactivation
82 tor (PAF)-like lipids in L5 by a recombinant PAF acetylhydrolase prevented both FGF-2 downregulation
85 A crystal structure is also presented of PAF acetylhydrolase reacted with the organophosphate com
86 -BB rats were treated with human recombinant PAF acetylhydrolase (rPAF-AH), which efficiently inactiv
88 inflammatory activities of recombinant human PAF-acetylhydrolase (rPAF-AH), which converts PAF to bio
90 internalized, and overexpression of PLA2g7 (PAF acetylhydrolase) that specifically hydrolyzes such o
91 inactive metabolite, lysoPAF, by the enzyme PAF acetylhydrolase, the activity of which has shown to
92 which can be prevented by co-incubation with PAF acetylhydrolase, the enzyme that catabolizes PAF in
93 rolase-LDL complex, we tested the ability of PAF acetylhydrolase to bind to lipoproteins containing t
94 PON1 purification by first depleting HDL of PAF acetylhydrolase to find PON1 purified in this way no
96 domains within the primary sequence of human PAF acetylhydrolase, tyrosine 205 and residues 115 and 1
98 e (LPS) significantly inhibited synthesis of PAF acetylhydrolase, whereas other cytokines, including
99 F acetylhydrolase were introduced into mouse PAF acetylhydrolase (which normally does not associate w
100 PAF is effectively and tightly regulated by PAF acetylhydrolases, which convert PAF back to lysoPAF.
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