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1 stics identical to those of human neutrophil flavocytochrome b558.
2 ery similar to those obtained for neutrophil flavocytochrome b558.
3 PH oxidase complex requires both subunits of flavocytochrome b558.
4 LPS increased plasma membrane association of flavocytochrome b558.
5 1-kDa subunit of the phagocyte NADPH oxidase flavocytochrome b558.
6 91(phox) is the sole heme binding subunit of flavocytochrome b558.
7 c factors (p47-phox, p67-phox, and Rac) plus flavocytochrome b558.
8 and Rac plus the phospholipid-reconstituted flavocytochrome b558.
9 ted p47(phox) and with p22phox, a subunit of flavocytochrome b558.
11 dox center of the phagocyte NADPH oxidase is flavocytochrome b558, a transmembrane protein with two s
12 ctions between p47phox and the transmembrane flavocytochrome b558 and also between the cytosolic comp
13 be reconstituted in a cell-free system using flavocytochrome b558 and the cytosolic proteins p47(phox
15 Specifically, nascent Hp phagosomes acquire flavocytochrome b558 but do not efficiently recruit or r
18 he heme spectrum in purified preparations of flavocytochrome b558 containing the p22(phox) derivative
19 evidence demonstrating the critical role of flavocytochrome b558 (Cyt b) in the NADPH-dependent oxid
20 correlated with phagosomal colocalization of flavocytochrome b558 (flavocytochrome b) and p47phox and
21 91 and Arg92 of gp91(phox) are essential for flavocytochrome b558 function in granulocytes and sugges
26 phagocytosis-induced superoxide production, flavocytochrome b558, p47(phox), p67(phox), and the Fcga
28 eptides to examine the relative role of each flavocytochrome b558 subunit in heme binding and O2- for
29 ted to the membrane where they interact with flavocytochrome b558 to form an activated microbicidal o
30 x) and p67(phox) and the membrane-associated flavocytochrome b558 to form the multicomponent respirat
31 hemical and functional features of wild type flavocytochrome b558 with those in cells co-expressing g
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