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1  with a lipid bilayer membrane incorporating cholesterol oxidase.
2 ains accessible to treatment with the enzyme cholesterol oxidase.
3 ted by increased susceptibility to exogenous cholesterol oxidase.
4 o HDL, and the sensitivity of membrane FC to cholesterol oxidase.
5 ced by increased susceptibility to exogenous cholesterol oxidase.
6 ity of membrane cholesterol to extracellular cholesterol oxidase.
7 rturbation using methyl-beta-cyclodextrin or cholesterol oxidase.
8 ility of this membrane fraction to exogenous cholesterol oxidase.
9 tigate the membrane disruption properties of cholesterol oxidase.
10 membrane cholesterol was also measured using cholesterol oxidase.
11 rane cholesterol to enzymatic oxidation with cholesterol oxidase.
12                     The crystal structure of cholesterol oxidase, a 56kDa flavoenzyme was anisotropic
13 ntially more rapidly than ent-cholesterol by cholesterol oxidase, a protein that contains a specific
14 ve product of cholesterol in the presence of cholesterol oxidase, a sensitive and selective method of
15 lesterol through methyl-beta-cyclodextrin or cholesterol oxidase abolished the protective effect of C
16 n binding without substantially altering the cholesterol oxidase-accessible cellular [(3)H]cholestero
17                                              Cholesterol oxidase and cholesterol esterase were assemb
18 ensing platform was developed by integrating cholesterol oxidase and cholesterol esterase with the hy
19 and fibroblasts were used: susceptibility to cholesterol oxidase and cholesterol transfer to cyclodex
20 o crucial redox enzymes for biosensors (i.e. cholesterol oxidase and glucose oxidase) are targeted.
21    (This was gauged by its susceptibility to cholesterol oxidase and its rate of transfer to cyclodex
22 sterol with two cholesterol-specific probes, cholesterol oxidase and saponin.
23 experiments before and after incubation with cholesterol oxidase and sphingomyelinase show that these
24                          Wild-type and E361Q cholesterol oxidases bind to vesicles with an apparent K
25                                          The cholesterol oxidase-BSA-AuNPs-metal-free organic framewo
26                    Our results indicate that cholesterol oxidase can metabolize phytosterols in vivo
27            We investigated the dependence of cholesterol oxidase catalytic activity and membrane affi
28                                              Cholesterol oxidase catalyzes the oxidation and isomeriz
29                                              Cholesterol oxidase catalyzes the oxidation and isomeriz
30  tobacco (Nicotiana tabacum) plants with the cholesterol oxidase choM gene and expressed cytosolic an
31                                              Cholesterol oxidase (ChOx) and catalase (CAT) were co-im
32 ose oxidase (GOx), lactate oxidase (LOx) and cholesterol oxidase (ChOx) by a new electron shuttling m
33 f H2O2 in the presence of O2/cholesterol and cholesterol oxidase (ChOx) by the fluorescence response
34                                 Furthermore, cholesterol oxidase (ChOx) is attached to G/PVP/PANI-mod
35                                              Cholesterol oxidase (ChOx), a member of the glucose-meth
36                                              Cholesterol oxidase (COase) is a bacterial enzyme cataly
37 olution at 37 degrees C by using an improved cholesterol oxidase (COD) activity assay.
38 acting enzyme was examined using a bacterial cholesterol oxidase (COD) as a model.
39 ng enzymes was addressed using soil bacteria cholesterol oxidase (COD) as a model.
40 ramide was investigated at 37 degrees C by a cholesterol oxidase (COD) reaction rate assay and by opt
41 total cholesterol using cholesterol esterase/cholesterol oxidase coupled with the luminol-H2O2-horser
42    The crystal structure of the redox enzyme cholesterol oxidase, determined at sub-angstrom resoluti
43           Transgenic leaf tissues expressing cholesterol oxidase exerted insecticidal activity agains
44 , magnetic nanoparticles functionalized with cholesterol oxidase (Fe(3)O(4)/APTES/ChOx), was develope
45  Degrading cholesterol in one monolayer with cholesterol oxidase first caused the boundary of the raf
46 eralfold; exposing the cells to mevinolin or cholesterol oxidase had the opposite effect.
47 e function of an active site loop (70-90) of cholesterol oxidase has been ascertained by deleting fiv
48               A neutron diffraction study of cholesterol oxidase has revealed an unusual elongated ma
49           The atomic resolution structure of cholesterol oxidase has revealed the presence of hydroge
50 lipid-modified surface, and incorporation of cholesterol oxidase in the electrode-supported thiolipid
51 solid-ordered state, the binding affinity of cholesterol oxidase increases approximately 10-fold.
52   The present work and our previous study on cholesterol oxidase-induced sterol oxidation suggest tha
53               These results demonstrate that cholesterol oxidase interacts directly with the lipid bi
54                                              Cholesterol oxidase is covalently linked to an 11-mercap
55             We conclude that the activity of cholesterol oxidase is directly and sensitively dependen
56 genic plants expressing chloroplast-targeted cholesterol oxidase maintained a greater accumulation of
57                             To elucidate the cholesterol oxidase-membrane bilayer interaction, a cyst
58                                              Cholesterol oxidase modified platinum microcavity electr
59   Experiments for direct contact between the cholesterol oxidase-modified electrode and the surface o
60                                          The cholesterol oxidase-modified electrodes show steady-stat
61                Enzymatic turnovers of single cholesterol oxidase molecules were observed in real time
62  cholesterol oxidation catalyzed by mediated cholesterol oxidase occurred at the anode.
63                                              Cholesterol oxidase represents a novel type of insectici
64 n with methyl-beta-cyclodextrin, filipin, or cholesterol oxidase resulted in an insulin-independent i
65 rs cholesterol within the membranes, or with cholesterol oxidase resulted in markedly reduced galanin
66 timulate the interaction of cholesterol with cholesterol oxidase, saponin and cyclodextrin, presumabl
67 e X-ray crystal structure of the flavoenzyme cholesterol oxidase, SCOA (Streptomyces sp.SA-COO) has b
68                              The loss of the cholesterol oxidase-sensitive FC pool and FC efflux to s
69  small unilamellar vesicles and an increased cholesterol oxidase-sensitive pool of membrane FC on the
70 spholipid vesicle acceptors and an increased cholesterol oxidase-sensitive pool of membrane free chol
71 a greatly reduced ability to: 1) enlarge the cholesterol oxidase-sensitive pool of membrane free chol
72 nspection of the X-ray crystal structures of cholesterol oxidase suggested that an active-site "lid"
73 hatidylcholine, previously shown to decrease cholesterol oxidase susceptibility, reduced the transfer
74                    The binding affinities of cholesterol oxidase to 100-nm unilamellar vesicles compo
75 differences were abolished by treatment with cholesterol oxidase to disrupt membrane rafts.
76 DHE ester synthesis is achieved by employing cholesterol oxidase to selectively render unesterified D
77                             Thus, binding of cholesterol oxidase to the membrane and partitioning of
78                                              Cholesterol oxidase was immobilized in a sol-gel matrix
79  the sensitivity of cellular FC to exogenous cholesterol oxidase was tested under conditions in which
80                       This acrylodan-labeled cholesterol oxidase was used to explore the pH, ionic st
81 rs that contain GOx, L-amino acid oxidase or cholesterol oxidase wherein the intrinsic FAD fluorescen
82 -one and therefore mimicking the activity of cholesterol oxidase, which is implicated in cardiovascul