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1 benzolamide or when the exogenous enzyme was heat inactivated.
2     Killing was abolished when the serum was heat inactivated.
3 gnificantly if the serum in the cultures was heat-inactivated.
4 ot seen with injection of HEPES buffer, with heat-inactivated 8-amino-cADPR, or in cells pretreated w
5 mice to intratracheal challenge with live or heat-inactivated A. fumigatus spores.
6  coli and subsequent in vitro reactions with heat-inactivated acceptor fractions derived from Mycobac
7 d by DAT blocker GBR12935 and is absent when heat-inactivated alpha-synuclein is dialyzed into these
8  at 1, 10, 25, or 50 hemolytic units (HU) or heat-inactivated alpha-toxin was intrastromally injected
9 hlaspi arvense L., 1753, and Thlaspi arvense-heat inactivated and three major chemical products of en
10                             The yeast can be heat-inactivated and delivered to mosquito larvae as rea
11 was dose and time dependent, was elicited by heat-inactivated and infectious viruses, and did not dep
12 ia coli) bacterial pathogens as well as with heat-inactivated and viable fungi (Candida albicans).
13 erived from an eIF4G2 mutant strain could be heat inactivated, and this inactivation could be reverse
14 and embryoid bodies dropped after culture in heat-inactivated anti-Neu5Gc antibody-negative human ser
15 division, whereas cells injected with either heat-inactivated antibodies or control scrambled peptide
16                                              Heat-inactivated antibody or control antibodies had a mu
17  nor secreted products were suppressive, and heat-inactivated, antibody-coated tachyzoites, which eff
18                           However, TFII-I is heat-inactivated at temperatures lower than that require
19 eclined over time when cells were exposed to heat-inactivated ATCV-1.
20                                        These heat-inactivated B. pertussis Ag/LPS-stimulated mast cel
21     Sensitivity for the POC molecular tests (heat-inactivated B3.13) ranged from 1.55 to 7.75 TCID(50
22            No PABA accumulation was noted by heat-inactivated bacteria or mammalian cells.
23                     Addition of EMD 57033 to heat-inactivated beta-cardiac myosin is followed by refo
24 ression in mast cells stimulated with LPS or heat-inactivated Bordetella pertussis Ag.
25                                      UV- and heat-inactivated C pneumoniae EBs also stimulated VSMC p
26                                 Formalin and heat-inactivated C. pneumoniae activated the transcripti
27                                              Heat-inactivated C. pneumoniae failed to stimulate produ
28         Parenteral immunization of dams with heat-inactivated C. rodentium reduces pathogen loads and
29 rly (IM) with MOMP, MOMP-ISCOMs, and live or heat-inactivated C. trachomatis serovar D.
30 cavengers, and catalytically active (but not heat-inactivated) catalase and SOD.
31 tibody is introduced into the cells, whereas heat-inactivated CE and antibodies are ineffective.
32                                              Heat-inactivated chronic-stage plasma can "neutralize" t
33      In this context, we have identified the heat inactivated coelomic fluid (HI-CF) of the earthworm
34 s observed when normal rabbit serum (NRS) or heat-inactivated complement was used.
35 y inhalation to A. fumigatus viable conidia, heat-inactivated conidia (HIC), or HEPA-filtered air twi
36 ells incubated with aHUS serum compared with heat-inactivated control, TTP, and normal serum.
37                          Upon treatment with heat-inactivated Corynebacterium parvum, urinary nitrite
38  volar forearm of 15 healthy volunteers with heat-inactivated cowhage spicules previously soaked in t
39 curred after treatment of colonic loops with heat-inactivated CPE, antibody alone, or bovine serum al
40 n contrast, control rabbits, inoculated with heat-inactivated culture supernatants from the same cell
41                                        Using heat-inactivated D39 (HI-D39) and sterile peritoneal dia
42 lture medium, purified DspB protein, but not heat-inactivated DspB, restored the ability of the mutan
43 d, intraperitoneal administration of live or heat inactivated E. coli JE5505 lacking the abundant out
44         In wild-type (Wt) mice injected with heat-inactivated E. coli, hepatic TLR4 and TLR2 proteins
45                                              Heat-inactivated elastase was used as control.
46 cubated with human uracil DNA N-glycosylase, heat-inactivated enzyme or buffer.
47 etectable in cells scanned with noncoated or heat-inactivated enzyme-coated tips (n = 9).
48 n SsoPox-W263I activity and could reactivate heat-inactivated enzyme.
49  to medium supplemented with 10% unheated or heat-inactivated fetal bovine serum and incubated at 37
50  S phase in the presence of cytokines and 5% heat-inactivated fetal calf serum (HI-FCS).
51                                              Heat-inactivated formulations and subunit vaccines are s
52 winged and unwinged aphids challenged with a heat-inactivated fungal pathogen, and found that immune
53                                 Live but not heat-inactivated fungal spores resulted in recruitment o
54 , gamma globulin-depleted ovine serum or 25% heat-inactivated, gamma globulin-depleted bovine serum.
55  mM MgCl2 or with this buffer and either 25% heat-inactivated, gamma globulin-depleted ovine serum or
56            We have previously shown that the heat-inactivated gram-negative bacterium Brucella abortu
57 imulated in an in vitro infection model with heat-inactivated Gram-positive (Staphylococcus aureus) a
58                       Inoculation of live or heat-inactivated gram-positive bacteria with macrophages
59                 HBECs were exposed to HDM or heat inactivated (hi)-HDM (20 mug/ml) for 24 h prior to
60  (AP) in normal human serum (NHS) but not by heat-inactivated (HI) serum.
61                         Liposomes containing heat-inactivated HindIII or an endonuclease specific for
62 th a reverse-transcriptase inhibitor or with heat-inactivated HIV-1.
63 ed with soluble CD4 (sCD4) or, as a control, heat-inactivated HIV.
64 artificial DNA and RNA both in buffer and in heat-inactivated human blood serum.
65 an neutrophils in the presence or absence of heat-inactivated human immune serum.
66 de inhibits the agglutination of pig RBCs by heat-inactivated human serum at concentrations similar t
67                            Incubation in 10% heat-inactivated human serum increased adherence to endo
68                                              Heat-inactivated IgE was less effective and the monoclon
69 e contralateral side that received saline or heat-inactivated IL1beta.
70     The active cytolysin, when compared with heat-inactivated ILY, did not appear to be chemotactic f
71                                              Heat-inactivated immune serum induced passive cutaneous
72                            Opsonization with heat-inactivated immune serum reduced the amount of atta
73 ither live (infection/inflammation model) or heat-inactivated (inflammation model) cultures in a thig
74            In contrast, PBMCs treated with a heat-inactivated inoculum exhibit normal susceptibility
75                                When FVIII is heat inactivated, it loses function and much of its immu
76 imed via intranasal inoculation with live or heat-inactivated Lactobacillus plantarum or Lactobacillu
77                                              Heat-inactivated, live attenuated varicella vaccine was
78  that E. coli Hsp90 promotes reactivation of heat-inactivated luciferase in a reaction that requires
79                                              Heat-inactivated M. bovis induced a slight increase in t
80                              Mouse serum and heat-inactivated mouse serum inhibited TNF-alpha product
81 had been pretreated with normal mouse serum, heat-inactivated mouse serum, or complement- deficient (
82 udy, two of eight badgers immunized with the heat-inactivated Mycobacterium bovis (HIMB) vaccine exhi
83                     However, upon removal of heat-inactivated mycoplasmas, 32D cells quickly became a
84                                    In vitro, heat-inactivated, naive or sensitized baboon sera contai
85  The synergy was reduced when SCP was either heat inactivated or coinstilled with a peptide inhibitor
86  and phagocytosis were still seen if PHS was heat inactivated or omitted altogether.
87 ese effects were attenuated if the serum was heat-inactivated or if hyaluronidase was added.
88 gammaR-expressing cells occurred with either heat-inactivated or non-heat-inactivated sera, was block
89 dition, the use of other vaccines, including heat-inactivated or replication-defective varicella-zost
90 TP plasma that was preincubated with EDTA or heat-inactivated, or to control plasma.
91 heat-inactivated ovine or bovine serum or in heat-inactivated ovine or bovine serum depleted of gamma
92 rain L011 were incubated in vitro for 2 h in heat-inactivated ovine or bovine serum from which gamma
93 Strains 82-25 and L101, incubated for 2 h in heat-inactivated ovine or bovine serum or in heat-inacti
94                Intranasal immunization using heat-inactivated P. acnes-based vaccines provided a simp
95                      Finally, DC-pulsed with heat-inactivated P. aeruginosa protected CD8(-/-) but no
96 mong them, miR393 and miR166 were induced by heat-inactivated P. sojae hyphae, indicating that they m
97                 We showed that live, but not heat-inactivated, P. aeruginosa inhibited phagocytosis a
98 tensive corneal epithelial erosions, whereas heat-inactivated PASP produced no erosions.
99                                     PASP and heat-inactivated PASP were injected into rabbit corneas,
100               The addition of PCSK9, but not heat-inactivated PCSK9, to the medium of cultured hepato
101 th pig IFN-gamma (but not human IFN-gamma or heat-inactivated pig IFN-gamma) induced human CD4(+) and
102               Neither ATP alone nor ATP with heat-inactivated PKC rescued a rundown of SOC.
103 ivated platelets and undetected in serum and heat-inactivated platelets, and in platelets prepared fr
104 ceptor (Ldlr(-/-) ) mice were immunized with heat-inactivated pneumococci, which were shown to induce
105 unized with control serum, antiserum against heat-inactivated pneumolysin (HI-PLY), or antiserum agai
106  killed Staphylococcus aureus opsonized with heat-inactivated pooled human serum significantly improv
107                                              Heat-inactivated PPE was used to generate a sham operati
108 n in mice that repeated administrations with heat-inactivated preparations of different immunoregulat
109 in or of oligonucleotide or when protein was heat-inactivated prior to forming proteoliposomes.
110     Injection of 20 ng active protease IV or heat-inactivated protease IV (200 ng) had no effect on o
111 ction with purified protease IV but not with heat-inactivated protease IV (P < or = 0.0001).
112                           Neither active nor heat-inactivated protease IV altered the growth of bacte
113 200 ng active purified protease IV or 200 ng heat-inactivated protease IV.
114 ignificantly reduced; neither PTX alone, nor heat-inactivated PTX had any effect on quinpirole-induce
115 Positive PCR results were also obtained with heat-inactivated pus (24 horses) and blood (23 horses) s
116 roduction scheme and compared to traditional heat-inactivated rAAV preparations in vitro and in vivo,
117 buffer media containing zymosan-activated or heat-inactivated rat sera in the presence of protein kin
118 mosan-activated (4 or 10 mg/mL) rat sera, or heat-inactivated rat sera.
119 r [Na+]i and [Na+]i/[K+]i ratios relative to heat-inactivated rat sera.
120 vival was not affected in mice that received heat-inactivated rmIL-13.
121 recombinant (r)PASP (10 microg/20 microL) or heat-inactivated rPASP was intrastromally injected into
122 culated with live RSV, UV light-treated RSV, heat-inactivated RSV, or medium.
123 augmented by recent RSV infection but not by heat-inactivated RSV.
124 d to SR after exposure to saline alone or to heat-inactivated RSV.
125 ammatory response in baboons challenged with heat-inactivated S aureus.
126 al mouse microglia and astrocytes exposed to heat-inactivated S. aureus in vitro.
127 lopment was demonstrated by the inability of heat-inactivated S. aureus to induce proinflammatory cyt
128                                    Analyzing heat-inactivated samples with a luciferase immunoprecipi
129 ubation in pH 4.5 buffer or by incubation of heat-inactivated segments in alpha-expansin or a fungal
130 essing cells exposed to human complement and heat-inactivated sera from 108 AQP4-IgG seropositive NMO
131 red with rabbit complement 10- to 60-fold in heat-inactivated sera from human vaccinees.
132                                              Heat-inactivated sera from rhesus monkeys that were natu
133                                              Heat-inactivated sera from skin grafted F344 rats were a
134 occurred with either heat-inactivated or non-heat-inactivated sera, was blocked by addition of purifi
135 ains were resistant to killing by normal and heat-inactivated sera.
136                          Passive transfer of heat-inactivated serum from infected and immune wild-typ
137 ons were performed in complement-depleted or heat-inactivated serum rather than control serum.
138 g untreated naive serum, but not C3-depleted heat-inactivated serum to the location of the parasites.
139  kill S. epidermidis when the gels contained heat-inactivated serum, C5-deficient serum, a streptococ
140 nectin increased by 511% after incubation in heat-inactivated serum, compared to that of organisms in
141 as determined by adding rabbit complement to heat-inactivated serum, using a two-color fluorescent dy
142 cidal activities of platelet-free plasma and heat-inactivated serum, while the activity of normal ser
143 get cells was blocked by human serum but not heat-inactivated serum.
144  fresh serum and only partially decreased in heat-inactivated serum.
145 EC by 58% compared to organisms incubated in heat-inactivated serum.
146                            Further, when the heat-inactivated set-point-stage plasma pool was mixed w
147 n of splicing extracts and reconstitution of heat-inactivated splicing extracts from strains carrying
148 ed patient sputum sediments were pooled, and heat inactivated, split in replicates, and treated by ei
149                                        While heat-inactivated spores did not induce detectable levels
150  in sera of mice following immunization with heat-inactivated spores.
151                 We show that both viable and heat-inactivated Staphylococcus aureus and lipoteichoic
152 systemic inflammation induced by infusion of heat-inactivated Staphylococcus aureus.
153 titis media with effusion, administration of heat-inactivated Streptococcus pneumoniae into the middl
154 exposed to medium, Stx1 (0.01-100 ng/mL), or heat-inactivated Stx1 or Stx1 B subunit (100 ng/mL).
155                    All seed meals except the heat inactivated T. arvense were toxic to mosquito larva
156 UV irradiation, whereas liposomes containing heat-inactivated T4 endonuclease V were ineffective.
157 UV-irradiated skin with liposomes containing heat-inactivated T4N5 did not restore immune function.
158 red with control cells or cells treated with heat-inactivated Tat.
159 ted by antibodies raised against Sug1, or by heat-inactivating temperature-sensitive Sug1 mutants wit
160 nfect the animals, and when such strains are heat inactivated they lose their ability to rescue the i
161 tive to the contralateral side that received heat-inactivated TNFalpha.
162 ity to restore the 'acid-growth' response to heat-inactivated tomato walls and by its similarity to e
163 nal toxin, because LT subunits, mutants, and heat-inactivated toxin were unable to trigger resistance
164 bit corneas (P < or = 0.05), whereas 1 HU or heat-inactivated toxin yielded negligible pathologic cha
165 RyRs to luminal Ca(2+) was not observed with heat-inactivated trypsin, indicating that digestion of l
166 i with potent ability to induce extension of heat-inactivated type I cell walls.
167 f C. albicans hyphae (Hyphae) but not by its heat-inactivated unicellular form.
168 idly lethal disease in N. vectensis and that heat-inactivated V. coralliilyticus and bacterial flagel
169 ricella vaccine (3625 pfu) or of a partially heat-inactivated vaccine (1125 or 439 pfu).
170 ed on the ability of a formaldehyde-treated, heat-inactivated vaccine to induce modest antibody respo
171                        The immunogenicity of heat-inactivated varicella vaccine and effects on VZV pa
172 trate the efficacy of our HUDSON protocol in heat-inactivating VHF viruses before SHERLOCK testing, e
173  envelope-modified, formaldehyde-stabilized, heat-inactivated virion vaccine could produce higher-tit
174 cating virus since they were not elicited by heat-inactivated virus and the anti-SIV antibody respons
175 ation, but monocyte cultures inoculated with heat-inactivated virus or infected in the presence of AZ
176                        Results obtained with heat-inactivated virus, neutralizing anti-EBV mAb 72A1 a
177                                 Extension of heat-inactivated walls from cucumber (Cucumis sativus cv
178               Mice were exposed to native or heat-inactivated white birch pollen extract (BPEx) intra
179 led to secrete TNF-alpha in response to both heat-inactivated whole bacteria and GBS-F, suggesting th
180                            We show that both heat-inactivated whole GBS and a secreted proteinaceous
181                                         Both heat-inactivated whole GBS bacteria and a heat-labile so
182            Serum IgG antibody levels against heat-inactivated whole P. gingivalis proved to be the pr
183 equired opsonization of hyphae with fresh or heat-inactivated whole plasma.
184                          Mice immunized with heat-inactivated, whole yeast-form cells (Y cells) of Ca
185       Helper adenoviruses can be effectively heat-inactivated with no effect on the infectivity of SV
186 ribose, raffinose, and maltose spiked into a heat-inactivated yeast culture broth supernatant that wa

 
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