戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 CoV-2 results in protective immunity against reexposure.
2 tion of a type 2 cytokine pattern with acute reexposure.
3 efficiently control infection in the case of reexposure.
4 ists and the other type under vehicle during reexposure.
5 otection from symptomatic disease on natural reexposure.
6 gain by 5-azacytidine exposure, washout, and reexposure.
7 tations in this assay to detect instances of reexposure.
8 lls that can assist in pathogen control upon reexposure.
9 revent disease in animal challenge models on reexposure.
10 ted their reactivation program upon allergen reexposure.
11 h cognitive deficits apparent with adult THC reexposure.
12 y when administered before a delayed context reexposure.
13 red either before or after the first context reexposure.
14 line or propranolol injection before context reexposure.
15  to the serum HLA antibody pool upon antigen reexposure.
16 he years between infections, possibly due to reexposure.
17 immunity and subsequent disease outcome upon reexposure.
18 pose health risks to patients requiring drug reexposure.
19  of DeltaFosB protein after repeated cocaine reexposure.
20 LT levels may be a useful clinical marker of reexposure.
21 posure but not in a group given eye shock US reexposure.
22  local and rapid protection against pathogen reexposure.
23 omycin was administered 25 min after a 5-min reexposure.
24 hanism of increased sensitivity to HBO(2) in reexposures.
25 igm followed by immediate or delayed context reexposures.
26 er of unformed stools passed was lower after reexposure (11.25 versus 8.62; P < 0.05).
27  accumulation of immunity following repeated reexposures; 2) partial protection that wanes over time;
28 nuation of therapy (continuous treatment) or reexposure after a therapy break (rechallenge treatment)
29 patterns during initial cocaine exposure and reexposure after withdrawal, which contrasted with disti
30  NAc AMPAR blockade with CNQX during cocaine reexposure and mimicked by intra-NAc infusions of AMPA,
31 o both deliver faster effector function upon reexposure and readapt to antigenically variant pathogen
32 es the risk of progressive disease following reexposure and reinfection is not known.
33 ntrast, mice given mAb to TNFR1 succumbed to reexposure, and the high mortality was accompanied by a
34 ating antibodies are no longer detectable at reexposure baseline and is recommended when heparin is t
35  received footshock exposure, rather than US reexposure, between extinction and test, and contextual
36 ody responses were elicited and boosted upon reexposure, but titers decreased rapidly, suggesting low
37  for rapid division independently of antigen reexposure by transiently inducing cell-cycle progressio
38           This means that short-term heparin reexposure can be safely performed if platelet-activatin
39          The rate of HCV clearance following reexposure depends on the cellular immune response, the
40                                      Heparin reexposure despite a history of previous heparin-induced
41 istration followed by a drug-free period and reexposure did not affect the conditioned behavior, but
42 tokine production, they do not reexpand upon reexposure due to increased apoptosis.
43 tance to such influences, and then retrieval/reexposure effects on either speaker or listener, with a
44 ome studies suggest that longer-term heparin reexposure (eg, for chronic hemodialysis) may also be re
45       Conversely, in SA-pretreated rats, the reexposure elevated the membrane excitability of NAcSh M
46  initial stimulation but exhibit anergy upon reexposure, group 1 CD1-restricted T cells exhibit delay
47 ficantly higher in vaccinated individuals on reexposure (&gt;1 week after diagnosis) than in vaccinated,
48    To determine if IFN-gamma is necessary in reexposure histoplasmosis, GKO and WT mice were inoculat
49 ences between these receptors for regulation reexposure histoplasmosis.
50 f 3.1 years (range, 0.4-5.6), with effective reexposure in 4 of 5 patients.
51  cells and their recall responses to antigen reexposure in a cell-intrinsic manner.
52 nfection induced protective immunity against reexposure in nonhuman primates.
53 l DNA methylation changes following nicotine reexposure in the F1 generation suggests that epigenetic
54  AMPARs is reversed or normalized on cocaine reexposure in withdrawal, but the mechanism for this AMP
55 ution in HIV infection may require antigenic reexposure, in addition to control of HIV replication.
56 e immunity following hepatitis C virus (HCV) reexposure is a prerequisite for the design of effective
57  of recurrent HIT 1 to 2 weeks after heparin reexposure is approximately 2% to 5% and is attributable
58  exposed to chronic nicotine, acute nicotine reexposure long after withdrawal potentiated reward resp
59 outbreaks, allows immunity to be lost before reexposure occurs.
60 nd episode of diarrhea, while a simultaneous reexposure of animals to C. difficile bacteria or spores
61               Memory recall triggered by the reexposure of mice to the sound cue did not lead to chan
62 (+)-K(+) pump current beyond steady state on reexposure of myocytes to K(+) after a period of exposur
63                                              Reexposure of the regular caffeine users to caffeine aft
64                                        After reexposure of the resulting solitary polyps to normal pH
65 f innate and adaptive immunity following HCV reexposure of two chimpanzees that had previously recove
66                                      Whether reexposure of varicella-immune persons to varicella-zost
67  adapted state and was not washed-out before reexposure on the second day.
68                              Whether through reexposure or the natural progression of infection, newl
69                            In the absence of reexposure, positive N. gonorrhoeae Aptima Combo 2 assay
70                                 In addition, reexposure-related c-Fos expression in the anterior cing
71          However, in the absence of constant reexposure, serum immunoglobulin (Ig) levels rapidly dec
72                                          How reexposure shapes humoral immunity to future norovirus s
73 e HIT undergoing repeated TPE before heparin reexposure should be tested by serial platelet activatio
74 on appears partial and can be overcome after reexposure, similar to what has been found in rodent mod
75 s' primed immunity was frequently boosted by reexposure, so maintaining herd immunity in the face of
76 into the basolateral amygdala shortly before reexposure to a cocaine-associated stimulus but not simp
77 ated the neuronal activation associated with reexposure to a discrete cocaine-associated stimulus usi
78 y CD8+ T cells increase protection following reexposure to a pathogen.
79       Although these quantitative effects of reexposure to Ag are well documented, little is known ab
80  that allergen-specific IgG-ICs, formed upon reexposure to allergen, promoted Th2 responses in two di
81 tive interneurons and returns to normal upon reexposure to amphetamine, suggesting that this paradoxi
82 to upregulate CD44 and LFA-1 expression upon reexposure to anti-CD3 mAb in vitro.
83 se can participate in a recall response upon reexposure to antigen even at protracted times postinfec
84 gen injection, and (2) hyporesponsiveness on reexposure to antigen.
85 prevented relapse to drug-seeking induced by reexposure to cannabinoids or cannabinoid-associated cue
86 ogenous boosting hypothesis" postulates that reexposure to circulating varicella zoster virus (VZV) o
87 s boosting hypothesis, which postulates that reexposure to circulating wild-type varicella delays the
88 entified a sequence of neural events whereby reexposure to cocaine activates a signaling cascade that
89                         Furthermore, after a reexposure to cocaine after long-term withdrawal, the me
90 rats, but AMPARs internalized after a single reexposure to cocaine or cocaine-related cues.
91 rimes Fosb for induction in this region upon reexposure to cocaine.
92 hanism for primed Fosb induction in NAc upon reexposure to cocaine.
93 er the tone), and tested for immobility upon reexposure to contextual stimuli or to one tone presenta
94  Expression could be repeatedly reinduced by reexposure to cytokines.
95 y, and shrink to near their original size on reexposure to dry air.
96 reinstatement of nicotine seeking induced by reexposure to either nicotine priming or nicotine-associ
97 -bred animals exhibited increased anxiety on reexposure to EPM but only if both trials were preceded
98 s recovered rapidly, however, within 1 hr of reexposure to ethanol liquid diet.
99 elta T cells to mediate a memory response on reexposure to ethylamine and to secrete IFN-gamma in res
100                                   Subsequent reexposure to heat shock results in the rapid relocaliza
101 ion in this enhanced transport was seen upon reexposure to heating, consistent with the development o
102 ed in relapse induced by footshock stress or reexposure to heroin.
103                                         Yet, reexposure to HIV-1 antigen during treatment discontinua
104 ent treatment of acute infection followed by reexposure to HIV-1 through supervised treatment interru
105 pressure elevation and renal inflammation on reexposure to hypertension stimuli.
106 ) T cells are critical for host defense upon reexposure to intracellular pathogens.
107                                              Reexposure to K(+) reproduced a transient current beyond
108 er photosynthetic activity more quickly upon reexposure to light.
109 plants with expression rapidly restored upon reexposure to light.
110 ce morbidity and mortality during subsequent reexposure to MHV-1.
111                                      Whether reexposure to mismatched HLA antigens (RMM) in the setti
112 e observe, however, that, during withdrawal, reexposure to nicotine doubles the frequency of pacemaki
113  hypoxia, or chronic hypoxia with subsequent reexposure to normoxia for different time points.
114                                           On reexposure to normoxia, chronic hypoxia-induced PH in mi
115 ch was demonstrated to functionally react to reexposure to P. gingivalis, as measured by a further in
116  T cells generated by chronic infection upon reexposure to parasite, we compared their responses to k
117 ery of antibodies was detected after natural reexposure to pathogens.
118 tor functions, which were restored following reexposure to rapamycin, demonstrating reversible effect
119 characterized, and converted to product upon reexposure to reaction conditions.
120                                              Reexposure to sutimlimab in a named patient program reca
121 ction, providing future host resistance upon reexposure to that pathogen.
122 ble to increased cognitive impairments after reexposure to THC in adulthood, which was correlated wit
123                                        After reexposure to the beverage and administration of a place
124                                   Subsequent reexposure to the cocaine or SCM S(D), but not the non-r
125                                 On test day, reexposure to the cocaine-associated Context A reinstate
126 /kg anisomycin immediately following a 5-min reexposure to the cocaine-conditioned context showed dec
127 isomycin was administered following a 30-min reexposure to the context or when anisomycin was adminis
128 st phase, all subjects underwent a test day (reexposure to the distinctively flavored beverage before
129  to cocaine use among human addicts is acute reexposure to the drug, which often precipitates cocaine
130  prolonged periods and can be reactivated on reexposure to the hypertensive stimulus.
131                                         Upon reexposure to the pathogen, the longevous Bmem, which ma
132                               The effects of reexposure to the S(D) on the recovery of responding at
133 profound, and specific T-cell tolerance upon reexposure to the same alloantigens.
134                            We find that upon reexposure to the same antigen, affinity-dependent selec
135  stronger response of an animal that follows reexposure to the same antigen.
136  and the number of new neurons responding to reexposure to the same environment.
137 om novel environments and is reinstated upon reexposure to the same familiar environment.
138 ent model, where reinstatement is induced by reexposure to the self-administered drug (drug priming),
139 he effect could be reactivated days later by reexposure to the stressful context.
140 ats were then tested for fearful behavior by reexposure to the tone without additional footshock.
141 extinguished conditioned response (CR) after reexposure to the unconditioned stimulus (US)--and spont
142 sed preparations needs to be reassessed, and reexposure to these agents should likely be avoided.
143                                              Reexposure to trauma reminders is an integral element of
144     Thus, the risk of zoster is decreased by reexposure to varicella-zoster virus, either by vaccinat
145 reactivation, and immunity-boosting, wherein reexposure to VZV boosts VZV-specific immunity to reinfo
146 ism of immunological boosting, through which reexposures to varicella-zoster virus are thought to red
147                                      Cocaine reexposure transiently reversed enhanced NAc AMPAR-media
148                          In Experiment 1, US reexposure was administered 24 hr prior to a reinstateme
149                          In Experiment 2, US reexposure was administered 5 min prior to a reinstateme
150 cination and unobserved natural infection or reexposure, which could result in overestimation of prot
151 th the ability to rapidly differentiate upon reexposure while maintaining the population over time.
152 YFP mice were administered a delayed context reexposure with either a saline or propranolol injection
153                                    After cue reexposure, Zif268 levels in the dentate gyrus of the hi

 
Page Top