ライフサイエンスコーパス: conditioning

1 freely behaving mice subjected to trace fear conditioning.

2 species, there were no benefits of parental conditioning.

3 enhanced conditioned approach and appetitive conditioning.

4 it plays an essential role in classical fear conditioning.

5 s than half the dose of Day 20 calves during conditioning.

6 tion trials are administered soon after fear conditioning.

7 nonautoimmune models required ablative host conditioning.

8 ard prediction error signal during Pavlovian conditioning.

9 ncluding cerebellum-dependent delay eyeblink conditioning.

10 t of rabbits before and after trace eyeblink conditioning.

11 ehavioral responses than tones even prior to conditioning.

12 5% (n = 3) were found to have a high risk of conditioning.

13 signaling phenomenon that may regulate soil conditioning.

14 the unconditioned stimulus (US) during fear conditioning.

15 ual complexity is involved, as in trace fear conditioning.

16 reflecting the laboratory paradigm of trace conditioning.

17 aviorally naive or trained on trace eyeblink conditioning.

18 g of 3D heart tissues with electromechanical conditioning.

19 al cortex of rats trained in contextual fear conditioning.

20 ive or busulfan-containing reduced intensity conditioning.

21 chain (TeLC) completely blocks auditory fear conditioning.

22 eference protocol so as to mediate Pavlovian conditioning.

23 stigated the role of octopamine in olfactory conditioning.

24 cooling issues for old buildings with no air conditioning.

25 onsidered up front or after bortezomib-based conditioning.

26 that change firing to cue and reward during conditioning.

27 veral mouse lines using Barnes maze and fear conditioning.

28 (65%) received myeloablative busulfan-based conditioning.

29 ed molds and after proper device washing and conditioning.

30 ling routes abrogated the salutary effect of conditioning.

31 emporal or contextual cues, as in trace fear conditioning.

32 nits, increased further) up to an hour after conditioning.

33 role in the acquisition of pavlovian threat conditioning.

34 ative or non-myeloablative-reduced intensity conditioning.

35 exhibit long term plasticity following fear conditioning.

36 he complex spike waveform is increased after conditioning.

37 ion impedes sucrose-driven flavor preference conditioning.

38 on memory of rats trained in contextual fear conditioning.

39 transplanted after optimized CT tolerogenic conditioning (1 x 25 mug [CT25]).

40 ty nine percent of sharks (n = 41) showed no conditioning, 36% (n = 25) showed a low risk and only 5%

41 a, this study (N = 186) tests the effects of conditioning a sales offer for a spare LPG cylinder on a

42 s upregulate excitability in delay eye-blink conditioning, a form of motor learning.

43 ng properties in response to contextual fear conditioning, a process called "remapping." In the prese

44 During fear conditioning, a sensory cue, such as a tone (the conditi

45 KO mice accounts for their impaired eyeblink conditioning across both animals and trials.

46 We recently reported that during cold conditioning, activation of alternative oxidase (AOX) oc

47 the transfer of a single major dominant gene conditioning all stage resistance, herein temporarily de

48 We propose that on conditioning, Amnesiac release from the MB allows, via a

49 Preclinical models of threat conditioning and extinction have provided an unparallele

50 Participants underwent discriminative threat conditioning and extinction in the clinic.

51 ith anxiety) completed a differential threat conditioning and extinction paradigm that has been valid

52 ggests that an "event boundary" between fear conditioning and extinction protects the conditioning me

53 nspiratory breathing load task, and (3) fear conditioning and extinction task.

54 demonstrated comparable differential threat conditioning and extinction.

55 ng the functional neuroanatomy of appetitive conditioning and identify specific brain regions that ar

56 avior by enhancing both appetitive Pavlovian conditioning and instrumental pursuit of CS.SIGNIFICANCE

57 amygdala (BLA) plays a critical role in fear conditioning and is extremely sensitive to ELS.

58 broad potential to disrupt conventional air conditioning and refrigeration as well as electronics co

59 ation (TBI), 2 Gy of TBI, 8 Gy of TBI, or no conditioning and treated by using transplantation with l

60 ovides the possibility to predict (Pavlovian conditioning) and control (operant conditioning) harmful

61 cell-specific CB1KOs exhibit normal eyeblink conditioning, and both global and granule-cell-specific

62 nced in Purkinje cells after delay eye-blink conditioning, and point toward a downregulation of SK ch

63 volume, voltage ramp, temperature, capillary conditioning, and rinsing procedure, etc.) were left to

64 was to examine developmental changes in fear conditioning, and to see whether these changes were impa

65 In "trace" fear conditioning, animals learn to associate a neutral cue w

66 The main genetic pathways for associative conditioning are known in experimental animals, but have

67 behavioral paradigms with Pavlovian cue-food conditioning are well established.

68 earning, such as in trace or delay eye-blink conditioning, are less well studied.

69 ral assays of anxiety, locomotion, and place conditioning, as well as c-Fos expression in 14 brain re

70 eived myeloablative versus reduced-intensity conditioning, as well as for patients whose allograft ca

71 ned by transient inflammation resulting from conditioning-associated damage and show that T cell para

72 in combination with short cycles of ischemic conditioning before and/or after clamping.

73 id not disrupt the acquisition of trace fear conditioning, but markedly increased the level of freezi

74 vmPFC in the acquisition of pavlovian threat conditioning by assessing skin conductance response (SCR

75 ore than 700 genes that modulate associative conditioning by molecular processes for synaptic plastic

76 d on a cohort of rabbits undergoing eyeblink conditioning can reveal functional brain connectivity ch

77 for context encoding during contextual fear conditioning causes maladaptively overgeneralized and in

78 ice were tested in a 3-shock contextual fear conditioning (CFC) paradigm to assess memory decline.

79 one (CORT) administration or contextual fear conditioning (CFC).

80 s and optional bridging therapy, followed by conditioning chemotherapy and a single infusion of KTE-X

81 Cyclophosphamide plus fludarabine conditioning chemotherapy was administered before CAR T

82 ng, and implemented in a two-stage efficient conditioning circuit for powering low-voltage devices us

83 ordingly, studies using appetitive Pavlovian conditioning confirm that environmental cues that are as

84 Conditioning consisted of fludarabine (90 mg/m2) and 2 t

85 Updating in the conditioning context alleviates overgeneralization and r

86 However, post-conditioning context exposure enables further context en

87 Unlike in context conditioning, cue conditioning (to an odor stimulus) occ

88 IL-12)- and Th17 (IL-23, IL-1beta, and IL-6)-conditioning cytokines by myeloid cells, which then cros

89 The threshold changes from pre to post-conditioning (DeltaMQST and DeltaTQST) were compared bet

90 respectively blocked or phenocopied enriched conditioning-dependent axon regeneration after SCI leadi

91 onditioning than fully reinforced fear (FRF) conditioning, despite an equivalent number of tone-shock

92 ings highlight the mechanisms of how operant conditioning develops the preference of ethanol-containi

93 the mouse DCN are diminished during eyeblink conditioning (EBC), a form of associative motor learning

94 (VOR) gain adaptation but impaired eyeblink conditioning (EBC), which relies on the ability to estab

95 This context-conditioning effect was entirely absent when participant

96 Conditioning electrical stimulation (CES) prior to nerve

97 Society for Heating, Refrigerating, and Air-Conditioning Engineers (ASHRAE).

98 The cohort of rabbits undergoing eyeblink conditioning exhibited increased functional connectivity

99 In contextual fear conditioning, experimental subjects learn to associate a

100 Participants also underwent a three-day fear conditioning, extinction learning, and extinction recall

101 cular deprivation (MD) or auditory-cued fear conditioning (FC) caused rapid spine elimination in V1 o

102 y processing; these show an increase in fear conditioning (FC), a reduction in prepulse inhibition (P

103 Seven cynomolgus macaques received immune conditioning followed by simultaneous donor bone marrow

104 thy participants underwent differential fear conditioning, followed by a generalization test in which

105 ) were associated with stent occlusion after conditioning for age, sex, and clinically relevant facto

106 se (GVHD) prophylaxis after nonmyeloablative conditioning for HLA class I or II mismatched hematopoie

107 nxiety, and motivational deficits in operant conditioning for palatable food rewards and in reward-ba

108 However, in mice, appetitive conditioning generally requires intensive training and t

109 ntrol group (n=2701) or the remote ischaemic conditioning group (n=2700).

110 Pavlovian conditioning) and control (operant conditioning) harmful events.

111 tal cortex (vmPFC) in human pavlovian threat conditioning has been relegated largely to the extinctio

112 mPFC) in the acquisition of pavlovian threat conditioning has been relegated largely to the inhibitio

113 e hippocampal activity supporting trace fear conditioning has long been mysterious, but a leading hyp

114 c plasticity plays a role in trace eye-blink conditioning; however, corresponding excitability change

115 Stepwise conditioning identified 67 non-MHC genes, of which 14 di

116 ll, our results demonstrate that hypoxia pre-conditioning impacts the pASC proteome signature and con

117 hippocampus but not PFC impaired trace fear conditioning in adult mice.

118 nriched in pathways activated by associative conditioning in animals, including the ERK, PI3K, and PK

119 tiviral gene therapy following myeloablative conditioning in first-in-human studies (trial registry n

120 In serial compound stimulus (SCS) conditioning in mice, repeated presentations of sequenti

121 ipatory behavioral responses in an odor fear conditioning in rats, while recording theta (5-15 Hz) an

122 ential pattern that is likewise observed for conditioning in the behavioral domain.

123 vely among patients receiving more intensive conditioning, including myeloablative regimens and highe

124 on potentiated CS-evoked port entries during conditioning, indicating enhanced conditioned approach a

125 Contextual fear conditioning induced selective strengthening of a subset

126 (a cellular substrate of memory erasure) of conditioning-induced potentiation at LA synapses, and th

127 ia (DRG) sensory neurons compared to EE or a conditioning injury alone, propelling axon growth well b

128 Conditioning intensity did not affect OS, but was associ

129 HLA match, sex match, cytomegalovirus match, conditioning intensity, type of T-cell depletion, and gr

130 graft-versus-host responses irrespective of conditioning intensity.

131 Conditioning is also performed with the enclosed DART.

132 tion.SIGNIFICANCE STATEMENT Pavlovian threat conditioning is an adaptive mechanism through which orga

133 tion resolution in the nerve is required for conditioning-lesion-induced neurorepair.

134 mice, inflammation resolution is delayed and conditioning-lesion-induced regeneration of DRG neuron c

135 phologic complete remission to myeloablative conditioning (MAC) or reduced-intensity conditioning (RI

136 ear conditioning and extinction protects the conditioning memory from interference by the extinction

137 In Pavlovian conditioning models, where cues predict reinforcer deliv

138 Air conditioning modulated HONO mixing ratios driven by cond

139 Flies fed after appetitive conditioning needed increased sleep for memory consolida

140 After EDU/SES conditioning, neuronal cell types were identified for ri

141 Operant conditioning of Hoffmann's reflex (H-reflex) is a non-in

142 ems that measure muscle activity for operant conditioning of spinal reflexes still use rigid metal el

143 Conditioning of the adults while they brood their larvae

144 that current ecotourism has no effect on the conditioning of the white sharks, and that all baits hav

145 its on the attraction, surface behaviour and conditioning of white sharks Carcharodon carcharias duri

146 Conditioning of white sharks was determined by the numbe

147 o 41 diseases and traits (average N = 320K), conditioning on a broad set of coding, conserved and reg

148 e informative for common disease, even after conditioning on a broad set of functional annotations.

149 We hypothesized that mechanically pre-conditioning on a soft matrix (soft priming) will delay

150 any cardiometabolic risk factors, even after conditioning on maternal GRS.

151 OC3, and CD300LG) remained significant after conditioning on the common index single-nucleotide polym

152 d single trial predictions improve most when conditioning on the experimentally measured local correl

153 Importantly, this signal remains despite conditioning on the lead class I and class II variants (

154 d type of ecological interactions changes by conditioning on the local environmental conditions.

155 rh-expressing cells (Crh neurons) after fear conditioning or extinction in mice using translating rib

156 JNJ-42165279 did not affect fear conditioning or within-session extinction learning as ev

157 tone coterminating with a periorbital shock (conditioning) or trials in which these stimuli were rand

158 adult polyps, may provide a form of hormetic conditioning, or environmental priming that elicits stim

159 e weight of evidence indicates that parental conditioning over generations is not a panacea to rescue

160 LA-to-FrA axons was the strongest in between conditioning pairings.

161 e final sample) completed a Pavlovian threat conditioning paradigm across two days.

162 ncies during a differential pavlovian threat-conditioning paradigm in eight patients with a bilateral

163 dults who completed a differential cued fear conditioning paradigm with 24 h delayed extinction while

164 rent, or a stranger, being exposed to a fear conditioning paradigm, and (2) the subsequent fear extin

165 rated elevated freezing in a contextual fear conditioning paradigm.

166 sensory cues paired with food in a classical conditioning paradigm.

167 essing amygdala-dependent memories using cue-conditioning paradigms in rodents, which were subsequent

168 s in rodents have predominantly used context conditioning paradigms, studies in humans have used comp

169 r the rotation trajectories across different conditioning parameters and different datasets?

170 acute grade 2-4 GVHD after reduced intensity conditioning PBSC h-HSCT, perhaps because of the combine

171 nical data extending from the pre-transplant conditioning period through stem cell engraftment were u

172 In the pre-conditioning phase, mice were conditioned for 3 days, an

173 In the conditioning phase, mice were given once-daily alternati

174 ed resistance to insect pests, their role in conditioning plant tolerance, the most durable and promi

175 cardioprotection induced by conventional pre-conditioning (PreCon) is decreased due to impaired AMP-a

176 rent's SCR during the actual process of fear conditioning predicted higher SCR for the child to the C

177 In locations with high air conditioning prevalence, simplified modeling approaches

178 Young children underwent an aversive conditioning procedure either in the parent's presence o

179 The parent was filmed while undergoing a conditioning procedure where one cue was paired with a s

180 mation alone, even after only a single-trial conditioning procedure, and that sleep is necessary to c

181 surgery, underwent a standard auditory fear conditioning procedure.

182 Here, we used operant conditioning procedures to examine the perceptual impact

183 four stages of developmental during the cold conditioning process.

184 The system includes signal conditioning, processing, and transmission parts for con

185 Fear conditioning produced an immediate and dramatic increase

186 genetic activation of the LC before the weak conditioning protocol increased conditioned freezing beh

187 The reflex-conditioning protocol uses electromyography (EMG) to mea

188 Here we report an antibody-based conditioning protocol with reduced toxicity and enhanced

189 onstrate its use in every step of the reflex-conditioning protocol.

190 In addition, L-EES may improve the reflex-conditioning protocol; it has potential to automatically

191 During conditioning, pupil and EEG markers related to heightene

192 ollowed by drying of nanodroplets and charge conditioning reaching Boltzmann charge equilibrium is a

193 patients received a uniform transplantation conditioning regimen (2 Gy of total-body irradiation, cy

194 Choice of conditioning regimen did not influence OS or EFS.

195 en used in combination with fludarabine as a conditioning regimen for allogeneic HSCT for older or co

196 The optimal conditioning regimen for older patients with acute myelo

197 AMSA-Bu), but the impact of this intensified conditioning regimen has not been studied in randomized

198 r modulation of the intensity of the alloHCT conditioning regimen in patients with AML who test posit

199 idence of interaction between MRD status and conditioning regimen intensity for relapse or survival.

200 ut there was no significant effect of either conditioning regimen or donor source on outcome.

201 iotepa; and receiving no pre-transplantation conditioning regimen prior to bone marrow transplant sig

202 with AML benefited from a reduced-intensity conditioning regimen with lower melphalan doses (FM100),

203 0/10 HLA-matched donor, with a myeloablative conditioning regimen, between Jan 1, 2000, and Dec 31, 2

204 The intensified RIC conditioning regimen, FLAMSA-Bu, did not improve outcome

205 Patients received a conditioning regimen, infusion of donor hematopoietic ce

206 , donor type, patient age, disease severity, conditioning regimen, patient and donor sex, and cytomeg

207 enty-one animals received a nonmyeloablative conditioning regimen.

208 atients who could not receive a more intense conditioning regimen.

209 reduce GVHD in cancer patients, but pre-HSCT conditioning regimens and GVHD create a challenging infl

210 from host T cells has not been explored, as conditioning regimens are believed to deplete host T cel

211 The use of total body irradiation as part of conditioning regimens for acute leukaemia is progressive

212 total marrow and lymphoid irradiation in new conditioning regimens seems dependent on its technologic

213 es, have led to the use of reduced-intensity conditioning regimens, in parallel with more aggressive

214 Among the 4 conditioning regimens, the FM100 group had a significant

215 h myeloablative (4) or reduced-intensity (1) conditioning regimens.

216 Both patients received reduced intensity conditioning regimens.

217 treated patients received 1 of the following conditioning regimens: (1) fludarabine+melphalan 100 mg/

218 ciation learning and suggest that trace fear conditioning relies on mechanisms that differ from persi

219 echanistically, we established that enriched conditioning relies on the unique neuronal intrinsic sig

220 f the two cultivars with very different cold conditioning requirements.

221 ystem for stress and anxiety disorders, fear-conditioning research has not yet characterized how thre

222 level of extinction learning of a trace fear conditioning response, a behavioral paradigm that requir

223 sistance exercise (BFRRE) or remote ischemic conditioning (RIC) could improve functional capacity and

224 Remote ischemic conditioning (RIC) has emerged as a promising tool in pr

225 Reduced-intensity conditioning (RIC) regimens have extended the curative p

226 Remote ischemic conditioning (RIC), transient restriction and recirculat

227 geting reperfusion injury is remote ischemic conditioning (RIC).

228 tive conditioning (MAC) or reduced-intensity conditioning (RIC).

229 udying podokinetic after-rotations following conditioning rotations not previously reported we have s

230 c time intervals between preconditioning and conditioning rTMS had stronger stimulation effects in bo

231 environmental enrichment (EE) followed by a conditioning sciatic nerve axotomy that precedes a spina

232 e we show that memory formation through fear conditioning selectively accelerates the degradation of

233 t an episode of restraint prior to the first conditioning session.

234 These rats then received instrumental conditioning sessions where they could press an inactive

235 During these Pavlovian conditioning sessions, we paired CS presentations with p

236 g 60-months of survival was examined in each conditioning set across strata of prognostic covariates,

237 This concept did not apply to the conditioning set of patients with recurrence, where CS e

238 neuronal activity and function, such as fear conditioning, shifts across the estrous cycle.

239 circuit, thereby regulating learning in fear conditioning.SIGNIFICANCE STATEMENT The central amygdala

240 Enriched conditioning significantly increases the regenerative ab

241 release in freely behaving mice during fear conditioning, social interaction, and sleep/wake transit

242 ntal collagen bonding without the additional conditioning step.

243 A 22N blunt probe (conditioning stimulus) was applied to the contralateral

244 Collectively, conditioning strategies reduced both renal and myocardia

245 act on the immune system and in the ischemic conditioning strategy.

246 -dependent transcription in response to fear conditioning stress, and the affected genes include many

247 al cortex as well as amygdala volume in fear conditioning studies.

248 rpart and, hence, may have a similar role in conditioning susceptibility to FHB in barley.

249 of optogenetic manipulations in a Pavlovian conditioning task and examining the influence on anticip

250 using light-field microscopy and an operant-conditioning task in larval zebrafish.

251 tiation and response rate in an instrumental conditioning task, but only when performance demand was

252 (critic) while monkeys performed a classical conditioning task.

253 tection by training mice on a novel eyeblink conditioning task.

254 fluenced learning in an appetitive pavlovian conditioning task.

255 e ~48 h after they learned a delay eye-blink conditioning task.

256 or 2 minutes, followed by MQST or TQST (post-conditioning test stimulus).

257 The pre-conditioning test stimulus, using mechanical/thermal qua

258 r 8 days and subsequently assessed in a post-conditioning test.

259 ituations (in the passive avoidance and fear conditioning tests) and an impairment of nonemotional co

260 Tone-elicited freezing was lower after PRF conditioning than fully reinforced fear (FRF) conditioni

261 amework that increases power of discovery by conditioning the FDR on overlapping associations.

262 re can thus propagate to mature communities, conditioning their functional repertoire.

263 ponsive to the aversive shock during context conditioning, their activity was necessary for memory en

264 S)-related information during classical fear conditioning, thereby having an indispensable role in le

265 in the absence of allergens due to Pavlovian conditioning to a specific cue.

266 caspase-autophagy pathway is engaged by fear conditioning to facilitate associative fear learning and

267 as a coincidence detector during associative conditioning to integrate calcium influx resulting from

268 We provide a novel test of coral parental conditioning to ocean acidification (OA) and tracking of

269 d 58 adults who received a reduced intensity conditioning to PBSC h-HSCT with cyclosporine and mycoph

270 Unlike in context conditioning, cue conditioning (to an odor stimulus) occurred independentl

271 oyed previously established cold temperature conditioning treatments for ripening of two pear cultiva

272 Gaussian noise (but not 8 kHz tone) between conditioning trials impaired the formation of auditory f

273 mice received tone-shock pairings on half of conditioning trials.

274 for adopting this compound into domestic air-conditioning units (ACUs).

275 Differential fear conditioning using FPS was tested in n = 63 children age

276 of this study asks: how does the podokinetic conditioning velocity affect the response velocity and h

277 slowing in a single session of context fear conditioning was found after HPC damage.

278 Cy/Flu conditioning was the probable cause for grade 3-4 hemato

279 Conditioning was treosulfanbased in 84% of patients; 84%

280 Trace eyeblink classical conditioning was used to assess the impact of neonatal a

281 clic voltammetry as rats underwent pavlovian conditioning, we demonstrate that a single stressful exp

282 In fear conditioning, where a conditioned stimulus predicts the

283 on the molecular mechanisms for associative conditioning, which are highly conserved in animals.

284 regenerative paradigm that we call enriched conditioning, which combines environmental enrichment (E

285 rform poorly in both aversive and appetitive conditioning, while individual heterozygous rutabaga/+ a

286 d a video of an adult stranger who underwent conditioning with a different cue reinforced (CS + Stran

287 Conditioning with a weaker footshock caused smaller incr

288 ilineage engraftment; we tested nongenotoxic conditioning with anti-CD45 mAbs conjugated with saporin

289 Conditioning with CD45-SAP allows multilineage engraftme

290 Conditioning with CD45-SAP enabled high levels of multil

291 r of body surface area after lymphodepleting conditioning with cyclophosphamide/fludarabine (Cy/Flu).

292 Conditioning with EDU/SES also revealed unidirectional c

293 onor were randomly assigned to myeloablative conditioning with fractionated 12 Gy TBI and etoposide v

294 We do so by combining Pavlovian conditioning with high-resolution behavioral tracking, o

295 aining, multiple trials of differential odor conditioning with rest intervals.

296 h(2) significantly increased by 20.23% after conditioning with SES.

297 aimed to evaluate the efficacy and safety of conditioning with treosulfan plus fludarabine compared w

298 nthetic niches reflect the immunosuppressive conditioning within a host that contributes to metastati

299 reward-predicting cue prevents second-order conditioning without affecting blocking.

300 Next, new rats received Pavlovian conditioning without photo-stimulation.