ライフサイエンスコーパス: unconditioned

1 s not necessary for the normal expression of unconditioned affective behavioral responses to taste st

2 d reached lymphoid and GVHD target tissue in unconditioned allogeneic RAG2(-/-) gamma-chain(-/-) reci

3 irectional, and immediate, resulting in both unconditioned and conditioned changes in brain and behav

4 Different nuclei of the amygdala mediate unconditioned and conditioned fear responses to threat i

5 d significant reductions in cat odor-induced unconditioned and conditioned fear-related behavior.

6 Nicotine has both unconditioned and conditioned stimulus properties.

7 t had at least 1 affected offspring and used unconditioned and DRB1-conditioned transmission disequil

8 e 14k are anxiolytic in both conditioned and unconditioned animal models of anxiety with minimal seda

9 periment 4 confirmed that the lesion reduced unconditioned anxiety in an elevated zero maze.

10 We found that BNST CRF-OE did not affect unconditioned anxiety-like responses in the elevated plu

11 ssion within BNST neurons on conditioned and unconditioned anxiety-related behavior by using a lentiv

12 isplayed reduced anxiety in several tests of unconditioned anxiety.

13 t or no effect on a range of conditioned and unconditioned appetitive behaviors known to depend on me

14 mplicit regulation of emotion in response to unconditioned auditory threat in healthy controls with E

15 a conditioned stimulus in the absence of the unconditioned aversive stimulus.

16 n between a conditioned stimulus (CS) and an unconditioned, aversive stimulus (US) but also involves

17 n, at least, the functional reengraftment of unconditioned bone marrow.

18 the BLA participates in the conditioned and unconditioned cat odor stimulus association that underli

19 xpression also drives formation of T-ALLs in unconditioned CD-1 nude mice, bypassing any requirements

20 nsplantation of purified exogenous HSCs into unconditioned congenic histocompatible strains of mice,

21 2-fold) and proliferation rates (21%) versus unconditioned constructs.

22 12,422 genes and ESTs from T and T- and the unconditioned control cells, 16 genes were found that ma

23 erate an antidonor humoral response, whereas unconditioned controls infused with similar numbers of B

24 posure to the saccharin cue also blunted the unconditioned dopamine response to morphine.

25 The unconditioned effects of more prolonged aversive states

26 than consummatory behavior maintained by the unconditioned effects of these substances.

27 tive of associative learning, but due to the unconditioned expression of estradiol's anorectic effect

28 Following conditioning, the unconditioned eyeblink response (UR) was analyzed in sub

29 of picrotoxin facilitated the expression of unconditioned eyeblinks evoked by trigeminal stimulation

30 mplete disappearance of both conditioned and unconditioned eyelid responses, and a progressive decrea

31 Modulators of unconditioned fear are potential targets for developing

32 However, 8-OHDPATs potential role in unconditioned fear has yet to be elucidated.

33 lesions of the PMd have been shown to reduce unconditioned fear in rats presented with either a cat o

34 Predator odors induce unconditioned fear in rats; however, the synthetic preda

35 he amygdala participate in the modulation of unconditioned fear induced by predator odor.

36 in shock-induced conditioned or TMT-induced unconditioned fear paradigms.

37 the freezing deficit during training or the unconditioned fear response to predator odor.

38 amygdala is involved in mediating some acute unconditioned fear responses but challenge the notion th

39 the CeL enhanced fear learning and elicited unconditioned fear responses.

40 Thus, TMT is a robust unconditioned fear stimulus in rats, and prior negative

41 n to achieve this effect, particularly to an unconditioned fear stimulus, is incomplete.

42 a contextual fear conditioning paradigm and unconditioned fear to a predator odor.

43 Whether the PMd, AHN and VMH are involved in unconditioned fear to another predator odor derived from

44 The neural circuits for unconditioned fear to predator odors (e.g., cat fur odor

45 neurotoxic lesions of MHDC nuclei in rats on unconditioned fear to TMT and shock-induced contextually

46 Unconditioned fear was also diminished in neuroD2 hetero

47 and oxytocin modulate brain regions involved unconditioned fear, processing of social stimuli and the

48 nts that examined maternal responses to this unconditioned fear-inducing odor were carried out in a s

49 -dihyrdo-2,4,5-trimethylthiazoline (TMT), an unconditioned fear-inducing stimulus.

50 from fear expressed during training and from unconditioned fear.

51 ical systems associated with conditioned and unconditioned fear.

52 t, CeA lesions had no significant effects on unconditioned fear.

53 jor role in modulating predator odor-induced unconditioned fear.

54 articipation of the medial amygdala (MeA) in unconditioned fear.

55 ng in conditioned fear situations but not in unconditioned fear.

56 avioral response during both conditioned and unconditioned fear.

57 Nevertheless, frontal control of basic unconditioned feeding responses remains poorly understoo

58 Confirming modulation of incentive salience, unconditioned food intake was similarly increased by DAM

59 ased release of norepinephrine evoked by the unconditioned footshock stimulus.

60 and VMH, and not cells in the MHDC, mediate unconditioned freezing to the predator odor TMT.

61 information of different modalities, mediate unconditioned freezing, and may be involved in developme

62 ocedures (81% vs 54%; P < .003), although in unconditioned haploidentical donor HCT, nonengraftment w

63 spective data on patients who have undergone unconditioned HCT from either URDs (n = 37) or MSDs (n =

64 e surviving patients and was seen even after unconditioned HCT.

65 one marrow stromal conditioned media (CM) or unconditioned media (UCM) with increasing concentrations

66 Cs (Tx), conditioned media (CM), or vehicle (unconditioned media) at 3 h after TBI.

67 Here we demonstrate that hESCs cultured in unconditioned medium (UM) are subjected to high levels o

68 conditioned MEP at each interval to the mean unconditioned MEP: the higher the ratio, the less inhibi

69 In unconditioned mice, there was decreased survival with an

70 Pentobarbital anesthesia abolished the unconditioned motor response to tap, but failed to aboli

71 nguished behaviorally by the US producing an unconditioned motor response whose form resembles that o

72 habit formation, striatal processing during unconditioned movements (i.e., licking) was characterize

73 scent protein (GFP) transgenic BM cells into unconditioned newborn STAT5ab(-/-) recipients of either

74 asured in the forced swim test, responses to unconditioned nociceptive stimuli, and elevated plus maz

75 of wild-type bone marrow-derived cells into unconditioned, nonirradiated Col4A3 knockout mice during

76 usion of unfractionated wild-type blood into unconditioned, nonirradiated Col4A3 knockout mice improv

77 show that odor exposure during STFP, but not unconditioned odor exposure, induces glomerulus-specific

78 one-mimicking microenvironment compared with unconditioned or myoblast containing matrices.

79 Unconditioned orienting (rearing to nonreinforced presen

80 sing male and female SHR rats exhibited more unconditioned orienting behavior than Wistar-Kyoto rats.

81 ned food-related responses or the display of unconditioned ORs.

82 alcohol or were novel, while also increasing unconditioned port-entries during the intertrial interva

83 BAP but not BLA increased unconditioned port-entries, while both manipulations pre

84 oduced more cue-trial omissions and elevated unconditioned port-entries.

85 To test this hypothesis, unconditioned, prediabetic female NOD mice were given a

86 The startle reflex is an unconditioned, quantifiable behavior used to study senso

87 On transplantation into unconditioned Rag2-/-Il2rgammac-/- recipients, both pre-

88 Heroin and cocaine have very different unconditioned receptor-mediated actions; however, in the

89 hocyte numbers were better in conditioned vs unconditioned recipients (P, .06).

90 fication suggests that learning modifies the unconditioned reflex pathway.

91 ged and older adults displayed reductions in unconditioned responding, discriminant conditioning, and

92 However, learning-related changes in the unconditioned response (UCR) produced by a predictable U

93 responses to cocaine self-administration, an unconditioned response to cocaine itself and a condition

94 lids consistently showed high percentages of unconditioned responses (UR) to the US, and the UR ampli

95 lowing a preconditioning test to measure any unconditioned responses to odor, mice received 5 pairing

96 Overgeneralization of unconditioned responses to unconditioned stimuli similar

97 Unconditioned rewarding stimuli evoke phasic increases i

98 gs demonstrate conditioned diminution of the unconditioned SCR.

99 neural circuits responsible for transforming unconditioned sensory stimuli and generating defensive b

100 g-related reductions in the magnitude of the unconditioned skin conductance response (SCR).

101 at fetal ethanol exposure results in a tuned unconditioned sniffing and neurophysiological olfactory

102 encode associations between conditioned and unconditioned stimuli (CS and US, respectively).

103 generally aversive but socially nonspecific unconditioned stimuli (e.g., unpleasant odors and painfu

104 LA about the conditioned (learned fear) and unconditioned stimuli (innate fear).

105 s a temporal gap between the conditioned and unconditioned stimuli (the trace interval), requires per

106 pleasant, neutral, or unpleasant odors [the unconditioned stimuli (UCS)] in a partial reinforcement

107 presentation of conditioned stimuli (CS) and unconditioned stimuli (US).

108 odors associated with aversive or appetitive unconditioned stimuli (US).

109 ed state transitions; these stimuli included unconditioned stimuli (USs) (liquid rewards and aversive

110 he representations of rewarding and aversive unconditioned stimuli (USs) in the basolateral amygdala

111 Ss) predicted the occurrence of one of three unconditioned stimuli (USs): a large liquid reward, a sm

112 s on the balance between the strength of the unconditioned stimuli and on the motivational state of t

113 ng following two pairings of conditioned and unconditioned stimuli but appear normal following a more

114 same animals using the same conditioned and unconditioned stimuli for eyeblink and fear conditioning

115 d responses when paired with corneal airpuff unconditioned stimuli in rabbits.

116 i without the association of conditioned and unconditioned stimuli in the multisensory thalamic nucle

117 ng tasks where the timing of conditioned and unconditioned stimuli is not optimal for the induction o

118 ing paradigm consisting of socially relevant unconditioned stimuli of critical facial expressions and

119 onditioning stimuli, and presentation of the unconditioned stimuli on sleep-wake states.

120 generalization of unconditioned responses to unconditioned stimuli similar to the trauma may also be

121 Neural representations of conditioned and unconditioned stimuli therefore ultimately connect to US

122 derscore the importance of disorder-relevant unconditioned stimuli when studying the conditioning cor

123 ned is whether generalization occurs between unconditioned stimuli with overlapping features.

124 g only 50% of conditioned stimuli with their unconditioned stimuli), and extinction (unpaired conditi

125 ociative learning, but not single context or unconditioned stimuli, induces rapid dephosphorylation (

126 (conditioned stimuli, CS), aversive events (unconditioned stimuli, US), and their relationship.

127 ) inputs with neuromodulatory reinforcement (unconditioned stimuli, US), which for aversive learning

128 the temporal gap between the conditioned and unconditioned stimuli.

129 imulus-free time gap between conditioned and unconditioned stimuli.

130 al and the association of these neurons with unconditioned stimuli.

131 uff to the wrist, or nothing, which acted as unconditioned stimuli.

132 ls that experienced unpaired conditioned and unconditioned stimuli.

133 ich was paired with one of three audiovisual unconditioned stimuli: negative insults with critical fa

134 or in determining the reinforcement value of unconditioned stimuli: poorly predicted ("surprising") o

135 ditioned stimulus (30 s; 85 dB white noise)--unconditioned stimulus (2 s; 0.57 mA foot shock) pairing

136 us was paired with a periorbital stimulation unconditioned stimulus (750-ms delay paradigm).

137 us was paired with a periorbital stimulation unconditioned stimulus (750-ms delay paradigm).

138 ial, the conditioned stimulus (tone) and the unconditioned stimulus (corneal airpuff) were presented

139 different effects of various conditioned and unconditioned stimulus (CS-US) preexposure conditions on

140 e in the measurement of conditioned stimulus-unconditioned stimulus (CS-US) time intervals during cla

141 he context and associate the context with an unconditioned stimulus (footshock).

142 to a conditioned stimulus (click CS) and an unconditioned stimulus (glabella tap US) were studied in

143 , in which the conditioned stimulus (CS) and unconditioned stimulus (UCS) coterminate.

144 t study, skin conductance response (SCR) and unconditioned stimulus (UCS) expectancy were measured co

145 n between a conditioned stimulus (CS) and an unconditioned stimulus (UCS) has been learned.

146 fail to produce aversive conditioning as an unconditioned stimulus (UCS) when presented in large amo

147 ditioned stimulus is paired with an aversive unconditioned stimulus (UCS).

148 s (CS) is repeatedly paired with an aversive unconditioned stimulus (UCS).

149 ivated when the sucrose reward was received [unconditioned stimulus (UCS)].

150 An unpleasant sound served as unconditioned stimulus (US) and pictures of neutral male

151 auditory nerve that immediately precedes an unconditioned stimulus (US) applied to the trigeminal ne

152 a conditioned stimulus (CS) must precede the unconditioned stimulus (US) by at least about 100 ms for

153 lus (CS) previously paired with a grid shock unconditioned stimulus (US) can greatly enhance the earl

154 owed 250 ms later by a 100 ms air puff as an unconditioned stimulus (US) coterminating with it.

155 tine stimulus could be diminished through an unconditioned stimulus (US) devaluation procedure.

156 onditional stimulus; CS) paired with a shock-unconditioned stimulus (US) does not emerge until postna

157 ip between the conditioned stimulus (CS) and unconditioned stimulus (US) during reactivation is suffi

158 s highly lateralized to the eye to which the unconditioned stimulus (US) has been directed.

159 tal shock or a corneal airpuff served as the unconditioned stimulus (US) in separate groups of sham o

160 In this procedure, the delivery of the unconditioned stimulus (US) is made contingent on condit

161 a conditioned stimulus (CS) and an aversive unconditioned stimulus (US) is often assumed to be funda

162 ion of the conditioned stimulus (CS) and the unconditioned stimulus (US) is separated in time by an i

163 Parallel to this, a novel CS-unconditioned stimulus (US) pairing induced stronger Fos

164 e been widely hypothesized to be part of the unconditioned stimulus (US) pathway of odor-shock classi

165 oning, such as conditioned stimulus (CS) and unconditioned stimulus (US) pathway, is important for un

166 CSs) that have a pre-existing relation to an unconditioned stimulus (US) rather than learning about a

167 to provide the cerebellum with a "teaching" unconditioned stimulus (US) signal required for cerebell

168 ditory conditioned stimulus (CS) and a shock unconditioned stimulus (US) that are separated by a 20-s

169 ditory conditioned stimulus (CS) and a shock unconditioned stimulus (US) that are separated by a 20-s

170 stimulus (CS) followed by an air puff as an unconditioned stimulus (US) that coterminated with it.

171 Ss) were pictures of virtual lights, and the unconditioned stimulus (US) was an electric shock.

172 diated EBC deficits and the intensity of the unconditioned stimulus (US) was explored in the current

173 odification (CRM)--changes in the NMR to the unconditioned stimulus (US) when tested in the absence o

174 ) nictitating membrane responses (NMR) to an unconditioned stimulus (US) when the US is tested by its

175 tioned stimulus (CS) and the delivery of the unconditioned stimulus (US), and delay conditioning, in

176 (CS), light CS, and periorbital stimulation unconditioned stimulus (US), rats received associative t

177 of Pavlovian conditioning using food as the unconditioned stimulus (US), some rats (sign-trackers) c

178 rates the conditioned stimulus (CS) from the unconditioned stimulus (US), the association of which ha

179 tioned response (CR) after reexposure to the unconditioned stimulus (US)--and spontaneous recovery--t

180 ity only during the trace interval, and some unconditioned stimulus (US)-coding cells will shift in t

181 mulus (CS) was paired with an electric shock unconditioned stimulus (US).

182 ulus (CS) and a unilateral periorbital shock unconditioned stimulus (US).

183 ts is lateralized to the eye targeted by the unconditioned stimulus (US).

184 ponsive to the conditioned stimulus (CS) and unconditioned stimulus (US).

185 stimulus (CS) and a corneal air puff as the unconditioned stimulus (US).

186 stimulus (CS) by pairing it with an aversive unconditioned stimulus (US).

187 ditioned stimulus (CS) and an electric shock unconditioned stimulus (US).

188 nditioned stimulus (CS) and the onset of the unconditioned stimulus (US).

189 tap conditioned stimulus (CS) and tail shock unconditioned stimulus (US).

190 the auditory CS and periorbital stimulation unconditioned stimulus (US).

191 being reactivated by the presentation of the unconditioned stimulus (US).

192 CS+) was paired with sucrose delivery [i.e., unconditioned stimulus (US)], and the other stimulus (i.

193 that was previously paired with footshocks [unconditioned stimulus (US)].

194 0 seconds, 85 dB white noise) paired with an unconditioned stimulus (US, 2 seconds, 0.57 mA footshock

195 ustic conditioned (CS, tone) and an aversive unconditioned stimulus (US, electric shock).

196 mulus (CS; 3 sec) and a fear-producing shock unconditioned stimulus (US; 0.5 sec) separated by a sile

197 ker stimulation) from a behaviorally salient unconditioned stimulus (US; air puff to the eye).

198 onditioned stimulus, CS; e.g., a tone) to an unconditioned stimulus (US; e.g., a shock).

199 onditioned stimulus (CS; saccharin, SAC) and unconditioned stimulus (US; lithium chloride, LiCl).

200 timulus (CS) paired with a periorbital shock unconditioned stimulus (US; presented at 200- or 500-ms

201 he siphon (the CS+) is paired with a noxious unconditioned stimulus (US; tail shock), while a second

202 stimulus predictive of 10% sucrose solution (unconditioned stimulus [US]), but not during equally fre

203 ce of malaise (such as that induced by LiCl; unconditioned stimulus [US]).

204 We use this social reward as an unconditioned stimulus and pair it with a distinct visua

205 be related to the relative intensity of the unconditioned stimulus and somatic requirements of the t

206 Thus, specific features of the unconditioned stimulus appear to be encoded in the amygd

207 Although the CS and unconditioned stimulus are contiguous, this very long de

208 so suggest an early dopamine response to the unconditioned stimulus as training continues.

209 reater retention of the conditioned stimulus/unconditioned stimulus association at each follow-up ses

210 stores memories of the conditioned stimulus-unconditioned stimulus association, but the origin of UC

211 ) in subjects acquiring conditioned stimulus-unconditioned stimulus associations than in those presen

212 -conditioned stimulus with an electric shock-unconditioned stimulus causes new projection neuron syna

213 esentations of a conditioned stimulus and an unconditioned stimulus did not acquire conditioned respo

214 tone-conditioned stimulus (CS) and eye-shock unconditioned stimulus during acquisition training.

215 rons conveying the reinforcing effect of the unconditioned stimulus during associative learning to th

216 airing ACh with dopamine, which mediates the unconditioned stimulus in ganglia, decreased the excitab

217 sical conditioning modifies responding to an unconditioned stimulus in the absence of a conditioned s

218 We used amphetamine (AMPH) as the unconditioned stimulus in the conditioned place preferen

219 bility of the hormone estradiol to act as an unconditioned stimulus in the conditioned taste avoidanc

220 We found that exposure to the unconditioned stimulus initiates an unconditioned stimul

221 Dopamine receptor DopR mediates the unconditioned stimulus inputs onto MB.

222 -12 Hz depending on the conditioned stimulus-unconditioned stimulus intervals (1 s, 500 ms, 250 ms) s

223 link conditioning under conditioned stimulus?unconditioned stimulus intervals known to be optimal or

224 Climbing fibre activity elicited by an unconditioned stimulus is inhibited during the expressio

225 onship between a conditioned stimulus and an unconditioned stimulus is represented in the brain.

226 tone is repeatedly paired with a reinforcing unconditioned stimulus like periorbital stimulation, the

227 were examined as a function of two different unconditioned stimulus locations.

228 ing this contextual memory engram with a new unconditioned stimulus of an opposite valence.

229 vanilla odor was associated with a negative unconditioned stimulus of saline solution, cockroaches c

230 ppermint odor was associated with a positive unconditioned stimulus of sucrose solution and vanilla o

231 associative properties of nicotine from the unconditioned stimulus or reward to include the role of

232 ation of a conditioned stimulus (CS) with an unconditioned stimulus over a stimulus-free trace interv

233 ronal activation during conditioned stimulus-unconditioned stimulus pairing were assessed using Fos-l

234 Training consisted of 2 CS-footshock unconditioned stimulus pairings.

235 d stimulus like periorbital stimulation, the unconditioned stimulus promotes acquisition of condition

236 associative processes rather than increased unconditioned stimulus reactivity as the active mechanis

237 The ability to acquire CRs with IO unconditioned stimulus signals that were blocked or seve

238 nditioned stimuli that are predictive of the unconditioned stimulus than by conditioned stimuli that

239 ygdala, as they convey information about the unconditioned stimulus to lateral amygdala neurons durin

240 on PD 25 when nontarget conditioned stimulus-unconditioned stimulus training occurred prior to the te

241 ng (in which the conditioned stimulus CS and unconditioned stimulus US overlap and co-terminate) is i

242 ned stimulus was an auditory tone, while the unconditioned stimulus was a low-intensity, single or do

243 ts when a relatively intense (5 psi) airpuff unconditioned stimulus was paired with the CS.

244 onditioned stimulus) and the electric shock (unconditioned stimulus) in mushroom body (MB) neurons.

245 facilitate decreases in anxiety (even to an unconditioned stimulus) while potentially promoting pair

246 imulus (CS) alone] or a reinforced trial (CS-unconditioned stimulus).

247 s repeatedly presented in the absence of the unconditioned stimulus, and the expression of previously

248 were independent of levels of anxiety to the unconditioned stimulus, implicating associative processe

249 is, a "trace" period between conditioned and unconditioned stimulus, requires awareness of the associ

250 p between a conditioned stimulus (CS) and an unconditioned stimulus, so that synaptic plasticity and

251 timulus, amyl-acetate, paired with a salient unconditioned stimulus, sucrose, for feeding.

252 r the cardiac-unconditioning response to the unconditioned stimulus, suggesting a role for the claust

253 Using amphetamine (AMPH) as the unconditioned stimulus, the present study compared two p

254 r predicts delivery of a salient reinforcer (unconditioned stimulus, UCS).

255 ed stimulus, CS) associated with pain onset (unconditioned stimulus, US) provoke defensive responses

256 as no such effect on responding during food (unconditioned stimulus, US) responding or in the intertr

257 e response-independent presentation of food (unconditioned stimulus, US).

258 stimulus, CS) when it is paired with touch (unconditioned stimulus, US).

259 variable representing the prediction of the unconditioned stimulus, whereas activity in the dorsolat

260 that have received the same pairing with the unconditioned stimulus, yet have no predictive value.

261 They show that a primary function of the unconditioned stimulus-evoked activity of BLA neurons is

262 e to the unconditioned stimulus initiates an unconditioned stimulus-specific reconsolidation of learn

263 y conditioned stimulus (CS) with an aversive unconditioned stimulus.

264 esentations with a CS (tone or light) and an unconditioned stimulus.

265 ummatory procedure that used morphine as the unconditioned stimulus.

266 s pairing rates between a conditioned and an unconditioned stimulus.

267 ned stimulus (CS) and a behaviorally salient unconditioned stimulus.

268 n, head turn, etc.) learned with an aversive unconditioned stimulus.

269 ary somatosensory cortex, which mediates the unconditioned stimulus.

270 (CS+/CS-) and an aversive alarm noise as the unconditioned stimulus.

271 ivity in the dentate gyrus after exposure to unconditioned stimulus.

272 e to associative pairing of the short CS and unconditioned stimulus.

273 the assignment of motivational value to the unconditioned stimulus.

274 pendency of fear recovery with a shock as an unconditioned stimulus.

275 responses after presentations of an auditory unconditioned stimulus.

276 the inhibitory stimulus was paired with the unconditioned stimulus.

277 g visual conditioned stimuli and an auditory unconditioned stimulus.

278 ed with a mild electric shock serving as the unconditioned stimulus.

279 s signalled by presenting a tone without the unconditioned stimulus.

280 3 kHz tone conditioned stimulus and airpuff unconditioned stimulus.

281 a tone conditioned stimulus and an air puff unconditioned stimulus.

282 iative learning by pairing with a starvation unconditioned stimulus.

283 l was interposed between the conditioned and unconditioned stimulus.

284 ior to omission (extinction) of the aversive unconditioned stimulus.

285 y reinforcing associations between outcomes (unconditioned stimulus; US) and their predictors (condit

286 then experiences the symptoms of poisoning (unconditioned stimulus; US).

287 ptor actions are independent of the primary (unconditioned) stimulus (i.e., the opiate or the stimula

288 Here, we used a novel unconditioned-stimulus (US) reactivation paradigm to int

289 suggest that ferret odor produces a reliable unconditioned stress response and may be useful as a pro

290 We have shown previously that unconditioned stressors inhibit neurons of the lateral/c

291 ute lymphoblastic leukemia when infused into unconditioned syngeneic mice.

292 ation between conditioned visual stimuli and unconditioned taste stimuli, as well as the unexpected v

293 Unconditioned TDTs revealed overtransmission of shared e

294 Unconditioned trait-like anxiety-fear responses remained

295 clarified which conditions are receptive to unconditioned transplants and which require more myeloab

296 vival was also seen in patients who received unconditioned transplants in comparison with myeloablati

297 to 10msec (10 trials at each interval and 40 unconditioned trials).

298 s in which the H-reflex was simply measured [unconditioned (UC) subjects], and locomotion was reasses

299 Unconditioned URD HCT achieves excellent rates of donor

300 Unconditioned whisking patterns were quantitatively char