ライフサイエンスコーパス: hippocampal-dependent

1 performed TP and control tasks that are not hippocampal dependent.

2 In primates relatively few hippocampal-dependent abilities (e.g. some aspects of re

3 Interestingly, the hippocampal-dependent alterations were not present in ju

4 In the present study, we examined hippocampal-dependent and -independent working memory us

5 affect fear conditioning, a memory task with hippocampal-dependent and hippocampal-independent compon

6 eptors for the acquisition and expression of hippocampal-dependent and hippocampal-independent forms

7 cognitive assessments distinguishing between hippocampal-dependent and hippocampal-independent functi

8 ome circumstances, delay conditioning can be hippocampal-dependent and trace conditioning can be spar

9 Therefore, the effects of stress on working (hippocampal-dependent) and reference (hippocampal-indepe

10 ction in young or middle-aged animals in the hippocampal-dependent appetitive radial maze task.

11 critical regulator of synaptic function and hippocampal-dependent associative and spatial learning.

12 Importantly, CTRP4 deficiency impairs hippocampal-dependent associative learning and memory as

13 The results suggest a relationship between hippocampal-dependent behavior and experience-dependent

14 AP5 impaired measures of hippocampal-dependent behavior and increased locomotor a

15 es of synaptic strength were correlated with hippocampal-dependent behavior and synaptic plasticity f

16 rve injury (SNI) neuropathic pain in mice on hippocampal-dependent behavior and underlying cellular a

17 es adult hippocampal neurogenesis and alters hippocampal-dependent behavior in rodents.

18 Evaluation of hippocampal-dependent behavior revealed parallel finding

19 straint stress enhanced freezing to context (hippocampal-dependent behavior) and tone (hippocampal-in

20 LTP and LTD coincides with the emergence of hippocampal-dependent behavior, implying that Ras-GRF pr

21 ne and synapse densities, and impairments in hippocampal-dependent behavior.

22 campal lateralization may play a role in the hippocampal-dependent behavioral deficit.

23 accumulation, tau hyperphosphorylation, and hippocampal-dependent behavioral impairments.

24 compared to sham-irradiated controls in the hippocampal-dependent behavioral task.

25 tyrosine kinase adaptor protein 1 (NCK1), in hippocampal dependent behaviors and development.

26 sociability, olfaction, anxiety, or several hippocampal-dependent behaviors.

27 ns (Tiam1(fKO) ) and assessed the effects on hippocampal-dependent behaviors.

28 ed neuronal morphogenesis may be involved in hippocampal-dependent behaviors.

29 ult hippocampal neuron shape acquisition and hippocampal-dependent behaviors.

30 mpus, as hippocampal-independent and ventral hippocampal-dependent behaviours remained unaffected.

31 Behaviourally, Fmr1 KO rats show deficits in hippocampal-dependent, but not hippocampal-independent,

32 , the specific role of the D1R versus D5R in hippocampal dependent CFC has not been investigated.

33 These findings suggest hippocampal-dependent changes in contextual retrieval as

34 tablish SUMO as a novel regulator of LTP and hippocampal-dependent cognition and additionally implica

35 ic factor (BDNF), a growth factor central to hippocampal-dependent cognition and plasticity, instead

36 ration and increases synaptic plasticity and hippocampal-dependent cognition in aged mice.

37 y neurotransmitters, have been implicated in hippocampal-dependent cognition.

38 Hippocampal-dependent cognitive behavior, neurogenesis,

39 As a tool for studying the mechanisms of hippocampal-dependent cognitive decline, we developed a

40 transcriptional inflammatory activation and hippocampal-dependent cognitive decline.

41 -molecule inhibitor of the ISR, reversed the hippocampal-dependent cognitive deficits induced by TBI

42 n that chronic psychological stress produces hippocampal-dependent cognitive deficits that are consis

43 agonism resulted in a sparing of TBI-induced hippocampal-dependent cognitive dysfunction and reduced

44 potential explanation for the maintenance of hippocampal-dependent cognitive function after androgen

45 ally, or locally in the hippocampus, impairs hippocampal-dependent cognitive function and neurogenesi

46 , both M(1) agonists enhanced acquisition of hippocampal-dependent cognitive function but did not rev

47 amyloid-beta (Abeta) protein expression, and hippocampal-dependent cognitive function in an animal mo

48 hippocampal CA1 neurons and preservation of hippocampal-dependent cognitive function when examined a

49 uble-edged sword': mild stress might promote hippocampal-dependent cognitive function, whereas severe

50 (LTP) in hippocampal CA1 pyramidal cells and hippocampal-dependent cognitive function.

51 Circulating estrogen levels and hippocampal-dependent cognitive functions decline with a

52 ing of development of the hippocampus and of hippocampal-dependent cognitive functions in primates.

53 ippocampal neurogenesis and neuroplasticity, hippocampal-dependent cognitive functions, and behaviour

54 GIRK channels activity in the maintenance of hippocampal-dependent cognitive functions, their involve

55 olymorphism of the BDNF Val66Met may mediate hippocampal-dependent cognitive functions.

56 is crucial for preserving several aspects of hippocampal-dependent cognitive functions.

57 mice at midlife, but not young age, induced hippocampal-dependent cognitive impairment, dorsal hippo

58 flexibly navigate an environment relies on a hippocampal-dependent cognitive map.

59 ycle in female rats correlate with increased hippocampal-dependent cognitive performance in a manner

60 is may be associated with selective forms of hippocampal-dependent cognitive processes.

61 antation exhibited superior performance on a hippocampal-dependent cognitive task 4 months postirradi

62 expression, concomitant with impairments on hippocampal-dependent cognitive tasks, were observed in

63 vanol consumption can act as a driver of the hippocampal-dependent component of cognitive aging.

64 d mice exhibited significant improvements in hippocampal-dependent contextual fear conditioning compa

65 emonstrated that memory consolidation of the hippocampal-dependent contextual fear-conditioning task

66 e glucose group showed superior retention of hippocampal-dependent contextual learning at test relati

67 ng glucose consumption improves retention of hippocampal-dependent contextual learning but not cued l

68 rimentally examined the effect of glucose on hippocampal-dependent contextual learning versus cued fe

69 k2(-/-) mice exhibited a striking deficit in hippocampal-dependent (contextual) and hippocampal-indep

70 Impaired, hippocampal-dependent, contextual fear conditioning (CFC

71 ations may lead to therapeutic approaches to hippocampal-dependent dysfunctions, such as Alzheimer's

72 ness, faster conduction speeds, and enhanced hippocampal-dependent emotional learning.

73 episode after incidental encoding based upon hippocampal-dependent episodic memory.

74 prompts interest in the role of REM sleep in hippocampal-dependent episodic memory.

75 in relation to sleep-dependent memory tasks: hippocampal-dependent episodic verbal memory and nonhipp

76 drome (DS) patients exhibit abnormalities of hippocampal-dependent explicit memory, a feature that is

77 conditional knock-out mice exhibit impaired hippocampal-dependent fear learning.

78 rat postnatal day (P) 7 permanently impairs hippocampal-dependent function in mature (P60) rats beca

79 significant information on the emergence of hippocampal-dependent functions in humans, on the time c

80 nvolved in molecular alterations that govern hippocampal-dependent functions.

81 ssed animals were impaired in retention of a hippocampal-dependent hidden platform version of the Mor

82 beta (ERbeta) in mediating performance on a hippocampal-dependent, hormone-sensitive task, inhibitor

83 ptor protein tyrosine phosphatase Shp2, show hippocampal-dependent impairments in spatial learning an

84 These data indicate that hippocampal-dependent impairments in spatial processing

85 crosses the blood-brain barrier and promotes hippocampal dependent learning and memory in a BDNF-depe

86 us work shows that sleep deprivation impairs hippocampal-dependent learning and long-term potentiatio

87 road forebrain regions of adult mice impairs hippocampal-dependent learning and long-term potentiatio

88 inase II (CAMKII) are critical modulators of hippocampal-dependent learning and LTP.

89 arly gene that has been widely implicated in hippocampal-dependent learning and memory and is believe

90 of Hdac4 in brain results in impairments in hippocampal-dependent learning and memory and long-term

91 the hippocampus of middle-aged mice enhances hippocampal-dependent learning and memory and restores i

92 Hippocampal-dependent learning and memory deficits have

93 ing conditional knock-out mice, we show that hippocampal-dependent learning and memory deficits in CD

94 Consistently, the mutant mice displayed hippocampal-dependent learning and memory deficits.

95 ory synapse number, synaptic plasticity, and hippocampal-dependent learning and memory due to a failu

96 rch and theory point to the possibility that hippocampal-dependent learning and memory mechanisms tra

97 pal neurochemistry, neuronal morphology, and hippocampal-dependent learning and memory processes.

98 Exercise improves performance on hippocampal-dependent learning and memory tasks and incr

99 A1 synapses, and have no deficits in several hippocampal-dependent learning and memory tasks.

100 5-HT(1A)-KO animals showed a deficit in hippocampal-dependent learning and memory tests, such as

101 e experimental design was that the status of hippocampal-dependent learning and memory was documented

102 By contrast, hippocampal-dependent learning and memory were not affec

103 units/kg diet, respectively) vitamin D3, and hippocampal-dependent learning and memory were then test

104 Kcnj6 triploid mice exhibit deficits in hippocampal-dependent learning and memory, altered respo

105 Indeed, leptin influences hippocampal-dependent learning and memory, and more rece

106 f the hippocampus and significantly impaired hippocampal-dependent learning and memory, as assayed by

107 and suggest that the Syt IV mutation affects hippocampal-dependent learning and memory, as well as mo

108 tion of HCN1 from forebrain neurons enhances hippocampal-dependent learning and memory, augments the

109 ved in several forms of plasticity including hippocampal-dependent learning and memory, experience-de

110 rs hippocampus-related functions, we studied hippocampal-dependent learning and memory, synaptic plas

111 rtant for the synaptic plasticity underlying hippocampal-dependent learning and memory.

112 vival in the hippocampus as well as enhanced hippocampal-dependent learning and memory.

113 f D(1)/D(5) receptors is required for normal hippocampal-dependent learning and memory.

114 nscription factor in the CNS of mice impairs hippocampal-dependent learning and memory.

115 ion from the locus ceruleus are required for hippocampal-dependent learning and memory.

116 f synaptic connectivity and thus facilitates hippocampal-dependent learning and memory.

117 Nile virus (WNV) or Zika virus (ZIKV) impact hippocampal-dependent learning and memory.

118 ity and have been implicated as mediators of hippocampal-dependent learning and memory.

119 y, sensorimotor retardation, and deficits in hippocampal-dependent learning and memory.

120 ampal neurogenesis, synaptic plasticity, and hippocampal-dependent learning and memory.

121 -term depression (LTD), inducing deficits in hippocampal-dependent learning and memory.

122 in vivo are associated with improvements in hippocampal-dependent learning and memory.

123 c knockout mice, and further resolve loss of hippocampal-dependent learning and memory.

124 med feeding resulted in dramatic deficits in hippocampal-dependent learning and memory.

125 9, rescued Abeta-induced deficits in LTP and hippocampal-dependent learning and memory.

126 al suppressor of CA2 synaptic plasticity and hippocampal-dependent learning and memory.

127 an increasingly important role in supporting hippocampal-dependent learning and the modulation of moo

128 ke patterns and sleep EEGs and showed normal hippocampal-dependent learning as assayed by the Morris

129 ent causes hyperactivity and more pronounced hippocampal-dependent learning deficits.

130 eration in the cortex and hippocampus and in hippocampal-dependent learning has been demonstrated, it

131 nesis, with implications for amelioration of hippocampal-dependent learning impairments associated wi

132 We demonstrate that exercise enables hippocampal-dependent learning in conditions that are no

133 potential therapeutic strategy for improving hippocampal-dependent learning in patients with mesial t

134 In experiments with rats, we found that the hippocampal-dependent learning of new paired associates

135 creased after trace eyeblink conditioning, a hippocampal-dependent learning paradigm.

136 ative evidence of behavioral disruption in a hippocampal-dependent learning task following developmen

137 e exposed to the stressor and trained on the hippocampal-dependent learning task of trace conditionin

138 Rats were trained as adults on the hippocampal-dependent learning task of trace eyeblink co

139 ve function in arrhythmic animals by using a hippocampal-dependent learning task.

140 al forms of hippocampal LTP and a particular hippocampal-dependent learning task.

141 long-term potentiation (LTP), and results in hippocampal-dependent learning that seems more rigid and

142 neurotransmitter serotonin (5-HT) modulates hippocampal-dependent learning through serotonin 1A (5-H

143 ear extinction (e.g., appetitive extinction, hippocampal-dependent learning).

144 ormal response to context, indicating intact hippocampal-dependent learning, but reduced response to

145 Hippocampal-dependent learning, memory and ischemic neur

146 tic potentiation in hippocampus and regulate hippocampal-dependent learning.

147 fear conditioning, an indicator of defective hippocampal-dependent learning.

148 creases in neuronal activity associated with hippocampal-dependent learning.

149 hippocampus and consequently to deficits in hippocampal-dependent learning.

150 ication necessary for Hebbian plasticity and hippocampal-dependent learning.

151 asticity at Schaffer collateral synapses and hippocampal-dependent learning.

152 re, we focus primarily on genetic studies of hippocampal-dependent learning.

153 ejuvenates hippocampal function and improves hippocampal-dependent learning.

154 Acetylcholine critically influences hippocampal-dependent learning.

155 hanges are responsible for the impairment in hippocampal-dependent learning.

156 ion impairs long-term potentiation (LTP) and hippocampal-dependent learning.

157 were consistent across tasks, regardless of hippocampal-dependent learning.

158 However, the hippocampal-dependent list-learning performance was dire

159 on making that cannot be explained easily by hippocampal-dependent long-term memory or spatial cognit

160 that are critical for their contribution to hippocampal-dependent long-term memory.

161 of this inhibition lowers the threshold for hippocampal-dependent long-term synaptic potentiation an

162 euron population activity was increased in a hippocampal-dependent manner following acute restraint s

163 cted question after incidental encoding in a hippocampal-dependent manner, consistent with the use of

164 rative process supporting the integration of hippocampal-dependent memories into neocortical networks

165 We hypothesize that the consolidation of hippocampal-dependent memories might not depend on SWS p

166 to involve the gradual transfer of transient hippocampal-dependent memories to distributed neocortica

167 when" memory while preserving other forms of hippocampal-dependent memories.

168 r regulating gene expression associated with hippocampal-dependent memories.

169 cts in some forms of synaptic plasticity and hippocampal-dependent memories.

170 odulate both the encoding and the storage of hippocampal-dependent memories.

171 participate in the formation and storage of hippocampal-dependent memories.

172 Finally, LBP k.o. mice show impaired hippocampal-dependent memory and increased anxiety-like

173 Dopamine (DA) is required for hippocampal-dependent memory and long-term potentiation

174 in 3G (Sema3G) in endothelial cells impaired hippocampal-dependent memory and reduced dendritic spine

175 r-deficient mice and found that they develop hippocampal-dependent memory and synaptic dysfunction, w

176 the hippocampus and is reflected in enhanced hippocampal-dependent memory and synaptic plasticity.

177 1 reduces GluA1 and GluA2 levels and impairs hippocampal-dependent memory and synaptic plasticity.

178 That osteocalcin (OCN) is necessary for hippocampal-dependent memory and to prevent anxiety-like

179 DH E2 infusion enhances hippocampal-dependent memory by rapidly activating extra

180 Hippocampal-dependent memory consolidation during sleep

181 t CREB-mediated transcription is integral to hippocampal-dependent memory consolidation processes.

182 Since PAF is required for hippocampal-dependent memory consolidation, and since th

183 ation by low-dose anisomycin failed to block hippocampal-dependent memory consolidation.

184 vely support the idea that the transience of hippocampal-dependent memory directly reflects the turno

185 is underscored by behavioral impairments in hippocampal-dependent memory displayed by MMP-9 null-mut

186 However, the effect of dietary intake on hippocampal-dependent memory during childhood has remain

187 the role of apamin-sensitive SK channels on hippocampal-dependent memory encoding and retention was

188 ation of hippocampal synaptic plasticity and hippocampal-dependent memory encoding.

189 reported aberrant neurogenesis and impaired hippocampal-dependent memory following stroke.

190 investigated the role of mRNA methylation in hippocampal-dependent memory formation in mice.

191 patients experience cognitive deficits, and hippocampal-dependent memory impairment has been reporte

192 The hippocampal-dependent memory impairment was paralleled b

193 In contrast, hippocampal-dependent memory impairments were observed o

194 matase regulate inhibitory neurons (INs) and hippocampal-dependent memory in adult female mice, but n

195 (BDNF) modulates hippocampal plasticity and hippocampal-dependent memory in cell models and in anima

196 from forebrain glutamatergic neurons impairs hippocampal-dependent memory in male conditional knock-o

197 repression enhances, while Tet1(FL) impairs, hippocampal-dependent memory in male mice.

198 ults indicate that exogenous OCN can improve hippocampal-dependent memory in mice and identify molecu

199 pocampus, as transducing OCN's regulation of hippocampal-dependent memory in part through inositol 1,

200 th elevated anxiety and impaired working and hippocampal-dependent memory in these mice.

201 Hippocampal-dependent memory is thought to be supported

202 The latter, hippocampal-dependent memory loss occurred in the absenc

203 synaptic learning rule for distinct forms of hippocampal-dependent memory mediated by distinct hippoc

204 ion, and long-term plasticity, important for hippocampal-dependent memory processes.

205 and spatial recognition tasks are solved by hippocampal-dependent memory processes.

206 ation facilitates hippocampal plasticity and hippocampal-dependent memory storage by modulating the a

207 sed that performing the 2-Back WM prior to a hippocampal-dependent memory task would impair performan

208 'matching-to-place' Morris water maze test-a hippocampal-dependent memory task-without the convulsant

209 xFAD mice of the same age were impaired in a hippocampal-dependent memory task.

210 no behavioral abnormalities were detected in hippocampal-dependent memory tasks, which correlated wit

211 role for neurogenesis in some, but not all, hippocampal-dependent memory tasks.

212 are not only affected by the formation of a hippocampal-dependent memory, but also participate in it

213 relevance of journey-dependent activity for hippocampal-dependent memory, however, is not well under

214 ove neurocognitive functioning, particularly hippocampal-dependent memory, in children with FASDs.

215 ed long term potentiation (LTP) and impaired hippocampal-dependent memory, suggesting a 'detrimental'

216 o investigate the roles phosphatases play in hippocampal-dependent memory, we studied transgenic mice

217 ibit a spectrum of individual differences in hippocampal-dependent memory.

218 beta, regulated transcription and maintained hippocampal-dependent memory.

219 s an increase in sleep drive and deficits in hippocampal-dependent memory.

220 nizer that regulates synaptic plasticity and hippocampal-dependent memory.

221 ss and may be associated with enhancement of hippocampal-dependent memory.

222 nduced cognitive impairments have focused on hippocampal-dependent memory.

223 by suggesting that stress should also impair hippocampal-dependent memory.

224 intervals commensurate with the duration of hippocampal-dependent memory.

225 echanism underlying the action of ghrelin on hippocampal-dependent memory.

226 Feeding behavior is heavily influenced by hippocampal-dependent mnemonic functions, including epis

227 c acetylcholine receptors (mAChRs) influence hippocampal-dependent mnemonic processing.

228 rs consolidation of long-term memory, in the hippocampal-dependent Morris water maze spatial memory t

229 and contextual memory but were impaired in a hippocampal-dependent, nonmatching-to-place working memo

230 sgenic mice showed significant deficits in a hippocampal-dependent object location task and a prefron

231 lic pulse of estradiol prior to testing on a hippocampal-dependent object placement (OP) task to asse

232 Immediately after training in a hippocampal-dependent object recognition task, mice rece

233 sion levels of synaptic protein markers, and hippocampal-dependent object-placement memory as a behav

234 We developed a novel version of the hippocampal-dependent paired associate inference (PAI) p

235 In experiments using a hippocampal-dependent paired-associate task for rats, th

236 valuated brain activity at rest and during a hippocampal-dependent pattern separation task.

237 tly enhancing and attenuating, respectively, hippocampal-dependent place conditioning.

238 nvestigations to uncover the role of D2Rs in hippocampal-dependent plasticity and learning.

239 ing to occur, and aligns dreaming with other hippocampal-dependent processes such as episodic memory

240 sNS selectively impaired working memory in a hippocampal-dependent radial arm water-maze task without

241 g performance of more cognitively demanding, hippocampal-dependent recognition memory tasks.

242 of the hippocampus, but left performance on hippocampal-dependent reference and working memory tasks

243 3 (n-3) fatty acids, and refined sugar, with hippocampal-dependent relational memory in prepubescent

244 t it is paradoxically less active during the hippocampal-dependent relational memory phase relative t

245 e was selectively positively associated with hippocampal-dependent relational memory.

246 In parallel, we show a shift away from hippocampal-dependent representational patterns to distr

247 gth, however, the functional neuroanatomy of hippocampal-dependent scene perception is unknown.

248 By 6 months, deficits in hippocampal-dependent spatial (Morris water maze) and as

249 c transmission, the mutants displayed normal hippocampal-dependent spatial and contextual memory but

250 treated with apamin demonstrated accelerated hippocampal-dependent spatial and nonspatial memory enco

251 hened short- and long-term memory in several hippocampal-dependent spatial and nonspatial tasks.

252 NAc shell DA as being necessary for enabling hippocampal-dependent spatial information to gain contro

253 nduced, and VGF mutant mice were impaired in hippocampal-dependent spatial learning and contextual fe

254 a plays on LTP in hippocampus, as well as in hippocampal-dependent spatial learning and memory tasks,

255 pheral metabolism and cognition, deficits in hippocampal-dependent spatial learning and memory were e

256 xpression may play a role in the deficits in hippocampal-dependent spatial learning and sleep/wake st

257 Hippocampal-dependent spatial learning tasks such as the

258 The status of hippocampal-dependent spatial learning was evaluated in

259 impaired acquisition, but not retrieval, of hippocampal-dependent spatial learning, a deficit that i

260 t impact anxiety/depression-like behavior or hippocampal-dependent spatial learning, it leads to an a

261 and aged rats behaviorally characterized in hippocampal-dependent spatial learning.

262 ective defects in LTP and in the encoding of hippocampal-dependent spatial memories.

263 kinase A, which has been reported to improve hippocampal-dependent spatial memory in aged animals, ha

264 ation, synaptic plasticity, neurogenesis and hippocampal-dependent spatial memory in rodents, leading

265 contributing to the transformation of a new hippocampal-dependent spatial memory into a remote one a

266 Moreover, chronic restraint impaired hippocampal-dependent spatial memory on the Y maze (4-hr

267 ry using the T-maze, Y-maze, and water maze, hippocampal-dependent spatial memory tasks.

268 circuit is likely to mediate key aspects of hippocampal-dependent spatial memory.

269 urrently acquired in the same environment of hippocampal-dependent spatial navigation and striatal-de

270 Learning based on hippocampal-dependent spatial navigation in female rats

271 h concomitant hypercorticalism, and impaired hippocampal-dependent spatial orientation.

272 MK2/3 DKO mice have distinctive deficits in hippocampal-dependent spatial reversal learning.

273 improved recovery through the protection of hippocampal-dependent spatial working memory and reducti

274 improved recovery through the protection of hippocampal-dependent spatial working memory and reducti

275 levels were correlated with learning of the hippocampal-dependent spatial, but not hippocampal-indep

276 The threshold for hippocampal-dependent synaptic plasticity and memory sto

277 extends to the optimal phase for learning a hippocampal-dependent task and to the phase of hippocamp

278 t these effects extend to performance on the hippocampal-dependent task of trace conditioning.

279 altered NE transmission after learning of a hippocampal-dependent task on neural activity and spatia

280 ed aged rats behaviorally characterized in a hippocampal-dependent task to evaluate the status of lon

281 otor activity and decreased habituation in a hippocampal-dependent task.

282 tion would affect trace fear conditioning, a hippocampal-dependent task.

283 been systematically evaluated on a specific hippocampal-dependent task.

284 py rescues the early cognitive deficits on a hippocampal-dependent task.

285 r skill acquisition, as an exemplar of a non-hippocampal-dependent task.

286 of the literature in rodents has focused on hippocampal dependent tasks, studies suggest that tasks

287 lt neurogenesis supports performance in many hippocampal dependent tasks.

288 nd for behavioral phenotyping when nonvisual hippocampal-dependent tasks are utilized.

289 ayed by this important neuromodulator during hippocampal-dependent tasks in vivo.

290 se uptake observed during the performance of hippocampal-dependent tasks.

291 d to learning and memory capabilities during hippocampal-dependent tasks.

292 ology and function as well as performance on hippocampal-dependent tests of learning and memory in th

293 y generated neurons in the adult rat impairs hippocampal-dependent trace conditioning, a task in whic

294 g and memory function was assessed using the hippocampal-dependent trace eye-blink conditioning parad

295 in young and aged Long-Evans rats by using a hippocampal-dependent version of the Morris water maze.

296 ng communication partners, and the nature of hippocampal-dependent versus hippocampal-independent lea

297 separate explicit and implicit components of hippocampal-dependent visuomotor associative memories af

298 ack of contiguity renders trace conditioning hippocampal dependent, we designed a "contiguous trace c

299 ptic transmission and contextual learning is hippocampal dependent, we hypothesized that this deficit

300 lating neurogenesis caused an improvement of hippocampal-dependent working memory when repetitive inf