ライフサイエンスコーパス: hippocampal formation

1 terminalis, mesocortical structures and the hippocampal formation.

2 n neuronal and glial profiles throughout the hippocampal formation.

3 ression of BDNF and its receptor TrkB in the hippocampal formation.

4 e localized to extranuclear sites in the rat hippocampal formation.

5 as most evident in the ventral region of the hippocampal formation.

6 anied by permanent structural changes in the hippocampal formation.

7 rk including functional disconnection of the hippocampal formation.

8 nnectivity of the Macaca fascicularis monkey hippocampal formation.

9 that maintain prominent connections with the hippocampal formation.

10 and depth electrodes were placed within the hippocampal formation.

11 led lateral occipital complex (LOC), and the hippocampal formation.

12 corticoids on noradrenergic receptors in the hippocampal formation.

13 ular zone (SVZ) and the dentate gyrus of the hippocampal formation.

14 hosphorylation of GluR1 at serine 831 in the hippocampal formation.

15 nally diverse roles of these channels in the hippocampal formation.

16 lly passed on to different subregions of the hippocampal formation.

17 rds correlate with anatomical changes in the hippocampal formation.

18 osed of multiple regions associated with the hippocampal formation.

19 on dendrites of CA1 pyramidal neurons in the hippocampal formation.

20 hinal cortex functions as the gateway to the hippocampal formation.

21 ic spines and axon terminals, within the rat hippocampal formation.

22 structural and functional alterations in the hippocampal formation.

23 enomic transducer of estrogen actions in the hippocampal formation.

24 the subiculum-the major output region of the hippocampal formation.

25 deep layer neurons of the neocortex and the hippocampal formation.

26 of cholinergic systems by mu-opioids in the hippocampal formation.

27 continuous and later in time) depends on the hippocampal formation.

28 n of BCATc in the mossy fiber pathway of the hippocampal formation.

29 duration sufficient to sustain memory in the hippocampal formation.

30 e we report findings on the amygdala and the hippocampal formation.

31 ives substantial direct projections from the hippocampal formation.

32 bution with cholinergic afferents in the rat hippocampal formation.

33 place alone was found after ablation of the hippocampal formation.

34 um and brainstem, being most numerous in the hippocampal formation.

35 n experience-dependent firing pattern in the hippocampal formation.

36 icate that this process depends on an intact hippocampal formation.

37 oth the plasticity and the output of the rat hippocampal formation.

38 regulating early developmental events in the hippocampal formation.

39 he major source of thalamic afferents to the hippocampal formation.

40 nd dendrites of CA3 pyramidal neurons in the hippocampal formation.

41 level is long-term potentiation (LTP) in the hippocampal formation.

42 rnal representation of space provided by the hippocampal formation.

43 yrus, one of the principal structures of the hippocampal formation.

44 nt within the DG and CA of the rhesus monkey hippocampal formation.

45 on of high-frequency oscillations within the hippocampal formation.

46 cipient of these signals is the intermediate hippocampal formation.

47 unications between neocortical areas and the hippocampal formation.

48 are mediated through the MRs present in the hippocampal formation.

49 to the anatomy and electrophysiology of the hippocampal formation.

50 may underlie theta in different parts of the hippocampal formation.

51 at are critical for memory processing in the hippocampal formation.

52 h prominent theta oscillations in the rodent hippocampal formation.

53 igher CL signals than other areas within the hippocampal formation.

54 evastating disorders of the brain target the hippocampal formation.

55 the activity of place and grid cells in the hippocampal formation.

56 erally associated with malfunctioning of the hippocampal formation.

57 rats was recorded most frequently within the hippocampal formation.

58 s associated with damage to the non-dominant hippocampal formation.

59 entially regulated in several regions of the hippocampal formation.

60 as in the hilus of the dentate gyrus of the hippocampal formation.

61 y shuts down blood supply to the ipsilateral hippocampal formation.

62 unctional correlations between lpIPL and the hippocampal formation.

63 k nodes, but not between these nodes and the hippocampal formation.

64 epsy in adults and usually originates in the hippocampal formations.

65 one (GH) is produced endogenously within the hippocampal formation, a brain structure associated with

66 macrophages, which were concentrated in the hippocampal formation, a region necessary for learning a

67 s have signal intensity abnormalities in the hippocampal formation and amygdala and, contrary to prio

68 Volumes of the posterior and anterior hippocampal formation and amygdala were computed in 46 (

69 rget regions with greatest SREB2 expression (hippocampal formation and amygdaloid complex).

70 h human embryonic stem cells (hESC) into the hippocampal formation and analyzed for stem cell surviva

71 constitute one of the main cell types in the hippocampal formation and are widely believed to represe

72 by interstitial white matter neurons in the hippocampal formation and by all three cell types in the

73 f these two dynein light chains in adult rat hippocampal formation and cerebral cortex.

74 irection (HD) cells are neurons found in the hippocampal formation and connected areas that fire as a

75 tion was used to quantify reelin mRNA in the hippocampal formation and dorsolateral prefrontal cortex

76 its first foothold in specific parts of the hippocampal formation and entorhinal cortex, effectively

77 ic Abeta-induced synaptic impairments in the hippocampal formation and eventually led to synaptic dys

78 bodies: the postcommissural fornix from the hippocampal formation and Gudden's ventral tegmental nuc

79 ensively studied in the dentate gyrus of the hippocampal formation and in the subventricular zone adj

80 ased HO-1 immunoreactivity in neurons of the hippocampal formation and its connections including CA1-

81 llular localization of immunostaining in the hippocampal formation and neocortex.

82 cortex is the primary interface between the hippocampal formation and neocortical sources of sensory

83 eral regions within the brain, including the hippocampal formation and olfactory bulb.

84 phase precession is observed throughout the hippocampal formation and other areas of the brain.

85 Greater extent of activation within the hippocampal formation and parahippocampal gyrus (PHG) wa

86 ad injured group in the basal forebrain, the hippocampal formation and regions of the neocortex.

87 grid, border and head direction cells in the hippocampal formation and related structures.

88 BD showed reduced gray matter volumes in the hippocampal formation and the amygdala relative to indiv

89 there are no direct connections between the hippocampal formation and the cerebellum, and because th

90 A functional interaction between the hippocampal formation and the ventral striatum is though

91 ceptor-mediated synaptic transmission in the hippocampal formation and then explored the underlying c

92 recise sites of TrkB activation in the mouse hippocampal formation and to determine any changes in th

93 vily interconnected structures including the hippocampal formation and underlying entorhinal, perirhi

94 d were caudate, putamen, amygdaloid complex, hippocampal formation and various cerebral and cerebella

95 associated with a dose-dependent increase in hippocampal formation and ventrolateral prefrontal corte

96 literature on the development of the primate hippocampal formation and will facilitate further invest

97 ogenetic dissociation of function within the hippocampal formation and, at the same time, support the

98 1 transcripts in interneurons of the cortex, hippocampal formation, and amygdala suggest possible int

99 c spines in cerebral cortex, caudatoputamen, hippocampal formation, and cerebellum, irrespective of r

100 uinpirole increased CNTF mRNA in the SVZ and hippocampal formation, and in cultured astrocytes by 1.5

101 was almost no CARTp-ir in the pallium or the hippocampal formation, and little CARTp-ir in the cerebe

102 ergic and cholinergic neurons, innervate the hippocampal formation, and play a role in modulating hip

103 irin mRNA were found in the cerebral cortex, hippocampal formation, and Purkinje cells, with high lev

104 teroid, and later, estrogen receptors in the hippocampal formation, and subsequent discovery of dendr

105 ted in the dorsal and caudal portions of the hippocampal formation, and the modified version of the v

106 erebral cortex: the olfactory bulb (OB), the hippocampal formation, and the neocortex.

107 Circuits within the hippocampal formation are active during memory processin

108 velopment and maturation of both the PFC and hippocampal formation are characterized by progressive s

109 tial representations found in and around the hippocampal formation are interdependent.

110 al amygdala and the ventral subiculum of the hippocampal formation are two of the major limbic-relate

111 results in fewer excitatory synapses in the hippocampal formation as assessed morphologically and fu

112 Decades of research identify the hippocampal formation as central to memory storage and r

113 -I) and insulin receptor pathways within the hippocampal formation as well as other brain regions.

114 sia/ heterotopia of principal neurons in the hippocampal formation, as well as spontaneous behavioral

115 , significantly improved AD-type deficits in hippocampal formation basal synaptic transmission and lo

116 mossy fibers and Schaffer collaterals in the hippocampal formation, basket cell axons in the cerebell

117 ich is thought to reflect dysfunction of the hippocampal formation before the onset of full blown dem

118 vival of new cells that are generated in the hippocampal formation before the training experience, es

119 The great similarities in the hippocampal formation between nonhuman primates and huma

120 appear to be critically dependent not on the hippocampal formation but rather on the posterior parahi

121 ral lobe epilepsy display neuron loss in the hippocampal formation, but neuropathological changes als

122 ted neurogenesis in the dentate gyrus of the hippocampal formation, but not in the subventricular zon

123 CK-B receptors are widely distributed in the hippocampal formation, but the functions of CCK there ha

124 ites, and dendritic spines of neurons in the hippocampal formation, but the majority of pTrkB-ir loca

125 analyzed the localization of Ca(v)1.2 in the hippocampal formation by using antibodies against the po

126 In the hippocampal formation, Ca(v)1.2 (L-type) voltage-gated C

127 een cortical gray/white matter junction, and hippocampal formation (CA1 and CA3 regions).

128 ction of long-term potentiation (LTP) in the hippocampal formation can be modulated by different beha

129 Within the rat hippocampal formation, cholinergic afferents and mu-opio

130 tivity (-LI) neurons in the cerebral cortex, hippocampal formation, colliculi, and mesencephalic reti

131 ed to glutamatergic alterations in intrinsic hippocampal formation connections.

132 The hippocampal formation constitutes the primary target for

133 The hippocampal formation contains a distinct population of

134 The results indicate that the hippocampal formation contains representations of both t

135 essed as Fluoro-Jade B-positive cells in the hippocampal formation, cortical and hippocampal inflamma

136 arly, ZNF804A genotype modulated right DLPFC-hippocampal formation coupling in siblings and patients.

137 In the mammalian hippocampal formation, dendrotoxin-sensitive voltage-gat

138 knowledge base of neuron types in the rodent hippocampal formation (dentate gyrus, CA3, CA2, CA1, sub

139 the subiculum, a major output region of the hippocampal formation, double label for PV (intact = 97.

140 ng and pacing theta-band oscillations in the hippocampal formation during exploration, novelty detect

141 Early descriptions of the hippocampal formation emphasized the serial nature of it

142 Place cells of the hippocampal formation encode a spatial representation of

143 ual cell types within the normal adult human hippocampal formation, expression profile analysis was p

144 pothalamic paraventricular nucleus (PVN) and hippocampal formation following exposure to a chronic no

145 when required by the task, as well as to the hippocampal formation for categorical encoding and retri

146 Using in situ hybridization in sections of hippocampal formation from 10 patients with schizophreni

147 In the hippocampal formation, GAD25/GAD67 and NKCC1/KCC2 ratios

148 ived ibotenic acid lesions restricted to the hippocampal formation (group H), and the four others rec

149 s, monkeys with ibotenic acid lesions of the hippocampal formation (H), and monkeys with aspiration l

150 Although the hippocampal formation has been implicated in processing

151 For many years, the hippocampal formation has been implicated in the regulat

152 vestigation of spatial representation in the hippocampal formation has evolved in stages.

153 The dentate gyrus (DG), a part of the hippocampal formation, has important functions in learni

154 In addition to the age-related decline in hippocampal formation (HF) activation (p < .05; false di

155 The avian hippocampal formation (HF) and mammalian hippocampus sha

156 uch a demonstration here by showing that the hippocampal formation (HF) and, to a lesser degree, the

157 The hippocampal formation (HF) contains a neural representat

158 in-derived neurotrophic factor (BDNF) in the hippocampal formation (HF) in rats.

159 The avian hippocampal formation (HF) is a structure necessary for

160 The hippocampal formation (HF) is one of the hottest regions

161 recorded from single neurons (units) in the hippocampal formation (HF) of freely moving homing pigeo

162 Neuronal firing in the hippocampal formation (HF) of freely moving rodents show

163 The hippocampal formation (HF) of mammals and birds is cruci

164 Ralpha is found in extranuclear sites in the hippocampal formation (HF), four different antibodies to

165 ding the medial prefrontal cortex (mPFC) and hippocampal formation (HF), is known to shape adaptive r

166 In the hippocampal formation (HF), the enkephalin opioids and e

167 ssenger RNA (mRNA) in multiple brain regions-hippocampal formation (HF), ventral tegmental area/subst

168 rsolateral prefrontal cortex (DLPFC) and the hippocampal formation (HF).

169 lities, but grossly normal structure, in the hippocampal formation (HF).

170 their hidden food caches that depends on the hippocampal formation (HF).

171 ization of spatial learning within the avian hippocampal formation (HF).

172 , superficial and deep layers of the cortex, hippocampal formation (hippocampus, dentate gyrus, subic

173 These findings argue that the hippocampal formation houses a flexible guidance system

174 s following GLP-1R activation in the ventral hippocampal formation (HPFv), a region only recently hig

175 eases of late life differentially target the hippocampal formation, identify elevations in blood gluc

176 Within the hippocampal formation, immunoreactivities for VAChT and

177 Ablations of the hippocampal formation in 2-month-old infants tested shor

178 erate high-resolution functional maps of the hippocampal formation in 240 community-based nondemented

179 e to increased seizure susceptibility in the hippocampal formation in a temporal lobe epilepsy model.

180 een ascribed to the effects of damage to the hippocampal formation in adult nonhuman primates.

181 s and modulates synaptic transmission in the hippocampal formation in animal studies.

182 like immunoreactive cells within the macaque hippocampal formation in contrast to the high density ob

183 parison task depends on the integrity of the hippocampal formation in humans, monkeys, and, for an an

184 of amnesia, based on ablations aimed at the hippocampal formation in infant rhesus monkeys, provides

185 oth functional and structural effects in the hippocampal formation in infrahuman species.

186 RT task to examine the specific roles of the hippocampal formation in learning first- and second-orde

187 gated volumetric alterations of the anterior hippocampal formation in patients experiencing a first e

188 dala complex may be specific to the anterior hippocampal formation in patients experiencing a first e

189 actor (BDNF) messenger RNA (mRNA) within the hippocampal formation in rats selectively bred for 1) hi

190 ntegration between prefrontal cortex and the hippocampal formation in schizophrenia.

191 s (origin of the perforant path input to the hippocampal formation in the medial temporal lobe) have

192 the nucleus accumbens from the amygdala, the hippocampal formation (including the entorhinal cortex),

193 , the heaviest projections originated in the hippocampal formation, including the entorhinal cortex,

194 ng a cortical window implant that leaves the hippocampal formation intact and does not lead to obviou

195 The hippocampal formation is a brain region noted for its pl

196 The hippocampal formation is a brain structure integrally in

197 The hippocampal formation is a complex circuit of interconne

198 The hippocampal formation is a highly plastic brain region t

199 The hippocampal formation is a highly plastic brain structur

200 The hippocampal formation is a key structure for memory func

201 The hippocampal formation is a main site of synaptic plastic

202 The hippocampal formation is believed to be critical for the

203 The hippocampal formation is critical for the acquisition an

204 e findings demonstrate that the adult monkey hippocampal formation is critical for the establishment

205 The hippocampal formation is generally considered essential

206 cate that alpha1d ADR mRNA expression in the hippocampal formation is highly sensitive to circulating

207 The hippocampal formation is one of the brain regions most s

208 The hippocampal formation is one of the most extensively stu

209 strated that cell proliferation in the adult hippocampal formation is regulated by estrogen under bot

210 The subiculum as a part of the hippocampal formation is the principal target of CA1 pyr

211 y parallels the time period during which the hippocampal formation is thought necessary for memory, c

212 The hippocampal formation is traditionally viewed as having

213 4B) is an important phosphodiesterase in the hippocampal formation, is a major Disrupted in Schizophr

214 These findings indicate that the hippocampal formation itself plays an essential role in

215 Selective hippocampal formation lesions speeded performance and im

216 approaches revealed that most neurons in the hippocampal formation, many pyramidal cortical neurons,

217 t that some of progesterone's actions in the hippocampal formation may be mediated by direct and rapi

218 that impaired contextual conditioning in the hippocampal formation may mediate the association betwee

219 Finally, we propose that the hippocampal formation might implement a neural analogue

220 ntal-plane based information provided by the hippocampal formation, modified in primates by expansion

221 In the hippocampal formation, NAAGergic neurons comprise a subp

222 Within the hippocampal formation neuronal networks undergo major re

223 s in 2-DG uptake in limbic cortical regions, hippocampal formation, nucleus accumbens, basolateral am

224 ds to image the pattern of activation in the hippocampal formation of 14 rhesus monkeys performing co

225 5 (KCC2)] in the prefrontal cortex (PFC) and hippocampal formation of a large cohort of nonpsychiatri

226 tein (GFAP) content increase with age in the hippocampal formation of certain animal models, it is un

227 gies, we generated CBV maps over time in the hippocampal formation of exercising humans.

228 proach to generate CBV maps over time in the hippocampal formation of exercising mice.

229 n the cortex, amygdala, basal forebrain, and hippocampal formation of intact and ovariectomized (ovx)

230 hosphorylated at tyrosine 816 (pTrkB) in the hippocampal formation of male and female mice under cond

231 n of ovarian hormone receptors in the dorsal hippocampal formation of mice.

232 uropeptide Y mRNA in the hilar region of the hippocampal formation of patients with temporal lobe epi

233 microscopy to examine PR distribution in the hippocampal formation of proestrus rats.

234 spatial firing properties of neurons in the hippocampal formation of rats, that this region supports

235 spatial firing patterns of grid cells in the hippocampal formation offer a compact combinatorial code

236 ot differ in volumes of either the posterior hippocampal formation or amygdala.

237 keys with neonatal aspiration lesions of the hippocampal formation or the amygdaloid complex were tes

238 ory bulb and is not expressed in cerebellar, hippocampal formation, or olfactory bulb granule cells.

239 el systems, for example, have shown that the hippocampal formation participates in acquisition of dec

240 that the entorhinal cortex, rather than the hippocampal formation, participates in memory consolidat

241 The hippocampal formation performs two related but distinct

242 other well characterized cell classes in the hippocampal formation: place and head-direction cells.

243 Within the temporal lobe, the hippocampal formation plays a central role in short-term

244 The hippocampal formation plays key roles in representing an

245 lace-modulated activity among neurons in the hippocampal formation presents a means to organize conte

246 In the striatum, hippocampal formation, presubiculum and parasubiculum, a

247 Place, head-direction, and grid cells in the hippocampal formation provide allocentric representation

248 The mammalian hippocampal formation provides neuronal representations

249 ly with acetylcholinesterase activity in the hippocampal formation (r = 0.56, P < 0.0001), amygdala (

250 The hippocampal formation receives extensive noradrenergic p

251 ly associated with the perirhinal cortex and hippocampal formation, respectively.

252 may contribute to the impact of T2DM on the hippocampal formation, resulting in decreased verbal dec

253 Damage to the hippocampal formation results in a profound temporally g

254 ractionation of whole mouse brains and human hippocampal formations revealed that both dysbindin-1 an

255 Light microscopic examination of the mouse hippocampal formation showed sparse nuclear ERalpha and

256 cated in hippocampal cultures and rat dorsal hippocampal formation showing a neuronal location.

257 tions averaging 18-42% (P = 0.027-0.0001) at hippocampal formation sites lacking neuronal dystrobrevi

258 these studies have not clarified whether the hippocampal formation specifically is essential to this

259 staining) throughout the cerebral neocortex, hippocampal formation, striatum and cerebellum, with les

260 Dense labeling was also detected in the hippocampal formation, subiculum, and basolateral amygda

261 Cells in the mammalian hippocampal formation subserve neuronal representations

262 hese results support the hypothesis that the hippocampal formation supports contextual fear condition

263 In hippocampal formation, Tctex-1 immunoreactivity was most

264 cinity of the limbic/paralimbic areas (i.e., hippocampal formation, temporal pole), striatum (i.e., c

265 refrontal cortex, temporal cortex, amygdala, hippocampal formation, thalamus, and hypothalamus.

266 erform nest bookkeeping, females have larger hippocampal formations than males.

267 g the breeding season, parasites have larger hippocampal formations than nonparasites.

268 r extent of postsurgical damage to the right hippocampal formation that differed in two key features,

269 on throughout the rostrocaudal extent of the hippocampal formation that was common to all behavioral

270 do not target any of the subdivisions in the hippocampal formation (the dentate gyus, the cornu ammon

271 st prominently the caudalmost portion of the hippocampal formation, the caudodorsal nidopallial shelf

272 eus (ADN) and its postsynaptic target in the hippocampal formation, the dorsal pre-subiculum (PrSd),

273 d 2 cortical regions interconnected with the hippocampal formation, the retrosplenial cortex (RSC) an

274 x, the caudate-putamen, globus pallidus, the hippocampal formation, the thalamus, the substantia nigr

275 t that novelty initiates a transition of the hippocampal formation to a mode that is particularly con

276 y infusing recombinant BDNF protein into the hippocampal formation to investigate whether this defici

277 gic fibres ramify extensively throughout the hippocampal formation to release acetylcholine upon a di

278 nal projections to other fields of the adult hippocampal formation, very little is known about the de

279 The ventral hippocampal formation (vHF) seems to constrain diverse r

280 cAMP signaling in the ventral hippocampal formation (VHIPP) appears to be required for

281 mediated excitatory neurotransmission in the hippocampal formation via a decrease in glutamate releas

282 tly reduced total (right plus left) anterior hippocampal formation volume relative to healthy compari

283 .5-mm coronal magnetic resonance images, the hippocampal formation was divided into posterior and ant

284 left inferior prefrontal cortex and the left hippocampal formation was greater for subsequently recog

285 Evidence for temporally graded change in the hippocampal formation was mixed, suggesting it may parti

286 In addition, activity in right hippocampal formation was only seen in varepsilon4 carri

287 rior and anterior segments, and the anterior hippocampal formation was separated from the amygdala.

288 lesions of the cholinergic projection to the hippocampal formation were added to the inferotemporal a

289 s of firing fields of principal cells in the hippocampal formation were generally preserved, but both

290 ossibility is insufficient inhibition in the hippocampal formation where seizures tend to initiate.

291 hat GH is endogenously produced in the adult hippocampal formation, where it is regulated by age, est

292 the hippocampus and binds to neurons of the hippocampal formation, where it promotes dendritic spine

293 complement component C1q is confined to the hippocampal formation, whereas glial fibrillary acidic p

294 ective lamination in the cerebral cortex and hippocampal formation, whereas homozygous mutations resu

295 e multiple sites across the long axis of the hippocampal formation while subjects performed different

296 n the networks is that one is coupled to the hippocampal formation while the other is not.

297 The dentate gyrus (DG) is a region in the hippocampal formation whose function declines in associa

298 ectrophysiological dysfunction of the rodent hippocampal formation with aging, the structural basis o

299 The effect was specific for the hippocampal formation, with levels of alpha1d mRNA unalt

300 ADR) mRNA is expressed at high levels in the hippocampal formation, within cells that express MR or G