ライフサイエンスコーパス: hippocampal formation

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

2 evastating disorders of the brain target the hippocampal formation.

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

4 rats was recorded most frequently within the hippocampal formation.

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

6 entially regulated in several regions of the hippocampal formation.

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

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

9 unctional correlations between lpIPL and the hippocampal formation.

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

11 n neuronal and glial profiles throughout the hippocampal formation.

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

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

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

15 anied by permanent structural changes in the hippocampal formation.

16 rk including functional disconnection of the hippocampal formation.

17 nnectivity of the Macaca fascicularis monkey hippocampal formation.

18 that maintain prominent connections with the hippocampal formation.

19 and depth electrodes were placed within the hippocampal formation.

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

21 corticoids on noradrenergic receptors in the hippocampal formation.

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

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

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

25 rds correlate with anatomical changes in the hippocampal formation.

26 osed of multiple regions associated with the hippocampal formation.

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

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

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

30 structural and functional alterations in the hippocampal formation.

31 enomic transducer of estrogen actions in the hippocampal formation.

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

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

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

35 tial adaptive evolutionary plasticity of the hippocampal formation.

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

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

38 duration sufficient to sustain memory in the hippocampal formation.

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

40 bution with cholinergic afferents in the rat hippocampal formation.

41 lives had fewer DCX(+) neurons in the caudal hippocampal formation.

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

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

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

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

46 man literature regarding the function of the hippocampal formation.

47 adulthood and contributes to sustaining the hippocampal formation.

48 terminalis, mesocortical structures and the hippocampal formation.

49 h prominent theta oscillations in the rodent hippocampal formation.

50 erally associated with malfunctioning of the hippocampal formation.

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

52 ives substantial direct projections from the hippocampal formation.

53 rnal representation of space provided by the hippocampal formation.

54 cipient of these signals is the intermediate hippocampal formation.

55 to the anatomy and electrophysiology of the hippocampal formation.

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

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

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

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

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

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

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

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

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

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

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

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

68 synapses in the isocortex, olfactory areas, hippocampal formation and cortical subplate.

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

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

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

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

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

74 biculum is the major output structure of the hippocampal formation and is involved in learning and me

75 biculum is the major output structure of the hippocampal formation and is involved in spatial navigat

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

77 (average read depth 584x) in 111 postmortem hippocampal formation and matched blood samples from 52

78 wed diffuse positive staining throughout the hippocampal formation and neocortex.

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

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

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

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

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

84 lenial and parietal cortices, as well as the hippocampal formation and striatum, provide a plethora o

85 alamic nuclei might be key partners with the hippocampal formation and that, respectively, they are p

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

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

88 tegorization task.SIGNIFICANCE STATEMENT The hippocampal formation and the medial prefrontal cortex o

89 the major sources of thalamic inputs to the hippocampal formation and the medial prefrontal cortex.

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

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

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

97 1 transcripts in interneurons of the cortex, hippocampal formation, and amygdala suggest possible int

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

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

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

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

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

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

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

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

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

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

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

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

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

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

112 e.org defines 122 neuron types in the rodent hippocampal formation based on their somatic, axonal, an

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

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

115 verall variation in the functionality of the hippocampal formation between the species, and in compar

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

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

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

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

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

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

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

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

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

125 ed to glutamatergic alterations in intrinsic hippocampal formation connections.

126 The hippocampal formation constitutes the primary target for

127 The hippocampal formation contains a distinct population of

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

129 t of the basal forebrain that innervates the hippocampal formation, contains high- and low-rhythmic-f

130 The four major portions of the hippocampal formation (cornu Ammonis, dentate gyrus, sub

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

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

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

134 rn of SCGN immunostaining in the adult human hippocampal formation (DG, CA1, CA2, CA3, subiculum, pre

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

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

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

138 The hippocampal formation encodes maps of space and a key qu

139 Distinct regions, layers, and cells of the hippocampal formation exhibit different profiles of stru

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

141 ial information by neurons in and around the hippocampal formation, far from the sensory periphery.

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

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

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

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

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

147 Although the hippocampal formation has been implicated in processing

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

149 The cetacean hippocampal formation has been noted to be one of the sm

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

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

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

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

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

155 The hippocampal formation (HF) contains a neural representat

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

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

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

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

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

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

162 ypothesise that the caudal pole of the avian Hippocampal Formation (HF) presents a homologous subregi

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

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

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

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

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

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

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

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

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

172 The hippocampal formation (HPF) is a focus of intense experi

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

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

175 Within the hippocampal formation, immunoreactivities for VAChT and

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

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

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

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

180 tive maps of environments are encoded in the hippocampal formation in an allocentric reference frame,

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

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

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

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

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

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

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

188 taining demonstrated cytoarchitecture of the hippocampal formation in the AWSD comparable to that rep

189 techniques, we analyzed the structure of the hippocampal formation in the banded mongoose and domesti

190 mical stains we provide a description of the hippocampal formation in the brain of the tree pangolin.

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

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

193 only a minority of potential synapses in the hippocampal formation, including those involving long-ra

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 become available.SIGNIFICANCE STATEMENT The hippocampal formation is a crucial functional substrate

199 The hippocampal formation is a highly plastic brain region t

200 The hippocampal formation is a highly plastic brain structur

201 The hippocampal formation is a key structure for memory func

202 The hippocampal formation is a main site of synaptic plastic

203 erved in the tree pangolin indicate that the hippocampal formation is an anatomically and neurochemic

204 The hippocampal formation is believed to be critical for the

205 The hippocampal formation is critical for the acquisition an

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

207 The hippocampal formation is generally considered essential

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

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

210 The hippocampal formation is one of the most extensively stu

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

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

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

214 The hippocampal formation is traditionally viewed as having

215 4B) is an important phosphodiesterase in the hippocampal formation, is a major Disrupted in Schizophr

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

217 Selective hippocampal formation lesions speeded performance and im

218 nal cortex (EC) is a critical element of the hippocampal formation located within the medial temporal

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

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

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

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

223 In the hippocampal formation, NAAGergic neurons comprise a subp

224 Within the hippocampal formation neuronal networks undergo major re

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

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

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

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

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

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

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

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

233 bution of acetylcholinesterase (AChE) in the hippocampal formation of terrestrial mammals with the go

234 rchitecture, and distribution of AChE in the hippocampal formation of the Atlantic white-sided dolphi

235 rvation, neural pathways and function of the hippocampal formation of the AWSD is conserved, similar

236 relationships of the component parts of the hippocampal formation of the tree pangolin were consiste

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

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

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

240 naptic input to cNTS PPG neurons include the hippocampal formation, paraventricular thalamus, and pre

241 scribe single-neuron recordings in the human hippocampal formation, performed in epileptic patients f

242 The hippocampal formation performs two related but distinct

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

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

245 The hippocampal formation plays key roles in representing an

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

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

248 Place and grid cells in the hippocampal formation provide foundational representatio

249 The mammalian hippocampal formation provides neuronal representations

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

251 The hippocampal formation receives extensive noradrenergic p

252 tal cortex and the entorhinal portion of the hippocampal formation represent the distances and the mo

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

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

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

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

257 It is widely assumed that the hippocampal formation seen in laboratory rodents and in

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

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

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

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

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

263 Cells in the mammalian hippocampal formation subserve neuronal representations

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

265 A quantitative description of the hippocampal formation synaptic architecture is essential

266 CX(+)) multipolar and bipolar neurons in the hippocampal formation than focal hens with minimal fract

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

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

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

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 We found wide variation in the form of the hippocampal formation, the most extreme examples of whic

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

275 In the hippocampal formation, there was substantial cell loss i

276 6K, ERK and CREB) in the cerebral cortex and hippocampal formation throughout of a sedentary period o

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

278 Map-like representations as supported by the hippocampal formation to encode physical space during na

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

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

281 Disrupting information flow from the hippocampal formation to the anterior thalamic nuclei an

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

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

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

285 .5-mm coronal magnetic resonance images, the hippocampal formation was divided into posterior and ant

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 ructural and functional heterogeneity of the hippocampal formation, we sought to characterize the sub

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

290 m the anterior thalamic nuclei to the dorsal hippocampal formation were inhibited, followed by separa

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

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

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

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

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

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

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

300 postmortem brain tissue, OXTR binding in the hippocampal formation would differ between parents and n