ライフサイエンスコーパス: retrosplenial

1 or, midcingulate (MCC), posterior (PCC), and retrosplenial.

2 ions, the lateral entorhinal cortex, and the retrosplenial agranular cortex.

3 To delineate the subdivisions of the retrosplenial and adjacent cortices, we conducted a cyto

4 ad connections with limbic cortex, including retrosplenial and caudal cingulate cortex as well as aud

5 rtex, and also increased interaction between retrosplenial and medial frontal cortex.

6 bule VII receives a prominent input from the retrosplenial and orbitofrontal cortices.

7 ex included the frontal, anterior cingulate, retrosplenial and perirhinal cortices, and the claustrum

8 e bregma to examine cell degeneration in the retrosplenial and piriform regions.

9 sed of an area (area 23v) that resembles the retrosplenial and posterior cingulate cortices but has a

10 suggested that posterior cortical areas, the retrosplenial and posterior parietal cortex, are involve

11 When examining only successful trials, the retrosplenial and posterior parietal cortices were recru

12 heightened immunodensities were specific to retrosplenial and temporal cortices.

13 ons that normally establish connections with retrosplenial and visual cortex, sites of early postnata

14 of left posterior parahippocampal, bilateral retrosplenial, and bilateral posterior inferior parietal

15 os labeling in medial prefrontal, cingulate, retrosplenial, and insular cortices.

16 ical regions, including posterior cingulate, retrosplenial, and lateral parietal cortex.

17 ual network consists of the parahippocampal, retrosplenial, and medial prefrontal cortices.

18 frontal (mPFC), agranular insular, piriform, retrosplenial, and parahippocampal cortices.

19 ipsilateral motor, secondary somatosensory, retrosplenial, and perirhinal cortex and contralateral S

20 t of brain areas, including medial temporal, retrosplenial, and posterior parietal cortices, that ove

21 motor, posterior parietal, lateral agranular retrosplenial, and temporal association cortices.

22 " pathway provides disynaptic input from the retrosplenial, anterior cingulate, and orbital cortex to

23 epwise laminar differentiation starting from retrosplenial area 30 towards the isocortical regions of

24 r transition zone includes both area 23d and retrosplenial area 30.

25 These results suggest that the retrosplenial area supramammillary nucleus may be parts

26 tion c-Fos positive nuclei were found in the retrosplenial area the posterior hypothalamus including

27 Histologic studies of retrosplenial areas 29 and 30 identify them on the ventr

28 S1 and S2, as well as parietal association, retrosplenial, auditory, ectorhinal, motor, and visual c

29 nment, the effects of hippocampal lesions on retrosplenial cells, and on head direction coding in dif

30 actions between group and age, were found in retrosplenial cingulate gyrus, found to be metabolically

31 d in brain regions known to participate with retrosplenial cingulate in networks contributing to spat

32 e also identified (eg, thalamus, cerebellum, retrosplenial cingulate), which suggests an imbalance in

33 Left orbitofrontal, right retrosplenial cingulate, and medial temporal cortex thic

34 he superior frontal cortex, the anterior and retrosplenial cingulate, and the anterior temporal pole;

35 V and, to a lesser extent, III and mainly in retrosplenial, cingulate, primary somatosensory and audi

36 at specific regions of the scene network-the retrosplenial complex (RSC) and occipital place area (OP

37 ltivoxel pattern analyses indicated that the retrosplenial complex (RSC) was the anatomical locus of

38 g: the parahippocampal place area (PPA), the retrosplenial complex (RSC), and a region around the tra

39 rns in the parahippocampal place area (PPA), retrosplenial complex (RSC), and occipital place area (O

40 l environments (VE) have reported effects in retrosplenial complex and (pre-)subiculum, but not the t

41 osterior visually responsive regions such as retrosplenial complex and the parahippocampal place area

42 alyses indicated that the left presubiculum, retrosplenial complex, and parietal-occipital sulcus cod

43 ons, the transverse occipital sulcus and the retrosplenial complex.

44 cuneus complex (PCC) and posterior cingulate/retrosplenial cortex (pC/Rsp)] showed strong retrieval s

45 , V1aR expression in the posterior cingulate/retrosplenial cortex (PCing) and laterodorsal thalamus (

46 (VS), rostral and dorsal anterior cingulate, retrosplenial cortex (RC), midbrain and hippocampus.

47 few limbic cortical structures including the retrosplenial cortex (RSC) and anterior cingulate cortex

48 t only a few limbic structures including the retrosplenial cortex (RSC) and anterior cingulate cortex

49 Distinct brain regions, the retrosplenial cortex (RSC) and thalamus, code for visual

50 onnected with the hippocampal formation, the retrosplenial cortex (RSC) and the medial prefrontal cor

51 eives corticocortical axons from the rostral retrosplenial cortex (RSC) and these form monosynaptic e

52 The rat parahippocampal region (PHR) and retrosplenial cortex (RSC) are cortical areas important

53 connectivity between the parahippocampus and retrosplenial cortex (RSC) correlated strongly with rati

54 and long-range top-down projections from the retrosplenial cortex (RSC) during associative learning o

55 lly reactivate a specific neural ensemble in retrosplenial cortex (RSC) engaged by context fear condi

56 the parahippocampal place area (PPA) and the retrosplenial cortex (RSC) for visual and haptic explora

57 The involvement of retrosplenial cortex (RSC) in human autobiographical mem

58 ippocampus, we tested the involvement of the retrosplenial cortex (RSC) in this process using a chemo

59 Retrosplenial cortex (RSC) is a dorsomedial parietal are

60 The retrosplenial cortex (RSC) is part of a network of inter

61 Of these sites, the retrosplenial cortex (RSC) is robustly activated during

62 tmentalization of complex routes, individual retrosplenial cortex (RSC) neurons exhibited periodic ac

63 tylcholine and glutamate onto the vulnerable retrosplenial cortex (RSC) neurons.

64 Retrosplenial cortex (RSC) played a central and highly s

65 ea V1, the parahippocampal place area (PPA), retrosplenial cortex (RSC), and lateral occipital comple

66 in the parahippocampal place area (PPA) and retrosplenial cortex (RSC), but no such extrapolation of

67 area (PPA), transverse occipital sulcus, and retrosplenial cortex (RSC), key regions associated with

68 al areas, including a prominent one from the retrosplenial cortex (RSC), likely targeting basal dendr

69 indicated that these areas, specifically the retrosplenial cortex (RSC), were functionally disrupted

70 he parahippocampal place area (PPA), and the retrosplenial cortex (RSC).

71 Our analyses focused on the retrosplenial cortex (RSC)/parietal-occipital sulcus reg

72 PPA), transverse occipital sulcus (TOS), and retrosplenial cortex (RSC)], which have been linked to h

73 The retrosplenial cortex (RSP) and postrhinal cortex (POR) a

74 The retrosplenial cortex (RSP) and the posterior parietal co

75 Lesions of retrosplenial cortex (RSP) disrupt spatial and contextua

76 The retrosplenial cortex (RSP) is highly interconnected with

77 The retrosplenial cortex (RSP), a brain region frequently li

78 emonstrated that electrolytic lesions of the retrosplenial cortex (RSP), a posterior region of cingul

79 These connections are consistent with the retrosplenial cortex acting as an interface between the

80 ucidate the topographic configuration of the retrosplenial cortex and adjacent structures, we have ma

81 GluM in regions of the default mode network (retrosplenial cortex and cingulate gyrus) and secondary

82 In this way, the retrosplenial cortex and hippocampus may be part of an i

83 ortex resulted in labeled neurons within the retrosplenial cortex and in areas 23 and 31 (approximate

84 ction information was expressed in the right retrosplenial cortex and posterior HC and was only sensi

85 nformation about heading direction, found in retrosplenial cortex and posterior HC, favored the verti

86 generation occurred at 8 h postimpact in the retrosplenial cortex and pre- and parasubiculum.

87 s this drug blocks PCP-induced damage of the retrosplenial cortex and RU38486 (corticosteroid recepto

88 e investigated the cortical afferents of the retrosplenial cortex and the adjacent posterior cingulat

89 sitional zone, area 30v, located between the retrosplenial cortex and the prestriate visual cortex.

90 Parameter estimates extracted from retrosplenial cortex and the thalamus revealed significa

91 Little is known about the function of the retrosplenial cortex and until recently, there was no ev

92 elated with striatal atrophy, while striatum-retrosplenial cortex connectivity is negatively correlat

93 ed and is further located between V1 and the retrosplenial cortex consistent with a role in processin

94 The fact that the retrosplenial cortex contains spatial and movement-relat

95 se memory to reduce such errors and that the retrosplenial cortex contributes to this process.

96 Inactivation of the retrosplenial cortex disrupted this search preference.

97 t decreases in orbitofrontal, cingulate, and retrosplenial cortex during partial seizures, and increa

98 networks, including posterior cingulate and retrosplenial cortex early in its progression, often bef

99 en together, these results indicate that the retrosplenial cortex engages in the formation and storag

100 g consistently predicted DMN activity in the retrosplenial cortex for resting-state functional magnet

101 Recognition that the retrosplenial cortex has a prominent role in the process

102 Thus, the retrosplenial cortex has the requisite dynamics to serve

103 These drugs also produce injury to cingulate-retrosplenial cortex in adult rodents that can be preven

104 To understand further the role of the retrosplenial cortex in navigation, we combined temporar

105 retrosplenial cortex, and the involvement of retrosplenial cortex in navigation.

106 ve lesions of the dysgranular portion of the retrosplenial cortex in rats.

107 Together, the findings implicate retrosplenial cortex in the extraction of path sub-space

108 Retrosplenial cortex inactivation impaired accuracy in d

109 A second experiment revealed that retrosplenial cortex inactivation impaired spatial learn

110 Furthermore, parahippocampal and retrosplenial cortex involvement in this coordination re

111 unctional neuroimaging studies show that the retrosplenial cortex is consistently activated by emotio

112 Retrosplenial cortex is densely interconnected with the

113 As retrosplenial cortex is itself vital for memory, this di

114 for extinction of the updated memory but the retrosplenial cortex is no longer required for retrieval

115 Subregional flat maps show that retrosplenial cortex is on the CGv, most of the surface

116 The retrosplenial cortex is strongly connected with brain re

117 usly overlooked pattern of observations: the retrosplenial cortex is the cortical region most consist

118 The retrosplenial cortex may provide mnemonic information, w

119 Here, retrosplenial cortex neurons were recorded as rats trave

120 ioral results confirmed that inactivation of retrosplenial cortex only impairs radial maze performanc

121 ateral amygdala, reticular thalamic nucleus, retrosplenial cortex or primary somatosensory cortex.

122 We suggest that the retrosplenial cortex provides mnemonic spatial informati

123 Injections involving the retrosplenial cortex resulted in labeled neurons within

124 nd previously that temporary inactivation of retrosplenial cortex results in dark-selective impairmen

125 cal environment, some neurons in dysgranular retrosplenial cortex showed bidirectional firing pattern

126 h the hippocampal CA fields and the granular retrosplenial cortex showed borderline increases in c-fo

127 asticity [long-term depression (LTD)] in rat retrosplenial cortex slices months following an anterior

128 integration, which recruits hippocampus and retrosplenial cortex to track movement relative to home.

129 e parahippocampal cortex and a region in the retrosplenial cortex together comprise a system that med

130 study in which recordings were made from the retrosplenial cortex while rats navigated through a comp

131 uced brain activation, including the NAS and retrosplenial cortex with motor cortex, hippocampus, and

132 ation, we combined temporary inactivation of retrosplenial cortex with recording of complex spike cel

133 ation of the posterior limbic (including the retrosplenial cortex) and parahippocampal regions simila

134 between cortical areas (particularly S1 and retrosplenial cortex) had a striking resemblance to the

135 in direct (prefrontal cortex) and indirect (retrosplenial cortex) targets of nbm corticopetal cholin

136 ective areas transverse occipital sulcus and retrosplenial cortex), although all three scene-selectiv

137 In the retrosplenial cortex, 93% of identified postsynaptic tar

138 rtmentalization processes could occur within retrosplenial cortex, a structure whose neurons simultan

139 ater interaction between the hippocampus and retrosplenial cortex, and also increased interaction bet

140 % less c-fos ir-cells in the insular cortex, retrosplenial cortex, and dentate gyrus.

141 tex (PMC) including the posterior cingulate, retrosplenial cortex, and medial parietal cortex/precune

142 In medial prefrontal cortex, retrosplenial cortex, and NAC shell, however, MK-801 ind

143 that dynamic processes recruit hippocampus, retrosplenial cortex, and parahippocampal cortex in supp

144 port of a homing vector system, hippocampus, retrosplenial cortex, and parahippocampal cortex were re

145 In addition, hippocampus, retrosplenial cortex, and parahippocampal cortex, as wel

146 home location, supported by the hippocampus, retrosplenial cortex, and parahippocampal cortex.

147 ctions between the posterior hippocampus and retrosplenial cortex, and prefrontal regions.

148 nection from the anterior thalamic nuclei to retrosplenial cortex, and the involvement of retrospleni

149 n the hippocampus/parahippocampal cortex and retrosplenial cortex, and to sustained activity in prefr

150 ent located at the juncture of the PoS, PaS, retrosplenial cortex, and visual cortex appears to be th

151 ons between the anterior thalamic nuclei and retrosplenial cortex, another region vital for memory.

152 prominently included the posterior cingulate/retrosplenial cortex, as in each previously-analyzed mod

153 also that LD projects upon the cingulate and retrosplenial cortex, but has only sparse projections to

154 ere found in contralateral cortical regions, retrosplenial cortex, dentate gyrus, subiculum, tenia te

155 hip between the anterior thalamic nuclei and retrosplenial cortex, given how dysfunctions in the latt

156 regions, including medial prefrontal cortex, retrosplenial cortex, hippocampus, nucleus accumbens, ba

157 ation and connectivity of the macaque monkey retrosplenial cortex, i.e., areas 29 and 30.

158 As in the retrosplenial cortex, injections of area 23 led to many

159 cludes the posterior cingulate cortex (PCC), retrosplenial cortex, lateral parietal cortex/angular gy

160 e entorhinal, parahippocampal, and cingulate/retrosplenial cortex, may be involved in emotion and oth

161 vely correlated to mPFC FC with the PCC/PCu, retrosplenial cortex, medial thalamus, and periaqueducta

162 tion and necrosis in the posterior cingulate/retrosplenial cortex, neither dose of ACEA 1021 had any

163 mann's map understates the rostral extent of retrosplenial cortex, overstates its caudoventral extent

164 s) which targeted the contralateral PreS and retrosplenial cortex, respectively.

165 during rest, some PMC sites, proximal to the retrosplenial cortex, responded selectively to autobiogr

166 ell as a region related to scene processing (retrosplenial cortex, RSC).

167 Within the retrosplenial cortex, scopolamine lowered PCP-induced ap

168 ed in a number of brain areas, including the retrosplenial cortex, subiculum, medial habenula, interp

169 ez' circuit, of place-by-direction coding in retrosplenial cortex, the anatomical connection from the

170 This relationship was observed in the retrosplenial cortex, the orbitofrontal cortex, the infe

171 ions were functionally connected to the left retrosplenial cortex, the region most activated in funct

172 In other sites, e.g., the subiculum and retrosplenial cortex, there was often less overlap of ce

173 associated signaling pathways in the in the retrosplenial cortex, we demonstrated that extinction of

174 ds" was changed by temporary inactivation of retrosplenial cortex, whereas other electrophysiological

175 task in right posterior hippocampus and left retrosplenial cortex, which could be related to self-loc

176 n between primary visual cortex (V1) and the retrosplenial cortex, which further projects to the hipp

177 reduced activity in frontal, cingulate, and retrosplenial cortex.

178 ding hippocampus, parahippocampal gyrus, and retrosplenial cortex.

179 dala, parahippocampal cortex, cingulate, and retrosplenial cortex.

180 rimary recipient of visual inputs to the rat retrosplenial cortex.

181 gyrus (STG) and dorsal bank of STS, and the retrosplenial cortex.

182 araventricular nucleus, the amygdala, and in retrosplenial cortex.

183 posterior thalamus, as well as in the right retrosplenial cortex.

184 and TF, whereas only area TF projects to the retrosplenial cortex.

185 esponses before, and during, inactivation of retrosplenial cortex.

186 that is made up, in part, of portions of the retrosplenial cortex.

187 uced neuronal damage in the striatum and the retrosplenial cortex.

188 posterior cingulate region that includes the retrosplenial cortex.

189 cortex and caudally directed projections to retrosplenial cortex.

190 and necrosis in the rat posterior cingulate/retrosplenial cortex.

191 nd layers II-III of the caudal neocortex and retrosplenial cortex.

192 esentation of head direction and location in retrosplenial cortex.

193 entation of place and head directions in the retrosplenial cortex.

194 /- 1% loss of dendritic spines in layer 1 of retrosplenial cortex.

195 ial and lateral entorhinal cortices, and the retrosplenial cortex.

196 halamus, which followed active states of the retrosplenial cortex.

197 r cingulate cortex (PCC)/precuneus (PCu) and retrosplenial cortex.

198 pocampal cortex, and posterior cingulate and retrosplenial cortex.

199 hippocampus was strongly correlated with the retrosplenial cortex.

200 event-specific reactivation was found in the retrosplenial cortex.

201 eral functional connectivity specifically in retrosplenial cortex.

202 e expressed throughout medial (cingulate and retrosplenial) cortex well before neocortex.

203 Moreover, suppression of retrosplenial cortical activity, which normally impairs

204 al surface of the isthmus are covered by the retrosplenial cortical areas 29l, 29m, and 30, whereas m

205 luded exacerbated damage in limbic cortices, retrosplenial cortical damage, and reduced inhibition in

206 ty to neurodegeneration [posterior cingulate/retrosplenial cortices (PCC/RSC) and parietal cortex, re

207 ased in cortical layer V of the temporal and retrosplenial cortices but not in parietal cortex despit

208 he medial parietal, posterior cingulate, and retrosplenial cortices collectively constitute a region

209 odegeneration in the posterior cingulate and retrosplenial cortices of female adolescent rats produce

210 or brain regions such as parahippocampal and retrosplenial cortices provide critical inputs that allo

211 Parahippocampal and retrosplenial cortices respond strongly to visual scenes

212 rconnectivity of the posterior cingulate and retrosplenial cortices with predominately medial and ant

213 n in the infralimbic, anterior cingulate and retrosplenial cortices, and in the hippocampus.

214 colliculus, zona incerta, and the visual and retrosplenial cortices.

215 pic organization that extend into barrel and retrosplenial cortices.

216 e parolfactory, cingulate, pericingulate and retrosplenial cortices.

217 ontal, ventrolateral orbital, cingulate, and retrosplenial cortices.

218 medial, insular, ectorhinal, perirhinal, and retrosplenial cortices; CA1/subiculum of hippocampus; cl

219 on brain activity; (3) a striking pattern of retrosplenial deactivation was observed in 7 cases mainl

220 , ventrolateral and lateral orbital, ventral retrosplenial, dorsal and posterior agranular insular, v

221 Retrosplenial ensembles robustly encoded conjunctions of

222 ory olfactory bulbs, the cerebellum, and the retrosplenial granular cortex.

223 tion in the rat brain that is limited to the retrosplenial granular cortex.

224 left posterior hippocampus, parahippocampal-retrosplenial gyrus and left superior frontal cortex reg

225 In particular, rats with dysgranular retrosplenial lesions were less reliant on distal visual

226 involved the parahippocampal cortex, whereas retrosplenial-medial prefrontal cortices synchrony was e

227 e progressive and preferential reductions in retrosplenial metabolism in PSAPP mice, these reductions

228 al cortex is areas 23a, 23b, and 31, and the retrosplenial/parahippocampal border is at the ventral e

229 (GluR1 and GluR2) subunits were analyzed in retrosplenial, parietal and temporal cortices during the

230 specific to cortical layer V throughout the retrosplenial, parietal, and temporal cortices, with no

231 layers III and IV of the posterior cingulate/retrosplenial (PC/RS) cortex in 50% and 100% of the mice

232 injury of neurons in the posterior cingulate/retrosplenial (PC/RS) cortex.

233 al cortex (MPFC), posterior cingulate cortex/retrosplenial (PCC/Rsp), inferior parietal lobule, later

234 d representations in the cortex (entorhinal, retrosplenial, perirhinal) and the amygdala could not be

235 frontal, lateral temporal and parietal, and retrosplenial PiB-PET tracer uptake.

236 Increases in 1CGU of 62-98% were found in retrosplenial, piriform and entorhinal cortex of dizocil

237 ts in limbic areas of the cortex (cingulate, retrosplenial, piriform, and entorhinal), in the visual

238 es, but also receives minor projections from retrosplenial, posterior parietal, and visual associatio

239 served electrophysiological co-activation of retrosplenial/posterior cingulate cortex (RSC/PCC) and a

240 ortex, posterior parahippocampal cortex, and retrosplenial/posterior cingulate cortex.

241 trophy and hypometabolism, restricted to the retrosplenial/posterior cingulate cortex.

242 ons between the anterior thalamic nuclei and retrosplenial/pre- and parasubicular neurons.

243 f precuneus, posterior cingulate cortex, and retrosplenial region), an intriguing territory currently

244 antagonist-induced neurodegeneration in the retrosplenial region.

245 labeled cells in the posterior cingulate and retrosplenial regions (approximately 67% of total labele

246 h changes with location, is mapped onto this retrosplenial representation.

247 timulated ACh efflux in the frontal (FC) and retrosplenial (RSC) cortices.

248 ere placed in the posterior cingulate (PCC), retrosplenial (RSC), medial parietal cortices (MPC), and

249 of motor, somatosensory, posterior parietal, retrosplenial, temporal, and occipital cortices; to nucl

250 ampal region of mice was retained within the retrosplenial tract of the dorsal 3rd ventrical and surr

251 ctory bulb, limbic, parietal, somatosensory, retrosplenial, visual, motor, and temporal regions, as w