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 The parahippocampal, retrosplenial and parietal cortices, as well as the hipp

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

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

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

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

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

13 heightened immunodensities were specific to retrosplenial and temporal cortices.

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

15 dial prefrontal, inferotemporal, entorhinal, retrosplenial, and anterior cingulate cortices, the subi

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

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

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

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

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

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

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

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

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

25 l stimulation and spread through the ventral retrosplenial area (VRA) with vibrissa air-puff stimulat

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

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

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

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

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

31 associated with greater connectivity between retrosplenial areas and the rest of the cortex, specific

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

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

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

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

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

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

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

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

40 y from the parahippocampal place area (PPA), retrosplenial complex (RSC) and occipital place area (OP

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

42 a (OFA), amygdala, fusiform body area (FBA), retrosplenial complex (RSC) and parahippocampal place ar

43 ce in future work.SIGNIFICANCE STATEMENT The retrosplenial complex (RSC) has been implicated in visio

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

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

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

47 Human retrosplenial complex (RSC), located in medial parietal

48 nother scene-selective region of cortex, the retrosplenial complex (RSC), showed the exact opposite p

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

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

51 g the "proto" parahippocampal place area and retrosplenial complex) by adulthood, already show domain

52 e regions (the parahippocampal place area or retrosplenial complex) or a motion-selective region (MT)

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

54 cally place-selective parahippocampal gyrus, retrosplenial complex, and transverse occipital sulcus.

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

56 ively to scenes: parahippocampal place area, retrosplenial complex/medial place area, and occipital p

57 to its anatomical positioning, the granular retrosplenial cortex (gRSC) may be a bridge for this hip

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

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

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

61 patial and contextual memories depend on the retrosplenial cortex (RSC) [1-5].

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

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

64 he relationship between neurons in the rat's retrosplenial cortex (RSC) and entorhinal cortex (MEC) t

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

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

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

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

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

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

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

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

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

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

75 Retrosplenial cortex (RSC) is a dorsomedial parietal are

76 As the retrosplenial cortex (RSC) is critical for episodic memo

77 The retrosplenial cortex (RSC) is involved in a broad range

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

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

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

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

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

83 Studies in humans and rodents suggest that retrosplenial cortex (RSC) plays a key role in these com

84 In expert mice, the retrosplenial cortex (RSC) uniquely encoded history- and

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

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

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

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

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

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

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

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

93 Hippocampus, granular retrosplenial cortex (RSCg), and anterior thalamic nucle

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

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

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

97 The retrosplenial cortex (RSP) is highly interconnected with

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

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

100 quency stimulation of these ensembles in the retrosplenial cortex 1 day after learning produced a rec

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

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

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

104 head-direction cells in the rodent thalamus, retrosplenial cortex and cingulum fiber bundle are tuned

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

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

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

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

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

110 onal connectivity in the posterior cingulate/retrosplenial cortex and precuneus and both ageing and A

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

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

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

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

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

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

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

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

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

120 Inactivation of the retrosplenial cortex disrupted this search preference.

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

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

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

124 on of the learned environment persisted, but retrosplenial cortex exhibited significantly increased c

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

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

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

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

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

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

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

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

133 Retrosplenial cortex inactivation impaired accuracy in d

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

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

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

137 Retrosplenial cortex is densely interconnected with the

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

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

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

141 The retrosplenial cortex is strongly connected with brain re

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

143 ound that rhythmic optogenetic activation of retrosplenial cortex layer 5 neurons recapitulated disso

144 The retrosplenial cortex may provide mnemonic information, w

145 Here, retrosplenial cortex neurons were recorded as rats trave

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

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

148 We suggest that the retrosplenial cortex provides mnemonic spatial informati

149 Injections involving the retrosplenial cortex resulted in labeled neurons within

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

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

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

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

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

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

156 ith the default mode network and centered on retrosplenial cortex was the most associated with hippoc

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

158 ity probes revealed rhythmic coupling of the retrosplenial cortex with anatomically connected compone

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

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

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

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

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

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

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

166 In the retrosplenial cortex, a core DMN region, we identify two

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

168 ing increased in bilateral temporal lobe and retrosplenial cortex, accompanied by atrophy in the same

169 endrites and their respective cell bodies in retrosplenial cortex, an area that encodes multi-modal n

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

171 % less c-fos ir-cells in the insular cortex, retrosplenial cortex, and dentate gyrus.

172 epilepticus, motor and somatosensory cortex, retrosplenial cortex, and insular cortex also contained

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

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

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

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

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

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

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

180 tional connectivity in the cingulate cortex, retrosplenial cortex, and thalamus consistent with brain

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

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

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

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

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

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

187 consolidation of memory: entorhinal cortex, retrosplenial cortex, cingulate gyrus, midline thalamic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 hippocampus, the subicular complex, and the retrosplenial cortex, suggesting a specialized role for

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

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

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

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

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

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

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

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

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

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

214 pocampal cortex, and posterior cingulate and retrosplenial cortex.

215 hippocampus was strongly correlated with the retrosplenial cortex.

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

217 eral functional connectivity specifically in retrosplenial cortex.

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

219 ding hippocampus, parahippocampal gyrus, and retrosplenial cortex.

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

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

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

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

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

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

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

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

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

229 posterior cingulate region that includes the retrosplenial cortex.

230 cortex and caudally directed projections to retrosplenial cortex.

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

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

233 trikingly resemble those observed within the retrosplenial cortex.

234 ty and plasticity within the hippocampus and retrosplenial cortex.

235 20 mice, plaques were densest in the ventral retrosplenial cortex.

236 b is at the junction of the presubiculum and retrosplenial cortex.

237 /- 1% loss of dendritic spines in layer 1 of retrosplenial cortex.

238 ed a 1-3-Hz rhythm in layer 5 neurons of the retrosplenial cortex.

239 esentation of head direction and location in retrosplenial cortex.

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

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

242 the largest SWR-related modulation occurs in retrosplenial cortex; however, contrary to the unidirect

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

244 een left posterior cingulate (PCC) and right retrosplenial cortical activity were reduced in children

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

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

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

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

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

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

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

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

253 Parahippocampal and retrosplenial cortices respond strongly to visual scenes

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

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

256 e parolfactory, cingulate, pericingulate and retrosplenial cortices.

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

258 tical areas, including visual, parietal, and retrosplenial cortices.

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

260 pic organization that extend into barrel and retrosplenial cortices.

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

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

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

264 Retrosplenial ensembles robustly encoded conjunctions of

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

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

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

268 Local retrosplenial hyperpolarization-activated cyclic-nucleot

269 C revealed a significant loss of sensory and retrosplenial inputs to the PPC while contralateral and

270 lar mechanisms underlying hippocampo-thalamo-retrosplenial interactions, we investigated the potentia

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

289 Our findings establish retrosplenial-projecting CA1 neurons as a distinct class

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

291 antagonist-induced neurodegeneration in the retrosplenial region.

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

293 cortical composite of frontal, lateral, and retrosplenial regions (FLR) was measured by PiB-PET in 1

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

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

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

297 piking of neurons in primary visual (V1) and retrosplenial (RSP) cortex to activity across dorsal cor

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

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

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