ライフサイエンスコーパス: dorsolateral

1 difficult tasks, we observed bilaterality in dorsolateral and anterior prefrontal cortex across WM do

2 t anterior insula, left ventral hippocampus, dorsolateral and dorsomedial prefrontal cortex, and caud

3 g, and counterfactual choice, rather than on dorsolateral and medial prefrontal areas involved in sev

4 ular-default network state involving insula, dorsolateral and medial prefrontal cortex, and posterior

5 Dorsolateral and polar prefrontal areas that are associa

6 s (increased recruitment and integration) in dorsolateral and ventrolateral prefrontal cortex, which

7 in three postmortem cortical tissue regions: dorsolateral and ventromedial prefrontal cortices and mo

8 ilateral, sparse, and primarily targeted the dorsolateral and ventromedial sectors of contralateral l

9 tex, including orbitofrontal, ventrolateral, dorsolateral, and ventromedial sectors, along with the a

10 , and a U-shaped digestive tract ending in a dorsolateral anus.

11 Deletion of C1ql3 in the dorsolateral AON impaired synaptic AON->OB connections a

12 egeneration is moderate and still ongoing in dorsolateral areas.

13 rinsic dynamics, one spanning a ventromedial-dorsolateral axis and dominated by measures of signal au

14 ations of neurons in the lateral CeA and the dorsolateral bed nucleus of the stria terminalis (dlBST)

15 immediate early gene mapping highlighted the dorsolateral bed nucleus of the stria terminalis (dlBST)

16 verall motor improvement, resided around the dorsolateral border of the STN.

17 (PreCaTs) in DA terminals and DA release in dorsolateral (Caudato-Putamen, DLS) and ventromedial (Nu

18 , MCH and ORX neurons by the dorsomedial and dorsolateral divisions of the BNST.

19 x; mPFC), a cognitive control network [e.g., dorsolateral (dl)PFC], and a salience network (e.g., ins

20 rons in the nucleus accumbens (NAc) core and dorsolateral (DLS) striatum in Npas2 mutant females afte

21 matter volume (GMV) and surface area (SA) in dorsolateral/dorsomedial prefrontal cortex and caudal an

22 somatosensory cortex, ectorhinal cortex, and dorsolateral entorhinal cortex.

23 e presence of APOE epsilon4, we examined the dorsolateral frontal cortex from deceased participants w

24 e have examined gene expression in the human dorsolateral frontal cortex using RNA- Seq to populate a

25 m; visual hallucinations (VH) with bilateral dorsolateral-frontal cortex, posterior cingulate, and pa

26 evidence has revealed that neurons in mouse dorsolateral geniculate nucleus (dLGN) can undergo rapid

27 ctions from the primary visual cortex to the dorsolateral geniculate nucleus (first-order) and pulvin

28 c inhibitory corticothalamic pathways to the dorsolateral geniculate nucleus and pulvinar, as well as

29 s synapse elimination in the postnatal mouse dorsolateral geniculate nucleus of the thalamus and sens

30 ll GABAergic neurons that express FoxP2; and dorsolateral glutamatergic neurons that express FoxP2 in

31 ed by SRP sources within the motor system-in dorsolateral hand motor areas for expected hand-related

32 medial, central, centrolateral, dorsomedial, dorsolateral) identifiable throughout development.

33 ves inhibitory inputs from the contralateral dorsolateral IP, and mainly excitatory inputs from the i

34 We acquired dorsolateral/medial prefrontal cortex samples from indiv

35 TD, terminate in specific cell groups in the dorsolateral nTTDo and in PrV.

36 olateral orbital area, lateral orbital area, dorsolateral orbital area, and agranular insular areas.

37 The major pathways are recursive: the dorsolateral pallium (DL) projects strongly to DDi, with

38 tive melanoblasts were not restricted to the dorsolateral pathway as in birds and mammals but were al

39 Significant dorsolateral PFC (DLPFC) activations were observed durin

40 related with functional connectivity between dorsolateral PFC (DLPFC) and temporal lobe that mediated

41 c receptor agonist carbachol onto neurons in dorsolateral PFC (DLPFC) of male rhesus macaques perform

42 between the amygdala and ventral PFC (VPFC), dorsolateral PFC (DLPFC), and dorsal anterior cingulated

43 this region's functional connectivity to the dorsolateral PFC (pgACC-dlPFC), and mediated of the asso

44 s and to functional connectivity between the dorsolateral PFC and caudate in pre-HD participants.

45 levels were also detected in the postmortem dorsolateral PFC of individuals with depression.

46 correlations with FC between the hCd and the dorsolateral PFC, hippocampus, and precuneus.

47 ed grasp to lift effort is shown to be under dorsolateral (PMv and AIP) more than dorsomedial control

48 ll positive GABAA receptor subunits from the dorsolateral pole to ventromedial extremities.

49 f GABAergic (Vgat-expressing) neurons in the dorsolateral portion of the dorsal raphe nucleus (DRN),

50 al posterior area (VLP) in marmosets and the dorsolateral posterior area (DLP) in owl monkeys, and re

51 neurons (L3PNs) differ significantly between dorsolateral prefrontal (DLPFC) and sensory areas.

52 fer significantly between primary visual and dorsolateral prefrontal (DLPFC) cortices.

53 ring processing of neutral faces and reduced dorsolateral prefrontal activity during failed inhibitio

54 In most other cortical regions, including dorsolateral prefrontal and anterior cingulate cortex, t

55 EF was uniquely associated with caudal left dorsolateral prefrontal and lateral temporo-parietal cor

56 tivation in executive control regions (e.g., dorsolateral prefrontal and supramarginal gyri; p = 0.01

57 d, whereas connectivity with regions such as dorsolateral prefrontal cortex (associated with emotion

58 e predicted expression or splicing levels in dorsolateral prefrontal cortex (DLFPC) and peripheral mo

59 f 561 immune genes and 20 immune pathways in dorsolateral prefrontal cortex (DLPFC) (144 schizophreni

60 Smaller right dorsolateral prefrontal cortex (DLPFC) (i.e., middle and

61 n distributed neural circuitry including the dorsolateral prefrontal cortex (DLPFC) and appear to ari

62 sis showed greater connectivity between left dorsolateral prefrontal cortex (dlPFC) and left inferior

63 ted with the age of onset of SCZ in both the dorsolateral prefrontal cortex (DLPFC) and orbitofrontal

64 ne density on layer 3 pyramidal cells in the dorsolateral prefrontal cortex (DLPFC) appears to contri

65 and functional alterations of neurons in the dorsolateral prefrontal cortex (dlPFC) are thought to co

66 cusing on the bilateral thalami and the left dorsolateral prefrontal cortex (DLPFC) as our regions of

67 posterior superior temporal sulcus (pSTS) or dorsolateral prefrontal cortex (DLPFC) before having par

68 er a temporary neural disruption of the left Dorsolateral Prefrontal Cortex (DLPFC) can improve impli

69 t-induced mGluR5 signaling in the postmortem dorsolateral prefrontal cortex (DLPFC) derived from 17 p

70 o for group differences in activation of the dorsolateral prefrontal cortex (DLPFC) during WM perform

71 For example, dendritic spines in the primate dorsolateral prefrontal cortex (dlPFC) express the molec

72 ceive either active or sham rTMS to the left dorsolateral prefrontal cortex (dlPFC) for 20 consecutiv

73 n expression and/or phosphorylation state in dorsolateral prefrontal cortex (DLPFC) from 22 pairs of

74 od-oxygen-level-dependent (BOLD) signal, and dorsolateral prefrontal cortex (DLPFC) glutamate+glutami

75 ndrial functional pathways were obtained for dorsolateral prefrontal cortex (DLPFC) gray matter and l

76 tively), and the role of the hippocampus and dorsolateral prefrontal cortex (dlPFC) in mediating such

77 tudies in adults highlighted the role of the dorsolateral prefrontal cortex (DLPFC) in regulating agg

78 Dorsolateral prefrontal cortex (dlPFC) is associated wit

79 Dorsolateral prefrontal cortex (DLPFC) maintains goal re

80 curring de novo, in brain-expressed genes of dorsolateral prefrontal cortex (DLPFC) neurons.

81 tic and total tissue fractions obtained from dorsolateral prefrontal cortex (dlPFC) of 15 MDD and 15

82 states of UPR sensor pathway proteins in the dorsolateral prefrontal cortex (DLPFC) of 22 matched pai

83 s no systematic overview of glutamate in the dorsolateral prefrontal cortex (DLPFC) of patients with

84 e analyzed expression levels of these TFs in dorsolateral prefrontal cortex (DLPFC) of SCZ patients.

85 We examined bioenergetic pathways in the dorsolateral prefrontal cortex (DLPFC) of subjects with

86 mation relevant for credit assignment in the dorsolateral prefrontal cortex (dlPFC) of two male rhesu

87 n activity in a high-level, executive area - dorsolateral prefrontal cortex (dlPFC) of unrestrained m

88 ial magnetic stimulation (rTMS) of the right dorsolateral prefrontal cortex (DLPFC) on working memory

89 The dorsolateral prefrontal cortex (DLPFC) plays a pivotal r

90 The primate dorsolateral prefrontal cortex (dlPFC) subserves top-dow

91 activity of neural circuitry in the primate dorsolateral prefrontal cortex (DLPFC) supports a range

92 Here we find cells in the dorsolateral prefrontal cortex (dlPFC) that reflect vari

93 ermined that HDAC2 mRNA levels were lower in dorsolateral prefrontal cortex (DLPFC) tissue from donor

94 tion, and 3) precision targeting of the left dorsolateral prefrontal cortex (DLPFC) to subgenual ante

95 ical inhibition (LICI) was measured from the dorsolateral prefrontal cortex (DLPFC) using combined tr

96 en quantify spatial gene expression in human dorsolateral prefrontal cortex (DLPFC) using spectral im

97 We hypothesized that the hippocampus and dorsolateral prefrontal cortex (dlPFC) would play a key

98 ree latent brain factors (amygdala, pACC and dorsolateral prefrontal cortex (DLPFC)) to test the effe

99 ilateral superior parietal lobule, bilateral dorsolateral prefrontal cortex (DLPFC), and bilateral mi

100 ional connectivity (FC) between amygdala and dorsolateral prefrontal cortex (DLPFC), and had increase

101 ed activity in primary auditory cortex (AC), dorsolateral prefrontal cortex (dlPFC), and the basolate

102 sorders generally involve dysfunction of the dorsolateral prefrontal cortex (dlPFC), but there are fe

103 xon-exon junctions in multiple brain regions-dorsolateral prefrontal cortex (DLPFC), hippocampus, and

104 this study, we tested the involvement of the dorsolateral prefrontal cortex (dlPFC), in anxiety expre

105 rnal rhythms in gene expression in the human dorsolateral prefrontal cortex (dlPFC), in schizophrenia

106 e found that threat affected activity in the dorsolateral prefrontal cortex (dlPFC), rather than the

107 l lobe circuits, with a central role for the dorsolateral prefrontal cortex (DLPFC), relatively intac

108 clude the striatum of the basal ganglia, the dorsolateral prefrontal cortex (DLPFC), the dorsal anter

109 recorded extracellular spiking activity from dorsolateral prefrontal cortex (dlPFC), the frontal eye

110 ,000 circRNAs species were identified in the dorsolateral prefrontal cortex (DLPFC), we observed lowe

111 ells in layer 3 (L3) and layer 5 (L5) of the dorsolateral prefrontal cortex (DLPFC), we sought to det

112 Working memory relies on the dorsolateral prefrontal cortex (dlPFC), where microcircu

113 to directly measure evoked activity from the dorsolateral prefrontal cortex (DLPFC), which is of cons

114 eas the mesocortical DA system-including the dorsolateral prefrontal cortex (dlPFC)-is critical for s

115 dorsal anterior cingulate cortex (dACC) and dorsolateral prefrontal cortex (dlPFC).

116 emory, an executive function mediated by the dorsolateral prefrontal cortex (dlPFC).

117 frontal lobe with decreased activity in the dorsolateral prefrontal cortex (DLPFC).

118 d after a session of 10 Hz rTMS to the right dorsolateral prefrontal cortex (dlPFC).

119 that flexibility is mainly subserved by the dorsolateral prefrontal cortex (DLPFC).

120 s3749034 and with the expression of GAD25 in dorsolateral prefrontal cortex (DLPFC).

121 a (SZ) is associated with dysfunction of the dorsolateral prefrontal cortex (DLPFC).

122 ts involve dysfunction of the newly evolved, dorsolateral prefrontal cortex (dlPFC).

123 in-positive (PV) interneurons in the primate dorsolateral prefrontal cortex (DLPFC).

124 t stimulation (HD-tDCS) to the left or right dorsolateral prefrontal cortex (DLPFC).

125 articular, it did impact the FC between left dorsolateral prefrontal cortex (DLPFC)/inferior frontal

126 100 kb of the lead SNP are expressed in the dorsolateral prefrontal cortex (DLPFC): UNC5C, ENC1, and

127 ere, we found that, in common marmosets, the dorsolateral prefrontal cortex (dlPFC; peak at A8aD) has

128 e (Glx), were measured by 1H MRS in the left dorsolateral prefrontal cortex (l-DLPFC) and bilateral h

129 Left dorsolateral prefrontal cortex (L-DLPFC) tDCS induced an

130 renia risk and expression at 89 genes in the dorsolateral prefrontal cortex (P <= 9.43 x 10-6), inclu

131 We found increased lactate in the dorsolateral prefrontal cortex (p = 0.043, n = 16/group)

132 fied a specific network including medial and dorsolateral prefrontal cortex (PFC) in default mode net

133 nnectivity between the hippocampus and right dorsolateral prefrontal cortex (PFC), which in turn was

134 l executive" (FPN) network anchored in right dorsolateral prefrontal cortex (rDLPFC) and posterior pa

135 odulatory effects of trait anger on amygdala-dorsolateral prefrontal cortex and amygdala-lateral orbi

136 mmonMind Consortium, comprising two regions: dorsolateral prefrontal cortex and anterior cingulate co

137 uted to saccadic action selection, including dorsolateral prefrontal cortex and anterior cingulate co

138 stribution of the NT5C2 protein in the human dorsolateral prefrontal cortex and cortical human neural

139 le total uncertainty is represented in right dorsolateral prefrontal cortex and drives random explora

140 her microglial activation is elevated in the dorsolateral prefrontal cortex and hippocampus of untrea

141 )], that span the lateral prefrontal cortex (dorsolateral prefrontal cortex and inferior frontal gyru

142 vortioxetine reduced activation in the right dorsolateral prefrontal cortex and left hippocampus duri

143 er volumes relative to controls in the right dorsolateral prefrontal cortex and left hippocampus, alo

144 changes were predicted from activity in left dorsolateral prefrontal cortex and precuneus while makin

145 of structure (decreased grey matter in right dorsolateral prefrontal cortex and right inferior tempor

146 ed functional connectivity between the right dorsolateral prefrontal cortex and right superior occipi

147 or parietal cortex, less deactivation of the dorsolateral prefrontal cortex and thalamus, and increas

148 ddiction-relevant brain regions, such as the dorsolateral prefrontal cortex and the angular and cingu

149 r of self-gathered information activated the dorsolateral prefrontal cortex and the midbrain, whereas

150 ed functional connectivity between the right dorsolateral prefrontal cortex and the parietal cortex i

151 ion, changes in the connectivity between the dorsolateral prefrontal cortex and the posterior default

152 etically predicted proteins derived from the dorsolateral prefrontal cortex and these outcomes.

153 rts, we tested whether GMV and NAA/Cr in the dorsolateral prefrontal cortex are associated with fatig

154 te stimulation was associated with increased dorsolateral prefrontal cortex beta power following feed

155 EF and DB were associated with the rostral dorsolateral prefrontal cortex bilaterally.

156 ex while recalling resulted in activation in dorsolateral prefrontal cortex bilaterally.

157 We found that neuronal activity in the dorsolateral prefrontal cortex conveyed the necessary in

158 Interestingly, activity in the dorsolateral prefrontal cortex correlated with gait impa

159 Both caudate and dorsolateral prefrontal cortex demonstrated a beta power

160 We stimulated over the left dorsolateral prefrontal cortex during a declarative memo

161 ignificant differences localized to the left dorsolateral prefrontal cortex during response selection

162 Notably, [oxy-Hb] change in the left dorsolateral prefrontal cortex during SAT showed a posit

163 When applied to subcutaneous adipose and dorsolateral prefrontal cortex expression datasets with

164 The optimal target in the dorsolateral prefrontal cortex for treating depression w

165 olymerase chain reaction in human postmortem dorsolateral prefrontal cortex from 286 nonpsychiatric c

166 We performed proteomic sequencing of dorsolateral prefrontal cortex in 438 older individuals

167 DoC patients with the anode placed over left-dorsolateral prefrontal cortex in a prospective open-lab

168 nal connectivity between the putamen and the dorsolateral prefrontal cortex in OCD patients, as well

169 eakdown between the cerebellum and the right dorsolateral prefrontal cortex is associated with negati

170 ng (MRI)-guided coil positioning to the left dorsolateral prefrontal cortex method was also compared.

171 lation and histone acetylation data from the dorsolateral prefrontal cortex of 411 older adults who h

172 associated with increased FOLH1 mRNA in the dorsolateral prefrontal cortex of brains from unaffected

173 18 and TNF, is increased in the amygdala and dorsolateral prefrontal cortex of children with ASD as c

174 lternating current stimulation over the left dorsolateral prefrontal cortex of human participants [n

175 riptomics to examine ~80,000 nuclei from the dorsolateral prefrontal cortex of male individuals with

176 predictor of both GMV and NAA/Cr in the left dorsolateral prefrontal cortex of patients with CFS.

177 associated with neuronal alterations in the dorsolateral prefrontal cortex of patients with CFS.

178 tial cues and choice-related activity before dorsolateral prefrontal cortex or the amygdala.

179 as indexed by [(18)F]FEPPA VT, in either the dorsolateral prefrontal cortex or the hippocampus.

180 Here, we investigated whether neurons in dorsolateral prefrontal cortex process risk derived from

181 isual networks after stimulation of the left dorsolateral prefrontal cortex resulted in faster task p

182 RNA sequencing data of human dorsolateral prefrontal cortex revealed relatively high

183 tients with major depression undergoing left dorsolateral prefrontal cortex rTMS and to determine ass

184 ross-validate in hundreds of non-overlapping dorsolateral prefrontal cortex samples.

185 ze 10,559 high-quality circRNAs in 589 human dorsolateral prefrontal cortex samples.

186 ramidal neuron dendrites in Brodmann area 46 dorsolateral prefrontal cortex using the Golgi-Cox techn

187 Seeds in the amygdala and dorsolateral prefrontal cortex were explored.

188 tivity profiles of the medial prefrontal and dorsolateral prefrontal cortex while GAD was specificall

189 s resulted in significant activation in left dorsolateral prefrontal cortex while recalling resulted

190 oncentration of lactate in postmortem brain (dorsolateral prefrontal cortex) in subjects with schizop

191 iatal and midbrain) and prefrontal cortical (dorsolateral prefrontal cortex) regions during reward an

192 gulate cortex), frontoparietal network (left dorsolateral prefrontal cortex), and salience network (r

193 ional 10-Hz rTMS or iTBS rTMS applied to the dorsolateral prefrontal cortex, 5 days/week over 4-6 wee

194 ace pupillary changes, infants recruited the dorsolateral prefrontal cortex, a brain region linked to

195 ce, a scarcity mindset decreased activity in dorsolateral prefrontal cortex, an area well known for i

196 ivity in behaving monkeys from the amygdala, dorsolateral prefrontal cortex, and auditory cortex.

197 the sgACC and the default mode network, left dorsolateral prefrontal cortex, and insula, and reduced

198 nt brain regions (anterior cingulate cortex, dorsolateral prefrontal cortex, and primary visual corte

199 l cortex, the dorsal anterior cingulate, the dorsolateral prefrontal cortex, and the lateral orbitofr

200 n the anterior cingulate cortex and later in dorsolateral prefrontal cortex, caudate and ventral stri

201 Seed-based (bilateral dorsolateral prefrontal cortex, DLPFC) rsFC analysis was

202 Although working memory tasks often engage dorsolateral prefrontal cortex, few studies have investi

203 RNA-seq datamining (hippocampus, dorsolateral prefrontal cortex, fusiform gyrus and super

204 nual anterior cingulate cortex [sgACC], left dorsolateral prefrontal cortex, hippocampus, and basolat

205 Moreover, in 6 out of 11 tissues (aorta, dorsolateral prefrontal cortex, hippocampus, pancreas, s

206 tal-striatal activation, specifically in the dorsolateral prefrontal cortex, inferior frontal gyrus,

207 y associated with MD values in the bilateral dorsolateral prefrontal cortex, left orbitofrontal corte

208 , hypometabolism and/or hypoperfusion in the dorsolateral prefrontal cortex, the anterior and middle

209 work of areas, including the dorsomedial and dorsolateral prefrontal cortex, the intraparietal sulcus

210 In dorsolateral prefrontal cortex, this difference increase

211 fortful DM) leading to activation across the dorsolateral prefrontal cortex, whereas experts are expe

212 the primary visual cortex and highest in the dorsolateral prefrontal cortex, whereas the GABA measure

213 novices showed significant activation of the dorsolateral prefrontal cortex, whereas this activation

214 rontal gyrus, the frontal eye field, and the dorsolateral prefrontal cortex, which are implicated in

215 le patients trait anger positively modulated dorsolateral prefrontal cortex-amygdala coupling.

216 were assessed in four frontostriatal tracts (dorsolateral prefrontal cortex-associative striatum, dor

217 nd fewer normalized streamlines in the right dorsolateral prefrontal cortex-sensorimotor striatum and

218 hermore, normalized streamlines in the right dorsolateral prefrontal cortex-sensorimotor striatum neg

219 rmalized streamlines in the right-hemisphere dorsolateral prefrontal cortex-sensorimotor striatum pre

220 eral prefrontal cortex-associative striatum, dorsolateral prefrontal cortex-sensorimotor striatum, ve

221 A breakdown of connectivity in a specific dorsolateral prefrontal cortex-to-cerebellum network dir

222 ns in the anterior hippocampus, amygdala and dorsolateral prefrontal cortex.

223 ilin receptor is reduced in the amygdala and dorsolateral prefrontal cortex.

224 re significantly preferentially expressed in dorsolateral prefrontal cortex.

225 coding of reward magnitude by neurons in the dorsolateral prefrontal cortex.

226 ortex, dorsal anterior cingulate cortex, and dorsolateral prefrontal cortex.

227 ferent periods of a delayed-response task in dorsolateral prefrontal cortex.

228 ct current stimulation (tDCS) over the right dorsolateral prefrontal cortex.

229 were generated using frozen tissue from the dorsolateral prefrontal cortex.

230 hibitory control signal originating from the dorsolateral prefrontal cortex.

231 nterior cingulate, medial frontal gyrus, and dorsolateral prefrontal cortex.

232 red, in up to 40 daily sessions, to the left dorsolateral prefrontal cortex.

233 ons including the amygdala, hypothalamus and dorsolateral prefrontal cortex.

234 with stronger connectivity between sgACC and dorsolateral prefrontal cortex.

235 insula, left inferior parietal lobule, left dorsolateral prefrontal cortex/superior frontal gyrus, a

236 esponse inhibition, connectivity between the dorsolateral prefrontal cortex/supramarginal gyrus and s

237 la induced by single TMS pulses to the right dorsolateral prefrontal cortex; and 4) greater ventromed

238 We performed RNA-seq in hippocampi and dorsolateral prefrontal cortices (DLPFCs) from 551 indiv

239 Here, we show that tRNS over the bilateral dorsolateral prefrontal cortices (dlPFCs) improved learn

240 er activity in the lateral orbitofrontal and dorsolateral prefrontal cortices compared with healthy m

241 associated with the responses of insula and dorsolateral prefrontal cortices to the receipt of large

242 ciative-limbic subthalamic nucleus and right dorsolateral prefrontal functional connectivity in healt

243 reduction is most marked in dorsomedial and dorsolateral prefrontal regions for compulsivity and in

244 remotor regions in the marmoset, rather than dorsolateral prefrontal regions, which are often suggest

245 x, including visual, posterior parietal, and dorsolateral prefrontal regions.

246 mary) and higher-order (posterior-dorsal and dorsolateral prefrontal) auditory regions.

247 etwork connectivity (encompassing aspects of dorsolateral prefrontal, dorsomedial prefrontal, lateral

248 tients showed disorder-specific reduced left dorsolateral-prefrontal activation and reduced posterior

249 es the generation of dopaminergic neurons by dorsolateral progenitors through inhibition of Pax6 expr

250 In the dorsolateral putamen, sensorimotor putamen atrophy corre

251 and a lower degree of atrophy (-20%) in the dorsolateral putamen.

252 ontextual fear discrimination identified the dorsolateral septum (DLS) as a relay of the dentate gyru

253 or correlates with broad reconfigurations of dorsolateral striatal (DLS) circuit properties that incr

254 tic and chemogenetic approaches to show that dorsolateral striatal PV interneurons influence the init

255 ze-running tasks, we demonstrate that phasic dorsolateral striatum (DLS) activity occurring at the on

256 Here, we studied the role of dorsolateral striatum (DLS) and dorsomedial striatum (DM

257 siology reveals disrupted action encoding in dorsolateral striatum (DLS) associated with altered habi

258 orts have been made to understand "what" the dorsolateral striatum (DLS) does for habitual behavior,

259 t functions to striatal subregions, with the dorsolateral striatum (DLS) especially implicated in hab

260 um (DMS) mediating goal-directed actions and dorsolateral striatum (DLS) mediating habitual actions.

261 posterior dorsomedial striatum (DMS) and the dorsolateral striatum (DLS) on a touchscreen visual seri

262 mate release from M2 cortex terminals in the dorsolateral striatum (DLS) was undetectable in HD mice

263 In "response learning," associated with the dorsolateral striatum (DLS), decisions are anchored to a

264 of striosome compartments restricted to the dorsolateral striatum (DLS), where less dopamine release

265 orsal hippocampus (DH)-dependent spatial and dorsolateral striatum (DLS)-dependent cued-response memo

266 co-striatal projection neuron (dSPN)] in the dorsolateral striatum (DLS).

267 ypes, and ischemic stroke was induced in the dorsolateral striatum (DLS).

268 rience in specific ways, the hippocampus and dorsolateral striatum can transcend their attributed rol

269 localized to astrocytes, and are enriched in dorsolateral striatum compared to accumbens core.

270 ral activity in the primary motor cortex and dorsolateral striatum during reach-to-grasp skill learni

271 Meanwhile, DREADD-mediated inhibition of the dorsolateral striatum enhanced response-outcome conditio

272 inactivation of the primary motor cortex and dorsolateral striatum had distinct effects on skilled fi

273 The dorsolateral striatum provides the basis for habits that

274 Retrograde tracing from the dorsolateral striatum reveals that both layer II/III and

275 The dorsomedial and dorsolateral striatum support goal-directed and habitual

276 How ethanol targets dorsolateral striatum to drive compulsive consumption is

277 urrent work reveals that the hippocampus and dorsolateral striatum use distinct and complementary pri

278 in male Long-Evans rats, the hippocampus and dorsolateral striatum use time and space in distinct and

279 e core of the nucleus accumbens (but not the dorsolateral striatum).

280 lutamate release from cortical inputs to the dorsolateral striatum, a brain structure critical for ac

281 e also assessed spine density on WD36 in the dorsolateral striatum, a region that is not implicated i

282 We reveal that DA release in mouse dorsolateral striatum, but not nucleus accumbens core, i

283 propose that anxiety (amygdala) and habits (dorsolateral striatum, DLS) may be causally linked.

284 how two memory networks, the hippocampus and dorsolateral striatum, may accomplish such a goal.

285 The results reveal that representations in dorsolateral striatum, prefrontal and secondary motor co

286 162 into the nucleus accumbens core, but not dorsolateral striatum, selectively reduced cue-controlle

287 and sensorimotor inputs from motor cortex to dorsolateral striatum, we show that associative and sens

288 on's disease (PD) preferentially affects the dorsolateral striatum.

289 corticostriatal synaptic transmission in the dorsolateral striatum.

290 burst firing among DA neurons projecting to dorsolateral striatum.

291 in the indirect, striatopallidal pathway in dorsolateral striatum.

292 e in the dorsomedial striatum but not in the dorsolateral striatum.

293 became dependent on both the hippocampus and dorsolateral striatum.

294 In contrast, a dorsolateral subsystem includes the lateral forebrain bu

295 superior occipital (cue-alpha) and the left dorsolateral superior frontal gyri (item-gamma) on permu

296 erior nidopallium, and medial portion of the dorsolateral thalamic nucleus (DLM).

297 scent neurons organized in bilateral columns dorsolateral to the central canal in segments L1-L5, the

298 A common tonotopy with a dorsolateral to ventromedial gradient of low to high fre

299 striatum is functionally segregated across a dorsolateral/ventromedial axis.

300 ther segregated based on those targeting the dorsolateral versus the dorsomedial subdivisions.