ライフサイエンスコーパス: dentate

1 There were 5,421 eligible dentate adults aged 21 to 74 y with complete relevant da

2 tolerated and was associated with a reduced dentate and caudate nucleus iron content compared to pla

3 statistically significant difference between dentate and edentulous quadrants (P < 0.001).

4 rsal on MRI (100%), with cerebral atrophy or dentate and pontine T2 hyperintensities observed in 28%.

5 (in inverse seconds [sec(-1)]) values of the dentate (case participants: 0.06 ppm +/- 0.04 and 23.87

6 In contrast, reducing dentate CCK induces reactive astrocytes, which correlate

7 peptide cholecystokinin (CCK), released from dentate CCK interneurons, in regulating neurogenic niche

8 croelectrode array (MEA) was used to monitor dentate (DG), CA3, and CA1 hippocampal extracellular glu

9 reover, the TLR4-dependent early increase in dentate excitability is causally associated with epilept

10 complementary neural codes: a rate code for dentate fast-spiking interneurons, a burstiness code for

11 Mean susceptibility and R2* values of the dentate (first MRI: 0.06 ppm +/- 0.05 and 25.78 sec(-1)

12 GABA is a key regulator of adult-born dentate granule cell (abDGC) maturation so mapping the f

13 romote seizures.SIGNIFICANCE STATEMENT Adult dentate granule cell (DGC) neurogenesis is altered in ro

14 tify that TLR4 signaling in neurons augments dentate granule cell calcium-permeable alpha-amino-3-hyd

15 outing of hippocampal mossy fiber axons onto dentate granule cell dendrites creates a recurrent excit

16 ly modified by the integration of adult-born dentate granule cells (abDGCs).

17 us subregion of the hippocampus give rise to dentate granule cells (DGCs) and astrocytes throughout l

18 Newborn dentate granule cells (DGCs) are continuously generated

19 Newborn dentate granule cells (DGCs) are generated in the hippoc

20 knockout mice in which the vast majority of dentate granule cells (DGCs) fail to develop - including

21 Most dentate granule cells (DGCs) generated in response to an

22 nce of striking morphological alterations in dentate granule cells (DGCs) of FTD patients and in a mo

23 tate gyrus (DG) of rodents generates newborn dentate granule cells (DGCs) throughout life.

24 Cs) in the dentate gyrus receive inputs from dentate granule cells (GCs) and project back to GCs loca

25 ns between perforant path (PP) afferents and dentate granule cells (GCs), a circuit involved in memor

26 ered action potential firing in postsynaptic dentate granule cells after single light pulses.

27 an electrophysiology-based classification of dentate granule cells and mossy cells in mice that we va

28 ppocampal adult neurogenesis, and adult-born dentate granule cells contribute to the pathologic retro

29 of varied [GABA] onto nucleated patches from dentate granule cells demonstrated a deactivation rate o

30 at the dynamic dispersion of newly generated dentate granule cells in the neurogenic zone is a requir

31 ssy cells are significantly more active than dentate granule cells in vivo, exhibit spatial tuning du

32 ime to our knowledge, that the population of dentate granule cells is disconnected from other regions

33 ss of circuit integration of newly-generated dentate granule cells of the hippocampus has been presum

34 ologically isolated delta receptors in mouse dentate granule cells to explore IPSCs.

35 manently marked activated mature hippocampal dentate granule cells using conditional Fos-TRAP mice.

36 hat are important for regulating activity of dentate granule cells.

37 of inhibitory neurotransmission measured in dentate granule cells.

38 ne possibility is insufficient inhibition of dentate granule cells.

39 Furthermore, tetrodes in the dentate granule layer and pCA3 pyramidal layer can also

40 to a novel stimulus, SINEs are activated in dentate granule neurons in a time course that is similar

41 a new experience increased firing of active dentate granule neurons rapidly and robustly.

42 We find that inhibition of Tiam1 function in dentate granule neurons reduces synaptic AMPA receptor f

43 the regulation of glutamatergic synapses in dentate granule neurons using a combination of molecular

44 By coupling in vivo Ca(2+) imaging of dentate granule neurons with a novel, unrestrained virtu

45 ogram of glutamatergic synapse regulation in dentate granule neurons.

46 ogram of glutamatergic synapse regulation in dentate granule neurons.SIGNIFICANCE STATEMENT Several l

47 iated with better L&M performance and larger dentate gyri.

48 strongest effects on the CA3 region and the dentate gyrus (CA3-DG) of the hippocampus, alongside ass

49 on of D1R-expressing cells within the dorsal dentate gyrus (dDG), but not the dorsal CA1 (dCA1).

50 NSCs in the dentate gyrus (DG(have enigmatic elaborated apical cellu

51 r perturbation expressed only in hippocampal dentate gyrus (DG) and assessed its association with hip

52 r representations for unexpected items, with dentate gyrus (DG) and CA3 being more sensitive to expec

53 n processes instantiated upstream within the dentate gyrus (DG) and CA3 subregions.

54 ; they innervated interneurons mostly in the dentate gyrus (DG) and CA3.

55 The dentate gyrus (DG) and proximal CA3 (pCA3) regions have

56 tion of computational circuits involving the dentate gyrus (DG) and proximal CA3.

57 heta-band short range communications between dentate gyrus (DG) and the Ammon's horn (CA1) within the

58 Mossy cells (MCs) of the dentate gyrus (DG) are a major group of excitatory hilar

59 on.SIGNIFICANCE STATEMENT Mossy cells in the dentate gyrus (DG) are an integral component of the DG/p

60 The dentate gyrus (DG) controls information flow into the hi

61 g advantage of the fact that the hippocampal dentate gyrus (DG) gives rise to newborn DGCs throughout

62 Moreover, we investigated the dentate gyrus (DG) granule cell reactivity and synaptic

63 The dentate gyrus (DG) has a key role in hippocampal memory

64 Within the mammalian hippocampus, the dentate gyrus (DG) has the unique characteristic of exhi

65 oung adult-born granule cells (abGCs) in the dentate gyrus (DG) have a profound impact on cognition a

66 ferent regions and layers of the hippocampus dentate gyrus (DG) in an electric stimulation rodent mod

67 The reorganization of the dentate gyrus (DG) in TLE may create pathological conduc

68 The hippocampal dentate gyrus (DG) is a unique brain region maintaining

69 emory impairments.SIGNIFICANCE STATEMENT The dentate gyrus (DG) is important for learning, memory, pa

70 on from the supramammillary nucleus (SuM) to dentate gyrus (DG) is needed for contextual memory, soci

71 Adult neurogenesis in the dentate gyrus (DG) is strongly influenced by drug-taking

72 Adult hippocampal dentate gyrus (DG) neural stem cells (NSCs) continuously

73 rylated tau in GABAergic interneurons in the dentate gyrus (DG) of AD patients and mice.

74 Neuronal hyperactivity was found in the dentate gyrus (DG) of leuprolide-treated females, but no

75 imuli.SIGNIFICANCE STATEMENT The hippocampal dentate gyrus (DG) of rodents generates newborn dentate

76 ells (DGCs) are generated in the hippocampal dentate gyrus (DG) of rodents through a process called a

77 roblasts and neuronal differentiation in the dentate gyrus (DG) of the hippocampus and significantly

78 Sparse populations of neurons in the dentate gyrus (DG) of the hippocampus are causally impli

79 he animal analog of ECT, neurogenesis in the dentate gyrus (DG) of the hippocampus is observed.

80 nd DISC1 influence adult neurogenesis in the dentate gyrus (DG) of the hippocampus, we hypothesized t

81 sis in the subventricular zone (SVZ) and the dentate gyrus (DG) of the hippocampus, whereas the impla

82 Dentate gyrus (DG) of the mammalian hippocampus gives ri

83 Theoretical work suggests that the dentate gyrus (DG) performs this role for memory process

84 DD) and suicide risk and potentially affects dentate gyrus (DG) plasticity.

85 The dentate gyrus (DG) plays a central role in the process o

86 brain varied between 6.6 +/- 0.7 muM in the dentate gyrus (DG) region of the hippocampus and 22.1 +/

87 elopment, in particular with assembly of the dentate gyrus (DG) region of the hippocampus.

88 The CA3 and dentate gyrus (DG) regions of the hippocampus are consid

89 Neural stem cells (NSCs) in the dentate gyrus (DG) reside in a specialized local niche t

90 their proliferation in the adult hippocampus dentate gyrus (DG) subgranular zone.

91 affer collateral synapses and perforant path-dentate gyrus (DG) synapses of the hippocampus.

92 attern separation processes supported by the dentate gyrus (DG) to prevent interference from overlapp

93 Synapses from the dentate gyrus (DG) to the CA3 area of the hippocampus ar

94 Acute neuronal activation of the dentate gyrus (DG) using cFos immunohistochemistry was m

95 rant path (PP) to the molecular layer of the dentate gyrus (DG) where information is filtered and con

96 Dentate gyrus (DG), a "gate" that controls information f

97 ocused on the hippocampus and especially the dentate gyrus (DG), a vulnerable brain region and one of

98 s and impaired GABAergic transmission in the dentate gyrus (DG), accompanied by schizophrenia-like be

99 (MCs), a major cell type in the hilus of the dentate gyrus (DG), are unique in providing extensive lo

100 subfields cornu ammonis 2/3 (CA2/3) and CA4/dentate gyrus (DG), as well as impaired hippocampal micr

101 ch of the three major hippocampal subfields, dentate gyrus (DG), CA3, and CA1, has a unique function

102 of neural stem cells (NSCs) in the postnatal dentate gyrus (DG), drastically increased perinatal apop

103 ltered inputs from the entorhinal cortex and dentate gyrus (DG), the proximal CA3 region of aged rats

104 nts of adult neurogenesis in the hippocampal dentate gyrus (DG), while the effects of antidepressants

105 ncement, but whether, and to what extent can dentate gyrus (DG)-resident neural stem cells drive rege

106 n the function of neurons in the hippocampal dentate gyrus (DG).

107 s, and aberrant mossy fiber sprouting in the dentate gyrus (DG).

108 ks between behavior and transcription in the dentate gyrus (DG).

109 ically profile the granule cell layer of the dentate gyrus (DG-GCL) in human hippocampus and contrast

110 ar delineation in SUVr between groups in the dentate gyrus (p = 0.009).

111 in the CA1 and CA3 fields, the hilus of the dentate gyrus (with sparing of granule cells), and the e

112 immunoreactive for reelin and project to the dentate gyrus [17, 18].

113 emonstrate that dopamine D1 receptors in the dentate gyrus act as a pivotal mediator of antidepressan

114 y neurons in the dentate hilus that regulate dentate gyrus activity and function.

115 d transcriptomic-wide changes in the ventral dentate gyrus after SDS.

116 heories of hippocampal function suggest that dentate gyrus and CA(2,3) (DG/CA(2,3)) are biased to dif

117 Here we find this distributed code in the dentate gyrus and CA1 subregions of the hippocampus.

118 nments may not be recognized as different by dentate gyrus and CA1 without LC input.

119 We changed the conductances of simulated dentate gyrus and CA3 hippocampal neurons according to o

120 ions in the synaptic connections between the dentate gyrus and CA3, which are thought to be critical

121 se in neuronal cytoplasmic inclusions in the dentate gyrus and cornu ammonis regions 1 and 2 of patie

122 4 (TLR4) on excitability of the hippocampal dentate gyrus and epileptogenesis after brain injury.

123 Adult neurogenesis persists in the rodent dentate gyrus and is stimulated by chronic treatment wit

124 eurogenesis in the granule cell layer of the dentate gyrus and rescues hippocampal memory defects in

125 GABAergic LRNs preferentially innervate the dentate gyrus and the CA3 area of the hippocampus, regio

126 ongly related to microglia activation in the dentate gyrus and the prefrontal cortex.

127 In the banded mongoose the dentate gyrus appears to be comprised of up to seven lam

128 h TLE display loss of PV interneurons in the dentate gyrus but questions persist.

129 contextual fear memory engrams in the mouse dentate gyrus contain functionally distinct neuronal ens

130 Neuroblasts within the aged dentate gyrus display a senescence-associated secretory

131 Within the dentate gyrus evidence for adult hippocampal neurogenesi

132 del of temporal lobe epilepsy, the epileptic dentate gyrus excessively recruits granule cells in beha

133 The dentate gyrus expressed synaptic function and neurogenes

134 (2020) report that human tau accumulation in dentate gyrus GABAergic interneurons disrupts AHN and st

135 We further demonstrate that in dentate gyrus GCs these conductance correlations are lik

136 bors and dendritic spines in newly generated dentate gyrus granule cell neurons of the hippocampus af

137 We recorded populations of dentate gyrus granule cells (DG GCs) and lateral entorhi

138 we characterized threshold K(+) currents in dentate gyrus granule cells (DGGCs) and CA1 pyramidal ce

139 in-positive (DCX(+)) ABGCs as well as DCX(-) dentate gyrus granule cells 2 weeks after a stroke or sh

140 d a hyperexcitability phenotype displayed in dentate gyrus granule neurons derived from patients with

141 Having previously studied the phenotype of dentate gyrus granule neurons, we turned our attention t

142 logical mechanisms involving the hippocampal dentate gyrus have been proposed.

143 ignificantly associated with smaller CA3 and dentate gyrus hippocampal subfield volumes but not with

144 pus, a widely accepted model posits that the dentate gyrus improves learning and memory by enhancing

145 evidence of disrupted microstructure of the dentate gyrus in children with OSAS that may help explai

146 We demonstrate lower mean diffusivity of the dentate gyrus in children with OSAS, which correlates wi

147 nized interneuron firing between the CA1 and dentate gyrus in epileptic mice.

148 we simultaneously recorded from the CA1 and dentate gyrus in pilocarpine-treated epileptic mice with

149 al and incorporation of neurons in the adult dentate gyrus increases after chronic stress and suggest

150 gest that stimulation of D1 receptors in the dentate gyrus is a potential adjunctive approach to impr

151 hypothesized that adult neurogenesis in the dentate gyrus is an ongoing process that maintains norma

152 We tested the hypothesis that human dentate gyrus is critical for pattern separation, wherea

153 ing to test the hypothesis that aging of the dentate gyrus is linked to impaired beacon discriminatio

154 AV-Cre mediated ablation of Shh in the adult dentate gyrus led to a marked degeneration of MCs.

155 In addition, ablation of Shh in the adult dentate gyrus led to increased neural precursor cell pro

156 Decreased dentate gyrus mean diffusivity correlated with a higher

157 s of pathway-tracing experiments showing the dentate gyrus mossy fiber projection, and its relationsh

158 20) reveal that post-tetanic potentiation at dentate gyrus mossy fiber synapses is induced by natural

159 irm that deficits are specifically linked to dentate gyrus neurogenesis since cyclin D2(-/-) mice als

160 ampus, cerebellum and cortex besides reduced dentate gyrus neurogenesis.

161 ls of the innate immune system reside in the dentate gyrus neurogenic niche of aged brains in humans

162 The computationally simulated BD dentate gyrus neurons had a hyperexcitability phenotype

163 on-touchscreen task and (56)Fe decreased new dentate gyrus neurons relative to Sham.

164 n, similar to what we previously reported in dentate gyrus neurons.

165 ortin immunohistochemistry) cells within the dentate gyrus of adult Egyptian fruit bats from three di

166 Elevated MAALIN in the dentate gyrus of impulsive-aggressive suicides was assoc

167 in developing neural cultures and in vivo in dentate gyrus of P4 mouse brain.

168 e of a dramatic shift in excitability in the dentate gyrus of Pafah1b1(+/-) mice that may contribute

169 on of Ephexin5 expression using shRNA in the dentate gyrus of presymptomatic adolescent hAPP mice was

170 (Nav 1.1, Nav 1.2, Nav 1.6) in area CA1 and dentate gyrus of rat hippocampus.

171 Adult neurogenesis occurs in the dentate gyrus of the hippocampus during adulthood and co

172 umber of newborn neurons incorporated in the dentate gyrus of the hippocampus during the 10-week post

173 Adult neurogenesis in the dentate gyrus of the hippocampus is highly regulated by

174 anced deposition of perineuronal nets in the dentate gyrus of the hippocampus of AS mice in the absen

175 on and the action of antidepressants, in the dentate gyrus of the hippocampus.

176 ddressed whether mossy fiber inputs from the dentate gyrus onto CA3 principal cells are affected in a

177 albumin-expressing interneurons (PVs) in the dentate gyrus provide activity-dependent regulation of a

178 ion channel agonist, we studied the role of dentate gyrus PV cells in regulating anxiety-like behavi

179 Activation of the Kv3.1 channel in dentate gyrus PV cells may represent a target for the de

180 e behavior, whereas upregulation of Kv3.1 in dentate gyrus PV cells or acute activation of Kv3.1 usin

181 The activity of dentate gyrus PV cells plays a major role in the behavio

182 enuated capacity of high-frequency firing in dentate gyrus PV cells, and altered short-term plasticit

183 ucidate the function and mechanism of p11 in dentate gyrus PV cells.

184 Excitatory hilar mossy cells (MCs) in the dentate gyrus receive inputs from dentate granule cells

185 rtin-labeled maturing newborn neurons in the dentate gyrus subgranular zone, and a single-Reelin infu

186 al glia-like neural stem cells (RGLs) in the dentate gyrus subregion of the hippocampus give rise to

187 development of glutamatergic perforant path-dentate gyrus synapses, but not in commonly studied in S

188 d progressive microstructural changes in the dentate gyrus translate to the severity of hippocampal s

189 s observed in hippocampus region CA3 and the dentate gyrus under both conditions.

190 nockout granule neurons integrating into the dentate gyrus using a variety of methods to examine thei

191 between parental education level and CA3 and dentate gyrus volumes; lower parental education level wa

192 abelled cells in the subgranular zone of the dentate gyrus was observed.

193 ocampal subfield CA3 (but less pronounced in dentate gyrus) correlated with this form of mnemonic pat

194 piriform cortex, 0.24 ug . g(-1) +/- 0.04 in dentate gyrus, 0.17 ug . g(-1) +/- 0.04 in hippocampus)

195 rties of netfeedback inhibition in the mouse dentate gyrus, a region critically involved in pattern s

196 4 mRNA, being highest in the olfactory bulb, dentate gyrus, and cerebellum.

197 substructures: the cornu ammonis (CA1-CA4), dentate gyrus, and subiculum.

198 prominently expressed on the neurons of the dentate gyrus, but its role in mediating behavioral resp

199 00 distinct neuron type pairs throughout the dentate gyrus, CA3, CA2, CA1, subiculum, and entorhinal

200 granule cells, the projection neurons of the dentate gyrus, can exhibit both pattern separation and i

201 nt developed more neuronal inclusions in the dentate gyrus, cornu ammonis regions 1, 2 and 4, and the

202 more neuronal cytoplasmic inclusions in the dentate gyrus, cornu ammonis regions 1-4 and entorhinal

203 This region, comprised of the dentate gyrus, hippocampus proper, subiculum, presubicul

204 cognitive functions and neurogenesis (e.g., dentate gyrus, hypothalamus, olfactory areas, cerebellum

205 In the central hilus (CH) of the dentate gyrus, Nav 1.1 immunoreactivity was selectively

206 Furthermore, deletion of Bdnf in the dentate gyrus, or specifically in LepRb-expressing neuro

207 duced with decreased size of the hippocampal dentate gyrus, partial agenesis of the corpus callosum,

208 map reset and a familiar map emerged in the dentate gyrus, proximal and distal CA1, and CA3c.

209 of the hippocampal formation (cornu Ammonis, dentate gyrus, subicular complex, and entorhinal cortex)

210 binding in the hippocampus (CA1, CA2/3, CA4, dentate gyrus, subiculum) and presubiculum layers (PSB1,

211 In the dentate gyrus, the summative effect of these pathologies

212 ampus, neurogenesis was nearly absent in the dentate gyrus, which was due to inhibited proliferation

213 ce of NLGN1 decreased neuronal counts in the dentate gyrus, which was not the case in wild-type anima

214 s fibres in the medial entorhinal cortex and dentate gyrus, with no frank noradrenergic cell body los

215 tformin enhanced the recovery of NPCs in the dentate gyrus, with sex-dependent effects on neurogenesi

216 The dentate gyrus-CA3 circuit of the hippocampus is continuo

217 etical models and the known functions of the dentate gyrus-CA3 circuit, acute or chronic manipulation

218 dorsolateral septum (DLS) as a relay of the dentate gyrus-CA3 circuit.

219 ls and differentiated these into hippocampal dentate gyrus-like neurons and astrocytes.

220 ower motor neurons, iPSC-derived hippocampal dentate gyrus-like neurons and primary astrocytes.

221 (56)Fe irradiation improved performance on a dentate gyrus-reliant pattern separation task; irradiate

222 the cells and the majority of spines in the dentate gyrus.

223 emarkably enriched in granule neurons of the dentate gyrus.

224 ber of granule cells and PV interneurons per dentate gyrus.

225 neurogenesis and synaptic plasticity in the dentate gyrus.

226 ion, up to seven laminae were evident in the dentate gyrus.

227 oimmune, and epigenetic changes in the adult dentate gyrus.

228 tions of fear and extinction memories in the dentate gyrus.

229 forant pathway in the molecular layer of the dentate gyrus.

230 y was observed in dendritic zones of CA1 and dentate gyrus.

231 ominent and dynamic source of Shh within the dentate gyrus.

232 sed microvascular blood-flow velocity in the dentate gyrus.

233 the proportion of adult-born neurons in the dentate gyrus.

234 ulates adult neurogenesis in the hippocampal dentate gyrus.

235 neurogenesis and synaptic plasticity in the dentate gyrus.

236 n susceptible mice could not be found in the dentate gyrus.

237 cerebellar cortex, insect mushroom body, and dentate gyrus.

238 or expression in mature granule cells in the dentate gyrus.

239 rogenesis and dendritic spine density in the dentate gyrus.

240 lt lateral ventricle subventricular zone and dentate gyrus.

241 ocampal CA3 area bypassing CA1, CA2, and the dentate gyrus.

242 affected by PD except for a decrease in the dentate gyrus.

243 cal layers II-III, IV, and V, as well as the dentate gyrus.

244 ng the function of neurogenesis in the adult dentate gyrus.

245 resentations for overlapping memories in the dentate gyrus/CA(2,3) and subiculum subfields of the hip

246 projecting pyramidal cells, but not putative dentate gyrus/CA3-projecting stellate cells, represented

247 Mossy cells are excitatory neurons in the dentate hilus that regulate dentate gyrus activity and f

248 Dentate individuals underwent a full-mouth periodontal e

249 e rigidity, one of the tpy units of the tris-dentate ligand was preblocked by stable <tpy-Ru(2+)-tpy>

250 cular intestinal tumour originating from the dentate line.

251 events, and these mice fail to perform on a dentate-mediated spatial discrimination task.

252 mma2, and delta were highly expressed in the dentate molecular layer, whereas alpha1, alpha2, alpha3,

253 of termination in the inner one-third of the dentate molecular layer.

254 The impact of dentate mossy cells on hippocampal activity remained unc

255 g in vivo shortly after brain injury reduced dentate network excitability and seizure susceptibility.

256 opx(+) embryonic, early postnatal, and adult dentate neural progenitors further reveal common molecul

257 we show that Hopx(+) precursors in the mouse dentate neuroepithelium at embryonic day 11.5 give rise

258 We hypothesized that the main function of dentate neurogenesis is long-term memory formation becau

259 Adult dentate neurogenesis may therefore represent a lifelong

260 by magnetic resonance (MR) imaging, reduced dentate neurogenesis moderately correlated with deficits

261 enitor population exclusively contributes to dentate neurogenesis throughout development and adulthoo

262 (-/-)) mouse model of endogenously deficient dentate neurogenesis to test this hypothesis.

263 avioral endpoints thought to be dependent on dentate neurogenesis, including memory acquisition, shor

264 d that Bax deletion in developing and mature dentate neurons increased EPSCs and prevented neurogenes

265 magnetic resonance (MR) imaging, cerebellar dentate nuclei (DNs) functional connectivity abnormaliti

266 eglumine on the signal intensity (SI) of the dentate nucleus (DN) of the pediatric brain on nonenhanc

267 (GBCAs) on the signal intensity (SI) of the dentate nucleus (DN) on unenhanced T1-weighted magnetic

268 d T1 signal intensities were measured in the dentate nucleus (DN), globus pallidus (GP), crus anterio

269 age, 49 years; age range, 25-73 years), the dentate nucleus (DN)-to-middle cerebral peduncle (MCP) S

270 timulating electrodes targeted to the dorsal dentate nucleus and tested a spectrum of frequencies ran

271 easured in regions of interest placed in the dentate nucleus and the pons, and we calculated the dent

272 Silencing activity in dentate nucleus by photoactivating inhibitory Purkinje c

273 decay times of the GABAergic currents to the dentate nucleus can facilitate sustained oscillatory act

274 pallidus, putamen, substantia nigra and the dentate nucleus compared to PD and controls.

275 oning task, cerebellar output neurons in the dentate nucleus exhibit preparatory activity similar to

276 uditory hallucinations were connected to the dentate nucleus in the cerebellum.

277 to determine whether signal intensity in the dentate nucleus is increased in unenhanced T1-weighted i

278 hyperintensity of the globus pallidus and/or dentate nucleus on unenhanced T1-weighted magnetic reson

279 ation of alpha(2/3)-receptor subunits in the dentate nucleus, and correspondingly, we studied the evo

280 , ventral intermediate thalamic nucleus, and dentate nucleus, and observed abnormal functional connec

281 T1 mapping showed no changes for dentate nucleus, pons, and thalamus.

282 rior cerebellar peduncle and the ipsilateral dentate nucleus, which correspond to the ipsilateral por

283 The difference in the dentate nucleus-pons signal intensity ratio between the

284 umine administrations and an increase in the dentate nucleus-to-middle cerebral peduncle signal inten

285 sity ratios (globus pallidus-to-thalamus and dentate nucleus-to-pons ratios), and T1 and T2 relaxatio

286 nucleus and the pons, and we calculated the dentate nucleus-to-pons signal intensity ratios and the

287 -based therapy for DCAs targeting the dorsal dentate nucleus.

288 rojections from the cerebellar cortex to the dentate nucleus.

289 iated with increased signal intensity in the dentate nucleus.

290 Data from 10,713 dentate participants aged >=30 years in NHANES 2009-2014

291 Participants were aged 30 to 65 years, dentate, periodontally healthy, and did not have diabete

292 Hopx(+) neural progenitors in the primitive dentate region, and they, in turn, generate granule neur

293 As the dentate's principal signalling population, the granule c

294 s dorsal spinose sclerites and dorso-lateral dentate sclerites.

295 y induced by CA3 activity, we refer to it as dentate sharp wave (DSW).

296 is, only bleeding on probing at the adjacent dentate sites was identified to be increased.

297 ypes of LFP events in the DG: high-amplitude dentate spikes (DSs), and a novel event type whose curre

298 pression and that proliferative cells in the dentate subgranular zone express cyclin A2.

299 etae) and two sets of sclerites (spinose and dentate) suggest that in a pre-annelid an earlier and mo

300 g us to cluster sharp waves (SWs) in the DG [dentate SWs (DSWs)] during sleep.