ライフサイエンスコーパス: dentate

1 gonist on limbic seizures induced by maximal dentate activation (MDA) acute kindling.

2 compared with a single environment, promoted dentate activation and enhanced the addition of new hipp

3 We used data from 1,702 dentate adults who participated in at least 2 of 3 surve

4 riodontal conditions were assessed for 1,911 dentate adults with a full-mouth periodontal examination

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

6 were assessed in the substantia nigra (SNc), dentate and caudate nucleus, red nucleus, putamen and gl

7 hite adult individuals, dentate or partially dentate and seeking dental therapy at a university clini

8 es to ongoing synaptic refinement within the dentate circuit.

9 C-GC recurrent circuit and may contribute to dentate-dependent forms of learning and epilepsy.

10 ks to assess experience-dependent changes in dentate field potentials in the presence and absence of

11 neurons, but the influence of mossy cells on dentate function is often overlooked.

12 the integration and functions of adult-born dentate granule cell (DGCs) are poorly understood.

13 Furthermore, new dentate granule cell number, morphology and excitatory s

14 tand how monosynaptic inputs onto adult-born dentate granule cells (DGCs) are altered in experimental

15 h CA3 interneurons peak when adult-generated dentate granule cells (DGCs) are approximately 4 weeks o

16 New dentate granule cells (DGCs) are continuously generated,

17 Dentate granule cells (DGCs) have a single, complex, api

18 the developing dendrites of adult-born mouse dentate granule cells (DGCs) in vivo and found that they

19 systems-based mechanisms by which adult-born dentate granule cells (DGCs) modulate pattern separation

20 Local application of FGF22 on the axons of dentate granule cells (DGCs), which are presynaptic to C

21 The continuous addition of new dentate granule cells (DGCs), which is regulated exquisi

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

23 for a novel, highly detailed active model of dentate granule cells (GCs) replicating a wide palette o

24 ect link between the primary cilia of mature dentate granule cells and behavior will require further

25 ins IFT20 and Kif3A (respectively) in mature dentate granule cells and investigated hippocampus-depen

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

27 ong-standing hypothesis that newly generated dentate granule cells are pro-epileptogenic and contribu

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

29 The mossy fiber (MF) axons of the dentate granule cells convey strong excitatory drive to

30 Silenced dentate granule cells develop with input-specific decrea

31 port chain of mitochondria, from hippocampal dentate granule cells in mice does not affect low-freque

32 primary cultures of rat hippocampal neurons, dentate granule cells in mouse organotypic slices, and l

33 res of rat hippocampal and cortical neurons, dentate granule cells in mouse organotypic slices, and l

34 ll proliferation and neuronal development of dentate granule cells in the hippocampus.

35 mRNA: cerebellar granule cell precursors and dentate granule cells in the hippocampus.

36 -lasting GABAergic inhibition of hippocampal dentate granule cells in vivo and in vitro.

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

38 mpal neurons in vitro and in vivo Adult-born dentate granule cells lacking Trim9 similarly exhibited

39 required for structural synapse formation in dentate granule cells or for Shh-dependent neuronal prec

40 However, its role in the function of mature dentate granule cells remains unknown.

41 Genetic ablation of AKAP7 specifically from dentate granule cells results in disruption of MF-CA3 LT

42 SnRNA-seq of mouse dentate granule cells reveals large-scale changes in the

43 e glutamatergic cell types, including mature dentate granule cells, area CA1-3 pyramidal cells and mo

44 imary cilia in the memory function of mature dentate granule cells, which may result from abnormal mo

45 ce despite normal dendritic spine density on dentate granule cells.

46 were unchanged following COX10 removal from dentate granule cells.

47 timulation-induced activation of hippocampal dentate granule cells.

48 outons, but rather to all synapses formed by dentate granule cells.

49 ptic release of both glutamate and GABA onto dentate granule cells.

50 assess synaptic function in Ptchd1-deficient dentate granule cells.

51 The synaptic changes in CA1 and dentate granule neurons are not observed when synaptic t

52 Reduced excitability of dentate granule neurons in response to strong depolarizi

53 atin accessibility landscapes of adult mouse dentate granule neurons in vivo before and after synchro

54 in vivo Embryonic hippocampal and adult-born dentate granule neurons lacking Trim9 exhibit several mo

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

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

57 s selectively increased in CA1 pyramidal and dentate granule neurons, as well as in microglia in mice

58 ogical approaches that Oxtrs in the anterior dentate gyrus (aDG) and anterior CA2/CA3 (aCA2/CA3) of m

59 ies have provided indirect evidence that the dentate gyrus (DG) and CA3 hippocampal subregions suppor

60 at mossy fiber (mf) connections between the dentate gyrus (DG) and CA3 neurons in vivo are still elu

61 tatin-expressing-interneurons (SOMIs) in the dentate gyrus (DG) control formation of granule cell (GC

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

63 rly gene (IEG) induction in stress-activated dentate gyrus (DG) granule neurons play a crucial role i

64 the cornu ammonis (CA) subfields CA1-4, the dentate gyrus (DG) including a granule cell layer (GCL)

65 CK) inhibitory interneurons of the mammalian dentate gyrus (DG) initiate the therapeutic response to

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

67 The hippocampal dentate gyrus (DG) is thought to be responsible for proc

68 Dentate gyrus (DG) is widely thought to provide a teachi

69 We recently reported that hippocampal dentate gyrus (DG) neurons differentiated from induced p

70 Infusions of adiponectin into the dentate gyrus (DG) of the hippocampus in fear-conditione

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

72 Cs resulted in fewer adult-born cells in the dentate gyrus (DG) overall, reducing populations across

73 spite abundant evidence that the hippocampal dentate gyrus (DG) plays a critical role in memory, it r

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

75 d S1 cortex, decreased NLGN2 mRNA in CA1 and dentate gyrus (DG) regions of the hippocampus, and incre

76 re indicative of a disrupted function of the dentate gyrus (DG) subregion of the brain, and they impr

77 The dentate gyrus (DG) subregion of the hippocampus is widel

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

79 The dentate gyrus (DG), a part of the hippocampal formation,

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

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

82 or, olfaction, and adult neurogenesis in the dentate gyrus (DG), olfactory bulb (OB), and the olfacto

83 neural progenitors in the adult hippocampal dentate gyrus (DG), one of the select regions of the mat

84 dult brain, like the subgranular zone of the dentate gyrus (DG), there is continuous production of ne

85 coding mechanism, pattern separation, in the dentate gyrus (DG)-CA3 circuit in resolving interference

86 hippocampal plasticity, particularly in the dentate gyrus (DG).

87 ee of calbindin reduction in the hippocampal dentate gyrus (DG).

88 ions strongly activated granule cells in the dentate gyrus (DG).

89 cal parvalbumin (PV) interneurons within the dentate gyrus (DG).

90 gressive neuron loss and astrogliosis in the dentate gyrus (DG).

91 thickness, and (ii) activity in ERC and the dentate gyrus (DG)/CA3 region.

92 with decreased mean diffusivity of the left dentate gyrus (p = 0.002; false discovery rate corrected

93 es 11 to 18 years forecasted diminished left dentate gyrus (simple slope, -14.20; standard error, 5.2

94 in hippocampal staining: CB(+) decreased in dentate gyrus (TBI = 2 +/- 0.382, Sham = 4 +/- 0.383, P

95 ify a role for the astroglial xCT in ventral dentate gyrus (vDG) in stress and antidepressant respons

96 In the dentate gyrus - a key component of spatial memory circui

97 d THY-Tau22 mice developed an atrophy of the dentate gyrus and a tau pathology characterized by Gally

98 ongly decreased stimulation-induced EPSPs in dentate gyrus and CA1 (up to 30 and 55%, respectively) v

99 late regions and showed trends toward larger dentate gyrus and CA1 regions of the hippocampus.

100 ion computations ascribed to the hippocampal dentate gyrus and CA3 fields.

101 ociation of years lived in poverty with left dentate gyrus and CA3 hippocampal subfields and left amy

102 f GAD67-cells in caudate-kindled rats in the dentate gyrus and CA3 hippocampal subfields.

103 We performed RNA sequencing analyses of the dentate gyrus and entorhinal cortex from each line and f

104 It is suggested that the dentate gyrus and hilar region in the hippocampus perfor

105 ChAT-ir fibers were seen throughout the dentate gyrus and hippocampus, in the mediodorsal, later

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

107 AMPAR-mediated synaptic transmission in the dentate gyrus and long-term potentiation in the CA1 regi

108 ffects of fluoxetine on proliferation in the dentate gyrus and on depressive behavior.

109 a thus support a sparse coding scheme in the dentate gyrus and provide a possible link between struct

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

111 gions of the vertebrate brain, including the dentate gyrus and rostral migratory stream in mammals, a

112 cantly reduced in the cortex, but not in the dentate gyrus and the amygdala.

113 Finally, we showed that adult dentate gyrus appears similar to immature CA1, demonstra

114 d incorporation of adult-born neurons in the dentate gyrus are critical for spatial learning and memo

115 Discharges of neurons in CA1 and dentate gyrus are modulated by both HRR and theta.

116 RK2 alone does not impair development of the dentate gyrus as animals expressing only ERK1 developed

117 ions in local inhibitory function within the dentate gyrus at time points where sparse activation was

118 born neurons are continually produced in the dentate gyrus but it is unclear whether synaptic integra

119 ride regulation was sufficient to elicit the dentate gyrus circuit collapse evident during epilepsy d

120 thin the local circuit generates the massive dentate gyrus circuit hyperactivation evident in animals

121 Mossy cells in the hilus of the dentate gyrus constitute a major excitatory principal ce

122 sy to test which pathological changes in the dentate gyrus correlate with seizure frequency and help

123 We identified distinct layers in the dentate gyrus corresponding to the granule cell layer an

124 nhibition of adult neurogenesis in the mouse dentate gyrus decreases hippocampal network activation a

125 We also demonstrate that an ablation of dentate gyrus engram cells containing restored spine den

126 m potentiation at perforant path synapses of dentate gyrus engram cells restores both spine density a

127 ve reduction in spine density of hippocampal dentate gyrus engram cells.

128 allowed targeted fatty acid analysis of the dentate gyrus granule cell layer and the CA1 pyramidal l

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

130 aGABAA receptor-mediated tonic inhibition in dentate gyrus granule cells (DGGCs), thereby contributin

131 e identified more than 40 lipid species from dentate gyrus granule cells and CA1 pyramidal neurons of

132 at allows for chronic, functional imaging of dentate gyrus granule cells in awake, behaving mice in a

133 ional' nature implies that burst activity in dentate gyrus granule cells is required for detonation.

134 g the activity of its principal neurons, the dentate gyrus granule cells, are missing.

135 citability by modulating tonic inhibition in dentate gyrus granule cells, in a process involving cros

136 berrant generation of excitatory synapses in dentate gyrus granule cells.

137 y encoded calcium indicators specifically to dentate gyrus granule cells.

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

139 all subfields, whereas TLE-G presented with dentate gyrus hypertrophy, focal increases in T2 intensi

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

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

142 s, we demonstrate distinct roles for CA3 and dentate gyrus in human memory and uncover the variegated

143 ced aberrant neurogenesis in the hippocampal dentate gyrus in the context of the blood-brain barrier

144 rphosphorylation of tau was increased in the dentate gyrus in THY-Tau22 mice, the development of neur

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

146 The hippocampal dentate gyrus is critically involved in learning and mem

147 Dentate gyrus is intimately connected to CA3 where, in a

148 The hippocampal dentate gyrus is often viewed as a segregator of upstrea

149 attenuated BDNF release and signaling in the dentate gyrus may account for cognitive and mental defic

150 verbal learning score correlated with lower dentate gyrus mean diffusivity (r = 0.54, p = 0.004).

151 hildren, as well as potential utility of the dentate gyrus mean diffusivity as an early marker of bra

152 Decreased dentate gyrus mean diffusivity correlated with a higher

153 Path analysis demonstrated that dentate gyrus mean diffusivity mediates the impact of OS

154 stic accuracy of a regression model based on dentate gyrus mean diffusivity reached 85.8% (cross vali

155 , we report that deletion of Drosha in adult dentate gyrus NSCs activates oligodendrogenesis and redu

156 5) mRNA levels were absent or reduced in the dentate gyrus of BDNF(Met/Met) mice.

157 rneuron-selective calretinin-ir cells in the dentate gyrus of hippocampal-kindled rats, which suggest

158 newly-incorporated DNA were observed in the dentate gyrus of hippocampus at the single cell level.

159 lial density and branching complexity in the dentate gyrus of hippocampus.

160 progenitor cells isolated directly from the dentate gyrus of MBD1 mutant (KO) and WT mice showed tha

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

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

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

164 pressed in neural stem cells residing in the dentate gyrus of the adult hippocampus (aNSCs) and MBD1

165 evelopmental stages are recapitulated in the dentate gyrus of the adult hippocampus, where neurons ar

166 ly, physical EE promoted neurogenesis in the dentate gyrus of the hippocampal formation, but not in t

167 Granule cells in the dentate gyrus of the hippocampus are thought to be essen

168 lished that new neurons are generated in the dentate gyrus of the hippocampus of almost all adult mam

169 ure neurons, and fewer mature neurons in the dentate gyrus of the hippocampus of the mouse brain.

170 STRACT: Exercise signals neurogenesis in the dentate gyrus of the hippocampus.

171 The dentate gyrus of the mammalian hippocampus continuously

172 eight paired helical filaments (PHFs) in the dentate gyrus of wild-type and mutant tau THY-Tau22 mice

173 t inhibitory synapses in hippocampus CA1 and dentate gyrus of young presymptomatic APPPS1 mice (1 to

174 t inhibition of the principal neurons of the dentate gyrus or CA3 via alpha2-containing GABAA recepto

175 infusion did not affect spine density in the dentate gyrus or ventromedial hypothalamus, suggesting s

176 Persistent neurogenesis in the dentate gyrus produces immature neurons with high intrin

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

178 al VitB12, mainly in the cornu ammonis 4 and dentate gyrus region (P= 0.029), which partially mediate

179 The dentate gyrus shows a novel phenotype: the infrapyramida

180 udy we investigate the relationships between dentate gyrus structure, hippocampus-dependent cognition

181 ynapses were frequently found in the CA3 and dentate gyrus sub-regions, corresponding to large thorny

182 ity in CA1 of pre-adolescent rodents, and in dentate gyrus throughout maturity.

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

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

185 hods to show that EE alters microglia in the dentate gyrus under physiological conditions and robustl

186 Critically, human dentate gyrus volume decreases with age whereas CA3 volu

187 pattern separation task, we demonstrate that dentate gyrus volume predicts accuracy and response time

188 Further, decreased dentate gyrus volume, and no other subfield volume, medi

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

190 of juxtacellularly recorded cells in CA1 and dentate gyrus were modulated by HRR and theta oscillatio

191 subfield (subiculum, cornu ammonis 1-3, and dentate gyrus) targets of immunomodulation-treated LGI1

192 We hypothesized that OSAS would affect the dentate gyrus, a hippocampal subdivision essential to ne

193 tic GABAA receptors in the mouse hippocampus dentate gyrus, a key region associated with epilepsy and

194 RNA sequencing of the ventral dentate gyrus, a mood-regulatory region, identified meta

195 The hippocampal dentate gyrus, a region with ongoing adult neurogenesis,

196 f inhibitory interneurons in the hippocampal dentate gyrus, an important area for seizure propagation

197 Young adults' whole hippocampal, dentate gyrus, and CA3 hippocampal subfields as well as

198 namely, granule cells and mossy cells of the dentate gyrus, and pyramidal cells of areas CA3, CA2, an

199 a critical role of the Ptchd1 protein in the dentate gyrus, but indicate that it is not required for

200 n- and somatostatin-positive interneurons in dentate gyrus, but no change in density of calretinin in

201 clude the basolateral amygdaloid nucleus and dentate gyrus, but the septohippocampal nucleus, lateral

202 s, alpha1 and alpha3 were accentuated in the dentate gyrus, CA1 region, and subiculum, whereas alpha5

203 HRR is most prominent in the dentate gyrus, especially when respiration is slower tha

204 ot suppress ECS-induced proliferation in the dentate gyrus, it blocks dendritic outgrowth of immature

205 e synapse remodeling and neurogenesis in the dentate gyrus, mechanistic studies have revealed both ge

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

207 ain injury can integrate abnormally into the dentate gyrus, potentially mediating temporal lobe epile

208 us.SIGNIFICANCE STATEMENT In the hippocampal dentate gyrus, seizures drive retrograde sprouting of gr

209 ows evidence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure.

210 A second excitatory cell type in the dentate gyrus, the mossy cell, forms an intricate circui

211 n the activation of neural stem cells in the dentate gyrus, their division, and differentiation of th

212 vious observations in the monkey hippocampal dentate gyrus, where MSBs comprised approximately 40% of

213 equency rhythm with largest amplitude in the dentate gyrus, which coupled to respiration-entrained os

214 s of neural stem cell differentiation in the dentate gyrus, with higher expression intensity in neuro

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

216 er and robust morphological sprouting in the dentate gyrus.

217 rging that human pattern separation requires dentate gyrus.

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

219 uption of synaptic transmission in the mouse dentate gyrus.

220 4 weeks led to volume reduction only in the dentate gyrus.

221 nergic terminals (fiber varicosities) in the dentate gyrus.

222 proliferation and neurogenesis in the adult dentate gyrus.

223 isplaced in the outer GCL of the hippocampal dentate gyrus.

224 tural and functional plasticity of the adult dentate gyrus.

225 rtin(+) cells in the subgranular zone of the dentate gyrus.

226 eased adult neurogenesis was observed in the dentate gyrus.

227 ysis of Nestin-GFP-positive RGL cells of the dentate gyrus.

228 of GABAergic interneurons in the hippocampal dentate gyrus.

229 hout the axon/dendrite layers of CA1 and the dentate gyrus.

230 ed slow rhythm with highest amplitude at the dentate gyrus.

231 , both lack a clear homolog of the mammalian dentate gyrus.

232 anisms, and network computation in the adult dentate gyrus.

233 c transmission and network inhibition in the dentate gyrus.

234 rted stress levels and reduced volume in the dentate gyrus.

235 d the glutamatergic rMF sprouting within the dentate gyrus.

236 ied within and between subregions of CA1 and dentate gyrus.

237 e of increasing neuronal excitability of the dentate gyrus.

238 he COX10 gene, in granule cells of the adult dentate gyrus.

239 s in the subventricular zone and hippocampal dentate gyrus.

240 pocampal size and decreased thickness of the dentate gyrus.

241 lt lateral ventricle subventricular zone and dentate gyrus.

242 agation pathway of ictal discharges from the dentate gyrus/hilus (DGH) to the medial entorhinal corte

243 e molecular layer, but it was reduced in the dentate hilus.

244 CA1 strata alveus/oriens/pyramidale and the dentate hilus.

245 yer and a parallel fiber retraction from the dentate hilus.

246 Therefore, control of dentate hyperactivity by cholinergic sprouting may be in

247 ntial role of both cholinergic sprouting and dentate hyperactivity in AD symptomatogenesis should be

248 Our results also suggest that dentate hyperactivity in MCI patients may be directly re

249 Dentate hyperactivity was abolished by optogenetic stimu

250 ing a terpyridine (tpy)-based, flexible tris-dentate ligand and characterized by single crystal X-ray

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

252 ation-inhibition coupled neural synchrony in dentate local field potentials was reduced in X-irradiat

253 epilepsy, involving fiber sprouting into the dentate molecular layer and a parallel fiber retraction

254 owth of immature granule cell neurons in the dentate molecular layer induced by ECS.

255 itory synapses in the inner one-third of the dentate molecular layer was Glu-CB1 -RS, 53.19% (glutama

256 rol rats in the inner and outer zones of the dentate molecular layer, but it was reduced in the denta

257 17) distinguish in vivo firing properties of dentate mossy cells from granule cells during behavior.

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

259 esion generates abnormal hyperactivity in EC/dentate networks.

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

261 significant number of Trim9(-/-) adult-born dentate neurons localized inappropriately.

262 nmt3a, is critical for the responsiveness of dentate neurons to environmental stimuli in terms of gen

263 s excitatory synaptic transmission to mature dentate neurons.

264 KEY POINTS: A cerebellar dentate nuclei (DN) contribution to volitional oculomoto

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

266 nfirmed in brain tissue, most notably in the dentate nuclei and globus pallidus.

267 teral cerebellum (cerebellar hemispheres and dentate nuclei, DN) is less well understood.

268 Neuronal tissues from the dentate nuclei, pons, globus pallidus, and thalamus were

269 images relative to reference tissues in the dentate nucleus (0.53% signal intensity increase per inj

270 ighted signal intensity (SI) increase in the dentate nucleus (DN) and globus pallidus (GP) in relatio

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

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

273 est for measurable visual enhancement of the dentate nucleus (DN) on unenhanced T1-weighted magnetic

274 ) in the globus pallidus (GP), thalamus (T), dentate nucleus (DN), and pons (P) were measured on unen

275 llowing five regions of interest (ROIs): the dentate nucleus (DN), pons, substantia nigra (SN), pulvi

276 minations had increased SI ratios within the dentate nucleus (mean SI ratio +/- standard error of the

277 wed visually detectable T1 shortening in the dentate nucleus (n = 13), globus pallidus (n = 13), subs

278 .026) and T2 of the whole brain (P = .004), dentate nucleus (P = .023), and thalamus (P = .002) show

279 rain (P < .001), globus pallidus (P = .002), dentate nucleus (P = .046), and thalamus (P = .026) and

280 en, pallidum, thalamus, midbrain, and in the dentate nucleus of the cerebellum (t's > 2.7, P's < 0.02

281 putamen, subthalamic nucleus, midbrain, and dentate nucleus relative to controls and PD patients (vo

282 [CI]: 0.03, 0.67; P = .03), but not between dentate nucleus SI and patient age (r = 0.23; 95% CI: -0

283 There was a significant correlation between dentate nucleus SI and total cumulative gadolinium dose

284 Unenhanced T1 signal intensities of the dentate nucleus were measured from magnetic resonance (M

285 red nucleus, cerebellar peduncle, colliculi, dentate nucleus, and globus pallidus.

286 The SI in the globus pallidus, thalamus, dentate nucleus, and pons was measured at unenhanced T1-

287 ior cingulate, inferior temporal lobule, the dentate nucleus, and the cerebellar lobules IV/V, VI, an

288 ls in the basal ganglia, midbrain, thalamus, dentate nucleus, cerebellar peduncles, cerebellar vermis

289 levated free-water in all regions except the dentate nucleus, subthalamic nucleus, and corpus callosu

290 terest were measured in the globus pallidus, dentate nucleus, thalamus, and pons.

291 Globus pallidus-thalamus and dentate nucleus-pons SI ratios were calculated and compa

292 ostnatally in the granule cell layer and the dentate nucleus.

293 Six hundred white adult individuals, dentate or partially dentate and seeking dental therapy

294 Surprisingly, dentate PV interneurons are depolarized by GABA signalin

295 medial septum (MS) as the major afferents to dentate PV interneurons.

296 urons to contribute to sparse and orthogonal dentate representations.

297 We evaluated these alternatives by using dentate-sensitive active place avoidance tasks to assess

298 disorders, interaction between human CA3 and dentate subfields is difficult to investigate due to sma

299 High-frequency dentate to CA3 glutamatergic synaptic transmission and f

300 cells in mice does not affect low-frequency dentate to CA3 glutamatergic synaptic transmission.