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1 proliferation and neurogenesis in the adult dentate gyrus.
2 isplaced in the outer GCL of the hippocampal dentate gyrus.
3 tural and functional plasticity of the adult dentate gyrus.
4 rtin(+) cells in the subgranular zone of the dentate gyrus.
5 eased adult neurogenesis was observed in the dentate gyrus.
6 ysis of Nestin-GFP-positive RGL cells of the dentate gyrus.
7 of GABAergic interneurons in the hippocampal dentate gyrus.
8 hout the axon/dendrite layers of CA1 and the dentate gyrus.
9 ed slow rhythm with highest amplitude at the dentate gyrus.
10 , both lack a clear homolog of the mammalian dentate gyrus.
11 anisms, and network computation in the adult dentate gyrus.
12 c transmission and network inhibition in the dentate gyrus.
13 rted stress levels and reduced volume in the dentate gyrus.
14 nd the maintenance of sparse activity in the dentate gyrus.
15 ctivity patterns in principal neurons of the dentate gyrus.
16 en in granule neurons of the murine neonatal dentate gyrus.
17 A3, and at P90 the reduction extended to the dentate gyrus.
18 diated, in part, by its aromatization in the dentate gyrus.
19 enitor cells required for development of the dentate gyrus.
20 sion, and an increase in neurogenesis in the dentate gyrus.
21 eurons, especially those in the hilus of the dentate gyrus.
22 t in the lateral perforant path input to the dentate gyrus.
23 milar to the pattern separation shown by the dentate gyrus.
24 naling during development of the hippocampal dentate gyrus.
25 d the glutamatergic rMF sprouting within the dentate gyrus.
26 of neural progenitor pools in the postnatal dentate gyrus.
27 hibition and neurosteroid sensitivity in the dentate gyrus.
28 t from CA3, but no detectable input from the dentate gyrus.
29 ied within and between subregions of CA1 and dentate gyrus.
30 d long-term potentiation specifically in the dentate gyrus.
31 lt lateral ventricle subventricular zone and dentate gyrus.
32 e of increasing neuronal excitability of the dentate gyrus.
33 he COX10 gene, in granule cells of the adult dentate gyrus.
34 s in the subventricular zone and hippocampal dentate gyrus.
35 pocampal size and decreased thickness of the dentate gyrus.
36 er and robust morphological sprouting in the dentate gyrus.
37 rging that human pattern separation requires dentate gyrus.
38 ocampal CA3 area bypassing CA1, CA2, and the dentate gyrus.
39 uption of synaptic transmission in the mouse dentate gyrus.
40 4 weeks led to volume reduction only in the dentate gyrus.
41 nergic terminals (fiber varicosities) in the dentate gyrus.
43 We hypothesized that OSAS would affect the dentate gyrus, a hippocampal subdivision essential to ne
44 tic GABAA receptors in the mouse hippocampus dentate gyrus, a key region associated with epilepsy and
47 ytes and microglia were also observed in the dentate gyrus across the different stages of tau patholo
48 ogical approaches that Oxtrs in the anterior dentate gyrus (aDG) and anterior CA2/CA3 (aCA2/CA3) of m
50 f inhibitory interneurons in the hippocampal dentate gyrus, an important area for seizure propagation
51 d THY-Tau22 mice developed an atrophy of the dentate gyrus and a tau pathology characterized by Gally
52 ongly decreased stimulation-induced EPSPs in dentate gyrus and CA1 (up to 30 and 55%, respectively) v
54 ranule and pyramidal cell neurons within the dentate gyrus and CA1 subfields of the hippocampus exhib
56 ociation of years lived in poverty with left dentate gyrus and CA3 hippocampal subfields and left amy
58 we report dysfunctional connectivity between dentate gyrus and CA3 networks in the transchromosomic T
59 cated pattern separation computations in the dentate gyrus and CA3 subregions of the hippocampus as a
60 We performed RNA sequencing analyses of the dentate gyrus and entorhinal cortex from each line and f
62 f the main cortical afferent pathways to the dentate gyrus and hippocampus are established by birth.
64 nlarged brains with an elongated hippocampal dentate gyrus and increased numbers of newborn neurons.
65 Adult neurogenesis persists in the rodent dentate gyrus and is stimulated by chronic treatment wit
66 AMPAR-mediated synaptic transmission in the dentate gyrus and long-term potentiation in the CA1 regi
67 ia-like neural stem cells in the adult mouse dentate gyrus and made the surprising discovery that pro
68 with preclinical models suggesting that the dentate gyrus and mPFC are especially vulnerable to stre
70 a thus support a sparse coding scheme in the dentate gyrus and provide a possible link between struct
71 eurogenesis in the granule cell layer of the dentate gyrus and rescues hippocampal memory defects in
72 gions of the vertebrate brain, including the dentate gyrus and rostral migratory stream in mammals, a
75 namely, granule cells and mossy cells of the dentate gyrus, and pyramidal cells of areas CA3, CA2, an
77 d incorporation of adult-born neurons in the dentate gyrus are critical for spatial learning and memo
80 RK2 alone does not impair development of the dentate gyrus as animals expressing only ERK1 developed
81 ions in local inhibitory function within the dentate gyrus at time points where sparse activation was
82 her, chronic aromatase inhibition within the dentate gyrus blocked the protective effects of testoste
83 born neurons are continually produced in the dentate gyrus but it is unclear whether synaptic integra
84 a critical role of the Ptchd1 protein in the dentate gyrus, but indicate that it is not required for
85 n- and somatostatin-positive interneurons in dentate gyrus, but no change in density of calretinin in
86 clude the basolateral amygdaloid nucleus and dentate gyrus, but the septohippocampal nucleus, lateral
87 s, alpha1 and alpha3 were accentuated in the dentate gyrus, CA1 region, and subiculum, whereas alpha5
89 n types in the rodent hippocampal formation (dentate gyrus, CA3, CA2, CA1, subiculum, and entorhinal
90 lities and impaired short-term plasticity at dentate gyrus-CA3 excitatory synapses culminate in impai
91 These results highlight the vulnerability of dentate gyrus-CA3 networks to aberrant human chromosome
93 pe mice, knocking down neuronal BRCA1 in the dentate gyrus caused increased DNA double-strand breaks,
94 ours in mice by optogenetically reactivating dentate gyrus cells that were previously active during a
95 cs and patch-clamp recordings, we found that dentate gyrus cells, long believed to not project to CA2
96 ride regulation was sufficient to elicit the dentate gyrus circuit collapse evident during epilepsy d
97 thin the local circuit generates the massive dentate gyrus circuit hyperactivation evident in animals
100 sy to test which pathological changes in the dentate gyrus correlate with seizure frequency and help
102 nhibition of adult neurogenesis in the mouse dentate gyrus decreases hippocampal network activation a
103 n-immunoreactive axons were exuberant in the dentate gyrus despite loss of immunopositive hilar neuro
106 ies have provided indirect evidence that the dentate gyrus (DG) and CA3 hippocampal subregions suppor
107 at mossy fiber (mf) connections between the dentate gyrus (DG) and CA3 neurons in vivo are still elu
108 tatin-expressing-interneurons (SOMIs) in the dentate gyrus (DG) control formation of granule cell (GC
109 y culture, neurons of the CA1 region and the dentate gyrus (DG) express high Np65 levels, whereas exp
112 rly gene (IEG) induction in stress-activated dentate gyrus (DG) granule neurons play a crucial role i
114 the cornu ammonis (CA) subfields CA1-4, the dentate gyrus (DG) including a granule cell layer (GCL)
115 CK) inhibitory interneurons of the mammalian dentate gyrus (DG) initiate the therapeutic response to
116 Here we show that PV-PIIs in rat and mouse dentate gyrus (DG) integrate their intrinsic activity ov
121 acid) content in reactive astrocytes in the dentate gyrus (DG) of a mouse model for AD (5xFAD) that
124 ) a population of cells in either the dorsal dentate gyrus (DG) of the hippocampus or the basolateral
125 nd DISC1 influence adult neurogenesis in the dentate gyrus (DG) of the hippocampus, we hypothesized t
126 Cs resulted in fewer adult-born cells in the dentate gyrus (DG) overall, reducing populations across
127 spite abundant evidence that the hippocampal dentate gyrus (DG) plays a critical role in memory, it r
129 brain varied between 6.6 +/- 0.7 muM in the dentate gyrus (DG) region of the hippocampus and 22.1 +/
130 d S1 cortex, decreased NLGN2 mRNA in CA1 and dentate gyrus (DG) regions of the hippocampus, and incre
131 ll proliferation and survival in the ventral dentate gyrus (DG) subgranular zone of Ghsr-null mice th
132 re indicative of a disrupted function of the dentate gyrus (DG) subregion of the brain, and they impr
136 s in the hippocampus and particularly in the dentate gyrus (DG), a region of active neurogenesis and
137 stimulation erased LTP in CA1 but not in the dentate gyrus (DG), although adenosine eliminated potent
138 subfields cornu ammonis 2/3 (CA2/3) and CA4/dentate gyrus (DG), as well as impaired hippocampal micr
139 of neural stem cells (NSCs) in the postnatal dentate gyrus (DG), drastically increased perinatal apop
141 or, olfaction, and adult neurogenesis in the dentate gyrus (DG), olfactory bulb (OB), and the olfacto
142 neural progenitors in the adult hippocampal dentate gyrus (DG), one of the select regions of the mat
143 dult brain, like the subgranular zone of the dentate gyrus (DG), there is continuous production of ne
144 irical evidence that tonic inhibition in the dentate gyrus (DG), which maintains sparseness of neuron
145 coding mechanism, pattern separation, in the dentate gyrus (DG)-CA3 circuit in resolving interference
152 l through the canonical trisynaptic circuit (dentate gyrus [DG] to CA3 to CA1), spontaneous GNA in th
153 ibute to pattern separation functions of the dentate gyrus due to their heightened excitability, wher
154 ress depression-like behaviours and point to dentate gyrus engram cells as potential therapeutic node
155 We also demonstrate that an ablation of dentate gyrus engram cells containing restored spine den
156 m potentiation at perforant path synapses of dentate gyrus engram cells restores both spine density a
159 allowed targeted fatty acid analysis of the dentate gyrus granule cell layer and the CA1 pyramidal l
160 bors and dendritic spines in newly generated dentate gyrus granule cell neurons of the hippocampus af
161 to SSRIs, but it is not known whether mature dentate gyrus granule cells (DG GCs) also contribute.
162 aGABAA receptor-mediated tonic inhibition in dentate gyrus granule cells (DGGCs), thereby contributin
163 e identified more than 40 lipid species from dentate gyrus granule cells and CA1 pyramidal neurons of
164 at allows for chronic, functional imaging of dentate gyrus granule cells in awake, behaving mice in a
165 ional' nature implies that burst activity in dentate gyrus granule cells is required for detonation.
166 e normal brain, the sparse activation of the dentate gyrus granule cells maintained by tonic inhibito
169 citability by modulating tonic inhibition in dentate gyrus granule cells, in a process involving cros
170 reduced the current amplitudes recorded from dentate gyrus granule cells, most likely by targeting pe
172 trophysiological recordings from hippocampal dentate gyrus granule cells, we show that synaptically r
175 growth, particularly hippocampus, where P21 dentate gyrus granule neurons were decreased 16%, sugges
176 circuit entorhinal cortex layer II (ECII)-->dentate gyrus-->CA3-->CA1 and the monosynaptic circuit E
178 orm connections with inhibitory cells in the dentate gyrus, hilus, and CA3 regions as they integrate
179 agation pathway of ictal discharges from the dentate gyrus/hilus (DGH) to the medial entorhinal corte
180 ppeared in several AD-related brain regions (dentate gyrus, hippocampal area CA1, piriform and pariet
181 hippocampal subfields including CA1, CA4 and dentate gyrus (HS ILAE Type 1), or predominant cell loss
182 in CA4 and partially affecting also CA3 and dentate gyrus (HS ILAE Type 3, n = 5) showed significant
183 all subfields, whereas TLE-G presented with dentate gyrus hypertrophy, focal increases in T2 intensi
185 ptic delta-containing GABAA receptors in the dentate gyrus in a mouse perimenstrual-like model of NSW
186 evidence of disrupted microstructure of the dentate gyrus in children with OSAS that may help explai
187 We demonstrate lower mean diffusivity of the dentate gyrus in children with OSAS, which correlates wi
188 s, we demonstrate distinct roles for CA3 and dentate gyrus in human memory and uncover the variegated
189 We recently demonstrated a role for the dentate gyrus in mediating testosterone's protective eff
190 ced aberrant neurogenesis in the hippocampal dentate gyrus in the context of the blood-brain barrier
192 rphosphorylation of tau was increased in the dentate gyrus in THY-Tau22 mice, the development of neur
193 aloid nucleus, hippocampal CA3 subfield, and dentate gyrus; in contrast, the level is greater in Cape
195 risoma-inhibiting interneurons (PIIs) of the dentate gyrus integrate rapidly correlated synaptic inpu
202 ot suppress ECS-induced proliferation in the dentate gyrus, it blocks dendritic outgrowth of immature
203 7.2 x 10(-6); right, p = 2.3 x 10(-6)), CA4/dentate gyrus (left, p = 1.4 x 10(-5); right, p = 2.3 x
204 gated the cellular phenotypes of hippocampal dentate gyrus-like neurons derived from iPSCs of patient
205 attenuated BDNF release and signaling in the dentate gyrus may account for cognitive and mental defic
206 information processing of cortical inputs in dentate gyrus, may participate in hippocampal-related co
207 verbal learning score correlated with lower dentate gyrus mean diffusivity (r = 0.54, p = 0.004).
208 hildren, as well as potential utility of the dentate gyrus mean diffusivity as an early marker of bra
211 stic accuracy of a regression model based on dentate gyrus mean diffusivity reached 85.8% (cross vali
212 e synapse remodeling and neurogenesis in the dentate gyrus, mechanistic studies have revealed both ge
213 llaterals (SC)-CA1 and medial perforant path-dentate gyrus (mPP-DG) synapses in juvenile and adult ra
214 Adult-generated granule cells (GCs) in the dentate gyrus must establish synapses with preexisting n
216 esis and glia in the subventricular zone and dentate gyrus neurogenic niches were evaluated using sin
218 Hsp60 was also increased in the hippocampal dentate gyrus neurons somata and neuropil and hippocampu
219 , we report that deletion of Drosha in adult dentate gyrus NSCs activates oligodendrogenesis and redu
223 rneuron-selective calretinin-ir cells in the dentate gyrus of hippocampal-kindled rats, which suggest
224 newly-incorporated DNA were observed in the dentate gyrus of hippocampus at the single cell level.
227 progenitor cells isolated directly from the dentate gyrus of MBD1 mutant (KO) and WT mice showed tha
229 e of a dramatic shift in excitability in the dentate gyrus of Pafah1b1(+/-) mice that may contribute
230 tion in the generation of new neurons in the dentate gyrus of patients with AD and severe neurofibril
231 d neurons significantly declined only in the dentate gyrus of patients with severe tau pathology.
232 on of Ephexin5 expression using shRNA in the dentate gyrus of presymptomatic adolescent hAPP mice was
234 pressed in neural stem cells residing in the dentate gyrus of the adult hippocampus (aNSCs) and MBD1
235 evelopmental stages are recapitulated in the dentate gyrus of the adult hippocampus, where neurons ar
237 ly, physical EE promoted neurogenesis in the dentate gyrus of the hippocampal formation, but not in t
238 tion into existing neuronal circuitry in the dentate gyrus of the hippocampus and subventricular zone
240 lished that new neurons are generated in the dentate gyrus of the hippocampus of almost all adult mam
241 ure neurons, and fewer mature neurons in the dentate gyrus of the hippocampus of the mouse brain.
242 retained significantly more new cells in the dentate gyrus of the hippocampus than those trained on t
243 ntrast, knocking down FGF9 expression in the dentate gyrus of the hippocampus using a lentiviral vect
244 hly expressed in the granular neurons in the dentate gyrus of the hippocampus, but it is undetectable
247 e status of beta adrenergic signaling in the dentate gyrus of the Ts65Dn mouse model of Down syndrome
248 eight paired helical filaments (PHFs) in the dentate gyrus of wild-type and mutant tau THY-Tau22 mice
249 t inhibitory synapses in hippocampus CA1 and dentate gyrus of young presymptomatic APPPS1 mice (1 to
250 t inhibition of the principal neurons of the dentate gyrus or CA3 via alpha2-containing GABAA recepto
251 infusion did not affect spine density in the dentate gyrus or ventromedial hypothalamus, suggesting s
252 with decreased mean diffusivity of the left dentate gyrus (p = 0.002; false discovery rate corrected
253 in the left hippocampus (cornu ammonis 1-3, dentate gyrus), parahippocampus (presubiculum, parasubic
254 of adrenals in the CA1 pyramidal cell layer, dentate gyrus polymorphic layer, bed nucleus of the stri
255 ain injury can integrate abnormally into the dentate gyrus, potentially mediating temporal lobe epile
256 We also developed a partial "whole-mount" dentate gyrus preparation and observed a dense plexus of
258 ate from the dentate ventricular zone to the dentate gyrus proper, resulting in premature depletion o
259 Excitatory hilar mossy cells (MCs) in the dentate gyrus receive inputs from dentate granule cells
260 umin, somatostatin and neuropeptide Y in the dentate gyrus, reduced aberrant neurogenesis with preser
261 al VitB12, mainly in the cornu ammonis 4 and dentate gyrus region (P= 0.029), which partially mediate
262 ed activity in the cornu ammonis 1 (CA1) and dentate gyrus regions of the hippocampus (P < 0.001, n =
264 us.SIGNIFICANCE STATEMENT In the hippocampal dentate gyrus, seizures drive retrograde sprouting of gr
266 ctrophysiological and molecular tests in the dentate gyrus showed that subAbeta rats or stressed rats
268 es 11 to 18 years forecasted diminished left dentate gyrus (simple slope, -14.20; standard error, 5.2
269 udy we investigate the relationships between dentate gyrus structure, hippocampus-dependent cognition
270 ynapses were frequently found in the CA3 and dentate gyrus sub-regions, corresponding to large thorny
271 breakdown in the hippocampus and its CA1 and dentate gyrus subdivisions worsened with mild cognitive
273 ed flexibly, and that these neurons regulate dentate gyrus synaptic and spiking responses to neocorti
274 subfield (subiculum, cornu ammonis 1-3, and dentate gyrus) targets of immunomodulation-treated LGI1
275 in hippocampal staining: CB(+) decreased in dentate gyrus (TBI = 2 +/- 0.382, Sham = 4 +/- 0.383, P
277 n the activation of neural stem cells in the dentate gyrus, their division, and differentiation of th
278 cluding the sprouting of mossy fibers in the dentate gyrus; they establish aberrant recurrent synapse
279 Reduction of fast phasic inhibition in the dentate gyrus through granule cell-selective knock-out o
280 New neurons continue to be generated in the dentate gyrus throughout life, providing this region of
282 w and high levels of kainic acid (KA) in the dentate gyrus to assess whether neuronal hyperexcitation
283 d progressive microstructural changes in the dentate gyrus translate to the severity of hippocampal s
285 hods to show that EE alters microglia in the dentate gyrus under physiological conditions and robustl
286 ify a role for the astroglial xCT in ventral dentate gyrus (vDG) in stress and antidepressant respons
288 pattern separation task, we demonstrate that dentate gyrus volume predicts accuracy and response time
290 n of testosterone's aromatization within the dentate gyrus was assessed by local infusion of the arom
292 of juxtacellularly recorded cells in CA1 and dentate gyrus were modulated by HRR and theta oscillatio
295 vious observations in the monkey hippocampal dentate gyrus, where MSBs comprised approximately 40% of
296 equency rhythm with largest amplitude in the dentate gyrus, which coupled to respiration-entrained os
297 ith enhanced novelty-induced activity in the dentate gyrus, which may be related to our findings that
298 Adult hippocampal neurogenesis provides the dentate gyrus with heterogeneous populations of granule
299 s of neural stem cell differentiation in the dentate gyrus, with higher expression intensity in neuro
300 s fibres in the medial entorhinal cortex and dentate gyrus, with no frank noradrenergic cell body los
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