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1 rovide the predominant synaptic input to the hippocampal dentate gyrus.
2 dent forebrain subventricular zone (SVZ) and hippocampal dentate gyrus.
3 l ventricle, and the subgranular zone of the hippocampal dentate gyrus.
4 nd new neurons in the olfactory bulb and the hippocampal dentate gyrus.
5 obustly stimulates adult neurogenesis in the hippocampal dentate gyrus.
6  necrosis in the cortex and apoptosis in the hippocampal dentate gyrus.
7  outer portion of the molecular layer of the hippocampal dentate gyrus.
8 aptic terminals, was infused into the dorsal hippocampal dentate gyrus.
9 rtin(+) cells in the subventricular zone and hippocampal dentate gyrus.
10  activation and enhanced neurogenesis in the hippocampal dentate gyrus.
11 SCs) generate neurons throughout life in the hippocampal dentate gyrus.
12 it persists only in the olfactory system and hippocampal dentate gyrus.
13 and became misplaced in the outer GCL of the hippocampal dentate gyrus.
14 egeneration of GABAergic interneurons in the hippocampal dentate gyrus.
15 e of ERK signaling during development of the hippocampal dentate gyrus.
16 reorganization of the circuitry in the aging hippocampal dentate gyrus.
17 ease in the number of newborn neurons in the hippocampal dentate gyrus.
18 ic lamina, the middle molecular layer of the hippocampal dentate gyrus.
19 ies in newborn neural precursor cells of the hippocampal dentate gyrus.
20 neurogenesis persists throughout life in the hippocampal dentate gyrus.
21  and increases adult neurogenesis in the rat hippocampal dentate gyrus.
22 to produce neurons are retained in the adult hippocampal dentate gyrus.
23 tion of neural progenitor cells in the adult hippocampal dentate gyrus.
24 e correlated with cellular dispersion in the hippocampal dentate gyrus.
25 eurons and in neural progenitor cells in the hippocampal dentate gyrus.
26 n the production of new neurons in the adult hippocampal dentate gyrus, a brain area integral in form
27 sed in cells of the subgranular layer of the hippocampal dentate gyrus, a brain region known to susta
28                                          The hippocampal dentate gyrus, a region with ongoing adult n
29                     Additionally, neurons in hippocampal dentate gyrus, a vulnerable region in epilep
30  loss in the granule cell layer (GCL) of the hippocampal dentate gyrus after experimental traumatic b
31  neocortical inputs, and that project to the hippocampal dentate gyrus, also send axon collaterals to
32 eurogenesis occurs in the adult brain in the hippocampal dentate gyrus, an area that contains neurons
33 citability of inhibitory interneurons in the hippocampal dentate gyrus, an important area for seizure
34 cells from the subgranular zone (SGZ) of the hippocampal dentate gyrus and alterations in new cell pr
35 lpha2 (-10%) and beta3 (+9%) subunits in the hippocampal dentate gyrus and CA1 regions, respectively.
36  and completion computations ascribed to the hippocampal dentate gyrus and CA3 fields.
37 on, fluoxetine reduced the metabolism of the hippocampal dentate gyrus and dorsomedial prefrontal cor
38 ike receptor 4 (TLR4) on excitability of the hippocampal dentate gyrus and epileptogenesis after brai
39 nance of long-term potentiation in the adult hippocampal dentate gyrus and for full NMDAR activity on
40 of BrdU-labeled cells were quantified in the hippocampal dentate gyrus and hilus and were related to
41 th sexes, we performed RNA-sequencing on the hippocampal dentate gyrus and identified differentially
42  mice with enlarged brains with an elongated hippocampal dentate gyrus and increased numbers of newbo
43 is persists throughout life in the mammalian hippocampal dentate gyrus and increases after epileptoge
44 les had more newly proliferated cells in the hippocampal dentate gyrus and protein levels of vascular
45 servoir supporting adult neurogenesis in the hippocampal dentate gyrus and subventricular zone of the
46 uroD1 is important in the development of the hippocampal dentate gyrus and the cerebellum, its functi
47 markers in the subgranular zone (SGZ) of the hippocampal dentate gyrus and the forebrain subventricul
48 gene 8-suggest that the granule cells of the hippocampal dentate gyrus and the pyramidal neurons in t
49  Neuropeptide Y (NPY) gene expression in the hippocampal dentate gyrus and throughout neocortex was a
50  particularly high levels in olfactory bulb, hippocampal dentate gyrus, and cerebellum.
51 Cs) are the principal cell population of the hippocampal dentate gyrus, and granule cells provide the
52 lso highly expressed in granule cells of the hippocampal dentate gyrus, and in a previous study we sh
53 ncluded the central nucleus of the amygdala, hippocampal dentate gyrus, and medial prefrontal cortex
54 vision in the mouse subventricular zone, the hippocampal dentate gyrus, and the corpus callosum.
55 ic niches, the subgranular zone (SGZ) of the hippocampal dentate gyrus, and the subependymal zone (SE
56                          Young adults' whole hippocampal, dentate gyrus, and CA3 hippocampal subfield
57 and the most medial field of the cortex, the hippocampal dentate gyrus, appears by cytoarchitecture t
58 ion by gamma-aminobutyric acid (GABA) in the hippocampal dentate gyrus are consistent with an augment
59                         Granule cells in the hippocampal dentate gyrus are generated throughout adult
60                    Adult-born neurons in the hippocampal dentate gyrus are important for flexibly usi
61 citatory, glutamatergic granule cells of the hippocampal dentate gyrus are presumed to play central r
62 dritic development of newborn neurons in the hippocampal dentate gyrus are still unclear.
63 ls (GCs), a minor population of cells in the hippocampal dentate gyrus, are highly active during the
64 n granule cells and GABAergic neurons in the hippocampal dentate gyrus both in vitro and in vivo.
65                     Surprisingly, a third of hippocampal -dentate gyrus, CA3, CA1 and subiculum- neur
66                    Genetic lesions of EC and hippocampal dentate gyrus, CA3 and CA1 regions have reve
67                                  Conversely, hippocampal dentate gyrus/CA3 demonstrated signals consi
68 l number and morphology were analyzed in the hippocampal dentate gyrus (cell proliferation and surviv
69 enesis in the rodent subgranular zone of the hippocampal dentate gyrus continues throughout adulthood
70 ike molecular perturbation expressed only in hippocampal dentate gyrus (DG) and assessed its associat
71                                          The hippocampal dentate gyrus (DG) and CA3 are known to cont
72 typed pruning of axons that originate in the hippocampal dentate gyrus (DG) and extend along the infr
73 brain continuously supply new neurons to the hippocampal dentate gyrus (DG) and the olfactory bulb (O
74  neural precursors and immature cells in the hippocampal dentate gyrus (DG) as well as in vivo magnet
75        Taking advantage of the fact that the hippocampal dentate gyrus (DG) gives rise to newborn DGC
76 re neurons and radial glia-like cells in the hippocampal dentate gyrus (DG) granular cell layer.
77                                          The hippocampal dentate gyrus (DG) is a unique brain region
78 ck the CXCR4 receptor, the morphology of the hippocampal dentate gyrus (DG) is dramatically altered.
79                                          The hippocampal dentate gyrus (DG) is thought to be responsi
80                                        Adult hippocampal dentate gyrus (DG) neural stem cells (NSCs)
81 nvestigate the formation of synapses between hippocampal dentate gyrus (DG) neurons and their target
82                    We recently reported that hippocampal dentate gyrus (DG) neurons differentiated fr
83  NMDAR synaptic function was enhanced in the hippocampal dentate gyrus (DG) of adult Low LG offspring
84 hia coli) stimuli.SIGNIFICANCE STATEMENT The hippocampal dentate gyrus (DG) of rodents generates newb
85 te granule cells (DGCs) are generated in the hippocampal dentate gyrus (DG) of rodents through a proc
86                      Convergent data suggest hippocampal dentate gyrus (DG) pathology in DS (Scn1a(+/
87 STATEMENT Despite abundant evidence that the hippocampal dentate gyrus (DG) plays a critical role in
88                       Granule neurons in the hippocampal dentate gyrus (DG) receive their primary inp
89 thway and restored adult neurogenesis in the hippocampal dentate gyrus (DG) to physiological levels.
90 tivate a set of "fear ensemble" cells in the hippocampal dentate gyrus (DG) whose reactivation is nec
91 entiation of neural progenitors in the adult hippocampal dentate gyrus (DG), one of the select region
92  Restricted Precursors (GRPs) into the adult hippocampal dentate gyrus (DG), or injected their secret
93  (SVZ) and the subgranular zone (SGZ) of the hippocampal dentate gyrus (DG), where VEGFR2/Flk-1 was c
94  to impairments of adult neurogenesis in the hippocampal dentate gyrus (DG), while the effects of ant
95 rs of pyramidal neurons and granule cells of hippocampal dentate gyrus (DG).
96 cts the degree of calbindin reduction in the hippocampal dentate gyrus (DG).
97 al changes in the function of neurons in the hippocampal dentate gyrus (DG).
98  forebrain subventricular zone (SVZ) and the hippocampal dentate gyrus (DG).
99 SCs) generate neurons throughout life in the hippocampal dentate gyrus (DG).
100  in the rodent subventricular zone (SVZ) and hippocampal dentate gyrus (DG).
101 cellular localization of two proteins in the hippocampal dentate gyrus (DG): the GluA2 subunit of the
102         Thus, effects of oxotremorine in the hippocampal dentate gyrus do not produce global changes
103 ion of adult neural stem cells (NSCs) in the hippocampal dentate gyrus during development.
104  a progressive reduction in spine density of hippocampal dentate gyrus engram cells.
105 ng was performed with anterior and posterior hippocampal dentate gyrus from adult female macaques (n
106 ned in the rat brain following lesion of the hippocampal dentate gyrus granular cells by intradentate
107 ypes within the limbic system, including the hippocampal dentate gyrus granule cells (dGCs) that are
108 l excitability, and synaptic transmission in hippocampal dentate gyrus granule cells (DGGCs).
109 a segregated zone on the distal dendrites of hippocampal dentate gyrus granule cells (i.e., outer mol
110  making electrophysiological recordings from hippocampal dentate gyrus granule cells, we show that sy
111  pathophysiological mechanisms involving the hippocampal dentate gyrus have been proposed.
112 rments and aberrant neuronal activity in the hippocampal dentate gyrus in AD-related mouse models and
113 source of the Abeta peptide deposited in the hippocampal dentate gyrus in Alzheimer's disease (AD) an
114 electroencephalograph (EEG) electrode in the hippocampal dentate gyrus in combination with an electro
115 imes more labeled cells were detected in the hippocampal dentate gyrus in ischemic animals than contr
116 ng) in the neurogenic stem-cell niche of the hippocampal dentate gyrus in male APP/PS1 transgenic AD
117 model for studying this process has been the hippocampal dentate gyrus in mice, where new neurons are
118 on METH-induced aberrant neurogenesis in the hippocampal dentate gyrus in the context of the blood-br
119 cells (but not in GABAergic interneurons) in hippocampal dentate gyrus in vitro, a key region for pat
120 ore, the number of DCX-positive cells in the hippocampal dentate gyrus increased in with G-CSF treatm
121 long-term potentiation (LTP) in intact mouse hippocampal dentate gyrus increased the neuron-specific,
122 antly enhanced long-term potentiation in the hippocampal dentate gyrus induced by high-frequency elec
123  PPD mice and overexpression of NLRP3 in the hippocampal dentate gyrus induced depression-like behavi
124                                          The hippocampal dentate gyrus is an important relay conveyin
125 mmature granule neurons (ABINs) in the mouse hippocampal dentate gyrus is both necessary and sufficie
126                                          The hippocampal dentate gyrus is critically involved in lear
127 tential of the subgranular zone (SGZ) of the hippocampal dentate gyrus is likely to be regulated by m
128 eneration and survival of new neurons in the hippocampal dentate gyrus is not involved with the cogni
129                                          The hippocampal dentate gyrus is often viewed as a segregato
130 urons in the adult rodent olfactory bulb and hippocampal dentate gyrus is widely accepted and stroke-
131    One of these, the subgranular zone of the hippocampal dentate gyrus, is of primary interest becaus
132 pical controls and differentiated these into hippocampal dentate gyrus-like neurons and astrocytes.
133 eurons and lower motor neurons, iPSC-derived hippocampal dentate gyrus-like neurons and primary astro
134  and investigated the cellular phenotypes of hippocampal dentate gyrus-like neurons derived from iPSC
135 d pluripotent stem cell modeling of BD using hippocampal dentate gyrus-like neurons derived from Li-r
136       Kainic acid-induced neuron loss in the hippocampal dentate gyrus may cause epileptogenic hypere
137 ignificantly reduced synaptic content in the hippocampal dentate gyrus molecular layer, with smaller,
138                                           In hippocampal dentate gyrus, MPH-receiving rats showed a 5
139                  We labelled a population of hippocampal dentate gyrus neurons activated during fear
140 l artery occlusion, and improved survival of hippocampal dentate gyrus neurons after systemic kainic
141              Hsp60 was also increased in the hippocampal dentate gyrus neurons somata and neuropil an
142 ons, oligodendrocytes, and astrocytes in the hippocampal dentate gyrus of adult macaque monkeys, usin
143         The generation of new neurons in the hippocampal dentate gyrus of adult mammals has been char
144 cell cycle exit in neural progenitors in the hippocampal dentate gyrus of adult mice.
145 cells were systematically quantitated in the hippocampal dentate gyrus of adult synapsin III knockout
146                                       In the hippocampal dentate gyrus of both COVID-19 hamsters and
147 filed the transcriptome and DNA methylome of hippocampal dentate gyrus of four prairie vole groups, n
148 c development of newly formed neurons in the hippocampal dentate gyrus of LRRK2 knockout mice.
149 lamic reuniens and centromedial nucleus, and hippocampal dentate gyrus of obese rats as compared to l
150 tiple markers of circuit organization in the hippocampal dentate gyrus of young adult monkeys (Macaca
151 decreased overall neurogenesis by 63% in the hippocampal dentate gyrus of young adult transgenic mice
152 porter 1 in the outer molecular layer of the hippocampal dentate gyrus on the first 157 participants
153 ificantly reduced with decreased size of the hippocampal dentate gyrus, partial agenesis of the corpu
154                          Neurogenesis in the hippocampal dentate gyrus persists throughout life and i
155 density and total granule cell number in the hippocampal dentate gyrus region are higher in the DFF45
156 led that 152 genes were downregulated in the hippocampal dentate gyrus region of mice lacking kmt2b.
157 neural stem cells in the subgranular zone of hippocampal dentate gyrus results in higher proliferatio
158             Immunocytochemistry of the adult hippocampal dentate gyrus revealed that synapsin III col
159 enic regions of the adult brain, such as the hippocampal dentate gyrus, rostral migratory stream, and
160 ic hippocampus.SIGNIFICANCE STATEMENT In the hippocampal dentate gyrus, seizures drive retrograde spr
161 dulthood in the mammalian olfactory bulb and hippocampal dentate gyrus, suggesting the hypothesis tha
162 is-dependent long-term potentiation (LTP) at hippocampal dentate gyrus synapses; conversely, Ngd depl
163 ed a preserved gene network in the posterior hippocampal dentate gyrus that was strongly associated w
164 anied by higher norepinephrine levels in the hippocampal dentate gyrus that were also reversed by pos
165 ch and reduced long-term potentiation in the hippocampal dentate gyrus that, as the hyperkinesis seen
166  of betaCaMKII activity is restricted to the hippocampal dentate gyrus, the region where long-term po
167       MEC and LEC were synchronized with the hippocampal dentate gyrus through high- and low-gamma-fr
168 e neurons within the subventricular zone and hippocampal dentate gyrus throughout adult life.
169                     Here we investigated the hippocampal dentate gyrus to determine if the FXS spine
170 ration and integration of new neurons in the hippocampal dentate gyrus, using dual pulse-chase, multi
171          Specific expression of TLX in adult hippocampal dentate gyrus via lentiviral transduction in
172 , the number of BrdU(+)/NeuN(+) cells in the hippocampal dentate gyrus was significantly elevated aft
173 t to our previous observations in the monkey hippocampal dentate gyrus, where MSBs comprised approxim
174                                   Unlike the hippocampal dentate gyrus, where proliferation of progen
175  temporal pattern separation within the left hippocampal dentate gyrus, which correlates with heighte
176 omponents in the processing of inputs to the hippocampal dentate gyrus, with distinct integrative rol
177 rils increased Lewy body accumulation in the hippocampal dentate gyrus, with heightened microglia and

 
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