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1 1 mice exhibit enhanced neurogenesis in both subgranular and subventricular zones.
2 ke that in adults, is mainly confined to the subgranular and subventricular zones.
3 l proliferation and their migration into the subgranular cell layer demonstrating that MCs-generated
4 features of nestin-GFP-positive cells in the subgranular cell layer of the dentate gyrus.
5     DCX-containing neurons were found in the subgranular hilus in adult rats and were more widespread
6 ogenitors of these new neurons reside in the subgranular layer (SGL) of the dentate gyrus.
7 oreactive fibers and puncta was located in a subgranular layer of the caudal anteroventral cochlear n
8 duced to proliferate and migrate outside the subgranular layer of the dentate gyrus.
9 in radial glia, such as those located in the subgranular layer of the dentate gyrus.
10 ed protein that is expressed in cells of the subgranular layer of the hippocampal dentate gyrus, a br
11     Active caspase-3 immunoreactivity in the subgranular layer was co-localized with an early neurona
12                                          The subgranular layers (layers 5 and 6) of primary sensory c
13  subclasses, and that thalamic inputs to the subgranular layers of cortex may combine with other, int
14 nd a few were found in the supragranular and subgranular layers of the dentate gyrus.
15  and interareal corticocortical cells in the subgranular layers represent largely independent populat
16 ayer 4, while SS+ cell density peaked in the subgranular layers.
17  and interareal corticocortical cells in the subgranular layers.
18 ncrease in cell proliferation in the dentate subgranular proliferative zone (SGZ), an area known to c
19 ted putative progenitor cells in the dentate subgranular proliferative zone.
20                           In the central and subgranular regions of the hilus, mossy cell axons estab
21 ly 50% fewer Ki67-positive stem cells in the subgranular zone (SGZ) and granular cell layer of the de
22 iding neural progenitor cells located in the subgranular zone (SGZ) as well as their derivatives incl
23 rdU) to label progenitors in the hippocampal subgranular zone (SGZ) during the synthesis phase.
24        Adult neurogenesis in the hippocampal subgranular zone (SGZ) is involved in learning and memor
25 plification of subventricular zone (SVZ) and subgranular zone (SGZ) neural precursors after neonatal
26 iferation and differentiation of hippocampal subgranular zone (SGZ) neuroblasts, and the dendritic ar
27                                     Abnormal subgranular zone (SGZ) neurogenesis is proposed to contr
28 n both the subventricular zone (SVZ) and the subgranular zone (SGZ) of adult brain.
29 ion is faithful to endogenous Tctex-1 at the subgranular zone (SGZ) of dentate gyrus, ventricular/sub
30 sion of Prominin-1 by precursor cells in the subgranular zone (SGZ) of the adult hippocampus has been
31 em cells (NSCs) in two discrete regions, the subgranular zone (SGZ) of the dentate gyrus and the subv
32       New neurons continue to be born in the subgranular zone (SGZ) of the dentate gyrus in the hippo
33 d neurogenesis throughout life occurs in the subgranular zone (SGZ) of the dentate gyrus in the hippo
34 ncreased precursor cell proliferation in the subgranular zone (SGZ) of the dentate gyrus in the monke
35                                          The subgranular zone (SGZ) of the dentate gyrus of the hippo
36 areas, the subventricular zone (SVZ) and the subgranular zone (SGZ) of the dentate gyrus, express hig
37 e (SVZ), rostral migratory stream (RMS), and subgranular zone (SGZ) of the dentate gyrus.
38 zone (SVZ) of the lateral ventricles and the subgranular zone (SGZ) of the dentate gyrus.
39 ated in regulating adult neurogenesis in the subgranular zone (SGZ) of the dentate gyrus; however, th
40                                          The subgranular zone (SGZ) of the DG contains dense vasculat
41 pression of immature neuronal markers in the subgranular zone (SGZ) of the hippocampal dentate gyrus
42 olve loss of neural precursor cells from the subgranular zone (SGZ) of the hippocampal dentate gyrus
43 lls in the subventricular zone (SVZ) and the subgranular zone (SGZ) of the hippocampal dentate gyrus
44              The neurogenic potential of the subgranular zone (SGZ) of the hippocampal dentate gyrus
45  life within two main neurogenic niches, the subgranular zone (SGZ) of the hippocampal dentate gyrus,
46 sis occurs in only two restricted areas, the subgranular zone (SGZ) of the hippocampus and the subven
47  in the subventricular zone (SVZ) and in the subgranular zone (SGZ) of the hippocampus in vivo.
48  the lateral ventricle and the dentate gyrus subgranular zone (SGZ) of the hippocampus.
49 l stages of neurogenesis were evident in the subgranular zone (SGZ) of wild-type (WT) mice (nestin-Cr
50 n be passaged long term, whereas hippocampal subgranular zone (SGZ) precursors are rapidly depleted b
51  from stem cells and their progeny in the DG subgranular zone (SGZ) prevented maturation of new neuro
52 cteristics that are typical of adult SVZ and subgranular zone (SGZ) stem cells/astrocytes.
53 ns and reduced neuronal cell survival in the subgranular zone (SGZ), as observed using doublecortin (
54 ss reduces neurogenesis in the dentate gyrus subgranular zone (SGZ), but it is unknown if stress-indu
55 ing in the subventricular zone (SVZ) and the subgranular zone (SGZ), is subject to complex regulation
56 a to promote neurogenesis in the hippocampal subgranular zone (SGZ), to reverse learning and memory d
57 l neuroplasticity, adult neurogenesis in the subgranular zone (SGZ), was regulated by cocaine self-ad
58 tricular-subventricular zone (V-SVZ) and the subgranular zone (SGZ), which are specialized niches in
59 tricular-subventricular zone (V-SVZ) and the subgranular zone (SGZ), with signaling pathways that con
60  region as expected, but also in the dentate subgranular zone (SGZ).
61  cells are the source for the LL-NSCs in the subgranular zone (SGZ).
62  originate from radial astrocytes within the subgranular zone (SGZ).
63 s and their progeny in the adult hippocampal subgranular zone (SGZ).
64 e effect was larger in the hilus than in the subgranular zone (SGZ).
65 iginates from multipotent progenitors in the subgranular zone (SGZ).
66 entate pole to produce a lifelong neurogenic subgranular zone (SGZ).
67 y in the adult subventricular zone (SVZ) and subgranular zone (SGZ).
68 d for neuronal maturation in the hippocampal subgranular zone (SGZ); these cells can be identified by
69 2-fold increase in cell birth in the dentate subgranular zone 1-2 weeks after 10 min bilateral common
70 largely taken up their final position in the subgranular zone along the hilar side of the dentate gra
71 in the dentate gyrus with cell bodies in the subgranular zone and processes extending into the granul
72 m cells resulted in defects in the postnatal subgranular zone and reduced neurogenesis.
73  dentate gyrus cradle newborn neurons in the subgranular zone and that their radial processes provide
74 responding to the granule cell layer and the subgranular zone and, contrary to previous reports, disc
75 her ablation of juvenile neurogenesis in the subgranular zone and/or the subventricular zone is respo
76 tion, granule cells born in the hilus or the subgranular zone begin to express NeuroD followed by Neu
77 aloric restriction increased apoptosis of DG subgranular zone cells in Ghsr-null mice, although it ha
78 c findings, in nuclei of a few pyramidal and subgranular zone cells.
79  and that proliferative cells in the dentate subgranular zone express cyclin A2.
80 r of Sox-2+ NPCs residing in the hippocampal subgranular zone following binge alcohol exposure.
81 at the newly divided cells migrated from the subgranular zone into the granule cell layer and matured
82        Adult neurogenesis in the hippocampus subgranular zone is associated with the etiology and tre
83              Neuroblasts born in the dentate subgranular zone migrate into the granule cell layer, wh
84 an important role during postnatal and adult subgranular zone neurogenesis, and it has been suggested
85 timately leading to the establishment of the subgranular zone neurogenic niche.
86  cells were observed in the GCL and adjacent subgranular zone of aged rats, indicative of a decrease
87 g cells in the subventricular zone (SVZ) and subgranular zone of dentate gyrus (SGZ) were counted 60
88 reduced progenitor cell proliferation in the subgranular zone of dentate gyrus in KO and OE mice.
89  postnatal cerebellum; and juvenile to adult subgranular zone of dentate gyrus, subventricular zone,
90 beling in the subventricular zone and in the subgranular zone of dentate gyrus, where EGFR/ErbB1 and
91 d survival in the ventral dentate gyrus (DG) subgranular zone of Ghsr-null mice than in that of wild-
92 ating Pten in adult neural stem cells in the subgranular zone of hippocampal dentate gyrus results in
93 analysis of Golgi-impregnated neurons in the subgranular zone of hippocampus.
94 ral stem-like and/or progenitor cells in the subgranular zone of rat dentate gyrus.
95 mature granular cells and astrocytes, in the subgranular zone of the adult dentate gyrus.
96 d cell proliferation and neurogenesis in the subgranular zone of the adult dentate gyrus.
97  produces an increase in neurogenesis in the subgranular zone of the adult hippocampus may be one of
98 rtin-positive neural progenitor cells in the subgranular zone of the dentate gyrus (DG) during the ea
99 zone (SVZ) of the lateral ventricles and the subgranular zone of the dentate gyrus (DG) show ongoing
100 estricted areas of the adult brain, like the subgranular zone of the dentate gyrus (DG), there is con
101  the animal in the subependymal zone and the subgranular zone of the dentate gyrus (DG).
102 lt neural stem cells (aNSCs) residing in the subgranular zone of the dentate gyrus (DG).
103 ranched doublecortin-positive neurons in the subgranular zone of the dentate gyrus and reduced BrdU i
104  cells in two neuroproliferative regions-the subgranular zone of the dentate gyrus and the rostral su
105                                          The subgranular zone of the dentate gyrus contains neural pr
106 d the generation of new neurons in the adult subgranular zone of the dentate gyrus contributes to lea
107  for immature hippocampal neurons within the subgranular zone of the dentate gyrus following TBI.
108 pocampal neural progenitor cell types in the subgranular zone of the dentate gyrus that were in trans
109 ew neurons are continuously generated in the subgranular zone of the dentate gyrus throughout adultho
110 y, an increase in BrdU-labelled cells in the subgranular zone of the dentate gyrus was observed.
111 -3 immunoreactivity was also detected in the subgranular zone of the dentate gyrus, a known region of
112 wly generated neurons, first detected in the subgranular zone of the dentate gyrus, that mature over
113 ling of immature neurons was detected in the subgranular zone of the dentate gyrus.
114 , Ki-67(+), and doublecortin(+) cells in the subgranular zone of the dentate gyrus.
115 ules tested enhanced neuron formation in the subgranular zone of the dentate gyrus.
116 ural progenitor cells (NPCs) residing in the subgranular zone of the DG are regulated by an array of
117 n of the number of BrdU-labeled cells in the subgranular zone of the DG revealed a significant decrea
118  established that neurogenesis in the rodent subgranular zone of the hippocampal dentate gyrus contin
119                            One of these, the subgranular zone of the hippocampal dentate gyrus, is of
120 cular zone of the lateral ventricle, and the subgranular zone of the hippocampal dentate gyrus.
121 ew neurons are generated continuously in the subgranular zone of the hippocampus and integrate into e
122 ew neurons are generated continuously in the subgranular zone of the hippocampus and integrate into e
123  or SB415286 also decreased apoptosis in the subgranular zone of the hippocampus in irradiated mice,
124                                          The subgranular zone of the hippocampus showed a significant
125  apoptosis and decreased neurogenesis in the subgranular zone of the hippocampus.
126 ntal cortices (layers II, III and V) and the subgranular zone of the hippocampus.
127 logical maturation of newborn neurons in the subgranular zone of the hippocampus.
128 cular zone of the anterior forebrain and the subgranular zone of the hippocampus.
129 l settlement of the neural precursors at the subgranular zone relies on a pertussis toxin-sensitive p
130 es of BrdU positive cells in the hippocampal subgranular zone revealed a significant increase in cell
131 ry processes follow a tortuous path from the subgranular zone through the granule cell layer and ensh
132 planted cells showed robust migration to the subgranular zone throughout the dentate gyrus, exhibitin
133 Both effects were bilateral, but that in the subgranular zone was more prominent on the ischemic side
134 terations in neurogenesis in the hippocampal subgranular zone were accompanied by decreased Notch-1,
135                    The dividing cells in the subgranular zone were identified as neurons since they e
136 hosphorylated IGF-I/insulin receptors in the subgranular zone were localized on immature neurons, sug
137 labeled RGS10-LIR cells in the dentate gyrus subgranular zone were not proliferating but that newly b
138 sis in the adult dentate gyrus occurs in the subgranular zone where newborn neurons (NNs) migrate a s
139 ating Sox2(+) neural progenitor cells in the subgranular zone yet reduced the number of doublecortin-
140 aturing newborn neurons in the dentate gyrus subgranular zone, and a single-Reelin infusion increased
141 lt tree shrews were primarily located in the subgranular zone, had morphological characteristics of g
142 s in the olfactory bulb, and the hippocampal subgranular zone, where they migrate and differentiate i
143  the proportion of radial glial cells in the subgranular zone, yet decreased the proportion of adult-
144 noreactivity was observed in the hippocampal subgranular zone-the site of adult neurogenesis--but was
145 des of newborn neurons to cradle them in the subgranular zone.
146 ther with a reduction in neurogenesis in the subgranular zone.
147  in the adult hippocampus dentate gyrus (DG) subgranular zone.
148 ring postnatal and adult neurogenesis of the subgranular zone.
149  depleted before proper establishment of the subgranular zone.
150 ot CB(2) receptor-deficient NPs of the mouse subgranular zone.
151 le subventricular zone and the dentate gyrus subgranular zone.
152   The number of newly generated cells in the subgranular zone/granule cell layer of the dentate gyrus
153 e mitotic doublecortin-positive cells in the subgranular zone; mRNA levels of brain-derived neurotrop
154 ated with neurons in the neuroproliferative (subgranular) zone of the dentate gyrus, the physiologica
155 lls obtained from the subventricular and the subgranular zones of adult mice brains, all compounds st
156 ng cells in the adult mouse subependymal and subgranular zones stopped the generation of immunohistoc
157  zones (including the subventricular and the subgranular zones).
158 adult ventricular-subventricular (V-SVZ) and subgranular zones, which contain neural stem cells (NSCs

 
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