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

 
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