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1  the specific enrichment of Tctex-1 at adult SGZ stem/progenitor cells.
2 ional program controls neurogenesis in adult SGZ as in embryonic cerebral cortex.
3 ges of neuronal lineage progression in adult SGZ.
4 odeoxyuridine incorporation studies of adult SGZ in four independent mouse lines showed that Tctex-1:
5  the dopaminergic innervation to the SVZ and SGZ in rodents.
6  to its exclusive restriction to the SVZ and SGZ or, for instance, to the inadequacy of the methods u
7  neural stem cells (NSC) in both the SVZ and SGZ that are capable of self-renewal and long-term neuro
8                    In addition, most SVZ and SGZ YFP+ cells became neurons, underscoring a link betwe
9 , in neurospheres in vitro and in newly born SGZ cells in vivo.
10                     In contrast to decreased SGZ cell birth, PDAPP mice had increased birth of immatu
11  SVZ, but not in contralateral SVZ or either SGZ, in both young adult (3-month-old) and aged (24-mont
12 nd 30 d post-TAM but had significantly fewer SGZ YFP+ cells 60 and 90 d post-TAM.
13 ll survival in the granular cell layer (GCL)/SGZ was observed in young animals and a slight augmentat
14 (SVZ) and subgranular zone of dentate gyrus (SGZ) were counted 60 days post-transplant.
15     However, the total number of hippocampal SGZ-derived new neurons was reduced bilaterally; in cont
16 , in a dose-dependent manner, BrdU+ cells in SGZ in 3xTgAD mice and restored SGZ proliferation to nor
17 d social avoidance was related to changes in SGZ proliferation and neurogenesis.
18                              The decrease in SGZ neurogenesis was not associated with an age-dependen
19       We report an age-dependent decrease in SGZ proliferation in homozygous PDAPP mice.
20  path stimulation resulted in an increase in SGZ mitotic activity similar to that seen with pilocarpi
21 63 genes selectively enriched in adult mouse SGZ.
22 CD44-expressing NSCs isolated from the mouse SGZ are self-renewing and capable of differentiating int
23 ny in nestin-CreER(T2)/R26R-YFP mice: 97% of SGZ stem-like cells (GFAP/Sox2 with radial glial morphol
24  of neurogenesis (via FACS and microarray of SGZ stem and progenitor cells) suggested the involvement
25 pment identified a highly overlapping set of SGZ-enriched genes, which can be divided based on tempor
26 self-administration enhanced the survival of SGZ BrdU cells, and methamphetamine seeking during protr
27 and T-maze and had a fewer number of 2-h-old SGZ BrdU cells than nondrug and I-ShA rats, suggesting t
28 e Y-maze and had a greater number of 2-h-old SGZ BrdU cells than nondrug controls.
29  did not reduce caspase-3 cleavage in SVZ or SGZ.
30 -immunopositive (+) neurons in the posterior SGZ and a normal number of adult-generated BrdU+ neurons
31 ed social avoidance) had fewer proliferating SGZ cells labeled with the S-phase marker BrdU.
32 rty-eight h after irradiation, proliferating SGZ cells were reduced by 93-96%; immature neurons were
33 paradoxically reacts to seizures by reducing SGZ proliferation.
34 dU+ cells in SGZ in 3xTgAD mice and restored SGZ proliferation to normal magnitude.
35 cal and electron microscopy demonstrate that SGZ astrocytes form baskets that hold clusters of D cell
36       Hypoxic niches were observed along the SGZ, composed of adult NSCs and early IPCs, and oxidativ
37      CSA decreased proliferation in both the SGZ and the subventricular zone (SVZ), a source of adult
38 eptor 4-dependent depletion of IPCs from the SGZ and suggest further pharmacological strategies to pr
39 ntly, depletion of LPS-induced IPCs from the SGZ is suppressed by cyclooxygenase inhibitors.
40 LPS-induced depletion of Tbr2+ IPCs from the SGZ.
41 ggest that p21 restrains neurogenesis in the SGZ and imipramine-induced stimulation of neurogenesis m
42 ntly expressed in the nuclei of cells in the SGZ and is colocalized with NeuN, a marker for neurons.
43  indomethacin increased proliferation in the SGZ and lateral SVZ.
44 lecular control of adult neurogenesis in the SGZ and SVZ, focusing on the role of specific transcript
45 ations of label-retaining cells exist in the SGZ and that Noggin overexpression increases their numbe
46 on and maturation of progenitor cells in the SGZ by enhancing GABA release, at least in part, from PV
47 ase the number of TUNEL-labeled cells in the SGZ compared to pair-fed rats (p<0.05).
48 wn to suppress postnatal neurogenesis in the SGZ in a cell-autonomous manner.
49      Transgenic Noggin overexpression in the SGZ increases multiple precursor cell populations but pr
50 igestion in wild type NSC cultures or in the SGZ induces increased NSC proliferation, and CD44-null a
51  differentiation, and HA accumulation in the SGZ may contribute to reductions in neurogenesis that ar
52  3 months, basal level of BrdU+ cells in the SGZ of 3xTgAD mice was significantly lower relative to n
53 ssed by a significant number of cells in the SGZ of adult mice in vivo and ex vivo, including postmit
54  by BrdU incorporation, was increased in the SGZ of p21(-/-) compared with WT mice.
55  show that while blood vessel density in the SGZ remained stable from initial layer formation (2 week
56 ally migrated to the neurogenic niche in the SGZ upon transplantation in vivo.
57  is synthesized by NSCs and increases in the SGZ with aging.
58 g 1 (Dlk1) is expressed biallelically in the SGZ, and both parental alleles are required for stem cel
59 tes to NSC maintenance in SVZ but not in the SGZ, and that this is regulated by the biallelic express
60 mber of adult-generated BrdU+ neurons in the SGZ, suggesting an enduring impact of CSA regardless of
61  up to 100 d after TAM in the OB, but in the SGZ, YFP+ cells reached a plateau 30 d after TAM.
62  NSCs, and draw comparisons with NSCs in the SGZ.
63  mediate the loss of neurogenic cells in the SGZ.
64 ion and maturation of newborn neurons in the SGZ.
65 strate increases in NSC proliferation in the SGZ.
66 ic reduction of NSC/NPC proliferation in the SGZ.
67 ate proliferation and differentiation in the SGZ.
68  nestin-expressing neural progenitors in the SGZ.
69  cell chronic lymphocytic lymphoma 2) in the SGZ.
70 er blade of the dentate gyrus, including the SGZ.
71 port that astrocytes in areas outside of the SGZ and SVZ of adult mice express high levels of ephrin-
72        Serial-section reconstructions of the SGZ, using confocal and electron microscopy demonstrate
73  BMP signaling in proliferative cells of the SGZ.
74 ts that subpial precursors contribute to the SGZ formation.
75 We propose that localized hypoxia within the SGZ contributes to the neurogenic microenvironment and d
76 n of IPCs away from hypoxic zones within the SGZ might result in oxidative damage, thus triggering ce
77 ompression of proliferating cells within the SGZ, and a gradual shift of quiescent neural stem cell s
78 Notch1 iKO mice had similar numbers of total SGZ YFP+ cells 13 and 30 d post-TAM but had significantl
79                                        While SGZ vessel density and NSPC association with vessels are
80 pic oGCL cells were still rare compared with SGZ proliferating cells, emphasizing that the primary ch
81 , such as the hippocampal sub-granular zone (SGZ).
82  the dentate subgranular proliferative zone (SGZ), an area known to contain neuronal precursor cells.
83 positive stem cells in the subgranular zone (SGZ) and granular cell layer of the dentate gyrus compar
84 nitor cells located in the subgranular zone (SGZ) as well as their derivatives including doublecortin
85 enitors in the hippocampal subgranular zone (SGZ) during the synthesis phase.
86 genesis in the hippocampal subgranular zone (SGZ) is involved in learning and memory throughout life
87 ventricular zone (SVZ) and subgranular zone (SGZ) neural precursors after neonatal brain injury.
88 erentiation of hippocampal subgranular zone (SGZ) neuroblasts, and the dendritic arborization of adul
89                   Abnormal subgranular zone (SGZ) neurogenesis is proposed to contribute to Alzheimer
90 ricular zone (SVZ) and the subgranular zone (SGZ) of adult brain.
91  endogenous Tctex-1 at the subgranular zone (SGZ) of dentate gyrus, ventricular/subventricular zone o
92  by precursor cells in the subgranular zone (SGZ) of the adult hippocampus has been available.
93  two discrete regions, the subgranular zone (SGZ) of the dentate gyrus and the subventricular zone (S
94 oughout life occurs in the subgranular zone (SGZ) of the dentate gyrus in the hippocampus and is hypo
95 continue to be born in the subgranular zone (SGZ) of the dentate gyrus in the hippocampus of adult ma
96  cell proliferation in the subgranular zone (SGZ) of the dentate gyrus in the monkey hippocampus.
97                        The subgranular zone (SGZ) of the dentate gyrus of the hippocampus is a brain
98 ricular zone (SVZ) and the subgranular zone (SGZ) of the dentate gyrus, express high levels of FGFR-2
99 igratory stream (RMS), and subgranular zone (SGZ) of the dentate gyrus.
100 lateral ventricles and the subgranular zone (SGZ) of the dentate gyrus.
101  adult neurogenesis in the subgranular zone (SGZ) of the dentate gyrus; however, the mechanism underl
102                        The subgranular zone (SGZ) of the DG contains dense vasculature where neural s
103 ricular zone (SVZ) and the subgranular zone (SGZ) of the hippocampal dentate gyrus (DG), where VEGFR2
104 l precursor cells from the subgranular zone (SGZ) of the hippocampal dentate gyrus and alterations in
105 re neuronal markers in the subgranular zone (SGZ) of the hippocampal dentate gyrus and the forebrain
106 eurogenic potential of the subgranular zone (SGZ) of the hippocampal dentate gyrus is likely to be re
107 ain neurogenic niches, the subgranular zone (SGZ) of the hippocampal dentate gyrus, and the subependy
108  two restricted areas, the subgranular zone (SGZ) of the hippocampus and the subventricular zone (SVZ
109 ular zone (SVZ) and in the subgranular zone (SGZ) of the hippocampus in vivo.
110 icle and the dentate gyrus subgranular zone (SGZ) of the hippocampus.
111 enesis were evident in the subgranular zone (SGZ) of wild-type (WT) mice (nestin-CreER(T2)/R26R-YFP/N
112  term, whereas hippocampal subgranular zone (SGZ) precursors are rapidly depleted by passaging.
113 nd their progeny in the DG subgranular zone (SGZ) prevented maturation of new neurons.
114 e typical of adult SVZ and subgranular zone (SGZ) stem cells/astrocytes.
115 ronal cell survival in the subgranular zone (SGZ), as observed using doublecortin (DCX) and 5-Bromo-2
116 nesis in the dentate gyrus subgranular zone (SGZ), but it is unknown if stress-induced changes in neu
117 ricular zone (SVZ) and the subgranular zone (SGZ), is subject to complex regulations.
118 genesis in the hippocampal subgranular zone (SGZ), to reverse learning and memory deficits in 3-month
119  adult neurogenesis in the subgranular zone (SGZ), was regulated by cocaine self-administration (CSA)
120 cular zone (V-SVZ) and the subgranular zone (SGZ), which are specialized niches in which young neuron
121 cular zone (V-SVZ) and the subgranular zone (SGZ), with signaling pathways that control the behavior
122 d, but also in the dentate subgranular zone (SGZ).
123 rce for the LL-NSCs in the subgranular zone (SGZ).
124 dial astrocytes within the subgranular zone (SGZ).
125 y in the adult hippocampal subgranular zone (SGZ).
126 r in the hilus than in the subgranular zone (SGZ).
127 ipotent progenitors in the subgranular zone (SGZ).
128 duce a lifelong neurogenic subgranular zone (SGZ).
129 ventricular zone (SVZ) and subgranular zone (SGZ).
130 uration in the hippocampal subgranular zone (SGZ); these cells can be identified by the expression of
131  and granule cell layer, or subgranule zone (SGZ), is an area of active proliferation within the adul

 
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