ライフサイエンスコーパス: subgranular

1 ke that in adults, is mainly confined to the subgranular and subventricular zones.

2 features of nestin-GFP-positive cells in the subgranular cell layer of the dentate gyrus.

3 DCX-containing neurons were found in the subgranular hilus in adult rats and were more widespread

4 ogenitors of these new neurons reside in the subgranular layer (SGL) of the dentate gyrus.

5 oreactive fibers and puncta was located in a subgranular layer of the caudal anteroventral cochlear n

6 duced to proliferate and migrate outside the subgranular layer of the dentate gyrus.

7 in radial glia, such as those located in the subgranular layer of the dentate gyrus.

8 ed protein that is expressed in cells of the subgranular layer of the hippocampal dentate gyrus, a br

9 Active caspase-3 immunoreactivity in the subgranular layer was co-localized with an early neurona

10 The subgranular layers (layers 5 and 6) of primary sensory c

11 subclasses, and that thalamic inputs to the subgranular layers of cortex may combine with other, int

12 nd a few were found in the supragranular and subgranular layers of the dentate gyrus.

13 and interareal corticocortical cells in the subgranular layers represent largely independent populat

14 ayer 4, while SS+ cell density peaked in the subgranular layers.

15 and interareal corticocortical cells in the subgranular layers.

16 ncrease in cell proliferation in the dentate subgranular proliferative zone (SGZ), an area known to c

17 ted putative progenitor cells in the dentate subgranular proliferative zone.

18 In the central and subgranular regions of the hilus, mossy cell axons estab

19 ly 50% fewer Ki67-positive stem cells in the subgranular zone (SGZ) and granular cell layer of the de

20 iding neural progenitor cells located in the subgranular zone (SGZ) as well as their derivatives incl

21 rdU) to label progenitors in the hippocampal subgranular zone (SGZ) during the synthesis phase.

22 Adult neurogenesis in the hippocampal subgranular zone (SGZ) is involved in learning and memor

23 plification of subventricular zone (SVZ) and subgranular zone (SGZ) neural precursors after neonatal

24 iferation and differentiation of hippocampal subgranular zone (SGZ) neuroblasts, and the dendritic ar

25 Abnormal subgranular zone (SGZ) neurogenesis is proposed to contr

26 n both the subventricular zone (SVZ) and the subgranular zone (SGZ) of adult brain.

27 ion is faithful to endogenous Tctex-1 at the subgranular zone (SGZ) of dentate gyrus, ventricular/sub

28 sion of Prominin-1 by precursor cells in the subgranular zone (SGZ) of the adult hippocampus has been

29 em cells (NSCs) in two discrete regions, the subgranular zone (SGZ) of the dentate gyrus and the subv

30 New neurons continue to be born in the subgranular zone (SGZ) of the dentate gyrus in the hippo

31 ncreased precursor cell proliferation in the subgranular zone (SGZ) of the dentate gyrus in the monke

32 The subgranular zone (SGZ) of the dentate gyrus of the hippo

33 areas, the subventricular zone (SVZ) and the subgranular zone (SGZ) of the dentate gyrus, express hig

34 e (SVZ), rostral migratory stream (RMS), and subgranular zone (SGZ) of the dentate gyrus.

35 zone (SVZ) of the lateral ventricles and the subgranular zone (SGZ) of the dentate gyrus.

36 ated in regulating adult neurogenesis in the subgranular zone (SGZ) of the dentate gyrus; however, th

37 pression of immature neuronal markers in the subgranular zone (SGZ) of the hippocampal dentate gyrus

38 olve loss of neural precursor cells from the subgranular zone (SGZ) of the hippocampal dentate gyrus

39 lls in the subventricular zone (SVZ) and the subgranular zone (SGZ) of the hippocampal dentate gyrus

40 The neurogenic potential of the subgranular zone (SGZ) of the hippocampal dentate gyrus

41 sis occurs in only two restricted areas, the subgranular zone (SGZ) of the hippocampus and the subven

42 in the subventricular zone (SVZ) and in the subgranular zone (SGZ) of the hippocampus in vivo.

43 the lateral ventricle and the dentate gyrus subgranular zone (SGZ) of the hippocampus.

44 l stages of neurogenesis were evident in the subgranular zone (SGZ) of wild-type (WT) mice (nestin-Cr

45 n be passaged long term, whereas hippocampal subgranular zone (SGZ) precursors are rapidly depleted b

46 from stem cells and their progeny in the DG subgranular zone (SGZ) prevented maturation of new neuro

47 cteristics that are typical of adult SVZ and subgranular zone (SGZ) stem cells/astrocytes.

48 ss reduces neurogenesis in the dentate gyrus subgranular zone (SGZ), but it is unknown if stress-indu

49 ing in the subventricular zone (SVZ) and the subgranular zone (SGZ), is subject to complex regulation

50 a to promote neurogenesis in the hippocampal subgranular zone (SGZ), to reverse learning and memory d

51 l neuroplasticity, adult neurogenesis in the subgranular zone (SGZ), was regulated by cocaine self-ad

52 tricular-subventricular zone (V-SVZ) and the subgranular zone (SGZ), with signaling pathways that con

53 region as expected, but also in the dentate subgranular zone (SGZ).

54 cells are the source for the LL-NSCs in the subgranular zone (SGZ).

55 originate from radial astrocytes within the subgranular zone (SGZ).

56 s and their progeny in the adult hippocampal subgranular zone (SGZ).

57 e effect was larger in the hilus than in the subgranular zone (SGZ).

58 iginates from multipotent progenitors in the subgranular zone (SGZ).

59 entate pole to produce a lifelong neurogenic subgranular zone (SGZ).

60 y in the adult subventricular zone (SVZ) and subgranular zone (SGZ).

61 d for neuronal maturation in the hippocampal subgranular zone (SGZ); these cells can be identified by

62 2-fold increase in cell birth in the dentate subgranular zone 1-2 weeks after 10 min bilateral common

63 largely taken up their final position in the subgranular zone along the hilar side of the dentate gra

64 in the dentate gyrus with cell bodies in the subgranular zone and processes extending into the granul

65 m cells resulted in defects in the postnatal subgranular zone and reduced neurogenesis.

66 dentate gyrus cradle newborn neurons in the subgranular zone and that their radial processes provide

67 responding to the granule cell layer and the subgranular zone and, contrary to previous reports, disc

68 her ablation of juvenile neurogenesis in the subgranular zone and/or the subventricular zone is respo

69 tion, granule cells born in the hilus or the subgranular zone begin to express NeuroD followed by Neu

70 aloric restriction increased apoptosis of DG subgranular zone cells in Ghsr-null mice, although it ha

71 c findings, in nuclei of a few pyramidal and subgranular zone cells.

72 r of Sox-2+ NPCs residing in the hippocampal subgranular zone following binge alcohol exposure.

73 at the newly divided cells migrated from the subgranular zone into the granule cell layer and matured

74 Adult neurogenesis in the hippocampus subgranular zone is associated with the etiology and tre

75 Neuroblasts born in the dentate subgranular zone migrate into the granule cell layer, wh

76 an important role during postnatal and adult subgranular zone neurogenesis, and it has been suggested

77 timately leading to the establishment of the subgranular zone neurogenic niche.

78 cells were observed in the GCL and adjacent subgranular zone of aged rats, indicative of a decrease

79 g cells in the subventricular zone (SVZ) and subgranular zone of dentate gyrus (SGZ) were counted 60

80 reduced progenitor cell proliferation in the subgranular zone of dentate gyrus in KO and OE mice.

81 postnatal cerebellum; and juvenile to adult subgranular zone of dentate gyrus, subventricular zone,

82 beling in the subventricular zone and in the subgranular zone of dentate gyrus, where EGFR/ErbB1 and

83 d survival in the ventral dentate gyrus (DG) subgranular zone of Ghsr-null mice than in that of wild-

84 ating Pten in adult neural stem cells in the subgranular zone of hippocampal dentate gyrus results in

85 analysis of Golgi-impregnated neurons in the subgranular zone of hippocampus.

86 ral stem-like and/or progenitor cells in the subgranular zone of rat dentate gyrus.

87 d cell proliferation and neurogenesis in the subgranular zone of the adult dentate gyrus.

88 mature granular cells and astrocytes, in the subgranular zone of the adult dentate gyrus.

89 rtin-positive neural progenitor cells in the subgranular zone of the dentate gyrus (DG) during the ea

90 zone (SVZ) of the lateral ventricles and the subgranular zone of the dentate gyrus (DG) show ongoing

91 estricted areas of the adult brain, like the subgranular zone of the dentate gyrus (DG), there is con

92 the animal in the subependymal zone and the subgranular zone of the dentate gyrus (DG).

93 ranched doublecortin-positive neurons in the subgranular zone of the dentate gyrus and reduced BrdU i

94 cells in two neuroproliferative regions-the subgranular zone of the dentate gyrus and the rostral su

95 The subgranular zone of the dentate gyrus contains neural pr

96 d the generation of new neurons in the adult subgranular zone of the dentate gyrus contributes to lea

97 for immature hippocampal neurons within the subgranular zone of the dentate gyrus following TBI.

98 pocampal neural progenitor cell types in the subgranular zone of the dentate gyrus that were in trans

99 y, an increase in BrdU-labelled cells in the subgranular zone of the dentate gyrus was observed.

100 -3 immunoreactivity was also detected in the subgranular zone of the dentate gyrus, a known region of

101 ling of immature neurons was detected in the subgranular zone of the dentate gyrus.

102 ules tested enhanced neuron formation in the subgranular zone of the dentate gyrus.

103 , Ki-67(+), and doublecortin(+) cells in the subgranular zone of the dentate gyrus.

104 ural progenitor cells (NPCs) residing in the subgranular zone of the DG are regulated by an array of

105 n of the number of BrdU-labeled cells in the subgranular zone of the DG revealed a significant decrea

106 established that neurogenesis in the rodent subgranular zone of the hippocampal dentate gyrus contin

107 One of these, the subgranular zone of the hippocampal dentate gyrus, is of

108 cular zone of the lateral ventricle, and the subgranular zone of the hippocampal dentate gyrus.

109 ew neurons are generated continuously in the subgranular zone of the hippocampus and integrate into e

110 ew neurons are generated continuously in the subgranular zone of the hippocampus and integrate into e

111 or SB415286 also decreased apoptosis in the subgranular zone of the hippocampus in irradiated mice,

112 The subgranular zone of the hippocampus showed a significant

113 logical maturation of newborn neurons in the subgranular zone of the hippocampus.

114 cular zone of the anterior forebrain and the subgranular zone of the hippocampus.

115 apoptosis and decreased neurogenesis in the subgranular zone of the hippocampus.

116 ntal cortices (layers II, III and V) and the subgranular zone of the hippocampus.

117 l settlement of the neural precursors at the subgranular zone relies on a pertussis toxin-sensitive p

118 es of BrdU positive cells in the hippocampal subgranular zone revealed a significant increase in cell

119 ry processes follow a tortuous path from the subgranular zone through the granule cell layer and ensh

120 planted cells showed robust migration to the subgranular zone throughout the dentate gyrus, exhibitin

121 Both effects were bilateral, but that in the subgranular zone was more prominent on the ischemic side

122 terations in neurogenesis in the hippocampal subgranular zone were accompanied by decreased Notch-1,

123 The dividing cells in the subgranular zone were identified as neurons since they e

124 hosphorylated IGF-I/insulin receptors in the subgranular zone were localized on immature neurons, sug

125 labeled RGS10-LIR cells in the dentate gyrus subgranular zone were not proliferating but that newly b

126 sis in the adult dentate gyrus occurs in the subgranular zone where newborn neurons (NNs) migrate a s

127 lt tree shrews were primarily located in the subgranular zone, had morphological characteristics of g

128 s in the olfactory bulb, and the hippocampal subgranular zone, where they migrate and differentiate i

129 noreactivity was observed in the hippocampal subgranular zone-the site of adult neurogenesis--but was

130 des of newborn neurons to cradle them in the subgranular zone.

131 ring postnatal and adult neurogenesis of the subgranular zone.

132 depleted before proper establishment of the subgranular zone.

133 ther with a reduction in neurogenesis in the subgranular zone.

134 ot CB(2) receptor-deficient NPs of the mouse subgranular zone.

135 le subventricular zone and the dentate gyrus subgranular zone.

136 The number of newly generated cells in the subgranular zone/granule cell layer of the dentate gyrus

137 e mitotic doublecortin-positive cells in the subgranular zone; mRNA levels of brain-derived neurotrop

138 ated with neurons in the neuroproliferative (subgranular) zone of the dentate gyrus, the physiologica

139 lls obtained from the subventricular and the subgranular zones of adult mice brains, all compounds st

140 ng cells in the adult mouse subependymal and subgranular zones stopped the generation of immunohistoc

141 zones (including the subventricular and the subgranular zones).