ライフサイエンスコーパス: subgranular zone

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

2 ring postnatal and adult neurogenesis of the subgranular zone.

3 depleted before proper establishment of the subgranular zone.

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

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

6 le subventricular zone and the dentate gyrus subgranular zone.

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

8 2-fold increase in cell birth in the dentate subgranular zone 1-2 weeks after 10 min bilateral common

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 The subgranular zone of the dentate gyrus contains neural pr

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

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

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

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

49 -3 immunoreactivity was also detected in the subgranular zone of the dentate gyrus, a known region of

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

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

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

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

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

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

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

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

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

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

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

61 The subgranular zone of the hippocampus showed a significant

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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