ライフサイエンスコーパス: hippocampal dentate gyrus

1 and became misplaced in the outer GCL of the hippocampal dentate gyrus.

2 necrosis in the cortex and apoptosis in the hippocampal dentate gyrus.

3 outer portion of the molecular layer of the hippocampal dentate gyrus.

4 aptic terminals, was infused into the dorsal hippocampal dentate gyrus.

5 egeneration of GABAergic interneurons in the hippocampal dentate gyrus.

6 rtin(+) cells in the subventricular zone and hippocampal dentate gyrus.

7 e of ERK signaling during development of the hippocampal dentate gyrus.

8 reorganization of the circuitry in the aging hippocampal dentate gyrus.

9 ease in the number of newborn neurons in the hippocampal dentate gyrus.

10 ic lamina, the middle molecular layer of the hippocampal dentate gyrus.

11 ies in newborn neural precursor cells of the hippocampal dentate gyrus.

12 neurogenesis persists throughout life in the hippocampal dentate gyrus.

13 and increases adult neurogenesis in the rat hippocampal dentate gyrus.

14 to produce neurons are retained in the adult hippocampal dentate gyrus.

15 tion of neural progenitor cells in the adult hippocampal dentate gyrus.

16 e correlated with cellular dispersion in the hippocampal dentate gyrus.

17 eurons and in neural progenitor cells in the hippocampal dentate gyrus.

18 rovide the predominant synaptic input to the hippocampal dentate gyrus.

19 dent forebrain subventricular zone (SVZ) and hippocampal dentate gyrus.

20 l ventricle, and the subgranular zone of the hippocampal dentate gyrus.

21 nd new neurons in the olfactory bulb and the hippocampal dentate gyrus.

22 sed in cells of the subgranular layer of the hippocampal dentate gyrus, a brain region known to susta

23 The hippocampal dentate gyrus, a region with ongoing adult n

24 loss in the granule cell layer (GCL) of the hippocampal dentate gyrus after experimental traumatic b

25 citability of inhibitory interneurons in the hippocampal dentate gyrus, an important area for seizure

26 cells from the subgranular zone (SGZ) of the hippocampal dentate gyrus and alterations in new cell pr

27 lpha2 (-10%) and beta3 (+9%) subunits in the hippocampal dentate gyrus and CA1 regions, respectively.

28 and completion computations ascribed to the hippocampal dentate gyrus and CA3 fields.

29 on, fluoxetine reduced the metabolism of the hippocampal dentate gyrus and dorsomedial prefrontal cor

30 nance of long-term potentiation in the adult hippocampal dentate gyrus and for full NMDAR activity on

31 of BrdU-labeled cells were quantified in the hippocampal dentate gyrus and hilus and were related to

32 mice with enlarged brains with an elongated hippocampal dentate gyrus and increased numbers of newbo

33 is persists throughout life in the mammalian hippocampal dentate gyrus and increases after epileptoge

34 les had more newly proliferated cells in the hippocampal dentate gyrus and protein levels of vascular

35 servoir supporting adult neurogenesis in the hippocampal dentate gyrus and subventricular zone of the

36 uroD1 is important in the development of the hippocampal dentate gyrus and the cerebellum, its functi

37 markers in the subgranular zone (SGZ) of the hippocampal dentate gyrus and the forebrain subventricul

38 gene 8-suggest that the granule cells of the hippocampal dentate gyrus and the pyramidal neurons in t

39 Neuropeptide Y (NPY) gene expression in the hippocampal dentate gyrus and throughout neocortex was a

40 particularly high levels in olfactory bulb, hippocampal dentate gyrus, and cerebellum.

41 Cs) are the principal cell population of the hippocampal dentate gyrus, and granule cells provide the

42 lso highly expressed in granule cells of the hippocampal dentate gyrus, and in a previous study we sh

43 vision in the mouse subventricular zone, the hippocampal dentate gyrus, and the corpus callosum.

44 Young adults' whole hippocampal, dentate gyrus, and CA3 hippocampal subfield

45 and the most medial field of the cortex, the hippocampal dentate gyrus, appears by cytoarchitecture t

46 ion by gamma-aminobutyric acid (GABA) in the hippocampal dentate gyrus are consistent with an augment

47 Granule cells in the hippocampal dentate gyrus are generated throughout adult

48 Adult-born neurons in the hippocampal dentate gyrus are important for flexibly usi

49 citatory, glutamatergic granule cells of the hippocampal dentate gyrus are presumed to play central r

50 dritic development of newborn neurons in the hippocampal dentate gyrus are still unclear.

51 ls (GCs), a minor population of cells in the hippocampal dentate gyrus, are highly active during the

52 Genetic lesions of EC and hippocampal dentate gyrus, CA3 and CA1 regions have reve

53 Conversely, hippocampal dentate gyrus/CA3 demonstrated signals consi

54 enesis in the rodent subgranular zone of the hippocampal dentate gyrus continues throughout adulthood

55 The hippocampal dentate gyrus (DG) and CA3 are known to cont

56 typed pruning of axons that originate in the hippocampal dentate gyrus (DG) and extend along the infr

57 brain continuously supply new neurons to the hippocampal dentate gyrus (DG) and the olfactory bulb (O

58 neural precursors and immature cells in the hippocampal dentate gyrus (DG) as well as in vivo magnet

59 re neurons and radial glia-like cells in the hippocampal dentate gyrus (DG) granular cell layer.

60 ck the CXCR4 receptor, the morphology of the hippocampal dentate gyrus (DG) is dramatically altered.

61 The hippocampal dentate gyrus (DG) is thought to be responsi

62 nvestigate the formation of synapses between hippocampal dentate gyrus (DG) neurons and their target

63 We recently reported that hippocampal dentate gyrus (DG) neurons differentiated fr

64 NMDAR synaptic function was enhanced in the hippocampal dentate gyrus (DG) of adult Low LG offspring

65 STATEMENT Despite abundant evidence that the hippocampal dentate gyrus (DG) plays a critical role in

66 Granule neurons in the hippocampal dentate gyrus (DG) receive their primary inp

67 thway and restored adult neurogenesis in the hippocampal dentate gyrus (DG) to physiological levels.

68 entiation of neural progenitors in the adult hippocampal dentate gyrus (DG), one of the select region

69 (SVZ) and the subgranular zone (SGZ) of the hippocampal dentate gyrus (DG), where VEGFR2/Flk-1 was c

70 forebrain subventricular zone (SVZ) and the hippocampal dentate gyrus (DG).

71 SCs) generate neurons throughout life in the hippocampal dentate gyrus (DG).

72 in the rodent subventricular zone (SVZ) and hippocampal dentate gyrus (DG).

73 cts the degree of calbindin reduction in the hippocampal dentate gyrus (DG).

74 rs of pyramidal neurons and granule cells of hippocampal dentate gyrus (DG).

75 cellular localization of two proteins in the hippocampal dentate gyrus (DG): the GluA2 subunit of the

76 Thus, effects of oxotremorine in the hippocampal dentate gyrus do not produce global changes

77 ion of adult neural stem cells (NSCs) in the hippocampal dentate gyrus during development.

78 a progressive reduction in spine density of hippocampal dentate gyrus engram cells.

79 ned in the rat brain following lesion of the hippocampal dentate gyrus granular cells by intradentate

80 a segregated zone on the distal dendrites of hippocampal dentate gyrus granule cells (i.e., outer mol

81 making electrophysiological recordings from hippocampal dentate gyrus granule cells, we show that sy

82 pathophysiological mechanisms involving the hippocampal dentate gyrus have been proposed.

83 rments and aberrant neuronal activity in the hippocampal dentate gyrus in AD-related mouse models and

84 source of the Abeta peptide deposited in the hippocampal dentate gyrus in Alzheimer's disease (AD) an

85 electroencephalograph (EEG) electrode in the hippocampal dentate gyrus in combination with an electro

86 imes more labeled cells were detected in the hippocampal dentate gyrus in ischemic animals than contr

87 on METH-induced aberrant neurogenesis in the hippocampal dentate gyrus in the context of the blood-br

88 ore, the number of DCX-positive cells in the hippocampal dentate gyrus increased in with G-CSF treatm

89 long-term potentiation (LTP) in intact mouse hippocampal dentate gyrus increased the neuron-specific,

90 antly enhanced long-term potentiation in the hippocampal dentate gyrus induced by high-frequency elec

91 The hippocampal dentate gyrus is critically involved in lear

92 tential of the subgranular zone (SGZ) of the hippocampal dentate gyrus is likely to be regulated by m

93 eneration and survival of new neurons in the hippocampal dentate gyrus is not involved with the cogni

94 The hippocampal dentate gyrus is often viewed as a segregato

95 urons in the adult rodent olfactory bulb and hippocampal dentate gyrus is widely accepted and stroke-

96 One of these, the subgranular zone of the hippocampal dentate gyrus, is of primary interest becaus

97 and investigated the cellular phenotypes of hippocampal dentate gyrus-like neurons derived from iPSC

98 Kainic acid-induced neuron loss in the hippocampal dentate gyrus may cause epileptogenic hypere

99 ignificantly reduced synaptic content in the hippocampal dentate gyrus molecular layer, with smaller,

100 In hippocampal dentate gyrus, MPH-receiving rats showed a 5

101 We labelled a population of hippocampal dentate gyrus neurons activated during fear

102 l artery occlusion, and improved survival of hippocampal dentate gyrus neurons after systemic kainic

103 Hsp60 was also increased in the hippocampal dentate gyrus neurons somata and neuropil an

104 ons, oligodendrocytes, and astrocytes in the hippocampal dentate gyrus of adult macaque monkeys, usin

105 The generation of new neurons in the hippocampal dentate gyrus of adult mammals has been char

106 cell cycle exit in neural progenitors in the hippocampal dentate gyrus of adult mice.

107 cells were systematically quantitated in the hippocampal dentate gyrus of adult synapsin III knockout

108 c development of newly formed neurons in the hippocampal dentate gyrus of LRRK2 knockout mice.

109 lamic reuniens and centromedial nucleus, and hippocampal dentate gyrus of obese rats as compared to l

110 tiple markers of circuit organization in the hippocampal dentate gyrus of young adult monkeys (Macaca

111 decreased overall neurogenesis by 63% in the hippocampal dentate gyrus of young adult transgenic mice

112 porter 1 in the outer molecular layer of the hippocampal dentate gyrus on the first 157 participants

113 Neurogenesis in the hippocampal dentate gyrus persists throughout life and i

114 density and total granule cell number in the hippocampal dentate gyrus region are higher in the DFF45

115 led that 152 genes were downregulated in the hippocampal dentate gyrus region of mice lacking kmt2b.

116 neural stem cells in the subgranular zone of hippocampal dentate gyrus results in higher proliferatio

117 Immunocytochemistry of the adult hippocampal dentate gyrus revealed that synapsin III col

118 enic regions of the adult brain, such as the hippocampal dentate gyrus, rostral migratory stream, and

119 ic hippocampus.SIGNIFICANCE STATEMENT In the hippocampal dentate gyrus, seizures drive retrograde spr

120 dulthood in the mammalian olfactory bulb and hippocampal dentate gyrus, suggesting the hypothesis tha

121 is-dependent long-term potentiation (LTP) at hippocampal dentate gyrus synapses; conversely, Ngd depl

122 ch and reduced long-term potentiation in the hippocampal dentate gyrus that, as the hyperkinesis seen

123 of betaCaMKII activity is restricted to the hippocampal dentate gyrus, the region where long-term po

124 e neurons within the subventricular zone and hippocampal dentate gyrus throughout adult life.

125 Here we investigated the hippocampal dentate gyrus to determine if the FXS spine

126 ration and integration of new neurons in the hippocampal dentate gyrus, using dual pulse-chase, multi

127 Specific expression of TLX in adult hippocampal dentate gyrus via lentiviral transduction in

128 , the number of BrdU(+)/NeuN(+) cells in the hippocampal dentate gyrus was significantly elevated aft

129 t to our previous observations in the monkey hippocampal dentate gyrus, where MSBs comprised approxim

130 Unlike the hippocampal dentate gyrus, where proliferation of progen

131 omponents in the processing of inputs to the hippocampal dentate gyrus, with distinct integrative rol