ライフサイエンスコーパス: cornu ammonis

1 more pyramidal cells in the CA3 subfield of cornus ammonis.

2 le recordings of neuronal populations in the cornu ammonis 1 (CA1) and CA3 regions of the hippocampus

3 us action potential-mediated activity in the cornu ammonis 1 (CA1) and dentate gyrus regions of the h

4 ection between TI and DND in the hippocampal cornu ammonis 1 (CA1) in an animal model of transient br

5 locking 5-HT signaling in dorsal hippocampal cornu ammonis 1 (CA1) in both male and female rats.

6 ction relationships in hippocampal pyramidal cornu ammonis 1 (CA1) neurons using morphologic, electro

7 zipper slice preparation was used to expose cornu ammonis 1 (CA1) pyramidal neurons for recording LT

8 n level changes, molecular fingerprinting of cornu ammonis 1 (CA1) pyramidal neurons was performed in

9 modulates dendritic spine plasticity in the cornu ammonis 1 (CA1) region of the hippocampus, and GPR

10 ining downregulation of hippocampal subfield cornu ammonis 1 (CA1).

11 lasticity at hippocampal Schaffer collateral-cornu ammonis 1 (SC-CA1) synapses have produced conflict

12 n within the apical dendrites of hippocampal cornu ammonis 1 and granule cell neurons, effects that w

13 n long-term potentiation in hippocampal area cornu ammonis 1 and on hippocampus-dependent contextual

14 amygdala, temporopolar cortex, and subiculum/cornu ammonis 1 hippocampal subfields.

15 Strikingly, cornu ammonis 1 NMDAR surface trafficking controls basal

16 is in coronal sections of the midhippocampus cornu ammonis 1 or subiculum, is an important pathology

17 d that NCLX knockdown within the hippocampal cornu ammonis 1 region in vivo causes substantial neurod

18 nal cell death in the lateral septum and the cornu ammonis 1 region of hippocampus after pilocarpine-

19 on was studied using field recordings in the cornu Ammonis 1 region of slices that were perfused with

20 The cornu ammonis 1 region of the hippocampus (CA1) sector o

21 ase only (control vector) were injected into cornu ammonis 1 region of the hippocampus 15 hours befor

22 We show that HSP72 overexpression protects cornu ammonis 1 region of the hippocampus neurons from g

23 of HSP72 in vivo and in vitro: (1) protected cornu ammonis 1 region of the hippocampus neurons from g

24 neocortex, sister excitatory neurons in the cornu ammonis 1 region of the hippocampus rarely develop

25 owed that neuronal injury in the hippocampal cornu ammonis 1 region was alleviated with LIP ultrasoun

26 ssion of growth-associated protein-43 in the cornu ammonis 1 region.

27 term potentiation at the Schaffer collateral/cornu ammonis 1 synapse in the dorsal hippocampus.

28 ermore, synaptic activity at cornu ammonis 3-cornu ammonis 1 synapses was significantly lower in AC3

29 n for E2-induced potentiation at hippocampal cornu ammonis 1 synapses.

30 of brain matter loss in the left hippocampal cornu ammonis 1 to cornu ammonis 3 and subiculum.

31 ivo medial temporal lobe volumes (subiculum, cornu ammonis 1) and cortical thickness (entorhinal cort

32 sk performance were significantly related to cornu ammonis 1-2 (CA1-CA2) stiffness (p = 0.018 and p =

33 Here, human hippocampal subfield (subiculum, cornu ammonis 1-3, and dentate gyrus) targets of immunom

34 ss all participants in the left hippocampus (cornu ammonis 1-3, dentate gyrus), parahippocampus (pres

35 all 4 neocortical regions, cornu ammonis 3, cornu ammonis 1/subiculum, and the entorhinal cortex spe

36 image taurine loss from the vulnerable CA1 (cornus ammonis 1) sector of the rat hippocampus followin

37 hyl-D-aspartate (0.12 M) lesions through the cornu ammonis-1 (CA1) field (7 microl in five sites), ma

38 The hippocampal cornu ammonis 2 (CA2) region is unique in being the only

39 The dorsal cornu ammonis 2 (dCA2) region of the hippocampus enables

40 aser-microdissected stratum oriens tissue of cornu ammonis 2/3 (CA2/3) and CA1 postmortem human hippo

41 ced hippocampal atrophy, including subfields cornu ammonis 2/3 (CA2/3) and CA4/dentate gyrus (DG), as

42 with the most prominent differences being in cornu ammonis 2/3 (P < .001).

43 Pathologically, cornu ammonis 2/3 hippocampal neuronal loss appears to b

44 Here, we propose a computational model of cornu ammonis 3 (CA3) and dentate gyrus (DG), where sens

45 blocked, norepinephrine reduces hippocampal cornu ammonis 3 (CA3) epileptiform activity through alph

46 dence from model organisms suggests that the cornu ammonis 3 (CA3) hippocampal subfield supports rece

47 hange in homeostatic plasticity processes in cornu ammonis 3 (CA3), accompanied by increased activity

48 ation-to-inhibition ratio in the hippocampal cornu ammonis 3 (CA3)-CA1 subcircuit toward hyperexcitab

49 ance and stiffness of both the dentate gyrus-cornu ammonis 3 (DG-CA3; p = 0.016) and subiculum (SUB;

50 lutamatergic activity in ventral hippocampal cornu ammonis 3 (vCA3) 1 week after injection.

51 s in the left hippocampal cornu ammonis 1 to cornu ammonis 3 and subiculum.

52 , we examined the time-dependent role of the cornu ammonis 3 DH subregion (dCA3) in cocaine-memory re

53 he stratum lacunosum, the dentate gyrus, and cornu ammonis 3 of the hippocampus, striatum, thalamus,

54 beta loads across all 4 neocortical regions, cornu ammonis 3, cornu ammonis 1/subiculum, and the ento

55 These relationships were specific to the Cornu Ammonis 3, Cornu Ammonis 4, dentate gyrus, and sub

56 Furthermore, synaptic activity at cornu ammonis 3-cornu ammonis 1 synapses was significant

57 tients with low-normal VitB12, mainly in the cornu ammonis 4 and dentate gyrus region (P= 0.029), whi

58 nships were specific to the Cornu Ammonis 3, Cornu Ammonis 4, dentate gyrus, and subiculum subfields.

59 ted tau accumulation in pyramidal neurons in cornu ammonis and in neocortical neurons.

60 This study demonstrates that the cornu ammonis area 1 (CA1) is capable of generating intr

61 at IPC in vivo increased tPA activity in the cornu ammonis area 1 (CA1) layer and Akt phosphorylation

62 The cornu ammonis area 1 (CA1) of the hippocampus receives g

63 In cornu ammonis area 1 hippocampal slices from wild-type m

64 frequency of pathological discharges in the Cornu Ammonis area 3 (CA3) area of freely moving epilept

65 amma frequency inputs from upstream regions (cornu ammonis area 3 and medial entorhinal cortex) and g

66 There was progressive loss of neurons in the cornu ammonis (CA) 1 and CA3 subfields of the hippocampu

67 alysis revealed selective volume loss in the cornu ammonis (CA) 1 region of the hippocampus in RRMS w

68 ell depletion and concomitant gliosis in the cornu Ammonis (CA) 1, CA2, CA3, and hilus.

69 Volumes of hippocampal subfields cornu ammonis (CA) 2+3, CA4+dentate gyrus, and subiculum

70 of spontaneous epileptiform burst firing in cornu ammonis (CA) 3 pyramidal neurons in brain slices.

71 ion and long-term synaptic plasticity at the Cornu Ammonis (CA) 3-CA1 synapses.

72 crostructural alterations in the hippocampal cornu ammonis (CA) 4 and dentate gyrus region, whereas C

73 The cornu ammonis (CA) fields 2 and 3 and the dentate gyrus

74 in the dentate gyrus and astrogliogenesis in Cornu Ammonis (CA) hippocampal subfields of rats, and wh

75 eakly detected in the dentate gyrus (DG) and Cornu Ammonis (CA) of the macaque hippocampus, whereas i

76 Hippocampal sharp-wave ripples (SWRs) in the cornu ammonis (CA) region and dentate spikes (DSs) in th

77 eptors (OXRs) and GPR103 particularly in the cornu ammonis (CA) subfield from AD patients suffering f

78 d consists of several subfields, such as the cornu ammonis (CA) subfields CA1-4, the dentate gyrus (D

79 Patient groups had smaller cornu ammonis (CA) subfields CA2/3 (left, p = 7.2 x 10(-

80 ne) was used to manually segment hippocampal cornu ammonis (CA) subfields, dentate gyrus (DG), and th

81 y/cognitive function [hippocampus proper, or cornu ammonis (CA), and dentate gyrus (DG)].

82 e gyrus (DG) and dendritic remodeling in the cornu ammonis (CA), particularly the CA3 subfield.

83 ropil and cell layer volumes were reduced in cornu ammonis (CA)1 and dentate gyrus (DG) of the anteri

84 e attrition of dendrite arbors and spines in Cornu Ammonis (CA)1 pyramidal neurons and exacerbated be

85 ip), decreased, and pyramidal neurons of the cornu-ammonis (CA) subfields showed the highest variatio

86 Trem2, developing neurons in the hippocampal cornus ammonis (CA)1 but not in CA3 subfield displayed c

87 hippocampal formation (the dentate gyus, the cornu ammonis [CA] fields 1, 2, and 3 and the subiculum)

88 in the hippocampal region, specifically the cornu Ammonis (CA1) region.

89 thin the transentorhinal region but also the cornu ammonis (CA1) subfield.

90 ts or medicated MDD participants and a lower cornu ammonis (CA1-3) volume in the hippocampal body sub

91 in principal hippocampal substructures: the cornu ammonis (CA1-CA4), dentate gyrus, and subiculum.

92 specifically in the right subiculum and left cornu ammonis (CA3).

93 major portions of the hippocampal formation (cornu Ammonis, dentate gyrus, subicular complex, and ent

94 roanterior hypothalamic nucleus (LA) and the cornu ammonis field 1 (CA1) of the dorsal hippocampus an

95 Specifically, place cells from dorsal cornu ammonis field 1 (CA1) were recorded while rats sea

96 cations) of place cells recorded from dorsal Cornu Ammonis field 1 in rats foraging freely on a novel

97 magnitude of Schaffer collateral/commissural-Cornu Ammonis field 1 long-term potentiation in vitro, a

98 d excitatory synapses between the DG and the cornu ammonis field 3 (CA3) field of the hippocampus wer

99 ayer (GL), hilus of the dentate gyrus (DGH), cornu ammonis fields (CA)2/3, CA1, and subiculum (SUB)].

100 rya of neurons in sectors CA3 and CA4 of the cornu Ammonis, less intensive staining in the cytoplasm

101 in Purkinjie cells in the cerebellum and the cornu ammonis of the hippocampus.

102 midbrain and agranular retrosplenial cortex; Cornu Ammonis receives input from a single class of pres

103 Specifically, we determined the cornu ammonis region 1 (CA1) field excitatory postsynapt

104 educed in Alzheimer disease (AD) hippocampal cornu ammonis region 1, but not in the thalamus or occip

105 y postsynaptic potential (fEPSP) response to cornu ammonis region 3 (CA3) stimulation and examined th

106 EC originated from pyramidal neurons in the cornu ammonis region CA1 and the subiculum.

107 he presence of the CA2 and CA4 fields of the cornu Ammonis region.

108 oplasmic inclusions in the dentate gyrus and cornu ammonis regions 1 and 2 of patients with normal co

109 re neuronal inclusions in the dentate gyrus, cornu ammonis regions 1, 2 and 4, and the subiculum comp

110 cytoplasmic inclusions in the dentate gyrus, cornu ammonis regions 1-4 and entorhinal cortex.

111 naptic loop-comprising the dentate gyrus and cornu ammonis regions CA3 and CA1-and back to cortex, wh

112 ow directional information is encoded in the cornu ammonis remains unresolved.

113 ramidal cell layers, reduced somal volume in cornu ammonis sector 2/3, reduced number of somatostatin

114 We observed increases in bilateral cornu ammonis volume (CA1-3) following the 3 months comp