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

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

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

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

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

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

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

12 Strikingly, cornu ammonis 1 NMDAR surface trafficking controls basal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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