ライフサイエンスコーパス: hippocampal pyramidal cell

1 in controlling the rate, burst and timing of hippocampal pyramidal cells.

2 age gradient for fast synaptic inhibition in hippocampal pyramidal cells.

3 rents by the muscarinic agonist carbachol in hippocampal pyramidal cells.

4 es at the GABAergic synapses in dendrites of hippocampal pyramidal cells.

5 e slightly fewer dendritic spines in the CA1 hippocampal pyramidal cells.

6 utside-out patches from acutely isolated CA1 hippocampal pyramidal cells.

7 es dendritic hyperexcitability in entorhinal-hippocampal pyramidal cells.

8 AMPA receptor-mediated synaptic responses in hippocampal pyramidal cells.

9 he biophysical and integrative properties of hippocampal pyramidal cells.

10 l patch clamp techniques on acutely isolated hippocampal pyramidal cells.

11 s back-propagate into the dendritic arbor of hippocampal pyramidal cells.

12 te in small spots along the dendrites of CA1 hippocampal pyramidal cells.

13 imulation of the Schaffer collaterals in CA1 hippocampal pyramidal cells.

14 F) mRNA levels occurred in granule cells and hippocampal pyramidal cells.

15 of dentate granule cells, hilar neurons, and hippocampal pyramidal cells.

16 te granule cells, dentate hilar neurons, and hippocampal pyramidal cells.

17 ows brief membrane depolarization in rat CA1 hippocampal pyramidal cells, a process called depolariza

18 In hippocampal pyramidal cells, a prominent elevation of Ca

19 In hippocampal pyramidal cells, a rise in Ca(2+) releases e

20 pecific gamma oscillations, implemented onto hippocampal pyramidal cells along their somato-dendritic

21 Hippocampal pyramidal cells also exhibit spatial selecti

22 In hippocampal pyramidal cells, AMPA receptors are heterome

23 translation of GluA1-4 mRNAs in dendrites of hippocampal pyramidal cells and CA1 interneurons but not

24 ligands are synthesized by neurons, such as hippocampal pyramidal cells and cerebellar granule cells

25 een described for principal neurons, such as hippocampal pyramidal cells and cerebellar Purkinje cell

26 By using both immunofluorescence of cultured hippocampal pyramidal cells and EM postembedding immunog

27 uses a rapid exocytosis of AMPA receptors in hippocampal pyramidal cells and is constitutively requir

28 We found that many hippocampal pyramidal cells and most interneurons discha

29 the spatial signal carried by the firing of hippocampal pyramidal cells and specifically reduces the

30 ound transform the integrative capacities of hippocampal pyramidal cells and their dendrites.

31 l-4-isoxazole propionate (AMPA) receptors in hippocampal pyramidal cells, and on glutamate transporte

32 Hippocampal pyramidal cells are called place cells becau

33 Many hippocampal pyramidal cells are scattered in the plexifo

34 ecific intracellular immunoreactive sites in hippocampal pyramidal cells, astroglia, and in microglia

35 y TBPB potentiates NMDA receptor currents in hippocampal pyramidal cells but does not alter excitator

36 ptors increases membrane excitability in CA1 hippocampal pyramidal cells by reducing the slow calcium

37 from the soma into dendrites was studied in hippocampal pyramidal cells by simultaneous extracellula

38 Hippocampal pyramidal cells can be divided into place ce

39 Here we find that the spike times of hippocampal pyramidal cells can be predicted more accura

40 rominent injury to dentate hilar neurons and hippocampal pyramidal cells, dentate granule cells of an

41 rchitecture and lineage relationships of the hippocampal pyramidal cells, dentate granule cells, and

42 ing KA administration, the large majority of hippocampal pyramidal cells die in the FVB/N (FVB) mouse

43 stargazin lacking the PDZ-binding domain in hippocampal pyramidal cells disrupts synaptic AMPA recep

44 In hippocampal pyramidal cells, dopamine acts at D1 recepto

45 semble activity correlations expressed among hippocampal pyramidal cells during behavior persists dur

46 The correlated activity of rat hippocampal pyramidal cells during sleep reflects the ac

47 Place fields of hippocampal pyramidal cells expand asymmetrically when a

48 ial segment (AIS) in low-density cultures of hippocampal pyramidal cells following GABAergic and glut

49 ts indicate that the amplitude of the AHP in hippocampal pyramidal cells from aged animals is depende

50 By contrast, the firing of hippocampal pyramidal cells from slices of the same age

51 In the actively foraging rat, hippocampal pyramidal cells have strong spatial correlat

52 rescue using whole-cell recordings from CA1 hippocampal pyramidal cells in brain slices.

53 s inhibition of the M-current in rat CA1/CA3 hippocampal pyramidal cells in primary neuron cultures.

54 conducted in excised patches collected from hippocampal pyramidal cells indicated that thiocyanate d

55 The firing of rat hippocampal pyramidal cells is determined both by the an

56 GluR-induced change in the firing pattern of hippocampal pyramidal cells is thus the result of multip

57 hat KChIP2, which is abundantly expressed in hippocampal pyramidal cells, is essential for IA regulat

58 s recorded from both below and above the CA1 hippocampal pyramidal cell layer became highly coherent.

59 ty and mRNA are found at lower levels in the hippocampal pyramidal cell layer, dentate granule cell l

60 lopregnanolone administration on spontaneous hippocampal pyramidal cell neural activity.

61 The inhibition of hippocampal pyramidal cells occurs via inhibitory intern

62 lta GABA(A) receptors (GABARs) occurs in the hippocampal pyramidal cells of female mice at pubertal o

63 eptors (mGluRs), are shown to coexist in CA1 hippocampal pyramidal cells of juvenile (11-35 day-old)

64 e genes undergo a sustained up-regulation in hippocampal pyramidal cells only of mice and rats that h

65 Hippocampal pyramidal cells (PCs) express many GABAAR su

66 he synaptic excitation and inhibition of CA1 hippocampal pyramidal cells (PCs), cells known to partic

67 The dendritic trees of hippocampal pyramidal cells play important roles in the

68 otentials back-propagating into dendrites of hippocampal pyramidal cells provide sufficient postsynap

69 The activity of hippocampal pyramidal cells reflects both the current po

70 The phase of spikes of hippocampal pyramidal cells relative to the local field

71 and GABA-negative dentate hilar neurons and hippocampal pyramidal cells remained immunonegative.

72 Tests in CA1 hippocampal pyramidal cells reveal that a slow AHP is re

73 Cerebellar Purkinje cells and hippocampal pyramidal cells revealed substantial immunor

74 Modeling experiments in CA1 hippocampal pyramidal cells revealed that both mutations

75 atch clamp recordings of acutely dissociated hippocampal pyramidal cells revealed that the D1 dopamin

76 Hippocampal pyramidal cells show high expression of alph

77 However, in isolated hippocampal pyramidal cells, simulated ischaemia evokes

78 Here we show in mouse hippocampal pyramidal cells that LTP at individual synap

79 f the presynaptic contacts between a pair of hippocampal pyramidal cells that used biologically reali

80 In CA1 hippocampal pyramidal cells, the fAHP is carried by the

81 c transmission in retinal ganglion cells and hippocampal pyramidal cells to determine, at a cellular

82 xtrinsic factors modulate the sensitivity of hippocampal pyramidal cells to kainic acid.

83 f glutamate receptors in distal dendrites of hippocampal pyramidal cells triggers voltage-dependent C

84 In the brain, hippocampal pyramidal cells use temporal as well as rate

85 The activity of hippocampal pyramidal cells was recorded while adult (10

86 was insufficient to injure hilar neurons and hippocampal pyramidal cells, was nonetheless sufficient

87 ndritic and axonal arbors of biocytin-filled hippocampal pyramidal cells were reconstructed.

88 e pyramidal layers of cortex, and changes in hippocampal pyramidal cells were smaller.

89 entate granule cells, hilar mossy cells, and hippocampal pyramidal cells, were devoid of detectable S

90 Transfection of CA3 hippocampal pyramidal cells with BoNtE-resistant SNAP-25

91 The spike timing of hippocampal pyramidal cells with respect to the theta rh