ライフサイエンスコーパス: pyramidale

1 eep compared to superficial layer of stratum pyramidale.

2 the organization of the hippocampal stratum pyramidale.

3 rvalbumin-expressing cells mostly in stratum pyramidale.

4 ks and sources were localized to the stratum pyramidale.

5 d elongate rapidly within strata lucidum and pyramidale.

6 des were carried out in stratum radiatum and pyramidale.

7 1, ripples have maximum amplitude in stratum pyramidale.

8 pendent changes in neuron density in stratum pyramidale.

9 on their radial position within the stratum pyramidale.

10 isomatic perineuronal net in the CA2 stratum pyramidale.

11 pression was found mainly in the stratum (s) pyramidale (29-37%) and s. oriens (20-25%).

12 8%) and CA1 stratum oriens (78.87%), stratum pyramidale (40%), and stratum radiatum (56.6%).

13 rotection or increased damage in the stratum pyramidale 7 days after reperfusion.

14 This group was found in or near the stratum pyramidale and had axonal projections almost exclusively

15 d hippocampal CA1 field potentials in strata pyramidale and radiatum and assessed neuroplasticity by

16 synaptic sites on CA1 neurons in the stratum pyramidale and stratum oriens layers of KO hippocampus m

17 increases could be detected in both stratum pyramidale and stratum radiatum in area CA1.

18 and the slope of EPSP recorded from stratum pyramidale and stratum radiatum respectively.

19 hest density in the CA1 strata alveus/oriens/pyramidale and the dentate hilus.

20 GLAST staining was highest along the stratum pyramidale and was especially prominent in astrocytes at

21 otential oscillation recorded in the stratum pyramidale, and concomitantly recorded action potentials

22 strocytes in CA1 s. radiatum, CA2 and CA3 s. pyramidale, and molecular layer of the DG, was increased

23 ls), which terminate in the strata radiatum, pyramidale, and oriens, are present throughout the entir

24 rked loss of SP fibers in the strata oriens, pyramidale, and radiatum of the CA3a and CA2 subfields.

25 1 predominantly expressed in the CA3 stratum pyramidale, and ZIP3 primarily localized to the stratum

26 l, but not vertical, clusters in the stratum pyramidale, as revealed by both cell-type-specific retro

27 up to 150 neurons in the hippocampal stratum pyramidale at approximately 1-mm depth within an intact

28 f putative excitatory neurons in CA1 stratum pyramidale based on waveform sorting and validated via o

29 when stimulating in the strata radiatum and pyramidale but not in the stratum oriens.

30 The zeta-potentials of the CA1 stratum pyramidale, CA3 stratum pyramidal, and dentate gyrus are

31 urons in the superficial sublayer of stratum pyramidale displayed larger post-synaptic responses at e

32 ve current sources restricted to the stratum pyramidale during SWRs originate from the synaptic outpu

33 In contrast, stratum pyramidale fast-spiking PV cells do not appear affected.

34 s and nearby interneurons in the CA1 stratum pyramidale has been strongly implicated on the basis of

35 e primarily located in the stratum oriens or pyramidale, have sparsely spiny dendrites, and do not ty

36 lls and PV bistratified cells in the stratum pyramidale; in stratum oriens, HC PV cells were electrop

37 es of hippocampal stratum oriens and stratum pyramidale inhibitory interneurones, before and followin

38 ic IPSPs, dendritic burst firing and stratum pyramidale interneuron activity were all temporally corr

39 siological recordings were made from stratum pyramidale interneurons in which morphology and Kv3.1b-p

40 gest that spatial selectivity of CA1 stratum pyramidale interneurons is inherited from a small cluste

41 were identified using the GIN mice: stratum pyramidale interneurons with lacunosum-moleculare axon a

42 rom pyramidal cells and fast-spiking stratum pyramidale interneurons, we demonstrate that fast gamma

43 minent sprouting was seen in the CA3 stratum pyramidale layer in all rats having 15 daily seizures, r

44 abeling, Purkinje cells, hippocampal stratum pyramidale, locus coeruleus (alpha3); alpha4- discrete l

45 (1) receptor immunoreactivity in the stratum pyramidale neuropil and dentate gyrus inner molecular la

46 active neurons express GFR alpha-1 in the s. pyramidale of CA1 (72%), CA2 (70%) and CA3 (70%) subfiel

47 nificant reductions in the strata oriens and pyramidale of CA1, the stratum pyramidale of CA3, and th

48 ta oriens and pyramidale of CA1, the stratum pyramidale of CA3, and the dentate hilus.

49 atum of CA1, the strata oriens, radiatum and pyramidale of CA3, the dentate molecular layer, and the

50 cording the extracellular response from str. pyramidale of CA3.

51 -sensitive microelectrodes placed in stratum pyramidale of hippocampal subfield CA1.

52 u hybridization revealed that within stratum pyramidale of the CA1 area, mRNA expression of the Ca(v)

53 to the oscillations recorded in the stratum pyramidale of the CA1 region.

54 ular layer of the dentate gyrus, the stratum pyramidale of the CA1 subregion and subiculum, while the

55 entials and unit activity in the CA1 stratum pyramidale of the hippocampus in the behaving wild-type

56 urons, primarily in or bordering the stratum pyramidale, produced slow membrane potential (0.04 Hz) o

57 of GABAergic terminals at the stratum oriens-pyramidale (SO-SP) or stratum lacunosum-molecular (S-L-M

58 ndex of neuronal activation) in dCA3 stratum pyramidale (SP) glutamatergic and GABAergic neurons and

59 of dorsal CA1 (dCA1) neurons in the stratum pyramidale (SP) in head-fixed mice performing a go-no go

60 most of their axonal arbours in the stratum pyramidale (SP).

61 SCs) on non-pyramidal neurons in the stratum pyramidale (SP).

62 al-field potential recorded from the stratum pyramidale, stratum radiatum, and stratum lacunosum mole

63 d axons that ramified throughout the stratum pyramidale, suggesting that they are responsible for the

64 sleep/rest, we identified ripples in stratum pyramidale that feature current sinks in stratum radiatu

65 the superficial sublayer of the CA1 stratum pyramidale to whole-population activity.

66 ent, a current was injected into the stratum pyramidale via a tungsten electrode positioned within 15

67 NT-3 mRNA expression in CA2 s. pyramidale was increased by 80.0%, and CNN increased the

68 gamma oscillations generated around stratum pyramidale, where basket cells selectively innervate pyr