ライフサイエンスコーパス: moleculare

1 st immunoreactivity in the stratum lacunosum-moleculare.

2 ns were restricted primarily to s. lacunosum-moleculare.

3 t not in interneurons from stratum lacunosum-moleculare.

4 i.e. the local network of stratum lacunosum-moleculare.

5 information processing of stratum lacunosum-moleculare.

6 essed in the postnatal CA1 stratum lacunosum-moleculare.

7 stratum radiatum, and the stratum lacunosum-moleculare.

8 der between str. radiatum and str. lacunosum-moleculare.

9 both stratum radiatum and stratum lacunosum-moleculare.

10 they selectively innervate stratum lacunosum-moleculare.

11 axonal projections to the stratum lacunosum-moleculare.

12 abeling was highest in the stratum lacunosum-moleculare.

13 ly in stratum radiatum and stratum lacunosum moleculare.

14 all other laminae, notably stratum lacunosum-moleculare.

15 ular layer and hippocampal stratum lacunosum moleculare.

16 response which again had a source in stratum moleculare.

17 n of CA2/3 basket cells in stratum lacunosum moleculare (33% of length, 29% surface, and 24% synaptic

18 ites project deep into the stratum lacunosum-moleculare, a distance several hundred micrometres in ex

19 acilitating inputs onto 7/7 oriens-lacunosum moleculare and 5/5 burst firing, sparsely spiny neocorti

20 otoxin-positive neurons in stratum lacunosum-moleculare and decreased numbers in stratum oriens.

21 s located at the border of stratum lacunosum-moleculare and stratum radiatum.

22 ls target specifically the stratum lacunosum-moleculare and the dentate gyrus, but lack postsynaptic

23 tected in CA1/CA3 stratum radiatum/lacunosum moleculare and the dentate gyrus.

24 Within stratum lacunosum-moleculare and the superficial stratum radiatum, GIRK1-I

25 source in the most distal dendrites (stratum moleculare) and a sink near the cell body layer.

26 Interneurons in CA1/CA3 stratum radiatum and moleculare, and in the hilus region of the dentate gyrus

27 us, CA-3 stratum radiatum, stratum lacunosum moleculare, and presubiculum.

28 rimary theta dipole in CA1 stratum lacunosum moleculare, are conveyed by the temporoammonic pathway.

29 of oriens/alveus interneurons with lacunosum-moleculare axon arborization (O-LM cells).

30 ratum pyramidale interneurons with lacunosum-moleculare axon arborization (P-LM cells) and stratum ra

31 stratum radiatum interneurons with lacunosum-moleculare axon arborization (R-LM cells).

32 ns at the stratum radiatum-stratum lacunosum-moleculare border (R-LM interneurons) of the CA1 area ma

33 adiatum to its border with stratum lacunosum-moleculare, both fate maps of pioneer cells labeled with

34 ted neuromodulation of the stratum lacunosum-moleculare by directly comparing the properties of CXCR4

35 n CA1 stratum radiatum and stratum lacunosum-moleculare (CA1-SRLM)--two monosynaptically connected st

36 ort days decreased apical (stratum lacunosum-moleculare) CA1 spine density, as well as increased basi

37 currents from hippocampal stratum lacunosum-moleculare Cajal-Retzius cells of the CXCR4-EGFP mouse.

38 preferential innervation of oriens-lacunosum moleculare cells (OLMs) through dendritic synapses.

39 eceive GABAergic input from oriens lacunosum-moleculare cells and that this input has different physi

40 o-axonic, bistratified, and oriens-lacunosum moleculare cells, innervating different domains of pyram

41 pes--basket, axo-axonic and oriens-lacunosum-moleculare cells--visualized and defined by synaptic con

42 th signals, while those in stratum lacunosum-moleculare exclusively receive a glutamatergic signal.

43 Interneurons in stratum radiatum/lacunosum-moleculare express KARs both with and without the GluR5

44 ta-adrenergic receptors in stratum lacunosum-moleculare GABAergic networks reduces electrical synapti

45 area of this pathway, the stratum lacunosum-moleculare, has the highest concentration of dopamine re

46 he parietal sensory barrel fields, lacunosum moleculare hippocampi, and specific nuclei of the rostra

47 us Nissl-stained structures in CA1 lacunosum/moleculare in the adult.

48 o striatum radiatum or to striatum lacunosum-moleculare in the case of slow cells, suggesting targeti

49 tion, AA blocked st. oriens-alveus-lacunosum-moleculare interneuron transient currents but not curren

50 in paired recordings from stratum lacunosum-moleculare interneurons by approximately 40%.

51 coupling was abolished in stratum lacunosum-moleculare interneurons from knockout animals, epileptif

52 eceptor-mediated events in stratum lacunosum moleculare interneurons of the rat hippocampus.

53 y slow synaptic input from stratum lacunosum-moleculare interneurons, anatomically identified as neur

54 as absent in EGFP-negative stratum lacunosum-moleculare interneurons.

55 sy fiber (MF) synapses on area CA3 lacunosum-moleculare (L-M) interneurons are capable of undergoing

56 , we demonstrate MF LTP in stratum lacunosum-moleculare (L-M) interneurons induced by the same stimul

57 somata in strata radiatum (R) and lacunosum-moleculare (L-M) receive converging stimulation from the

58 of voltage-activated K+ current on lacunosum/moleculare (L/M) hippocampal interneurons, but not on CA

59 ons in SYN immunoreactivity in CA3 lacunosum-moleculare (LM) relative to either young controls or age

60 es of oriens interneurones, oriens lacunosum-moleculare (O-LM) and trilaminar cells, showed prominent

61 Oriens-lacunosum/moleculare (O-LM) cells are inhibitory cells in the hipp

62 erneurons, corresponding to oriens-lacunosum moleculare (O-LM) cells.

63 rizations (ADPs) of stratum oriens-lacunosum moleculare (O-LM) interneurones.

64 Excitatory synapses onto oriens-lacunosum moleculare (O-LM) interneurons are facilitating and have

65 vity of pyramidal cells and oriens-lacunosum-moleculare (O-LM) interneurons during ripples.

66 Oriens-lacunosum moleculare (O-LM) interneurons have been implicated as c

67 mGluR1-mediated EPSCs from oriens-lacunosum moleculare (O-LM) interneurons in acute hippocampal slic

68 In particular, the oriens lacunosum-moleculare (O-LM) interneurons were shown to synapse on

69 s has been characterized in oriens-lacunosum moleculare (O-LM) interneurons, which express parvalbumi

70 ivergence among hippocampal oriens-lacunosum moleculare (O-LM) projecting interneurons that have hith

71 d presynaptic interneurone, oriens-lacunosum moleculare (O-LMC), basket (BC), axo-axonic (AAC), bistr

72 ation of ChR2-labeled fibers in s. lacunosum-moleculare of CA1 and the dentate molecular layer elicit

73 intense activation of the stratum lacunosum-moleculare of CA1 and the subiculum, contrasting with ba

74 en the CA1 strata radiatum and the lacunosum moleculare of CA1 subfield.

75 ral septum, diagonal band, stratum lacunosum-moleculare of CA1, and various nuclei of the amygdala an

76 of the dentate gyrus, and stratum lacunosum-moleculare of field CA1 of Ammon's horn.

77 its normal position in the stratum lacunosum-moleculare of field CA2 to an alvear position in SRK.

78 n the strata oriens, radiatum, and lacunosum-moleculare of hippocampal CA1 and CA3 regions and in the

79 t path termination zone in stratum lacunosum-moleculare of the CA1 area as well as equivalent portion

80 al interneurons located in stratum lacunosum-moleculare of the CA1 hippocampus.

81 esses were also present in stratum lacunosum-moleculare of the CA1 region and all layers of the CA3 r

82 The stratum lacunosum-moleculare of the hippocampus is an area of integration

83 e dentate gyrus and in the stratum lacunosum-moleculare of the subfield CA3.

84 al dendritically projecting oriens lacunosum moleculare (OLM) cells.

85 ons [pyramidal, basket, and oriens-lacunosum moleculare (OLM) cells] generated theta and gamma oscill

86 that TRPV1 is expressed in oriens-lacunosum-moleculare (OLM) interneurons in the hippocampus, and pr

87 In contrast, in CA1 oriens lacunosum moleculare (OLM) interneurons, which do not contain any

88 (P < 0.005) and within the stratum lacunosum moleculare (P < 0.01), the stratum radiatum (P < 0.005),

89 potential implications for stratum lacunosum-moleculare processing of information in vivo, will be al

90 interneurons projecting to stratum lacunosum-moleculare (representing somatostatin/mGlu(1a)-expressin

91 Stratum lacunosum-moleculare (SL-M) stimuli that activate GABA(A,slow) inh

92 at the border between the stratum lacunosum-moleculare (SLM) and the SR (2).

93 ndria accumulations in the stratum lacunosum moleculare (SLM) layer, without loss of endogenous nucle

94 stratum radiatum (SR), and stratum lacunosum-moleculare (SLM).

95 electrical stimulus of the stratum lacunosum-moleculare (SLM, which contains the PP) had on excitatio

96 uropil layer [CA1-stratum radiatum lacunosum moleculare (SRLM)] thickness, and (ii) activity in ERC a

97 d dendritic development in stratum lacunosum-moleculare, thus impacting the integrative properties of

98 Light delivered to stratum lacunosum-moleculare triggered EPSCs both on local interneurons an

99 he synaptic network of the stratum lacunosum-moleculare via excitatory GABAergic input.

100 r axons which projected to stratum lacunosum-moleculare where they ramified extensively, in the regio

101 to dendritic spines in the stratum lacunosum-moleculare, which form synapses with presynaptic entorhi

102 ippocampal interneurons of stratum lacunosum-moleculare with different excitability is a novel findin