ライフサイエンスコーパス: stratum lacunosum-moleculare

1 but more frequently in stratum radiatum and stratum lacunosum moleculare.

2 gyrus outer molecular layer and hippocampal stratum lacunosum moleculare.

3 f the hippocampus, i.e. the local network of stratum lacunosum-moleculare.

4 ut that may impact information processing of stratum lacunosum-moleculare.

5 ha) is highly expressed in the postnatal CA1 stratum lacunosum-moleculare.

6 d distal thirds of stratum radiatum, and the stratum lacunosum-moleculare.

7 ratum radiatum, but not in interneurons from stratum lacunosum-moleculare.

8 and displaced into both stratum radiatum and stratum lacunosum-moleculare.

9 to O-LM cell, as they selectively innervate stratum lacunosum-moleculare.

10 um oriens, and had axonal projections to the stratum lacunosum-moleculare.

11 Terminal labeling was highest in the stratum lacunosum-moleculare.

12 n the neuropil in all other laminae, notably stratum lacunosum-moleculare.

13 on, with the highest immunoreactivity in the stratum lacunosum-moleculare.

14 dritic arborization of CA2/3 basket cells in stratum lacunosum moleculare (33% of length, 29% surface

15 e the apical dendrites project deep into the stratum lacunosum-moleculare, a distance several hundred

16 pus, particularly in the highly vascularized stratum lacunosum moleculare and stratum moleculare laye

17 125)I]alpha-bungarotoxin-positive neurons in stratum lacunosum-moleculare and decreased numbers in st

18 ls and interneurons located at the border of stratum lacunosum-moleculare and stratum radiatum.

19 Cajal-Retzius cells target specifically the stratum lacunosum-moleculare and the dentate gyrus, but

20 Within stratum lacunosum-moleculare and the superficial stratum

21 in the dentate gyrus, CA-3 stratum radiatum, stratum lacunosum moleculare, and presubiculum.

22 ving rise to the primary theta dipole in CA1 stratum lacunosum moleculare, are conveyed by the tempor

23 on-principal neurons at the stratum radiatum-stratum lacunosum-moleculare border (R-LM interneurons)

24 ate from stratum radiatum to its border with stratum lacunosum-moleculare, both fate maps of pioneer

25 SDF-1 alpha-mediated neuromodulation of the stratum lacunosum-moleculare by directly comparing the p

26 rtex (ERC) and then CA1 stratum radiatum and stratum lacunosum-moleculare (CA1-SRLM)--two monosynapti

27 Short days decreased apical (stratum lacunosum-moleculare) CA1 spine density, as well

28 spontaneous action currents from hippocampal stratum lacunosum-moleculare Cajal-Retzius cells of the

29 adiatum receive both signals, while those in stratum lacunosum-moleculare exclusively receive a gluta

30 , activation of beta-adrenergic receptors in stratum lacunosum-moleculare GABAergic networks reduces

31 The termination area of this pathway, the stratum lacunosum-moleculare, has the highest concentrat

32 ation of GABA(A) receptor-mediated events in stratum lacunosum moleculare interneurons of the rat hip

33 ion-based coupling in paired recordings from stratum lacunosum-moleculare interneurons by approximate

34 lthough electrical coupling was abolished in stratum lacunosum-moleculare interneurons from knockout

35 litude, kinetically slow synaptic input from stratum lacunosum-moleculare interneurons, anatomically

36 3100 (1 muM) and was absent in EGFP-negative stratum lacunosum-moleculare interneurons.

37 Here, we demonstrate MF LTP in stratum lacunosum-moleculare (L-M) interneurons induced

38 sinks in stratum radiatum (Rad(sink)) versus stratum lacunosum-moleculare (LM(sink)).

39 stimulation of temperoammonic (TA) inputs to stratum lacunosum moleculare of hippocampal area CA1 het

40 he stratum pyramidale, stratum radiatum, and stratum lacunosum moleculare of the CA1 subregion, consi

41 ttern consisted of intense activation of the stratum lacunosum-moleculare of CA1 and the subiculum, c

42 us coeruleus, lateral septum, diagonal band, stratum lacunosum-moleculare of CA1, and various nuclei

43 putamen, the hilus of the dentate gyrus, and stratum lacunosum-moleculare of field CA1 of Ammon's hor

44 r calretinin from its normal position in the stratum lacunosum-moleculare of field CA2 to an alvear p

45 ating the perforant path termination zone in stratum lacunosum-moleculare of the CA1 area as well as

46 between hippocampal interneurons located in stratum lacunosum-moleculare of the CA1 hippocampus.

47 ew KT-labeled processes were also present in stratum lacunosum-moleculare of the CA1 region and all l

48 The stratum lacunosum-moleculare of the hippocampus is an ar

49 ecular layer of the dentate gyrus and in the stratum lacunosum-moleculare of the subfield CA3.

50 the dentate gyrus (P < 0.005) and within the stratum lacunosum moleculare (P < 0.01), the stratum rad

51 gether with their potential implications for stratum lacunosum-moleculare processing of information i

52 aining cells) and interneurons projecting to stratum lacunosum-moleculare (representing somatostatin/

53 Stratum lacunosum-moleculare (SL-M) stimuli that activat

54 quitin and mitochondria accumulations in the stratum lacunosum moleculare (SLM) layer, without loss o

55 3), and SR (2) and at the border between the stratum lacunosum-moleculare (SLM) and the SR (2).

56 cells and other interneurons located within stratum lacunosum-moleculare (SLM) mediate powerful inhi

57 oximal and distal stratum radiatum (SR), and stratum lacunosum-moleculare (SLM).

58 act that a single electrical stimulus of the stratum lacunosum-moleculare (SLM, which contains the PP

59 ptic plasticity and dendritic development in stratum lacunosum-moleculare, thus impacting the integra

60 Light delivered to stratum lacunosum-moleculare triggered EPSCs both on loc

61 re integrated in the synaptic network of the stratum lacunosum-moleculare via excitatory GABAergic in

62 ns-alveus and their axons which projected to stratum lacunosum-moleculare where they ramified extensi

63 ifically targeted to dendritic spines in the stratum lacunosum-moleculare, which form synapses with p

64 l coupling among hippocampal interneurons of stratum lacunosum-moleculare with different excitability