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1 response which again had a source in stratum moleculare.
2 st immunoreactivity in the stratum lacunosum-moleculare.
3 ns were restricted primarily to s. lacunosum-moleculare.
4 i.e. the local network of stratum lacunosum-moleculare.
5 information processing of stratum lacunosum-moleculare.
6 t not in interneurons from stratum lacunosum-moleculare.
7 essed in the postnatal CA1 stratum lacunosum-moleculare.
8 stratum radiatum, and the stratum lacunosum-moleculare.
9 der between str. radiatum and str. lacunosum-moleculare.
10 both stratum radiatum and stratum lacunosum-moleculare.
11 they selectively innervate stratum lacunosum-moleculare.
12 axonal projections to the stratum lacunosum-moleculare.
13 abeling was highest in the stratum lacunosum-moleculare.
14 ly in stratum radiatum and stratum lacunosum moleculare.
15 all other laminae, notably stratum lacunosum-moleculare.
16 ular layer and hippocampal stratum lacunosum 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
21 in the highly vascularized stratum lacunosum moleculare and stratum moleculare layers of the dentate
23 ls target specifically the stratum lacunosum-moleculare and the dentate gyrus, but lack postsynaptic
27 Interneurons in CA1/CA3 stratum radiatum and moleculare, and in the hilus region of the dentate gyrus
29 rimary theta dipole in CA1 stratum lacunosum moleculare, are conveyed by the temporoammonic pathway.
31 ratum pyramidale interneurons with lacunosum-moleculare axon arborization (P-LM cells) and stratum ra
33 ns at the stratum radiatum-stratum lacunosum-moleculare border (R-LM interneurons) of the CA1 area ma
34 adiatum to its border with stratum lacunosum-moleculare, both fate maps of pioneer cells labeled with
35 ted neuromodulation of the stratum lacunosum-moleculare by directly comparing the properties of CXCR4
36 n CA1 stratum radiatum and stratum lacunosum-moleculare (CA1-SRLM)--two monosynaptically connected st
37 ort days decreased apical (stratum lacunosum-moleculare) CA1 spine density, as well as increased basi
38 currents from hippocampal stratum lacunosum-moleculare Cajal-Retzius cells of the CXCR4-EGFP mouse.
40 eceive GABAergic input from oriens lacunosum-moleculare cells and that this input has different physi
41 o-axonic, bistratified, and oriens-lacunosum moleculare cells, innervating different domains of pyram
42 pes--basket, axo-axonic and oriens-lacunosum-moleculare cells--visualized and defined by synaptic con
43 th signals, while those in stratum lacunosum-moleculare exclusively receive a glutamatergic signal.
44 Interneurons in stratum radiatum/lacunosum-moleculare express KARs both with and without the GluR5
45 ta-adrenergic receptors in stratum lacunosum-moleculare GABAergic networks reduces electrical synapti
46 area of this pathway, the stratum lacunosum-moleculare, has the highest concentration of dopamine re
47 he parietal sensory barrel fields, lacunosum moleculare hippocampi, and specific nuclei of the rostra
49 o striatum radiatum or to striatum lacunosum-moleculare in the case of slow cells, suggesting targeti
50 identified a population of oriens lacunosum-moleculare INs that predominantly targeted CA1 pyramidal
51 tion, AA blocked st. oriens-alveus-lacunosum-moleculare interneuron transient currents but not curren
53 coupling was abolished in stratum lacunosum-moleculare interneurons from knockout animals, epileptif
57 y slow synaptic input from stratum lacunosum-moleculare interneurons, anatomically identified as neur
59 sy fiber (MF) synapses on area CA3 lacunosum-moleculare (L-M) interneurons are capable of undergoing
60 , we demonstrate MF LTP in stratum lacunosum-moleculare (L-M) interneurons induced by the same stimul
61 somata in strata radiatum (R) and lacunosum-moleculare (L-M) receive converging stimulation from the
62 of voltage-activated K+ current on lacunosum/moleculare (L/M) hippocampal interneurons, but not on CA
65 ons in SYN immunoreactivity in CA3 lacunosum-moleculare (LM) relative to either young controls or age
66 es of oriens interneurones, oriens lacunosum-moleculare (O-LM) and trilaminar cells, showed prominent
70 to somatostatin expressing oriens-lacunosum-moleculare (O-LM) interneurons (INs), and the postsynapt
71 Excitatory synapses onto oriens-lacunosum moleculare (O-LM) interneurons are facilitating and have
73 d intrinsic potentiation in oriens-lacunosum moleculare (O-LM) interneurons following stimulation of
75 mGluR1-mediated EPSCs from oriens-lacunosum moleculare (O-LM) interneurons in acute hippocampal slic
78 s has been characterized in oriens-lacunosum moleculare (O-LM) interneurons, which express parvalbumi
79 ivergence among hippocampal oriens-lacunosum moleculare (O-LM) projecting interneurons that have hith
80 d presynaptic interneurone, oriens-lacunosum moleculare (O-LMC), basket (BC), axo-axonic (AAC), bistr
81 ation of ChR2-labeled fibers in s. lacunosum-moleculare of CA1 and the dentate molecular layer elicit
82 intense activation of the stratum lacunosum-moleculare of CA1 and the subiculum, contrasting with ba
84 ral septum, diagonal band, stratum lacunosum-moleculare of CA1, and various nuclei of the amygdala an
86 its normal position in the stratum lacunosum-moleculare of field CA2 to an alvear position in SRK.
87 peroammonic (TA) inputs to stratum lacunosum moleculare of hippocampal area CA1 heterosynaptically de
88 n the strata oriens, radiatum, and lacunosum-moleculare of hippocampal CA1 and CA3 regions and in the
89 t path termination zone in stratum lacunosum-moleculare of the CA1 area as well as equivalent portion
91 esses were also present in stratum lacunosum-moleculare of the CA1 region and all layers of the CA3 r
92 ale, stratum radiatum, and stratum lacunosum moleculare of the CA1 subregion, considering both speed
93 he RSG to the CA1 stratum radiatum/lacunosum-moleculare of the dorsal hippocampus and the superficial
98 ons [pyramidal, basket, and oriens-lacunosum moleculare (OLM) cells] generated theta and gamma oscill
99 that TRPV1 is expressed in oriens-lacunosum-moleculare (OLM) interneurons in the hippocampus, and pr
101 (P < 0.005) and within the stratum lacunosum moleculare (P < 0.01), the stratum radiatum (P < 0.005),
102 potential implications for stratum lacunosum-moleculare processing of information in vivo, will be al
103 interneurons projecting to stratum lacunosum-moleculare (representing somatostatin/mGlu(1a)-expressin
106 ndria accumulations in the stratum lacunosum moleculare (SLM) layer, without loss of endogenous nucle
107 nterneurons located within stratum lacunosum-moleculare (SLM) mediate powerful inhibition of CA1 pyra
108 ion in the stratum oriens (SO) and lacunosum-moleculare (SLM) of the dCA1 area, but not in the stratu
110 electrical stimulus of the stratum lacunosum-moleculare (SLM, which contains the PP) had on excitatio
111 uropil layer [CA1-stratum radiatum lacunosum moleculare (SRLM)] thickness, and (ii) activity in ERC a
112 d dendritic development in stratum lacunosum-moleculare, thus impacting the integrative properties of
115 r axons which projected to stratum lacunosum-moleculare where they ramified extensively, in the regio
116 to dendritic spines in the stratum lacunosum-moleculare, which form synapses with presynaptic entorhi
117 ippocampal interneurons of stratum lacunosum-moleculare with different excitability is a novel findin