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1 l network (CNN) to detect healthy neurons in acute slice.
2 induced by electrical stimulation of L5-6 in acute slice.
3 frequency in cortical neurons in culture and acute slice.
4 cites prefrontal thalamocortical synapses in acute slice.
5 esponse to novelty or tetanic stimulation in acute slices.
6 nd reduced MLI-evoked pauses in PC firing in acute slices.
7 or thalamus using an optogenetic strategy in acute slices.
8 ic responses were recorded by patch clamp in acute slices.
9 ellate cell synapses by electrophysiology in acute slices.
10 n of YFP, we identified 5-HT neurons in live acute slices.
11 c target neurons by whole-cell recordings in acute slices.
12 mined by whole-cell patch-clamp recording in acute slices.
13  migration by 27%, as previously reported in acute slices.
14 g ischemia, consistent with changes shown in acute slices.
15 ed by means of dual whole-cell recordings in acute slices.
16 odulating the spread of action potentials in acute slices.
17 on at CA3-CA1 synapses by tetanic stimuli in acute slices, a cellular model of long-term memory, lead
18 singly is underpinned by LHb hypoactivity in acute slices, accompanied by alterations in both excitat
19  spines on two distinct types of NAc MSNs in acute slices after 24 hours of cocaine withdrawal and af
20 n MAP1B and GRIP1 increased significantly in acute slices after treatment with DHPG and not NMDA.
21 ice such effects were markedly attenuated in acute slices and abolished in the dissociated Purkinje c
22 on content represented by such landscapes in acute slices and in vivo promises to unveil the hitherto
23 of the mouse hippocampus in cultured slices, acute slices and in vivo.
24 ents using in vitro whole cell recordings in acute slices and measured cystine and glutamate uptake i
25 current (mEPSC) amplitude in monocular V1 of acute slices and prevented the increase in visually evok
26 eous EPSC (sEPSC) frequency was increased in acute slices and primary hippocampal cultures prepared f
27 ulating functional pathways independently in acute slices and recording synaptic responses in RGCs, w
28 function, we performed functional imaging in acute slices and targeted eloquent circuits (specific su
29 Studies in reduced systems--tissue cultures, acute slices, and anesthetized rats--show that spontaneo
30 i, indicating that these native receptors in acute slices are significantly Ca2+-permeable, consisten
31 radiatum interneurons and pyramidal cells in acute slices by recording nAChR-mediated currents elicit
32                              Recordings from acute slices demonstrate that FFA reduces repetitive- an
33 uorescent detection of peptide elongation in acute slices demonstrates robust translation in distal p
34 ous firing of layer 2/3 pyramidal neurons in acute slices derived from monocular visual cortex.
35                                      Lastly, acute slice electrophysiology and morphological studies
36  marker, together with immunohistochemistry, acute slice electrophysiology, and optogenetic circuit m
37 rvation, electroencephalographic recordings, acute slice electrophysiology, immunohistochemistry, and
38 -out mice and analyzed synaptic responses by acute slice electrophysiology.
39                                     Finally, acute slice experiments revealed a reduced efficacy of p
40     In vitro recordings of 47 human cortical acute slices from 11 pediatric patients who received ope
41 midal cells and fast-spiking interneurons in acute slices from adult mice followed by quantal analysi
42       Here, we report a novel preparation of acute slices from adult mouse spinal cord, allowing visu
43                                           In acute slices from adult rats, coincident pre- and postsy
44                                           In acute slices from C57BL/6 mice, we find that co-activati
45                              In contrast, in acute slices from juvenile (P14) rats, TBS failed to ind
46 ly altered synaptic properties in the BL: in acute slices from juvenile (prepubertal) female rats, wa
47 pyramidal cells, effects which are absent in acute slices from M(1) receptor knock-out mice.
48 physiology and two-photon calcium imaging in acute slices from male and female juvenile mice.
49                                           In acute slices from male and female rats, CRF depolarized
50  recordings and two-photon Ca(2+) imaging in acute slices from male rats, we report that, unlike CA1P
51 idal neurons using patch clamp recordings in acute slices from mice at different ages.
52 hysiological and Ca2+ imaging experiments in acute slices from rat cerebella.
53 nsic excitability of PL pyramidal neurons in acute slices from rats exposed to either escapable stres
54 d voltage imaging with the Voltron sensor in acute slices from rats of either sex to test CA3PC conne
55 CA1 region of the rat hippocampus to compare acute slices from the third postnatal week with various
56 0 GFP-fluorescent cell aspirates obtained in acute slices from transgenic mice expressing green fluor
57  clamp recordings from dysplastic neurons in acute slices from TSC tubers demonstrated excitatory GAB
58  addition of protein synthesis inhibitors to acute slices (in which spines otherwise proliferate) blo
59                 Both in cultured neurons and acute slices, KO of Rab11Fip5 had no significant effect
60  of Thy1-GCaMP pyramidal cells in an ex vivo acute slice model of diffusely infiltrating glioma.
61 ity was analysed by patch-clamp recording in acute slices obtained from mice carrying a targeted null
62 icity at Schaffer collateral-CA1 synapses in acute slices of adult mice.
63  by recording from pairs of relay neurons in acute slices of developing ventrobasal nucleus (VBN) of
64     Here the authors study Up/Down states in acute slices of entorhinal cortex, and find that Up stat
65                                     Treating acute slices of GBM with a fatty acid synthesis inhibito
66 recordings were performed on DCN neurones in acute slices of juvenile rat cerebellum.
67                                           In acute slices of letrozole-treated female mice with reduc
68    Here, by making patch-clamp recordings in acute slices of macaque retina, we show that the bipolar
69 sed whole-cell recordings from Im neurons in acute slices of mouse amygdala.
70  recordings from LIII pyramidal neurons from acute slices of mouse medial entorhinal cortex, we find
71 velopment (P2-P12) in pyramidal neurons from acute slices of mouse neocortex.
72 ological and optical recording techniques in acute slices of rat cerebellum, along with modeling, we
73 estigate gain modulation in granule cells in acute slices of rat cerebellum.
74 a channel antagonists on Purkinje neurons in acute slices of rat cerebellum.
75 his issue in mature organotypic cultures and acute slices of rat cortex by recording spontaneous loca
76 h recordings from visualized interneurons in acute slices of rat hippocampus.
77                              Recordings from acute slices of rat locus coeruleus (LC) demonstrated th
78               Here, we recorded from RBCs in acute slices of rat retina and isolated lateral GABAergi
79 uts to neurons in the ganglion cell layer of acute slices of rat retina.
80 ice preparations as well as in synapses from acute slices of the auditory brainstem.
81                        We discovered that in acute slices of the avian OT, persistent (>100 ms) epoch
82 optogenetic suppression of PC firing, and in acute slices of the cerebellum, do not lead to large, su
83                      We mimicked activity in acute slices of the cochlear nucleus from mice of both s
84  investigated layer 2/3 pyramidal neurons in acute slices of the contralateral medial prefrontal cort
85 ally, we found that, in cultured neurons and acute slices of the hippocampus, extracellular sequences
86  Electron microscopy of potassium-stimulated acute slices of the lumbar cord showed that oxytocin-neu
87 cs to show that layer 2 pyramidal neurons in acute slices of the mouse mPFC receive excitatory inputs
88 r modulation of layer 5 pyramidal neurons in acute slices of the mouse prefrontal cortex.
89                      In cultured neurons and acute slices of the olfactory bulb, however, intracellul
90 clamp recording and intracellular filling in acute slices of ventral premotor cortex (vPMC) from rhes
91  abolish hippocampal LTD as measured both in acute slices or using a chemical LTD protocol in culture
92 of excitatory neurons, which we confirmed by acute slice physiology on independent biopsy specimens.
93                  However, in rat hippocampal acute slices, PolyP reduced ion flux through NMDA and AM
94 ampal neurons in vivo, followed by immediate acute slice preparation and electrophysiological quantif
95 on, studies were then performed in the adult acute slice preparation to examine changes in DA recepto
96                   Here, we show that, in the acute slice preparation, actin expression increases duri
97 pal input onto downstream septal cells in an acute slice preparation.
98 nsible for tonic conductance observed in the acute slice preparation.
99 -cell patch-clamp recordings from neurons in acute slice preparations from neonatal wild-type and hSO
100 netic activation of VPMpc afferents to GC in acute slice preparations from rats of both sexes to inve
101  and optogenetics to explore connectivity in acute slice preparations.
102 naptic currents in host pyramidal neurons in acute slice preparations.
103 nd external stimuli, and they proliferate in acute slice preparations.
104                                              Acute slices prepared at postnatal days (P) 14, 17 and 2
105  from individual corticostriatal synapses in acute slices prepared from mice of either sex that were
106                                              Acute slice recordings revealed that Kv3.3 channels are
107               Confocal time-lapse imaging in acute slices reveals that groups of mitral cells assembl
108         Electrophysiological recordings from acute slices showed that barium- and bupivacaine-sensiti
109                     However, live imaging in acute slices showed that Pten deletion did not cause a u
110           Stimulation and calcium imaging in acute slices showed that there is local excitatory conne
111                    Patch-clamp recordings in acute slices showed that, 1 week after the nerve injury,
112 e of the vessel constricting agent U46619 in acute slices, SMCs and EPs revealed only sparse calcium
113 in vitro and can be used in parallel with an acute slice system to model mature brain tissue to exami
114 e we demonstrate, in cultured neurons and in acute slices, that the NMDA receptor is both effector an
115  whole-cell recordings from granule cells in acute slices to assess synaptic function after Pten knoc
116   We used laser scanning photostimulation in acute slices to study the organization of local excitato
117 tes or B-cells led to a vascular response in acute slices using the P2Y(2/4) receptor (P2Y(2/4)R) ago
118 t notable difference between organotypic and acute slices was a four- to five-fold increase in the ab
119 t notable difference between organotypic and acute slices was a four- to five-fold increase in the ab
120 d optogenetic activation of LC fibers in the acute slice, we find evidence for monoamine release onto
121     Using electrophysiological recordings in acute slices, we demonstrate that knockout (KO) of Rab3B
122              Using patch-clamp recordings in acute slices, we examined developmental refinement of wh
123 ynapses in the rat hippocampal CA1 region of acute slices were studied using whole-cell patch-clamp t

 
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