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1 and cellular stress-gated switch function in cultured hippocampal neurons.
2 d cell-surface expression of the receptor in cultured hippocampal neurons.
3 excitatory postsynaptic currents (EPSCs) in cultured hippocampal neurons.
4 s undergoing dendrite-selective transport in cultured hippocampal neurons.
5 zing factor for axon/dendrite development in cultured hippocampal neurons.
6 fficient endocytosis of synaptic vesicles in cultured hippocampal neurons.
7 d the response of pH(i) to depolarization in cultured hippocampal neurons.
8 creases dendrite number when knocked down in cultured hippocampal neurons.
9 o regulate synapse structure and function in cultured hippocampal neurons.
10 -protein signaling in silencing induction in cultured hippocampal neurons.
11 A interference (RNAi) to knockdown AMPARs in cultured hippocampal neurons.
12 erol modulated Abeta-induced Tau cleavage in cultured hippocampal neurons.
13 ase machinery in neurosecretory cells and in cultured hippocampal neurons.
14 T1-R283W to stimulate PAK phosphorylation in cultured hippocampal neurons.
15 ed by blockade of AMPA receptors (AMPARs) in cultured hippocampal neurons.
16 exocytic fusion at the axon and dendrite of cultured hippocampal neurons.
17 ion induced predominant proBDNF secretion in cultured hippocampal neurons.
18 arize the initiation and turning of axons in cultured hippocampal neurons.
19 and the phosphorylation of IRS-1 and tau in cultured hippocampal neurons.
20 ynthase or CAPON) in dendritic patterning of cultured hippocampal neurons.
21 mulated above 25 Hz in both HEK293 cells and cultured hippocampal neurons.
22 ame mutations interfere with E-T coupling in cultured hippocampal neurons.
23 O enhance GABAergic synaptic transmission in cultured hippocampal neurons.
24 generation of a toxic 17 kDa tau fragment in cultured hippocampal neurons.
25 receptors (AMPARs) on the plasma membrane of cultured hippocampal neurons.
26 ephrin-B1-induced growth cone withdrawal in cultured hippocampal neurons.
27 id pathology and in Abeta42 oligomer-treated cultured hippocampal neurons.
28 duced occupancy of the promoter by BHLHB2 in cultured hippocampal neurons.
29 minal peptides increase synaptic activity in cultured hippocampal neurons.
30 obile FM1-43-labeled vesicles in synapses of cultured hippocampal neurons.
31 uces the density of presynaptic terminals in cultured hippocampal neurons.
32 -state accumulation during axon outgrowth in cultured hippocampal neurons.
33 presynaptic and postsynaptic compartments in cultured hippocampal neurons.
34 ough which BDNF increases synapse density in cultured hippocampal neurons.
35 y of glutamatergic and GABAergic synapses in cultured hippocampal neurons.
36 this Kv2.1 clustering in both HEK cells and cultured hippocampal neurons.
37 lphaCaMKII 5' and 3' untranslated regions in cultured hippocampal neurons.
38 rtical and hippocampal brain sections and in cultured hippocampal neurons.
39 AMPAR surface insertion was also observed in cultured hippocampal neurons.
40 in vivo, and brief glutamate stimulation of cultured hippocampal neurons.
41 , and prevent AbetaO-induced synapse loss in cultured hippocampal neurons.
42 activation of presynaptic silent synapses in cultured hippocampal neurons.
43 ntegrins are involved in spine remodeling in cultured hippocampal neurons.
44 s alpha1-chimaerin to the plasma membrane of cultured hippocampal neurons.
45 hRs by expressing epitope-tagged subunits in cultured hippocampal neurons.
46 ney 293 cells stably expressing CB(1) and in cultured hippocampal neurons.
47 ibitory, but not excitatory, postsynapses in cultured hippocampal neurons.
48 re used to disrupt SNARE protein function in cultured hippocampal neurons.
49 elayed the maturation of dendritic spines in cultured hippocampal neurons.
50 ls and on native non-L-type Ca2+ currents of cultured hippocampal neurons.
51 the neuromodulatory effects of serotonin in cultured hippocampal neurons.
52 t SNARE-mediated neurotransmitter release in cultured hippocampal neurons.
53 d the generation of a 17 kDa tau fragment in cultured hippocampal neurons.
54 element-binding protein (pCREB) signaling in cultured hippocampal neurons.
55 tes the growth and branching of dendrites in cultured hippocampal neurons.
56 ate Wnt-5a signaling and dendritic spines in cultured hippocampal neurons.
57 e loss of AMPA receptors from the surface of cultured hippocampal neurons.
58 c cytochrome c after NMDA overstimulation in cultured hippocampal neurons.
59 MKII is essential for synaptic plasticity in cultured hippocampal neurons.
60 reen fluorescent protein-tagged synapsins in cultured hippocampal neurons.
61 ocalizes with the NMDA receptor at spines of cultured hippocampal neurons.
62 etastin increased [Ca2+]i in a population of cultured hippocampal neurons.
63 wo kinds of GABAA receptors are expressed on cultured hippocampal neurons.
64 ippocampus, increases dendritic branching in cultured hippocampal neurons.
65 demonstrated by three independent assays in cultured hippocampal neurons.
66 ell surface to intracellular compartments in cultured hippocampal neurons.
67 ty of calpain to cleave the NMDA receptor in cultured hippocampal neurons.
68 channel molecules to the initial segment of cultured hippocampal neurons.
69 ASIC1 was not gated by synaptic activity in cultured hippocampal neurons.
70 agonist-induced internalization of GluRs in cultured hippocampal neurons.
71 beta-actin mRNA localization in dendrites of cultured hippocampal neurons.
72 ation-induced changes in cytosolic Ca(2+) in cultured hippocampal neurons.
73 ites lacking postsynaptic specializations in cultured hippocampal neurons.
74 alyze cell-surface Nav1.6 within the soma of cultured hippocampal neurons.
75 -5-methylisoxazole-4-propionate receptors in cultured hippocampal neurons.
76 1b for the morphology of dendritic spines of cultured hippocampal neurons.
77 t in E(GABA) values and increased spiking of cultured hippocampal neurons.
78 fferentiated living PC12 cells as well as in cultured hippocampal neurons.
79 embrane potential, exocytosis, and Ca(2+) in cultured hippocampal neurons.
80 afficking and activation of TrpC channels in cultured hippocampal neurons.
81 ed role in regulating synaptic plasticity in cultured hippocampal neurons.
82 essed in Xenopus oocytes, HEK 293 cells, and cultured hippocampal neurons.
83 e distribution of channels into dendrites of cultured hippocampal neurons.
84 particle tracking of individual GABA(A)Rs in cultured hippocampal neurons.
85 ession of c-Fos induced by depolarization of cultured hippocampal neurons.
86 state also exists for native Kv2.1 found in cultured hippocampal neurons.
87 inhibited physiological IRS-1pTyr in mature cultured hippocampal neurons.
88 urrent (mIPSC) amplitudes and GABA levels in cultured hippocampal neurons.
89 subdomains adjacent to activated synapses in cultured hippocampal neurons.
91 an additional sci-ATAC-seq preparation from cultured hippocampal neurons (899 high-quality cells, 43
94 rotrusions and at dendritic branch points in cultured hippocampal neurons--a distribution reminiscent
95 nal genetic approach to remove both genes in cultured hippocampal neurons after synapses are establis
98 surface expression in hippocampal slices and cultured hippocampal neurons, an effect mimicked by LP-2
99 ry postsynaptic currents (mIPSCs) in primary cultured hippocampal neurons, an effect opposite to that
101 in non-neuronal cells, and increased in both cultured hippocampal neurons and brain tissue from Fbxo2
102 ial steps for PFF formation, PFF addition to cultured hippocampal neurons and confirmation of aggrega
104 at the axon initial segment of AnkG-depleted cultured hippocampal neurons and fails to recruit neurof
105 study, we performed whole-cell recordings of cultured hippocampal neurons and found that NMDAR activa
107 GFP-tagged alpha1A subunit were expressed in cultured hippocampal neurons and HEK cells to understand
108 is phosphorylation reduced axon formation in cultured hippocampal neurons and impaired polarization o
109 al excitatory en passant boutons in axons of cultured hippocampal neurons and in hippocampal slices e
110 DNF downregulated the proteasome activity in cultured hippocampal neurons and in hippocampal synapton
111 thin synapses at key developmental stages in cultured hippocampal neurons and in hippocampus in vivo.
112 tection of synaptic and action potentials in cultured hippocampal neurons and intact leech ganglia.
113 ively localized to the axonal growth cone of cultured hippocampal neurons and is required for specifi
114 d PICK1 coimmunoprecipitate from extracts of cultured hippocampal neurons and P4 cortices, and immuno
116 e impairs activity-dependent BDNF release in cultured hippocampal neurons and predicts impaired memor
117 n became up-regulated during polarization of cultured hippocampal neurons and remained at high levels
119 pendent dendritic outgrowth and branching in cultured hippocampal neurons and slices is mediated thro
121 2, and analyzed RIM-BP-deficient synapses in cultured hippocampal neurons and the calyx of Held.
124 interacts with PSD-95 in dendritic spines of cultured hippocampal neurons, and as a GTPase-activating
125 glyceraldehyde-3-phosphate dehydrogenase in cultured hippocampal neurons, and directly compare their
126 actin is concentrated in dendritic spines of cultured hippocampal neurons, and the N-terminal half of
128 current methods of gene delivery for primary cultured hippocampal neurons are limited by toxicity, tr
130 observed that DHT rapidly activates CREB in cultured hippocampal neurons, as evidenced by CREB phosp
131 apping protein, in the dendrites and soma of cultured hippocampal neurons at different developmental
132 the same striking patterns of attachment to cultured hippocampal neurons, binding on dendrite surfac
133 morlin stimulated microtubule disassembly in cultured hippocampal neurons but had no significant effe
134 DNF translated from long 3' UTR Bdnf mRNA in cultured hippocampal neurons, but not from short 3' UTR
135 kers for synaptic function and plasticity in cultured hippocampal neurons by NaPB-treated astroglial
137 ion of the EphB receptor tyrosine kinases in cultured hippocampal neurons by their ephrinB ligands in
138 ibited F1Fo ATP synthase function in primary cultured hippocampal neurons by using non-lethal oligomy
140 of GRIP1 by small interfering RNA (siRNA) in cultured hippocampal neurons caused a loss of dendrites,
141 c activation of mu-opioid receptors (MOR) in cultured hippocampal neurons causes two forms of synapti
143 ols, respectively, when expressed in primary cultured hippocampal neurons, consistent with previous s
145 rsible fragmentation of the Golgi complex in cultured hippocampal neurons cultured in hyperexcitable
146 enhanced GABAergic synaptic transmission in cultured hippocampal neurons (days-in-vitro 10-14) prepa
147 genous Chmp2b reduced dendritic branching of cultured hippocampal neurons, decreased excitatory synap
148 ng pathways involved in axon formation using cultured hippocampal neurons demonstrates a role for Ca(
149 ive of synaptic homeostasis were observed in cultured hippocampal neurons derived from alpha(1A) (-/-
150 ich is homologous to human CRMP4 (S541Y), in cultured hippocampal neurons derived from Crmp4-knockout
151 and spontaneous neurotransmitter release in cultured hippocampal neurons derived from PS1 knock-out
152 r together as double or triple KDs (TKDs) in cultured hippocampal neurons, did not decrease synapse n
156 infusion of active CaM-kinase I (CaMKI) into cultured hippocampal neurons enhances miniature EPSC amp
158 ERbeta, DPN, to prevent neurodegeneration in cultured hippocampal neurons exposed to excitotoxic glut
159 mic domain, we find that all interneurons in cultured hippocampal neurons express high levels of Pcdh
161 letely and reversibly blocked by dynasore in cultured hippocampal neurons expressing the fluorescent
162 uorescence and digital imaging microscopy in cultured hippocampal neurons, FMRP and Fmr1 mRNA were lo
166 rates of Venus-PSD-95 mRNA was increased in cultured hippocampal neurons from Fmr1 KO mice compared
168 properties of synaptic transmission between cultured hippocampal neurons from MeCP2 knockout and wil
169 es of the proteolytic processing of Nrxns in cultured hippocampal neurons from mice and rats of both
170 ions to control RIM and Munc13-1 activity in cultured hippocampal neurons from mice of either sex and
171 ion of amino-terminal ligands, we first used cultured hippocampal neurons from N2A and N2B knock-out
172 esults demonstrate that agmatine can protect cultured hippocampal neurons from NMDA- or glutamate-ind
173 vectors expressing CAT or GPX still protect cultured hippocampal neurons from oxygen/glucose depriva
175 tracking of individual synaptic vesicles in cultured hippocampal neurons from rats of both sexes wit
176 lexes from hippocampal brain homogenates and cultured hippocampal neurons from Sprague Dawley rats.
177 introducing each isoform into glutamatergic cultured hippocampal neurons from synapsin triple knock-
178 nsfecting wild-type synaptotagmin I DNA into cultured hippocampal neurons from synaptotagmin I knock-
181 ective failure of BDNF-dependent survival in cultured hippocampal neurons from the trisomy 16 (Ts16)
182 s for Ca2+ stimulation of adenylyl cyclases, cultured hippocampal neurons from transgenic mice lackin
183 functional analyses in zebrafish embryos and cultured hippocampal neurons from wild-type and Ctnnd2 n
185 the formation of rods in a maximum of 19% of cultured hippocampal neurons in a time- and concentratio
186 V pools via V-Glut1-pHluorin fluorescence in cultured hippocampal neurons in response to alterations
188 We conclude that DIDS induces apoptosis in cultured hippocampal neurons, in spite of the fact that
189 lipid rafts exist abundantly in dendrites of cultured hippocampal neurons, in which they are associat
190 nduced enhancement of neurite outgrowth from cultured hippocampal neurons indicating an important fun
192 thermore, the expression of this fragment in cultured hippocampal neurons induced the formation of nu
195 otentiation of synaptic transmission between cultured hippocampal neurons is accompanied by an increa
196 ew release sites during potentiation between cultured hippocampal neurons is due to (a) conversion of
197 e show here that NMDAR stimulation of PLC in cultured hippocampal neurons is necessary for AKAP79/150
198 t that phosphorylation of endogenous KCC2 in cultured hippocampal neurons is regulated by PKC-depende
201 tudy vesicle dynamics inside the synapses of cultured hippocampal neurons labeled with the fluorescen
202 similar degree of protection is observed in cultured hippocampal neurons lacking caspase-2, which ar
205 a thorough analysis of neurotransmission in cultured hippocampal neurons lacking synaptic vesicle pr
207 ed high-frequency epileptiform discharges in cultured hippocampal neurons leads to caspase-dependent
208 at amyloid beta-peptide (Abeta) treatment of cultured hippocampal neurons leads to the inactivation o
211 potential (AP)-mediated network activity in cultured hippocampal neurons maintains eEF2 in a relativ
212 Here, we were able to reproduce in primary cultured hippocampal neurons many of the effects of in v
214 t both excitatory and inhibitory synapses in cultured hippocampal neurons, newly endocytosed vesicles
216 three Ca(V)2s using conditional knockout in cultured hippocampal neurons or at the calyx of Held, wh
219 ity-dependent endocytosis of AMPARs by using cultured hippocampal neurons prepared from knockout (KO)
220 essing chimeric KCC2-KCC4 cDNA constructs in cultured hippocampal neurons prepared from Sprague Dawle
222 P activities in undifferentiated neurites of cultured hippocampal neurons promote and suppress axon f
224 rdingly, knock-out or knockdown of KCTD12 in cultured hippocampal neurons reduces the magnitude of th
225 ction of the future axon among neurites of a cultured hippocampal neuron requires the activity of gro
226 mic reticulum (ER) to the plasma membrane of cultured hippocampal neurons requires Ca(2+) release fro
229 at various stages in the differentiation of cultured hippocampal neurons results in substantial loss
231 is of BDNF-induced synaptic strengthening in cultured hippocampal neurons revealed increased expressi
237 Immunocytochemistry in epithelial cells and cultured hippocampal neurons showed that endogenous neur
240 gomer-induced changes in dendritic spines of cultured hippocampal neurons, sparing mature spine class
241 endent regulation of GIRK channel density in cultured hippocampal neurons that requires activity of N
242 protein-tagged alpha1C subunits expressed in cultured hippocampal neurons, that Ca2+/CaM interaction
246 d Fyn are localized together in the axons of cultured hippocampal neurons, the mossy fibers of the hi
248 -20-one (C2-NBD 3alpha5alphaP), responses of cultured hippocampal neurons to 10 microM NMDA were pote
249 his study, we assessed the susceptibility of cultured hippocampal neurons to Abeta-dependent 17 kDa t
251 ce RNAs to eliminate Piccolo expression from cultured hippocampal neurons to assess its involvement i
252 assessed the effect of the S940A mutation in cultured hippocampal neurons to explore the mechanisms u
254 d and NH4(+)-induced pHi shifts were used in cultured hippocampal neurons to quantify the rate of KCC
255 ent light-induced membrane depolarization in cultured hippocampal neurons to trigger reliable repetit
256 ng techniques applied to both fixed and live cultured hippocampal neurons to visualize the localizati
259 afficking and regulated secretion of BDNF in cultured hippocampal neurons transfected with the met al
263 o be concentrated in the dendritic shafts of cultured hippocampal neurons under control conditions bu
264 cts of pregabalin on presynaptic function of cultured hippocampal neurons using a powerful technique
265 effects of estradiol on synaptic proteins in cultured hippocampal neurons using immunocytochemistry a
266 rin in regulating synapse function in rodent cultured hippocampal neurons using optical methods and e
267 the stability of synaptic NMDA receptors on cultured hippocampal neurons using the open-channel bloc
268 45 GFP-tagged synaptic proteins expressed in cultured hippocampal neurons, using fluorescence recover
269 RNA in differentiated axons and dendrites of cultured hippocampal neurons varying in developmental ma
270 emaphorin 3A-induced growth cone collapse in cultured hippocampal neurons was associated with the par
272 loring dynamic localization of APP/BACE-1 in cultured hippocampal neurons, we found that after synthe
273 expression of stargazin mutant constructs in cultured hippocampal neurons, we identified a novel doma
275 Through a loss-of-function genetic screen in cultured hippocampal neurons, we previously identified t
278 ivity and subdiffraction-limit resolution in cultured hippocampal neurons, we show that two molecules
281 lectin modulation, whereas AMPA receptors in cultured hippocampal neurons were insensitive, which cou
286 red the effects of changes in temperature in cultured hippocampal neurons, where higher average rates
288 lation of IRS-1 (Ser616) and tau (Ser422) in cultured hippocampal neurons, whereas JNK inhibition blo
289 ce of WT DCX reduces dendritic complexity of cultured hippocampal neurons, whereas neurons expressing
290 monitoring intracellular calcium [Ca2+]i in cultured hippocampal neurons, which are known to express
293 tudy synapse formation by neuroligins, we co-cultured hippocampal neurons with COS cells expressing w
298 from GABA-B-R1 knock-out mouse brains and in cultured hippocampal neurons with their GABA-B-R1 genes
300 at serine 31 are colocalized in the axons of cultured hippocampal neurons, with enrichment at the axo