ライフサイエンスコーパス: slice

1 ve fibroblastic subtypes was predicted using SLICE.

2 d across a whole 300 microm-thick myocardial slice.

3 DHK responses in the intact rat nTS and the slice.

4 n mouse dorsal horn neurons from spinal cord slices.

5 ar palsy and corticobasal degeneration brain slices.

6 e lamina I neurons in horizontal spinal cord slices.

7 tently with previous findings in hippocampal slices.

8 of a more heterogeneous vein coverage across slices.

9 ression in voltage-clamp recordings in brain slices.

10 vely profile single neurons from mouse brain slices.

11 o map nanoscale diffusivity in ex vivo brain slices.

12 f CA1 pyramidal neurons in mouse hippocampal slices.

13 us (LC) neurons contained in acute rat brain slices.

14 alcium signals in mouse acute cortical brain slices.

15 d for representative sections in RP specimen slices.

16 ordings and voltage-sensitive dye imaging in slices.

17 hysical properties have been well studied in slices.

18 with a vibratome and handling of myocardial slices.

19 toxylin-eosin-stained whole-mount histologic slices.

20 using whole-cell electrophysiology in brain slices.

21 settings and correct handling of myocardial slices.

22 nt is diminished in SynII-deleted (SynII(-)) slices.

23 NKL also induced TRAP activity in mouse lung slices.

24 es cAMP in neuronal cultures and hippocampal slices.

25 ed prostate cancers on whole-mount pathology slices.

26 ts, such as single dendritic spines in brain slices.

27 Fbxl3(Afh/Afh) compared with Fbxl3(+/+) SCN slices.

28 in order to prepare highly viable myocardial slices.

29 in cardiac myocyte cultures and murine heart slices.

30 of olfactory sensory neurons (OSNs) in bulb slices.

31 anaesthetized rat nTS or applied to rat nTS slices.

32 fter decellularization of human renal tissue slices.

33 ominent short-term plasticity, as studied in slices.

34 lux in ASMCs within mouse precision-cut lung slices.

35 action potentials in rat (both sexes) brain slices.

36 enerated by a cleavage reaction analogous to slicing.

37 icity and spine numbers in acute hippocampal slices 2-3 weeks later.

38 We developed SLICE, a novel algorithm that utilizes single-cell RNA-s

39 erform patch-clamp recordings from SCN brain slices across the projected day/night cycle.

40 Despite lacking efficient slicing activity, these fish have retained the ability t

41 A1 area of the mouse hippocampus in cultured slices, acute slices and in vivo.

42 tatively analyzed using a combination of 2-D slice analysis and 3-D visualization and counting.

43 specific study and (iii) generic methods to slice and dice data across different dimensions in one o

44 h normal and cancerous prostate tissues were sliced and cultured in the presence of the azide-functio

45 nologies for conducting IHC on intact tissue slices and has great potential to be used in the discove

46 By electrophysiological recordings in slices and histological analysis of the uptake of retrog

47 Multiple particle tracking in brain tissue slices and in vivo testing in orthotopic murine malignan

48 mouse hippocampus in cultured slices, acute slices and in vivo.

49 Despite extensive studies in hippocampal slices and incentive from computational theories, the sy

50 s, microglia, and astrocytes in WNV-infected slices and markedly decreased levels of inducible nitric

51 o no significant difference between MI size3-slices and MI sizefull LV (P = 0.93) with an excellent c

52 Furthermore, using AAR3-slices and MI sizefull LV resulted in 'negative' MSI in

53 hysiological recordings in acute hippocampal slices and primary hippocampal neuronal cultures showed

54 k channels also occurs in intact spinal cord slices and that it is carried out by adaptor protein-2 (

55 ysiological diversity of HA neurons in brain slices and the effect of their acute silencing in vivo i

56 by acute treatment of both tangential brain slices and the isolated guinea pig brain with the potass

57 neurons and Purkinje neurons in vitro (brain slices) and in vivo.

58 c transmission in young animals and cultured slices, and an increase in postsynaptic density protein

59 of THC was evaluated using acute hippocampal slices, and hippocampal cannabinoid receptor type 1 and

60 n small-diameter dorsal root ganglia, spinal slices, and in a mouse model of pain induced by NaV1.7 a

61 ning recordings and pharmacology in vivo, in slices, and in human embryonic kidney 293 cells, it was

62 Experiments in cultured cells, brain slices, and in living mice demonstrate single-neuron spa

63 luated in cultured human cells, liver tissue slices, and mice with acute-on-chronic liver injury.

64 ative in vivo autoradiography of human tumor slices, and on human data now supports a shift to sstr a

65 ific cell types in dissociated cortex, brain slices, and the brains of live mice.

66 les are firstly scanned to produce grayscale slices, and the corresponding fracture area, length, ape

67 T1 and T2 mapping are more accurate than a 3-slice approach for delineating the AAR, especially in th

68 ovascular magnetic resonance (CMR) using a 3-slice approach has been shown to accurately quantify the

69 ss the MOB and AOB, using an in vitro, brain slice approach in postnatal 15-30 day mice.

70 We aimed to compare the performance of a 3-slice approach to full left ventricular (LV) coverage fo

71 Adult ventricular myocardial slices are 100- to 400-mum-thick slices of living myocar

72 Furthermore, since tissue slices are routinely used for diagnostics in clinical se

73 sing the number of perivascular profiles per slice area accessed by IgG by approximately 50%.

74 ed on pyramidal neurons in acute hippocampal slices at 270 DAT, was reduced in epileptic mice but res

75 (SFT) were measured using T1-weighted axial slices at the level of the umbilicus and the upper borde

76 We used the in vitro entorhinal cortex slices bathed in 4-aminopirydine (4-AP) as an experiment

77 nsorial properties and volatile compounds of sliced bread during 90days of storage.

78 icity (STDP) has been studied extensively in slices but whether such pairings can induce plasticity i

79 in dissociated cultured neurons or in brain slices, but not in the intact living brain.

80 odies are captured from perfused mouse brain slices by patch clamping, and lipids are analyzed using

81 l nucleus of the amygdala (CeA) in brainstem slices by recording from retrogradely labelled NTS proje

82 all subjects using short axis and long axis slices by steady-state free precession (SSFP) sequences

83 o difference between the AARfull LV and AAR3-slices by T1 (P = 0.054) and T2-mapping (P = 0.092), wit

84 Virtual slicing by means of 2D XRF tomography, combined with hol

85 han acting on the nerves within the pancreas slice, CCK cellular actions directly affected human acin

86 s to infer ancient hominid behaviors such as slicing, chopping, and percussive actions during butcher

87 In spinal cord slices, clonidine reduced the frequency of capsaicin-ind

88 -induced increase in cAMP levels in midbrain slices, consistent with reported effects of inhibition o

89 ages of the perpendicular and parallel brain slices containing mesh electronics showed that the distr

90 Notably, images of sagittal brain slices containing nearly the entire mesh electronics pro

91 Slices containing Pten-deleted neurons showed increased

92 Slices containing the adhesive-dentin interface were cov

93 al of this work was to study drying of pequi slices (convective or vacuum drying at 40 degrees C and

94 All patients underwent multi-slice CT imaging with a triphasic protocol, which includ

95 Routine multi-slice CT of the paranasal sinuses was performed to look

96 t two radiology departments equipped with 64-slice CT scanners, Khartoum, Sudan.

97 ed 186 cases of NSCLC with preoperative thin-slice CT scans.

98 at 2260 m included CMS symptom score, multi-slice CT, perfusion CT, pulse oximetry (SpO2%), and hemo

99 th 19 pinhole collimators interfaced with 64-slice CT.

100 This hybrid Organotypic Slice Culture Assay coupled with RT-QuIC (OSCAR) permits

101 ative detection of prions from an infectious slice culture model on a reduced time scale.

102 stem coupled to an ex vivo prion organotypic slice culture model to rapidly advance rationale-based h

103 ibed a novel organotypic 3xTg-AD mouse brain slice culture model with key Alzheimer's disease-like ch

104 Organotypic brain slice culture models provide an alternative to early sta

105 l-induced demyelination model on organotypic slice culture, in a BDNF-dependent manner.

106 We utilized ex vivo spinal cord slice cultures (SCSC) to demonstrate that anti-inflammat

107 imaging of graded potentials in organotypic slice cultures and in Drosophila.

108 ng platform and that the prions generated in slice cultures are biologically active.

109 dings highlight the utility of 3xTg-AD brain slice cultures as a rapid and reliable in vitro method f

110 ng in vivo treatment are replicated in brain slice cultures from 3xTg-AD mice.

111 Similarly, in organotypic corticoamygdalar slice cultures from immature rats, treatment with letroz

112 Using organotypic brain slice cultures generated from embryonic mice of various

113 CA1 pyramidal neurons in mutant hippocampal slice cultures that are essentially devoid of presynapti

114 In brain slice cultures, Treg accelerated developmental myelinati

115 etection of action potentials in organotypic slice cultures.

116 We found that a slicing-defective AGO4 was unable to fully recover AGO4-

117 ent detection of peptide elongation in acute slices demonstrates robust translation in distal process

118 metimes also a G-A mismatch) enhances target slicing, despite disrupting seed pairing important for t

119 the protein level is found in patient tumor slices displaying a vasculogenic mimicry (VM) phenotype.

120 tivation of the pathway in acute mouse brain slices drove IN activity despite small amplitude synapti

121 ectroencephalographic (vEEG) monitoring, and slice electrophysiology outcomes were obtained up to 270

122 We used slice electrophysiology to measure connectivity changes

123 Slice electrophysiology was employed to measure excitabi

124 Slice electrophysiology was used to measure glutamatergi

125 r, together with immunohistochemistry, acute slice electrophysiology, and optogenetic circuit mapping

126 approach of gene transfer, systems and brain slice electrophysiology, behavior, and immunohistochemis

127 the addition of IGF1 to acute olfactory bulb slices elicited the GABAergic LTP in mitral cells by enh

128 ut also provides information on the electron slice emittance and energy spread.

129 ofile can be directly related to the derived slice emittance as a function of intra-bunch coordinate

130 ntal area (VTA) dopamine neurons in midbrain slices ex vivo.

131 P-AP delay in vivo and shorter AP latency in slice experiments, is consistent with increased synaptic

132 -AP delay in vivo, and shorter AP latency in slice experiments, is consistent with increased synaptic

133 nts in both cultured neurons and hippocampal slices exposed to E2, while their frequency was unaffect

134 tory cortical neurons supporting the present slice findings.

135 In slices, five pairings of subthreshold presynaptic activi

136 introduce a preparation of peripheral nerve slices for patch-clamp recordings.

137 nsgene-labeled markers in a 1-mm thick brain slice from adult mice, and 14 days were required for det

138 ved in layer II horizontal connections of EC slices from 2 month old mhAPP mice, whereas at later sta

139 s using whole-cell patch-clamp recordings in slices from adult rats.

140 argeted patch-clamp recording in spinal cord slices from adult transgenic mice that express enhanced

141 ting breast cancer cells in live acute brain slices from an experimental mouse model of breast cancer

142 We found, in acute rat OB slices from both sexes, that inhibitory synchrony is evi

143 In contrast, in hippocampal slices from calpain-1 knock-out (KO) mice, application o

144 Half of the slices from each animal were pre-incubated in normal art

145 tion in pyramidal neurons in rat hippocampal slices from either sex.

146 This dampening effect is lost in slices from GluA2 KO mice, indicating a requirement of G

147 ered synaptic properties in the BL: in acute slices from juvenile (prepubertal) female rats, wash-in

148 ation of SD in layers 2-3 of visual cortical slices from juvenile rats.

149 dal neurons and fast-spiking interneurons in slices from male and female mice and in the isolated fem

150 urons and POMC neurons was examined in brain slices from male and female mice.

151 In each case, imaging in brain slices from male or female animals revealed electrically

152 did not prevent the generation of LTP in the slices from males.

153 Blocking mGluRI in slices from mice lacking EAAC1 restores D1R expression a

154 Using acute hippocampal slices from mice of either sex with genetic conditional

155 Here we show in acute hippocampal slices from mice that endogenous NPY, released in respon

156 Here we use GCaMP Ca(2+) imaging in brain slices from mice to address how nerve terminal Ca(2+) is

157 gs from basal amygdala (BA) neurons in brain slices from mice with channelrhodopsin genetically targe

158 cordings from MSO principal neurons in brain slices from Mongolian gerbils.

159 nced by activation of protein kinase C or in slices from morphine-treated rats.

160 timuli, GFP-identified GnRH neurons in brain slices from OVX+E or OVX female mice were recorded durin

161 In acute cerebellar slices from postnatal day (P)12-14 mice, light-evoked EP

162 r paradigm, Arc-expressing IGCs in acute AOB slices from resident males displayed stronger excitation

163 on and repeated firing up to 100 Hz in brain slices from Swiss male mice.

164 dependent synaptic plasticity in hippocampal slices from Tg(CJD) mice, which model a genetic form of

165 f highly viable adult ventricular myocardial slices from the hearts of small and large mammals, inclu

166 echnique on contiguous T1-weighted axial MRI slices from the level of the prostate base to the apex.

167 ulation and an optogenetic approach in brain slices from the mouse, we investigated the synaptic prop

168 Using precision-cut slices from the porcine lung to passage the parental vir

169 In brain slices from these animals, single-trial hybrid optical v

170 l and anatomical approaches in ex vivo brain slices from transgenic mice, it was found that 2 weeks o

171 with cancer cell spheroids, and microtissue slices from tumors, and normal organs.

172 Dynamic clamp studies in cerebellar slices from weanling mice demonstrate that synaptic exci

173 confirmed in patch-clamp recordings in bulb slices from wild-type and connexin 36-knockout (KO) mice

174 ly increased following treatment of striatal slices from wild-type mice with quinpirole, a D2R agonis

175 Here, using hippocampal slices from young adult male rats and mice, we report th

176 Here we demonstrate that MILI slicing generates a 16-nt by-product that is discarded a

177 At 7 T, a single slice GluCEST technique was used to estimate in vivo glu

178 Studies in brain slices have led to a model in which rhythmic synchronize

179 pplicability and high predictive accuracy of SLICE in determining cellular differentiation states and

180 and function can be studied using myocardial slices in vitro.

181 We found that, in rat brain slices, increasing the supply of the physiological trans

182 mouse granule neurons and ex vivo cerebellar slices indicate that ZNHIT3 is indispensable for granule

183 ast partly because Argonaute2-catalyzed mRNA slicing is impaired.

184 Activation of PKA in striatal slices leads to phosphorylation of Ser88, and this is ac

185 Here, Gao et al. extend multi-slice methods to electrons in the multiple scattering re

186 ly integrate data collected in the 'fine phi-slicing' mode (in which the rotation angle per image is

187 culture, IL-34 expression in a rodent brain slice model with intact neuron-microglial networks exace

188 Using cyclic voltammetry in mouse brain slices, nAChR-dependent spontaneous dopamine transients

189 The smallest diameter of supra-slice objects in the Catphan phantom were taken into con

190 tic terminals using two photon microscopy in slices obtained from forebrain specific HCN1 deficient m

191 a of the greatest amount of effusion on each slice of the three slices used.

192 In slices of corpus callosum from mice subjected to a demye

193 re the authors study Up/Down states in acute slices of entorhinal cortex, and find that Up states pro

194 Tooth slices of human healthy extracted third molars were dece

195 ct, a data extraction tool to export defined slices of liquid chromatography/ion mobility/mass spectr

196 acted directly from the surface of ultrathin slices of liver tissue prior to detection by high-resolu

197 myocardial slices are 100- to 400-mum-thick slices of living myocardium that retain the native multi

198 trophysiological recordings from hippocampal slices of mice lacking PRMT8 reveal multiple defects in

199 cells, in primary neuronal culture, in brain slices of mouse and monkey, and in mouse brain in vivo.

200 h validation in cultured neuronal assays, in slices of mouse dorsal striatum, and in behaving mice.

201 dings from LIII pyramidal neurons from acute slices of mouse medial entorhinal cortex, we find that s

202 In acute brain slices of murine layer 2/3 cortical neurons, we determin

203 mensional infrared (2D IR) spectra on tissue slices of porcine eye lenses.

204 RP caused sustained excitation of neurons in slices of rat spinal cord.

205 teromer, could then be identified in situ in slices of rat ventral tegmental area (VTA) with MAPK act

206 sions of individuals with ASD made from thin slices of real-world social behavior by typically-develo

207 ted these forms of plasticity in hippocampal slices of rodents.

208 P-TOFMS images relative to the corresponding slices of the 3D mu-CT reconstruction.

209 In slices of the central amygdala, DCUK-OEt acted primarily

210 ocaine-induced inhibition of DA clearance in slices of the nucleus accumbens.

211 his paradigm was then used in layers I-IV of slices of the rat motor cortex to determine the percent

212 hoton Ca(2+) imaging in male rat acute brain slices of the somatosensory neocortex, we found that the

213 lf a bowl (65g) of breakfast cereal and four slices of toasted (122g) or untoasted bread (160g).

214 nderstood adaptive pathway links cytoplasmic slicing of target RNA by the PIWI protein MILI to loadin

215 Electrochemical etching is used to slice off single-crystalline AlGaN/GaN layers while pres

216 heir pattern of spread in disinhibited brain slices over millimeters.

217 ne major challenge is to extract tomographic slice parameters instead of projected electron beam prop

218 as determined via whole animal and brainstem slice patch clamp experiments.

219 I was similar between the 2 approaches, MSI3-slices performed poorly when MSI was <0.50.

220 Using the brain slice preparation for cellular recordings, superfusion o

221 We have developed an organotypic slice preparation of the normal portions of human pancre

222 tudy, we established an in vitro mouse brain slice preparation that retains connectivity across the e

223 ll patch-clamp recordings in the spinal cord slice preparation with attached dorsal roots also demons

224 ayer V pyramidal neurons in an ex vivo brain slice preparation, we found that operant self-administra

225 On the basis of studies in cell cultures and slice preparations, it is hypothesised that synaptic rem

226 ynapses have been performed largely in brain slice preparations, without consideration of physiologic

227 ptogenetics to explore connectivity in acute slice preparations.

228 zation of neurons in the rostral Re of brain slices prepared from adult male mice.

229 aw circuits, as revealed by both spinal cord slice recordings and behavior assays.

230 Using slice recordings and modeling of synaptic activity at ce

231 Using slice recordings before hearing onset and in vivo record

232 Through in vitro slice recordings coupled with laser-scanning photostimul

233 Using in vitro slice recordings, we have analysed postsynaptic function

234 overy from AP depression that we observed in slice recordings.

235 Human pancreas slices represent excellent preparations to examine pancr

236 R agonist [Thr(4),Gly(7)]-OXT to hippocampal slices resulted in an acute and lasting potentiation of

237 n Scn8a(N1768D/+) pyramidal neurons in brain slices revealed early afterdepolarization (EAD)-like AP

238 N2B S1413L in GluN2A/B-deficient mouse brain slices revealed only partial rescue of synaptic current

239 Whole-cell patch-clamp recordings in brain slices revealed that intrinsic excitability of DG granul

240 proteins, AGO4 is an endonuclease that can 'slice' RNAs.

241 In this implementation, the slice selectivity depends on the conductivity of the mat

242 , our experimental data in mouse hippocampal slices show that acetylcholine biases STDP toward synapt

243 ordings from mEC stellate cells in rat brain slices showed that GTx inhibited delayed-rectifier K(+)

244 Patch clamp experiments on hypothalamic slices showed that the mean amplitude of the putative EN

245 stochemical staining of mice and human brain slices shows DAM with intracellular/phagocytic Abeta par

246 rophysiology, activation of mGlu5 in ex vivo slices significantly reduced KCa2 channel currents in la

247 ated secretory responses from human pancreas slices similar to those previously observed in dispersed

248 distances using a mathematical model termed SLICE (statistical inference of co-segregation).

249 tically from transcripts, informed by a thin-slicing study of participant ratings of officer utteranc

250 SLICE successfully measured the differentiation states o

251 AGOs use miRNAs as guides to slice target mRNAs to produce truncated 5' and 3' RNA fr

252 litude increase was observed in neurons from slices that had been pre-incubation in gabapentin.

253 we investigated whether in mice hippocampal slices these distinct forms of LTP are specifically regu

254 120 kVp, current tube time product - 86 mAs, slice thickness 1 mm.

255 We then applied SLICE to scRNA-seq of embryonic mouse lung at E16.5 to i

256 ippocampal neurons or ex vivo human cortical slices to AbetaOs transiently decreased intracellular AT

257 rdings in rat (both sexes) neocortical brain slices to assess the ionic mechanisms supporting persist

258 electrophysiology in acute mouse hippocampal slices to dissect the roles of P/Q- and N-type VGCCs.

259 ure and multielectrode recordings from brain slices to explore intrinsic excitatory connectivity of t

260 xtracellular field recordings in hippocampal slices to investigate adaptations in synaptic function a

261 uangxitoxin-1E (GTx; 10-100 nm) in rat brain slices to investigate Kv2 channel functions in mEC layer

262 ically evoked NMDAR responses in acute brain slices to investigate mechanisms by which channel blocke

263 omerular stimulation in mouse olfactory bulb slices to measure the synaptic dynamics of afferent-evok

264 d whole-cell patch-clamp recordings in brain slices to reveal how nanomolar concentrations of KYNA al

265 of ultrapure silicon is lost as kerf during slicing to produce wafers.

266 2+) measurements in mouse precision-cut lung slices, to simulate Ca(2+) oscillations and changes in m

267 ippocampal LTP, and this effect is absent in slices treated with either a glial toxin or an adenosine

268 We found that slice treatment with hyaluronidase occluded the effect o

269 mount of effusion on each slice of the three slices used.

270 tage changes in acutely prepared mouse brain slices using 2P illumination.

271 rticobasal degeneration patient brain tissue slices using autoradiography studies.

272 2beta1gamma1 GABAAR pentamers in hippocampal slices using cell-surface cross-linking, followed by Wes

273 with microelectrode arrays and ex vivo brain slices, using whole-cell voltage clamp.

274 universal detection power, and (b) in REMPI-slice velocity map ion imaging (VMI) detection technique

275 failure are shown, demonstrating myocardial slice viability, maximum contractility, Ca(2+) handling

276 and the excitability of LHb neurons in brain slices was higher, whereas the amplitude of medium after

277 Time-lapse two-photon microscopy in adult slices was used to determine the precise molecular-event

278 electrophysiological techniques on in vitro slices, we investigated gamma-aminobutyric acidergic (GA

279 me-lapse superresolution microscopy in brain slices, we report that axons grow wider after high-frequ

280 In cultured neurons and brain slices, we show that Cal-Light drives expression of the

281 s of PKA activity in acute mouse hippocampus slices, we show that endogenous Galphaq-coupled muscarin

282 Here, using mouse organotypic hippocampal slices, we show that the extracellular AMPAR N-terminal

283 n hippocampal CA1 pyramidal neurons in brain slices, we showed that the effects of INaP on Rin and ta

284 Here, in acute mouse olfactory bulb slices, we test how the two major classes of olfactory b

285 ramidal neurons of both primary cultures and slices, we triggered a unique form of AIS plasticity by

286 The potato slices were fried in rapeseed oil under vacuum at 125 de

287 For most species, only a few 2D slices were needed to accurately estimate Sm within 10%

288 Subsequently, nucleus accumbens brain slices were prepared, and we tested for changes in the r

289 In adulthood, hippocampal slices were prepared.

290 Then the 2-D slices were stacked to create a complete 3-D image using

291 Beef slices were wrapped in special three-layer sheets of pac

292 ional circuit mapping in ex vivo acute brain slices, which preserve in vivo-like connectivity of axon

293 endogenous dynorphin from D1R-SPNs in brain slice while using whole-cell patch recording to measure

294 sectioning of a nanostructured material into slices with 0.34 nm lateral resolution and with a corres

295 adiographic labelling of Alzheimer's disease slices with 11C-PBB3 and 18F-AV-1451 were noted.

296 as well as normal and cancer cells in tissue slices with high accuracy.

297 bined two-photon imaging microscopy in brain slices with in vivo work in rats and C57BL/6J mice to ex

298 novel preparation of living peripheral nerve slices with preserved cellular architecture and used a p

299 mory in young mice, while treatment of brain slices with TIMP2 antibody prevents long-term potentiati

300 for heart explantation, tissue preparation, slicing with a vibratome and handling of myocardial slic