ライフサイエンスコーパス: slice

1 n vivo and show non-specific connectivity in slice.

2 andmarks through the image sequence for each slice.

3 lesion segmentations on a single transversal slice.

4 second for a typical perfusion scan of three slices.

5 d TTFL time-keeping in the corresponding SCN slices.

6 ynaptic currents (mEPSCs) in rat hippocampal slices.

7 d interpretation time in the absence of 1-mm slices.

8 in synthetic HA matrix and organotypic brain slices.

9 terns in mouse hippocampal-entorhinal cortex slices.

10 AMP8 was also observed in murine hippocampal slices.

11 rtical tissue blocks were sampled from these slices.

12 ng fast-scan cyclic voltammetry in rat brain slices.

13 r oscillations in skin fibroblasts and liver slices.

14 er content of 3-MCPD esters in toasted bread slices.

15 a histological and microcomputed tomographic slices.

16 macaques, anesthetized mice, and acute brain slices.

17 cultured hepatocytes and forebrain cortical slices.

18 validated in cortical neurons of acute brain slices.

19 ble to delay post-cut browning of lotus root slices.

20 urrents were recorded from day and night SCN slices.

21 hysiological responses, in acute mouse brain slices.

22 rway contraction in human precision-cut lung slices.

23 icrovasculature) of optically cleared tissue slices.

24 aints for shelf-life extension of lotus root slices.

25 Adult male mice and hippocampal brain slices.

26 n histological and microcomputed tomographic slices.

27 n CA1 pyramidal neurons in acute hippocampal slices.

28 ution and EM in intact brain and acute brain slices.

29 n SCI sites in vivo and in adult spinal cord slices.

30 enhanced synaptic plasticity in hippocampal slices.

31 ssed these two key points in mouse subicular slices.

32 tructures in unlabeled live cells and tissue slices.

33 ring spreading depression in rat hippocampal slices.

34 ction in 6-month-old 5xFAD mouse hippocampal slices.

35 matter in chimpanzee and macaque cerebellum slices.

36 gic axons in the mouse cortex in acute brain slices.

37 ed increase in vesicle docking in cerebellar slices.

38 ly to resolve errors at the basal and apical slices.

39 and dorsal root ganglion neurons, and brain slices.

40 ass spectrometry to locate sterols in tissue slices (10 um) of mouse brain.

41 t atrial fibrillation (1-3 mm interspace per slice, 20-200 slices for each patient, ranging from the

42 which were used as benchmark primers, namely slicing (5.0 +/- 0.6 umol glyceollins/g DW) and sonicati

43 performed zero padding on more than 99.2% of slices (9828 of 9907).

44 ll and free DNA resolution within mouse lung slices, a difficult to achieve task with available subst

45 protein lysate extracted from 2 x 5 um FFPE slices absolutely and quantitatively using QDB method in

46 segments, and AR-SMS imaging with four times slice acceleration.

47 g and cell tracking data from ex vivo tissue slices acquired from a growth-factor driven glioblastoma

48 ly defined progenitor subpopulations in live slices across key stages of mouse DG development, testin

49 Therefore, the intrinsic slicing activity of AGO3 remains controversial and a lon

50 ynaptic currents in heterozygous hippocampal slices also showed a prolonged deactivation time course.

51 Slice and in vivo electrophysiology and Western blots we

52 trophysiological recordings from hippocampal slices and activity measurements of glutamic acid decarb

53 Vertical slices and horizontal layers of the CX are formed by col

54 ollagen production in IPF precision cut lung slices and in the bleomycin model.

55 the extracellular D-serine concentration in slices and in vivo by microdialysis.

56 pment of fibrosis both in vitro in the liver slices and in vivo in a rodent model.

57 The cilia-beating deficit observed in brain slices and in vivo is caused by elevated levels of dopam

58 dynamics of GLU and GABA in rat hippocampal slices and observed a significant, nonlinear shift in th

59 Patch-clamp recordings in slices and RNAscope showed that oxytocin affects S1 exci

60 e used electrophysiological studies in brain slices and structural analysis of post-mortem tissues ob

61 oradiography was performed on resected brain slices and subsequently stained with cresyl violet to en

62 Correlation between the AOA of slices and suspensions is found.

63 on, we performed functional imaging in acute slices and targeted eloquent circuits (specific subcircu

64 ted and reference values on per-patient, per-slice, and per-segment analyses.

65 This classification was performed for each slice, and the slice scores were combined by using a ful

66 ry cultured spinal cord neurons, spinal cord slice, and Xenopus laevis oocytes expressing recombinant

67 hanced bone resorption when cultured on bone slices, and altered mRNA expression of related chemokine

68 R GECIs in cultured cells, acute mouse brain slices, and Caenorhabditis elegans and Xenopus laevis in

69 ed long-term potentiation in the hippocampal slices, and L-655,708 attenuated this reduction.

70 ine cells; in D1 medium spiny neurons of NAc slices; and in either male or female mouse brain in a re

71 se inhibition properties and fresh-cut apple slices antibrowning effect when compared to kojic acid.

72 escent images of optically cleared pathology slices are acquired with a preclinical in vivo optical i

73 Addition of microalga reduced the slice area and increased the crumb hardness, but it coul

74 We also establish human precision-cut lung slices as a platform for modeling early host/pathogen in

75 s classified fibrosis on spectral-domain OCT slices, as type A if located underneath the RPE, as type

76 l tracing and functional assays in intact or sliced assembloids, we show that cortical neurons send a

77 Furthermore, brain-slice autoradiography studies demonstrated the absence o

78 he motion of the landmarks and averaged on a slice basis.

79 ion dynamically quantified on representative slice before and after thrombin administration (22.20 +/

80 In brain slices, both of the mutations changed the electrical pro

81 ch-clamp and field recordings in mouse brain slices (C57Bl/6, male and female).

82 wders were reconstituted and applied to coat sliced cakes, a bakery product.

83 pal CA1 neurons from male rat or mouse brain slices causes intermittent, seconds long increases in th

84 of cyp1a in exposed precision-cut cod liver slices confirmed the activation of the Ahr signaling pat

85 GABA transporters (GATs) in acute rat brain slices containing key parts of the thalamocortical seizu

86 In rat brain slices containing the intercalated cells, we found that

87 LepR-expressing neurons in horizontal brain slices containing the NTS from male and female LepR-Cre

88 vitro patch-clamp electrophysiology in brain slices containing the OFC, we found that the mu-opioid a

89 pair (EVAR) relies on manual review of multi-slice CT angiography (CTA) by physicians which is a tedi

90 BLA principal neurons in a novel organotypic slice culture (OTC) model of male rat BLA, and examined

91 We recently developed an organotypic slice culture assay for sensitive detection of scrapie p

92 eveloped and characterized the ex vivo brain slice culture model for CWD, using a transgenic mouse mo

93 We used a novel organotypic slice culture model of BLA, complemented with in vivo st

94 nfectivity of biological samples in this CWD slice culture model.

95 size and shape to increase surface area and slice culture to maintain nutrient and oxygen access to

96 contains navigational cues for TCAs, we used slice culture transplants and gene expression studies.

97 nals in planar tissue including rodent brain slices, cultured cells, and brain regions with laminar s

98 Using a combination of in vitro gut slice cultures and ex vivo organ cultures, we determined

99 gical inhibition of JNK signaling in ex vivo slice cultures caused cortical interneurons to rapidly d

100 Slice cultures from Tg12, but not from prnp(-/-) mice, t

101 euronal cultures and organotypic hippocampal slice cultures from wild-type mice.

102 ice, and targeted reduction of Crb2/CRB2S in slice cultures reveal essential roles for transmembrane

103 Organotypic slice cultures were prepared from male and female ChAT-E

104 anced live imaging techniques of organotypic slice cultures, clonal analysis, and mathematical modeli

105 In organotypic slice cultures, repeated NPY treatment reduces the compl

106 Using primary neurons and brain slice cultures, we find that overexpression and knockdow

107 n provoke paranodal elongation in cerebellar slice cultures, which could be reversed by an N-methyl-D

108 can traverse ventricular walls in embryonic slice cultures.

109 imals and ex vivo in organotypic hippocampal slice cultures.

110 and fibrosis in Grp78 KO mouse and IPF lung slice cultures.Conclusions: These results support a caus

111 s of distal lung epithelium, and in IPF lung slice cultures.Measurements and Main Results: Grp78 dele

112 P (P = .002) and number of defects per image slice (defects/slice) (P = .0001) than children without

113 Using thalamic slices derived from adult mice of either sex, we recorde

114 iated Schaffer collateral (SC)-CA1 fEPSPs in slices derived from male and female rats.

115 ors resolve evoked DA release in mouse brain slices, detect evoked compartmental DA release from a si

116 and quality attributes of blanched eggplant slices during infrared drying.

117 ntermittent alcohol vapor exposure), ex vivo slice electrophysiology and ISH.

118 Employing slice electrophysiology and mice with a genetic deletion

119 In addition, ex vivo slice electrophysiology of transgenic Cre-inducible Rosa

120 n vHIP-NAc activity in vivo and used ex vivo slice electrophysiology to identify the mechanism of thi

121 We therefore used a combination of slice electrophysiology, in vivo two-photon calcium imag

122 Using slice electrophysiology, we measured how acute sleep dep

123 Through brain-slice electrophysiology, we show that subthreshold GAT15

124 we explore mOP-LTD in DMS using mouse brain slice electrophysiology.

125 g, and performed functional assessment using slice electrophysiology.

126 c5 knockout model was elaborated using brain slice electrophysiology.

127 d Methods Dedicated compressed sensing-based slice encoding for metal artifact correction 1.5-T MRI e

128 lity, which can cause variations in both the slice energy spread and longitudinal profile of electron

129 n vivo and examination of precision-cut lung slices ex vivo.

130 that 10 mmol L(-1) oxalic acid treated lotus slices exhibited reduced browning, superoxide anion, hyd

131 Finally, acute slice experiments revealed a reduced efficacy of perfora

132 with 12 GB RAM compared with 6-8 minutes per slice for the manual analysis.

133 llation (1-3 mm interspace per slice, 20-200 slices for each patient, ranging from the upper border o

134 pulmonary vein computed tomography geometric slices from 358 patients with nonrecurrent atrial fibril

135 epithelium (RPE) in 836 spectral-domain OCT slices from 44 eyes of 39 patients.

136 omatic dendrites of CA1 pyramidal neurons in slices from adult male rats.

137 long-term potentiation (LTP) in hippocampal slices from AS mice by enhancing SK2 internalization.

138 inergic afferents in prefrontal cortex brain slices from compound-transgenic wild-type and Chrna5 kno

139 two-photon microscopy in ex vivo spinal cord slices from CX3CR1-GFP mice complemented with confocal a

140 ases mediate desensitization of MOR in brain slices from drug-naive and morphine-treated animals.

141 stained with a fluorescent lectin in tissue slices from female and male epileptic patients diagnosed

142 tic spine motility in acutely prepared brain slices from female and male mice following METH-associat

143 nt in autoradiography (ARG) studies in brain slices from HD mouse models and postmortem human HD samp

144 gle or dual optogenetic stimulation in brain slices from male and female mice, we compared the proper

145 d 8% decrease in duration of SWRs in ex vivo slices from male and female three-month 5xFAD mice versu

146 While microglia in brain slices from male mice lack C3aR1 receptors, both recepto

147 res, and from acute hippocampal and cortical slices from male wild-type and amyloid precursor protein

148 ) to mimic background activity in cerebellar slices from mature mice of both sexes, I identified a pr

149 In PVN slices from mice expressing GCaMP6, leptin excites gluta

150 ngs from identified MOC neurons in brainstem slices from mice of either sex to demonstrate that in ad

151 entiated synaptic transmission in cerebellar slices from mice of either sex, an effect that was insen

152 ensitization of the somatostatin receptor in slices from morphine-treated animals.

153 In slices from naive animals, pharmacological inhibition of

154 receptor was also blocked by compound 101 in slices from naive but not morphine-treated animals.

155 lthough ZIP has no effect on accumbal LTD in slices from naive or yoked saline mice, it is able to re

156 duced glutamate neurotransmission in the BLA slices from panic-prone rats.

157 nzymatic toolkit to ascites fluid and tissue slices from patients with ovarian cancer facilitated cha

158 is question, we recorded from LSO neurons in slices from prehearing mice while stimulating MNTB affer

159 ell recordings in basolateral amygdala (BLA) slices from rats revealed higher frequency of miniature

160 ine did not increase the NMDAR potentials in slices from serine racemase knock-out mice, which are de

161 affic of DAT in intact brain and acute brain slices from the knock-in mouse expressing epitope-tagged

162 ed network excitability in acute hippocampal slices from the Mecp2 KO mice.

163 ts, pharmacologically disinhibited subicular slices generated hyper-synchronous discharges.

164 Slice-generated CWD prions transmitted efficiently to Tg

165 th asthma who had a higher number of defects/slice had a higher rate of health care utilization (r =

166 The 10 mmol L(-1) treated slices had better visual quality and higher ascorbic aci

167 s 6-mm slabs with 3-mm overlap, without 1-mm slices, had similar diagnostic performance compared with

168 lk, pizza, poultry, salmon, sausage, shrimp, sliced ham, tilapia, and vegetable oil.

169 l coverage (i.e. missing basal and/or apical slices), however most of them were limited to the first

170 rent culture conditions for human pancreatic slices (HPSs) have only been tested for short-term appli

171 gm, and spine were segmented in each CT scan slice images to construct the 3D morphology of the regio

172 Slices in the average brain image were then manually seg

173 5) is proposed to be responsible for precise slicing in many monocots to generate diverse 24-nt phase

174 studies in vivo and dynamic clamp studies in slice indicated that such brief PC suppression, as a res

175 plication of IL-1beta to ex vivo hippocampal slices induced non-synaptic depolarisation and irreversi

176 frozen or preserved with chemical fixatives, sliced into thin sections placed on microscope slides, s

177 n the sensor system is exposed to the sample slice is used as a source of information.

178 The culture of live pancreatic tissue slices is a powerful tool for the interrogation of physi

179 method based on HR-MAS NMR spectroscopy with slice localization (SLS) to achieve spatial resolution o

180 In vlPAG slices, mCbN terminals excite ~20% of neurons positive f

181 ed nerve-dependent airway reactivity in lung slices mediated via TrkB.

182 eable inter-slice motion (i.e. average inter-slice misalignment greater than 3.4 mm).

183 sults demonstrate that this integrated brain slice model of CWD enables the study of pathogenic mecha

184 sound parameters in a transgenic mouse brain slice model that enables calcium imaging as a quantitati

185 the stacks were affected by noticeable inter-slice motion (i.e. average inter-slice misalignment grea

186 mated quality metrics (heart coverage, inter-slice motion and image contrast in the cardiac region) a

187 Inter-slice motion was positively correlated with weight and b

188 as determined from the formalin-fixed tissue slices (n = 42; 17 patients).

189 Here, we report the sliced neocortical organoid (SNO) system, which bypasses

190 ormed on non-fixed coronal hemispheric brain slices of 23 patients with progressive multiple sclerosi

191 pamine secretion is abolished in acute brain slices of conditional knockout mice in which Synaptotagm

192 Whole-cell patch recordings from brainstem slices of mice of both sexes were performed.

193 of 31 patients based on the analysis of all slices of the chest CT scan.

194 resented in a compass-like manner across the slices of the CX.

195 lens allowing us to obtain optical vertical slices of the IPL, which provide a complete picture of t

196 ical texture features were extracted from CT slices of the liver for 34 patients with a diagnosis of

197 ron microscopy of potassium-stimulated acute slices of the lumbar cord showed that oxytocin-neurophys

198 a GABA 'sniffer' patch in acute hippocampal slices of the rat and document strong dependence of [GAB

199 recording and intracellular filling in acute slices of ventral premotor cortex (vPMC) from rhesus mon

200 mples such as cell culture, tissue histology slices, or living subjects.

201 In mouse precision-cut lung slices, osthole relaxed preconstricted airways, irrespec

202 eneanilines were bent to an arbitrary angle, sliced out from a bundle into individual crystals, cut i

203 d number of defects per image slice (defects/slice) (P = .0001) than children without asthma.

204 Precision-cut lung slices (PCLS) are ideal for measuring small airway contr

205 Precision-cut lung slices (PCLS) of allergen-exposed guinea pigs were used

206 ical field stimulation in precision cut lung slices (PCLS) were assessed.

207 primary human lung cells, precision-cut lung slices (PCLS), and a murine in vivo hyperoxia model.

208 s approximately 260 frames (approximately 13 slices) per second on a GPU with 12 GB RAM compared with

209 l5) expression, and dcl5-1 mutants unable to slice PHAS transcripts lack nearly all 24-nt phasiRNAs.

210 Here we use slice physiology and optogenetics to study vHPC-evoked f

211 ling in cultured cells and in an acute brain slice preparation.

212 requently observed in principal neurons from slice preparations of rodent medial entorhinal cortex (M

213 sured intracellular Ca(2+) and report APs in slice preparations of the goldfish retina.

214 active neurons and synapses in cell culture, slice preparations, and in vivo during behavior.

215 e obtained from Purkinje cells in cerebellar slices prepared from male mice ~48 h after they learned

216 e microscopy that involves: (i) a method for slicing rat brain tissue into sections with the same thi

217 period of bioluminescent TTFL rhythms in SCN slices recorded ex vivo Abrogation of circadian competen

218 In brain slice recordings, many NPY neurons fired spontaneously,

219 arse-view cone-beam acquisition with a multi-slice residual dense network (MS-RDN) reconstruction.

220 004 +/- 0.035 in the basal, mid-, and apical slices, respectively (mean +/- standard deviation of dif

221 on potential firing of GnRH neurons in brain slices.RESULTSIn healthy women, the amplitude of luteini

222 cell recordings of PCs from acute cerebellar slices revealed altered climbing fiber (CF)-evoked compl

223 rophysiological investigation in hippocampal slices revealed significantly reduced long-term potentia

224 hysiological recordings in hippocampal brain slices revealed that KA stimulated the activity of inhib

225 Recordings from PFC brain slices revealed that MK-801 exposure during adolescence

226 togenetics-assisted circuit mapping in brain slices revealed that POA(PAG) neurons directly inhibit P

227 Confocal time-lapse imaging in acute slices reveals that groups of mitral cells assemble into

228 In a brain slice, RhoVR-Halos provide exquisite labeling of defined

229 silenced primary human DPSCs seeded in tooth slice/scaffolds and transplanted into the subcutaneous s

230 cation was performed for each slice, and the slice scores were combined by using a fully connected ne

231 single pulse dose of 0.7 Gy via multi-energy slice selection from the broad input spectrum.

232 the extraction protocol in combination with slice-selection NMR experiments is suitable for metaboli

233 s and organic phases are determined by using slice-selective proton NMR experiments.

234 MVD ginger slices showed a higher shrinkage rate and a higher hardn

235 In addition, 10 mmol L(-1) treated slices showed reduced total bacterial count along with l

236 hysiological recordings on acute hippocampal slices showed that exogenous Amh protein addition increa

237 iological properties of Lm128C cell in brain slices showed that Lm128C cells exhibit elevated membran

238 e histological and microcomputed tomographic slices showed that melatonin significantly limits the li

239 xtracellular field recordings in hippocampal slices showed that syntaxin-3 cKO did not exhibit signif

240 Stimulation and calcium imaging in acute slices showed that there is local excitatory connectivit

241 immunostaining of mouse and human pancreatic slices shows that TSPAN-7 is highly expressed in beta- a

242 The obtained 7 slice spectra from each of the model samples (i.e., chic

243 pping (approximate duration, 3 minutes; five slices; spin-echo cardiac diffusion acquisition; b value

244 Combining brain slice studies and site-directed mutagenesis in HEK293T c

245 In brain slices, synaptically released dopamine increases astrocy

246 rotocol (10-mm slabs with 5-mm overlap, 1-mm slices, synthetic 2D mammogram) and an experimental prot

247 : 0.3 msec +/- 2.9; ECV: -0.3% +/- 1.7), per-slice (T2: 0.1 msec +/- 4.6; ECV: -0.3% +/- 2.5), and pe

248 .91; ECV: R = 0.91, 95% CI: 0.89, 0.93), per-slice (T2: R = 0.83, 95% CI: 0.81, 0.85; ECV: R = 0.84,

249 s; no effect on current is observed on brain slices taken from CLC-2 knockout mice.

250 However, in slices taken from morphine-treated animals, the combinat

251 cleaved passenger strand and degradation of sliced target RNA.

252 gnificantly higher VDP and number of defects/slice than healthy controls.

253 uniform moisture distribution in MVD ginger slices than that in splits in the original geometry.

254 Here, we show in mouse brain slices that alpha1-A(R)-mediated excitatory synaptic tra

255 gineered heart tissues and living myocardial slices that could help bridging the gap between in vivo

256 urther confirmed directly in living pancreas slices that sensory terminals in the islet were sensitiv

257 recordings in the cornu Ammonis 1 region of slices that were perfused with L-655,708 (100 nM).

258 GPC as a biomarker, we identified the tissue slices that were predominantly the cortex or medulla.

259 innocua was inoculated on the surface of ham slices that were vacuum-packaged and flashed with 2.1, 4

260 T's efficiency in application on big data by slicing the entire dataset into smaller sets of features

261 sulting technical variability (eg, different slice thicknesses, reconstruction kernels or timings aft

262 otein recovery for every pixel in a given 2D slice, thus moving FRAP measurements beyond these previo

263 s by using 3-T MRI with DR-CSI and were then sliced to create coregistered WMHP slides.

264 ere constructed and trained to map axial MRI slices to a set of bounding box predictions encompassing

265 Here we used mouse hippocampal slices to address how PVs signal to newborn neurons prio

266 pulmonary vein computed tomography geometric slices to create a prediction model for NPV triggers in

267 nt imaging approaches on fresh human adenoid slices to provide static and dynamic information on Tfh

268 pocampal neurons in culture and intact brain slices, to discover relationships between the speed of c

269 after serum incubation was assessed in mouse slices using molecular markers and electrophysiological

270 p to a depth of almost 400 um in acute brain slices using one-photon light-sheet imaging.

271 We tested for CWD infectivity in cultured slices using sensitive seeding assays such as real-time

272 ic phenotype, and optimal selection of tumor slices versus whole tumor.

273 to investigate the difference between ginger slices (vertically cut) and splits (horizontally cut) du

274 und that CB(1)-iLTD in acute rat hippocampal slices was associated with protein synthesis-dependent p

275 to specific neurons in human and mouse brain slices was evaluated ex vivo after incubation with serum

276 Tracer influx assessed in coronal slices was increased in agreement with previous reports

277 Fluorescence imaging of ex vivo mouse brain slices was used to quantify the delivery outcomes of 800

278 erative adversarial award, being generalized sliced Wasserstein, for chemically diverse molecules wit

279 cultured hepatocytes and precision-cut liver slices we demonstrated increased gene expression of prof

280 al cell model and HD mouse organotypic brain slices we found that D(1)R-induced cell death signaling

281 Recording from adult zebra finch brain slices we show that within each bird basal ganglia Area

282 Studying microglial cells in acute brain slices, we found that TLQP21 impaired metabotropic purin

283 ual-energy CT images of a juxtadiaphragmatic slice were obtained, gas and blood volume fractions with

284 onstrated that the VDP and number of defects/slice were predictive of increased health care utilizati

285 Donor-derived human precision-cut lung slices were exposed to leukotriene (LT) D(4), MCTRs, or

286 In addition, hippocampal slices were prepared 1 week after traumatic brain injury

287 h later for cue-induced reinstatement, or LA slices were prepared for electrophysiological recordings

288 n 47 distinct eyes, 4181 spectral-domain OCT slices were retrospectively reviewed to longitudinally a

289 Stacks of short-axis MRI slices were split into overlapping substacks that were s

290 nt thalamic discolorations in cm-thick brain slices were T2/fluid-attenuated inversion recovery (FLAI

291 In the present study, lotus roots slices were treated with 0, 5 and 10 mmol L(-1) oxalic a

292 f the heart, for a total of 23 683 images of slices) were used in the deep learning process, the ResN

293 ng working memory processing, in vitro brain slice whole-cell patching recordings and in vivo stereot

294 Cs) were 0.82 +/- 0.02 and 0.75 +/- 0.03 for slice-wise and participant-wise enhancement prediction,

295 % +/- 4.3 and 73% +/- 2.7, respectively, for slice-wise prediction.

296 otropic image volume composed of 256 coronal slices with 71 manually delineated structures and substr

297 ontrast tomography (XPCT), providing virtual slices with histology-matching resolution.

298 The superfusion of CeA slices with nociceptin/orphanin FQ peptide (N/OFQ; 500 n

299 from labeled cortical neurons in a rat brain slice, without the need for trial averaging.

300 escence intensities of formalin-fixed tissue slices yielded an optimal mean fluorescence intensity cu