ライフサイエンスコーパス: cryosection

1 nd colocalization of Iba1 and PSD95 in brain cryosection.

2 sion to cultured RA fibroblasts and to RA ST cryosections.

3 ted EPC adhesion to RA fibroblasts and RA ST cryosections.

4 -floating sections and on 1-microm ultrathin cryosections.

5 and immunofluorescence of retinal-choroidal cryosections.

6 n cavities/lacunae in supragingival calculus cryosections.

7 ntibody labeled the food vacuole in parasite cryosections.

8 d sections, and by TUNEL staining on retinal cryosections.

9 ded cells) and by counting pyknotic cells in cryosections.

10 al elemental concentrations were measured in cryosections.

11 nates and by immunohistochemistry of retinal cryosections.

12 itu hybridization and immunocytochemistry on cryosections.

13 cells of the ganglion cell layer in retinal cryosections.

14 and sex organs in both male and female worm cryosections.

15 ing on obtaining artifact-free, longitudinal cryosections.

16 RNA in situ hybridization studies of retinal cryosections.

17 es by immunoelectron microscopy of ultrathin cryosections.

18 ic (glycolmethacrylate) sections, but not in cryosections.

19 confocal microscopy of immunofluorescence in cryosections.

20 ed with light and fluorescence microscopy of cryosections.

21 detect ecto-apyrase in immunolabeled gizzard cryosections.

22 f Schwann cells cultured on peripheral nerve cryosections.

23 ightly stained LC on human neonatal foreskin cryosections.

24 DNA content from thin (about 220 nm) nuclear cryosections.

25 ative abundance of metabolites across tissue cryosections.

26 for assessing CI activity directly in tissue cryosections.

27 crodissection (LCM) in porcine and human eye cryosections.

28 ized in Masson's trichrome and immunostained cryosections.

29 lipid distribution in human coronary artery cryosections.

30 London Resin White, and avoids the need for cryosections.

31 alyzed using immunohistochemistry on retinal cryosections.

32 Binding of Epo-Cy5.5 was validated on tumor cryosections.

33 nick end labeling (TUNEL) were evaluated in cryosections.

34 the CE precursor proteins Tg-1 and Muc5AC in cryosections.

35 gglutinin staining in retinal flatmounts and cryosections.

36 d by immunohistochemical analysis of retinal cryosections.

37 roteins and immune cell subsets in placental cryosections.

38 eyes were preserved <4 hours postmortem and cryosectioned.

39 mples were fixed in 4% paraformaldehyde, and cryosectioned.

40 me points, biologic samples were excised and cryosectioned.

41 ular tissues caused by formalin fixation and cryosectioning.

42 physical sectioning, in particular, Tokuyasu cryosectioning.

43 ue onto the chuck inside the cryostat during cryosectioning.

44 -minute and 24-hours post-fixation, and post-cryosectioning.

45 Cryosections (0.85 microm) of CBCECs were used for light

46 paraformaldehyde-fixed olfactory organs were cryosectioned (10 microm), double-labeled for Galpha(olf

47 d 5 dpf embryos were fixed and processed for cryosectioning, after which eye sections were screened f

48 Furthermore, fluorescence imaging of tissue cryosections allowed high-resolution visualization of in

49 h the cocktail of 6D1 and AP1 and studied in cryosections also failed to reveal uptake of GPIb/IX rec

50 a self-regularization constraint between the cryosectioned and FFPE images for the preservation of cl

51 retinal extracts, and confocal microscopy of cryosectioned and immunolabeled contralateral eyes.

52 In addition, on day 12, the eyes were cryosectioned and immunostained with a panel of neuronal

53 nd-embedded human eyes from 17 patients were cryosectioned and subjected to high-sensitivity digoxige

54 time points from 0 to 24 hours, corneas were cryosectioned and subsequently analyzed by immunofluores

55 d to the mouse ears, which were subsequently cryosectioned and thawed for the analyses.

56 Following exposure, prawns were cryosectioned and the spatial distribution of radionucli

57 ng to interpret due to artefacts from tissue cryosectioning and conventional staining.

58 Additionally, fully automated serial cryosectioning and fluorescence imaging of 1 tumor-beari

59 and 38 months through 1000 microns by serial cryosectioning and histochemical staining for cytochrome

60 gn, primary probe making, sample collection, cryosectioning and RNA/DNA primary probe hybridization c

61 lobes were prepared for either wholemount or cryosectioning and were stained using various primary an

62 tal multiphoton imaging, confocal imaging of cryosections and biochemical analysis revealed that loca

63 mmunofluorescence on retinal wholemounts and cryosections and by flow cytometry.

64 using immunofluorescence staining of retinal cryosections and found a significantly higher number of

65 Immunostained rat heart cryosections and HEK293 cells cotransfected with Kir2.1

66 We demonstrated both on cryosections and in cell cultures that in the human VZ/S

67 More intense staining of tuberin, in the cryosections and in paraffin sections, was observed in t

68 of human skeletal muscle were studied using cryosections and myotubes prepared from muscle biopsies

69 assessed by in situ hybridization on eyecup cryosections and real-time PCR.

70 estigated with a phosphospecific antibody on cryosections and retinal whole-mounts.

71 nodetection of RGCs was performed on retinal cryosections and RGCs and ONL nuclei rows were counted.

72 trixes were applied directly to 14-mum brain cryosections and spectra acquired.

73 Indirect immunofluorescent staining of SCC cryosections and Western blotting of cultured keratinocy

74 Tumors from imaged mice were harvested and cryosectioned, and alternating sections were analyzed by

75 n, and fibroproliferative pannus) or frozen, cryosectioned, and assayed for enzyme activity either by

76 Eyes and ocular adnexa were excised, cryosectioned, and evaluated for apoptosis by terminal d

77 growth, the radish plants were harvested and cryosectioned, and sections were imaged by positive-ion

78 mpletion of MRI, mouse eyes were enucleated, cryosectioned, and stained for assessing retinal layer t

79 fected cells for EM using chemical fixation, cryosectioning, and high-pressure freezing.

80 to bind to the synovial membrane surface on cryosections, and the protein was detected in cell lysat

81 sults demonstrate that formalin fixation and cryosectioning are good choices for studying ocular tiss

82 AID integrates a generative model to correct cryosection artefacts and a pathology foundation model t

83 rating an attention mechanism that rectifies cryosection artefacts and a self-regularization constrai

84 reserved in buffered 4% paraformaldehyde and cryosectioned at 10 microm.

85 ison of bacterial populations in lung tissue cryosections by immunofluorescent staining showed sparse

86 Cryosectioning can be used to prepare thin enough sectio

87 pper structures were also observed in fixed, cryosectioned cells expressing the Tsr receptor at high

88 Tomograms constructed from fixed, cryosectioned cells revealed that overproduction of Tsr

89 demonstrated by mapping glutamic acid from a cryosectioned chicken breast with a thallium spike depos

90 Fluorescence microscopy on cryosections colocalized near-infrared fluorescent osteo

91 Immunofluorescence microscopy of oocyte cryosections confirmed that MIT mutants were expressed o

92 tron microscopic studies with rat cerebellum cryosections demonstrated that the 34 kDa polypeptide co

93 Fresh snap-frozen (20 mum) cryosections dried at room temperature were scanned at 1

94 We used ORCA to study a Hox gene cluster in cryosectioned Drosophila embryos and labelled around 30

95 Frozen human lenses were cryosectioned equatorially and axially into 20-mum-thick

96 were obtained, with 10-20 consecutive 12-um cryosections extracted from each and imaged with an iQID

97 Interestingly, cryosectioning-FISH showed these two comammox species sp

98 Serial cryosections (five per eye) were immunohistochemically l

99 d to angiography; retinas were harvested for cryosections, flat-mount preparations, or trypsin digest

100 m applications, such as tissue embedding and cryosectioning followed by standard histology or immunof

101 ls, laser capture microdissection of retinal cryosections followed by qPCR, and RNA in situ hybridiza

102 studies of ASFV using chemical fixation and cryosectioning for electron microscopy (EM) have produce

103 fK)](2) peptide PET/CT, tumors were cut into cryosections for autoradiography, histology, and immunoh

104 or vascular occlusion; and analysis of tumor cryosections for endothelial cell damage, apoptosis, and

105 and whole eye globes were collected to make cryosections for immunohistochemical staining.

106 -fixed, paraffin-embedded sections or frozen cryosections for immunohistochemistry.

107 fication in diverse samples (cultured cells, cryosections, formalin-fixed paraffin-embedded sections

108 the hearts were excised and rapidly frozen, cryosectioned, freeze-dried, and examined by EPXMA in up

109 Retinal cryosections from cbs(-/-) mice and cbs(+/-) mice were e

110 ive energy-dispersive x-ray microanalysis of cryosections from hippocampal slice cultures rapidly fro

111 Slit2-alkaline phosphatase binding to kidney cryosections from mice with or without tamoxifen-inducib

112 roscopy performed on nondiseased nephrectomy cryosections from persons with normal kidney function re

113 Electron probe microanalysis of cryosections from rapidly frozen slice cultures has reve

114 eroxidase immunocytochemistry in 0.85-microm cryosections from rat inner medulla revealed discrete la

115 ano-organization using tau-STED nanoscopy in cryosections from the mouse primary somatosensory cortex

116 Cryosections from the optic nerve heads (ONH) of eyes is

117 The preparation of intact cryosections from whole insects presents a challenge due

118 Retinal cryosections from young, middle-aged, and senescent wild

119 tatuses (e.g., ATRX, H3K27M, and TP53) using cryosection images that were previously deemed disqualif

120 to predict molecular statuses directly from cryosection images.

121 Using the cryosection immunogold technique, we have found that the

122 Cryosectioning, immunohistochemistry, and fluorescence m

123 MLL tumor cryosections immunostained with anti-PECAM-1 showed that

124 e mouse brain is embedded, flash frozen, and cryosectioned in preparation for mass spectrometry imagi

125 hilles tendon matched that of the rat-tendon cryosections in backscattered geometry.

126 Cell size measured in transverse cryosections increased after 3 minutes of pacing (75+/-5

127 Cryosections indicated that tuberin is widely expressed

128 Examination of serial cryosections indicated that visceral podocytes migrated

129 muscles, snap-frozen at resting length, were cryosectioned, indirectly immunolabeled with fluorescent

130 we describe a novel method for preparing and cryosectioning invasive spheroids in a two-component (co

131 Tokuyasu cryosectioning is relatively rapid but is limited to sma

132 On the same series of pancreatic cryosections, islets were identified by dithizone beta-c

133 rpret virus structure in chemically fixed or cryosectioned material, and in the latter case the virus

134 ved that on wild-type embryonic day 10 (E10) cryosections, neurites generally failed to grow into r3

135 ique we term dual-hydrogel in vitro spheroid cryosectioning of three-dimensional samples (DISC-3D).

136 advantage of recently developed methods for cryosectioning of vitrified cells.

137 pture microdissection to isolate cement from cryosections of 6 h and 24 h tick attachment sites and t

138 Cryosections of A-Gl-prelabeled platelets labeled again

139 Cryosections of biofilms were treated with polyclonal an

140 Spectra of individual cells in situ in cryosections of bovine cornea were collected by using a

141 ng of cultured retinal endothelial cells and cryosections of bovine retina showed junctional localiza

142 cultured human retinal endothelial cells and cryosections of bovine retina.

143 reactivating virus in explanted ganglia and cryosections of DRG and the sacral sympathetic ganglia (

144 In cryosections of druse-enriched pellets (6-57 drusen per

145 st, when trigeminal neurons were seeded onto cryosections of E10 erbB4 -/- embryo heads their neurite

146 Adjacent cryosections of each tumor were analyzed in 3 ways: imag

147 aining for NCAM and polySia was conducted on cryosections of embryonic and adult corneas, whole embry

148 anglion neurons are cultured on longitudinal cryosections of embryonic mouse head.

149 ation of GFP in the grafts was determined in cryosections of enucleated eyes, and GFP expression in t

150 Cryosections of fetal week 11-18 retinas were immunostai

151 Cryosections of HCEC aggregates were subjected to immuno

152 Trx could also activate extracellular TG2 in cryosections of human and mouse small intestinal biopsie

153 Super-resolution imaging of axial cryosections of human cross-facial nerve grafts demonstr

154 Vertical cryosections of human retinas were immunostained with an

155 yte-dependent dermal-epidermal separation in cryosections of human skin.

156 oducing, and chief cells-were harvested from cryosections of infected and uninfected murine stomachs

157 Cryosections of infected cells revealed numerous membran

158 tron microscopy of immunogold-labeled thawed cryosections of infected cells revealed the association

159 cted in situ hybridization on slides bearing cryosections of late embryonic chicken heads, bodies, an

160 positive granulocyte infiltrates with IgA in cryosections of lesional skin of patients suffering from

161 Cryosections of LG were stained with cresyl violet, and

162 Ultrathin cryosections of lung tissue from rabbits given an infusi

163 MS imaging of cryosections of mature cotton embryos revealed a distinc

164 Super-resolution imaging of axial cryosections of murine sciatic nerves yielded robust vis

165 In cryosections of rat cerebellum and kidney, BWD is shown

166 two ezrin-binding proteins was performed in cryosections of rat eyes of various ages and in monolaye

167 Ultrathin cryosections of rat kidney were labeled with the mAbs an

168 ion were determined by immunofluorescence on cryosections of rat liver, pancreas, stomach, and small

169 particle size distribution of CeO(2) NPs in cryosections of rat spleen, CeO(2) NPs were found to rem

170 Cryosections of retina and choroid from the macula and t

171 Probes were hybridized to cryosections of retina and visualized with immunocytoche

172 nes, detergent-soluble membrane proteins, or cryosections of retina from adult bovine eyes.

173 sion was based on experimental work in which cryosections of SCCs from 10 people with RDEB all showed

174 cal ganglion (SCG) neurons in culture and in cryosections of SCG and heart.

175 Tissue ligand binding assays using cryosections of Sepp1-/- kidneys revealed that the proxi

176 Cryosections of six diabetic epiretinal tissues were eva

177 lue dye (EBD) was injected into animals, and cryosections of the brains were evaluated by autoradiogr

178 Cryosections of the explant and the outgrowth were detec

179 determinant of the repolarization waveform, Cryosections of the ferret atrium and ventricle were pre

180 nd immunohistological analysis of subsequent cryosections of the glioma revealed an enhanced infiltra

181 Cryosections of the macula and periphery of human eyes (

182 Methods: Xenograft cryosections of the prostate cancer cell line LNCaP trea

183 By using cryosections of tumor specimens and immunohistochemistry

184 nm and compared quantitatively with stained cryosections of unfixed retinas from the same locations.

185 hemical techniques were applied to ultrathin cryosections of washed platelets.

186 was studied by labeling cell monolayers and cryosections of whole rat lenses for clathrin or caveoli

187 Retinas harvested for cryosectioning or flat mount preparations were subjected

188 ice were killed, and eyes were harvested for cryosectioning or for DNA extraction.

189 identified by immunofluorescent staining of cryosections or tissue whole mounts.

190 Cryosection pathology is essential for intraoperative di

191 the higher levels of APOL1 protein in human cryosectioned podocytes may reflect both endogenous prot

192 Controls comprised heat treatment of cryosections prior to staining.

193 e was obtained after developing an embedding/cryosectioning protocol.

194 tensity of CXCR4 expression on corresponding cryosections (r(2) = 0.61; P < 0.05).

195 tituents of M-bands in freshly dissected and cryosectioned rectus extraocular muscles (EOMs) and tibi

196 post-fixing by 1 minute, 24 hours, and post-cryosectioning, respectively.

197 autoradiography with (99m)Tc-scVEGF of tumor cryosections revealed a 2.2- to 2.6-fold decrease in tra

198 In situ mRNA expression profiling in bone cryosections revealed a ~70-fold up-regulation of Fgfr3

199 f A-Gl-prelabeled platelets labeled again on cryosections revealed GPIb present on linings of the ope

200 In clofazimine-treated mice, skin cryosections revealed no evidence of CLDIs when analyzed

201 Epifluorescence of cryosections served as validation.

202 Analysis of cryosections showed diffuse homogeneous uptake of (124)I

203 Immunofluorescence microscopy of oocyte cryosections showed that MIT mutants were expressed on t

204 Electron microscopy of cryosections showed virus particles, identified by their

205 Here, we used en-face cryosectioning, spatial transcriptomics, and machine lea

206 Six samples were cryosectioned, stained with a bacterial viability kit, a

207 Histopathologic analysis of cryosections taken from mice treated with pAd-2S03 revea

208 Histological artefacts in cryosectioned tissue can hinder rapid diagnostic assessm

209 The rats were killed, and cryosectioned tissue sections were subjected to hematoxy

210 emistry and fluorescence microscopy of organ cryosections (tumor, kidney, spleen) were also performed

211 orescence determined by microscope images of cryosectioned tumors.

212 Tracer uptake was quantified on arterial cryosections using autoradiography and compared with CXC

213 nd co-localization with macrophages in aorta cryosections using autoradiography, histology, and immun

214 denaturation were investigated in rat-tendon cryosections using SHG and bright-field imaging.

215 tion (SHG) imaging of collagen in rat-tendon cryosections, using femtosecond laser scanning confocal

216 mbedding the tissue followed by freezing and cryosectioning, usually between 5 and 25 mum thick, depe

217 POL1 protein in kidney podocytes observed in cryosections versus the lesser abundance in podocyte cel

218 urther localization of cGK I and II mRNAs on cryosections was accomplished by in situ hybridization u

219 Binding of fluoresceinated PEDF to retina cryosections was detected by confocal microscopy.

220 tochemical localization of cGMP in mouse eye cryosections was performed using an anti-cGMP antibody,

221 yrian hamster ( Mesocricetus auratus ) brain cryosections, we show how our pipeline benefits from the

222 Tumor cryosections were analyzed with immunofluorescence and a

223 Cryosections were cut from the maculae of unfixed human

224 were fixed, cryoprocessed, and frozen; 80-nm cryosections were double labeled with combinations of CC

225 Cryosections were evaluated by standard histologic exami

226 Retinal cryosections were examined by TUNEL staining and outer n

227 ex vivo human model of BP, normal human skin cryosections were incubated with purified human peripher

228 Cryosections were prepared for autoradiography, hematoxy

229 Retinal cryosections were prepared for TUNEL analysis to determi

230 n micrographs and immunostained longitudinal cryosections were prepared from sciatic nerve during dem

231 This barrier was removed if cryosections were pretreated with chondroitinase or were

232 Cryosections were stained with antibodies against neutro

233 Cryosections were stained with antibodies against neutro

234 ed for light microscopy, and 800-A ultrathin cryosections were used for electron microscopy (EM).

235 however, usually still involves fixation and cryosectioning, which could deform the tissues.

236 enhances neurite outgrowth on adult cortical cryosections, which normally provide an unfavourable sub

237 -learning model that improves the quality of cryosectioned whole-slide images by transforming them in

238 d specimens are provided, including Tokuyasu cryosectioning, whole-cell mount, cell unroofing and pla

239 A correlation between VEGF and HSA in cryosections with angiopathic changes in the adenosine d

240 we combine electron cryotomography of serial cryosections with genetic and pharmacological perturbati

241 situ hybridization was performed on jejunal cryosections with probes to detect formyl peptide recept