ライフサイエンスコーパス: cryosection

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

2 and immunofluorescence of retinal-choroidal cryosections.

3 n cavities/lacunae in supragingival calculus cryosections.

4 ntibody labeled the food vacuole in parasite cryosections.

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

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

7 al elemental concentrations were measured in cryosections.

8 nates and by immunohistochemistry of retinal cryosections.

9 itu hybridization and immunocytochemistry on cryosections.

10 cells of the ganglion cell layer in retinal cryosections.

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

12 RNA in situ hybridization studies of retinal cryosections.

13 es by immunoelectron microscopy of ultrathin cryosections.

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

15 confocal microscopy of immunofluorescence in cryosections.

16 ed with light and fluorescence microscopy of cryosections.

17 detect ecto-apyrase in immunolabeled gizzard cryosections.

18 f Schwann cells cultured on peripheral nerve cryosections.

19 ightly stained LC on human neonatal foreskin cryosections.

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

21 ized in Masson's trichrome and immunostained cryosections.

22 lipid distribution in human coronary artery cryosections.

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

24 alyzed using immunohistochemistry on retinal cryosections.

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

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

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

28 gglutinin staining in retinal flatmounts and cryosections.

29 d by immunohistochemical analysis of retinal cryosections.

30 for assessing CI activity directly in tissue cryosections.

31 roteins and immune cell subsets in placental cryosections.

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

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

34 eyes were preserved <4 hours postmortem and cryosectioned.

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

36 me points, biologic samples were excised and cryosectioned.

37 ue onto the chuck inside the cryostat during cryosectioning.

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

39 ular tissues caused by formalin fixation and cryosectioning.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 Cryosectioning can be used to prepare thin enough sectio

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

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

73 Fluorescence microscopy on cryosections colocalized near-infrared fluorescent osteo

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

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

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

77 Serial cryosections (five per eye) were immunohistochemically l

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

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

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

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

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

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

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

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

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

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

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

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

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

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

92 Cryosectioning, immunohistochemistry, and fluorescence m

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

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

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

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

97 Cryosections indicated that tuberin is widely expressed

98 Examination of serial cryosections indicated that visceral podocytes migrated

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

100 Tokuyasu cryosectioning is relatively rapid but is limited to sma

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

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

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

104 Cryosections of A-Gl-prelabeled platelets labeled again

105 Cryosections of biofilms were treated with polyclonal an

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

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

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

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

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

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

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

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

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

115 Cryosections of fetal week 11-18 retinas were immunostai

116 Cryosections of HCEC aggregates were subjected to immuno

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

118 Vertical cryosections of human retinas were immunostained with an

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

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

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

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

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

124 Cryosections of LG were stained with cresyl violet, and

125 Ultrathin cryosections of lung tissue from rabbits given an infusi

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

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

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

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

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

131 Cryosections of retina and choroid from the macula and t

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

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

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

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

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

137 Cryosections of six diabetic epiretinal tissues were eva

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

139 Cryosections of the explant and the outgrowth were detec

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

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

142 Cryosections of the macula and periphery of human eyes (

143 By using cryosections of tumor specimens and immunohistochemistry

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

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

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

147 Retinas harvested for cryosectioning or flat mount preparations were subjected

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

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

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

151 Controls comprised heat treatment of cryosections prior to staining.

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

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

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

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

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

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

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

159 Epifluorescence of cryosections served as validation.

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

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

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

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

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

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

166 orescence determined by microscope images of cryosectioned tumors.

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

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

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

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

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

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

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

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

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

176 Tumor cryosections were analyzed with immunofluorescence and a

177 Cryosections were cut from the maculae of unfixed human

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

179 Cryosections were evaluated by standard histologic exami

180 Retinal cryosections were examined by TUNEL staining and outer n

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

182 Retinal cryosections were prepared for TUNEL analysis to determi

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

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

185 Cryosections were stained with antibodies against neutro

186 Cryosections were stained with antibodies against neutro

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

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

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

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

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