ライフサイエンスコーパス: hematoxylin

1 Kit and lightly counterstained with Mayer's hematoxylin.

2 verity of inflammation was assessed by eosin/hematoxylin.

3 clear marker (NeuN), and counterstained with hematoxylin.

4 In 12 cadavers, specimens were stained with hematoxylin and eosin (3 sections) or Masson trichrome (

5 ) previously had biopsies submitted for both hematoxylin and eosin (H & E) and direct IF testing.

6 Routine hematoxylin and eosin (H & E) staining and direct immuno

7 Hematoxylin and eosin (H & E) staining was performed to

8 Hematoxylin and eosin (H & E) staining was then performe

9 ove after repeated treatment trials, routine hematoxylin and eosin (H&E) and direct immunofluorescenc

10 dded lacrimal glands (LGs) were stained with hematoxylin and eosin (H&E) and evaluated with a stereom

11 Serial sections were then stained with hematoxylin and eosin (H&E) and subjected to detailed mo

12 tumor cells or cell aggregates identified by hematoxylin and eosin (H&E) and/or IHC.

13 novel OCT system and verified the results by hematoxylin and eosin (H&E) histology.

14 h recurrence and death compared with routine hematoxylin and eosin (H&E) histology.

15 The prognostic value of ultrastaging hematoxylin and eosin (H&E) negative LNs (N0) using pan-

16 The algorithm was tested using digitized hematoxylin and eosin (H&E) stained prostate cancer spec

17 scent staining images but not with classical hematoxylin and eosin (H&E) staining on the same tissue

18 Hematoxylin and eosin (H&E) staining, confocal microscop

19 s was performed using immunofluorescence and hematoxylin and eosin (H&E) staining.

20 Enucleated eyes were processed for hematoxylin and eosin (H&E) staining.

21 2 maps and were histologically identified by hematoxylin and eosin (H&E) staining.

22 icobacter pylori IgG-antibody titer changes, hematoxylin and eosin (H&E) stains, immunohistochemical

23 2,3,5-triphenyltetrazolium chloride (TTC) or hematoxylin and eosin (H&E) stains.

24 ct comparison between H&E alone and elastica Hematoxylin and Eosin (H&E) was made in 53 patients.

25 Tissue sections were stained with hematoxylin and eosin (H&E), and DNA was extracted from

26 These were compared with an adjacent hematoxylin and eosin (H&E)-stained section.

27 erial tissue sections that were stained with hematoxylin and eosin (H&E).

28 Hematoxylin and eosin (HE) staining of cerebral tissue w

29 ll lymph nodes were examined by conventional hematoxylin and eosin (HE) staining.

30 The SN was examined first by hematoxylin and eosin (HE), and if the SN was negative w

31 Liver damage was assessed by hematoxylin and eosin and alanine aminotransferase level

32 Every fifth section was stained with hematoxylin and eosin and analyzed histologically.

33 rized, as demonstrated by staining with both hematoxylin and eosin and antibodies to three different

34 Specimens were stained using hematoxylin and eosin and by immunohistochemistry for cy

35 were selected for histologic analysis using hematoxylin and eosin and dihydroxyphenylalanine oxidase

36 Brain sections at 7 days were examined via hematoxylin and eosin and Fluoro-Jade C (identifying dyi

37 the excised left kidney tissue stained with hematoxylin and eosin and Gomori's methenamine silver st

38 Hematoxylin and eosin and immunohistochemical analyses s

39 d at days 2, 7, and 56 and were evaluated by hematoxylin and eosin and immunohistochemical staining.

40 rwent frozen sectioning and were examined by hematoxylin and eosin and immunohistologic (cytokeratin)

41 ion of different regions of the retina using hematoxylin and eosin and immunostaining.

42 Hematoxylin and eosin and Oil Red O staining were perfor

43 cumulation and liver injury, as evidenced by hematoxylin and eosin and Oil Red O staining.

44 ns were routinely processed and stained with hematoxylin and eosin and periodic acid Schiff.

45 Hematoxylin and eosin and periodic acid-Schiff stained s

46 were assessed by means of flow cytometry and hematoxylin and eosin and periodic acid-Schiff staining,

47 and lung biopsy specimens were stained with hematoxylin and eosin and periodic acid-Schiff, visualiz

48 tions were stained with Masson trichrome and hematoxylin and eosin and subjected to the tartrate-resi

49 also performed on Tax(+) mouse tails, using hematoxylin and eosin and tartrate-resistant acid phosph

50 munohistochemistry (IHC) and inflammation by hematoxylin and eosin and trichrome staining, IHC, and i

51 were cultured, and microscopic analysis with hematoxylin and eosin and trichrome was performed.

52 Specimens were stained with hematoxylin and eosin and trichrome.

53 re made of each cut surface and stained with hematoxylin and eosin and/or Diff-Quik.

54 cted changes in histology were determined by hematoxylin and eosin as well as by Fluoro-Jade staining

55 fixed, sectioned, and stained with X-gal or hematoxylin and eosin for histochemical and histopatholo

56 site were examined by light microscopy using hematoxylin and eosin Goldner's trichrome stains, and po

57 specimens imaged using both SRH and standard hematoxylin and eosin histology.

58 ibiting close correlation with corresponding hematoxylin and eosin histology.

59 umor diagnostic imaging is commonly based on hematoxylin and eosin or immunohistochemical staining of

60 at 6 microns to 8 microns, and stained with hematoxylin and eosin or Masson's trichrome.

61 Thin sections (5 microm) were stained with hematoxylin and eosin or tartrate-resistant acid phospha

62 Hind limb sections were stained with hematoxylin and eosin or toluidine blue and scored for i

63 jury, as indicated by Sirius Red/Fast Green, hematoxylin and eosin quantification, and serum alanine/

64 In 319 patients with both frozen-section hematoxylin and eosin results and BLN Assay results, the

65 Anatomy was assessed by serial hematoxylin and eosin sections and scanning electron mic

66 Coded hematoxylin and eosin sections were evaluated for tumor

67 and can be readily identified using routine hematoxylin and eosin sections, we suggest that pathway

68 ASS1 + HCA combined with a typical hematoxylin and eosin stain aspect defined a new HCA sub

69 Hematoxylin and eosin stain revealed a paucity of connec

70 ally and clinically node-negative by routine hematoxylin and eosin stain, 100 patients were found to

71 The aortic valves were examined with hematoxylin and eosin stain, Masson trichrome, macrophag

72 were killed at 7 days and injured neurons in hematoxylin and eosin stained coronal brain sections thr

73 e staining, and morphology was studied using hematoxylin and eosin stained sections.

74 related with histopathological assessment of hematoxylin and eosin stained thin tissue sections obtai

75 of occult nodal metastases not identified by hematoxylin and eosin staining (H&E).

76 a motility, and histologic examination using hematoxylin and eosin staining and CD8/CD4 immunohistoch

77 Tissue architecture was determined after hematoxylin and eosin staining and cellular organization

78 Hematoxylin and eosin staining and histologic grading fo

79 he arteries were evaluated histologically by hematoxylin and eosin staining and immune staining with

80 ll-thickness wedge biopsy was performed, and hematoxylin and eosin staining and immunohistochemistry

81 omposition, and cytokine expression by using hematoxylin and eosin staining and immunohistochemistry.

82 osectioned tissue sections were subjected to hematoxylin and eosin staining and MALDI-MSI analyses.

83 Hematoxylin and eosin staining and smooth muscle actin (

84 Histological examination with hematoxylin and eosin staining and von Kossa staining co

85 changes that are identified by cytology with hematoxylin and eosin staining but also provided molecul

86 Hematoxylin and eosin staining confirmed marked synovial

87 hen stained to reveal tumor pathophysiology: Hematoxylin and eosin staining demonstrated viable and n

88 h categories were examined with conventional hematoxylin and eosin staining for epithelial, connectiv

89 eased apoptosis by both active caspase 3 and hematoxylin and eosin staining in both the intestinal ep

90 valuation by means of light microscopy after hematoxylin and eosin staining might not accurately refl

91 Hematoxylin and eosin staining of liver tissue of knocko

92 al signs of muscular dystrophy, as judged by hematoxylin and eosin staining of muscle biopsies taken

93 in whole eye flatmounts was quantified, and hematoxylin and eosin staining of paraffin sections was

94 and three quantitative characteristics from hematoxylin and eosin staining of prostate tissue.

95 Hematoxylin and eosin staining revealed intact colonic e

96 Furthermore, hematoxylin and eosin staining revealed necrotic cell de

97 Hematoxylin and eosin staining revealed similar nuclear

98 Hematoxylin and eosin staining revealed that moderate to

99 Hematoxylin and eosin staining showed clear signs of vas

100 Hematoxylin and eosin staining showed epithelial migrati

101 Hematoxylin and eosin staining showed no differences in

102 ymph nodes in 12 patients were identified by hematoxylin and eosin staining to have evidence of metas

103 leukocyte, liver, and jejunum DNA damage and hematoxylin and eosin staining to investigate macroscopi

104 Hematoxylin and eosin staining was done to verify the pr

105 Hematoxylin and eosin staining was performed in six anim

106 Blue-stained nodes that were negative by hematoxylin and eosin staining were further analyzed by

107 29%) whose lymphatic basins were negative by hematoxylin and eosin staining were upstaged by immunohi

108 biopsies were analyzed for histomorphology (hematoxylin and eosin staining) and DNA damage (terminal

109 biopsies were analyzed for histomorphology (hematoxylin and eosin staining) and markers of apoptosis

110 romote microglial activation as confirmed by hematoxylin and eosin staining, (3)H-PK11195 autoradiogr

111 levels of aspartate aminotransferase (AST), hematoxylin and eosin staining, and specific markers of

112 ,3,5-triphenyltetrazolium chloride staining, hematoxylin and eosin staining, and terminal deoxynucleo

113 Histological examination included hematoxylin and eosin staining, immunofluorescence, immu

114 ated for apoptotic and immunologic events by hematoxylin and eosin staining, immunohistochemical stai

115 ens and corneal development were assessed by hematoxylin and eosin staining, in situ hybridization, a

116 depleted allogeneic and allogeneic grafts by hematoxylin and eosin staining, terminal deoxynucleotidy

117 examined by immunohistochemical analysis and hematoxylin and eosin staining.

118 s; structural mucosal damage was measured by hematoxylin and eosin staining.

119 h slit lamp, digital confocal microscopy and hematoxylin and eosin staining.

120 l structure of the retina was examined using Hematoxylin and eosin staining.

121 Mouse eye morphology was assessed by hematoxylin and eosin staining.

122 y knee biopsy and assessed histologically by hematoxylin and eosin staining.

123 ally and neuronal integrity was assessed via hematoxylin and eosin staining.

124 d is usually incompatible with commonly used hematoxylin and eosin staining.

125 e stroma of mouse corneas was monitored with hematoxylin and eosin staining.

126 d-type control animals was examined by using hematoxylin and eosin staining.

127 ures closely resembling histopathology using hematoxylin and eosin staining.

128 ures and were processed histologically using hematoxylin and eosin to determine the degree of inflamm

129 Morphology (hematoxylin and eosin), apoptosis (M30), tight junctions

130 ic data (e.g., images of cell proliferation, hematoxylin and eosin).

131 ing an abdominal reexploration, stained with hematoxylin and eosin, and evaluated according to a semi

132 days, calvaria decalcified and stained with hematoxylin and eosin, and images digitized and measured

133 ning plastic sections with toluidine blue or hematoxylin and eosin, and show how to couple these stai

134 formalin, embedded in paraffin, stained with hematoxylin and eosin, and/or fresh frozen.

135 histopathologic evaluation of organ injury (hematoxylin and eosin, electron microscopy) and immunohi

136 cytokines, and osteoclasts was assessed from hematoxylin and eosin, immunohistochemical, or tartrate-

137 n, intracellular Ca(2+) handling, histology (hematoxylin and eosin, Masson trichrome), protein damage

138 Tissue of resected HCCs was stained for hematoxylin and eosin, Masson trichrome, alpha-smooth mu

139 reated mice as shown by transaminase levels, hematoxylin and eosin, Masson's trichrome staining, and

140 m) through the optic nerve were stained with hematoxylin and eosin, or incubated with anti-Hsp90, ant

141 Standard hematoxylin and eosin, periodic acid-Schiff and silver m

142 Tissue sections stained by hematoxylin and eosin, periodic acid-Schiff stain, and G

143 Gram staining, bright-field microscopy, hematoxylin and eosin, periodic acid-Schiff, Congo red,

144 Hematoxylin and eosin, Prussian blue and ED-1, a monoclo

145 Hematoxylin and eosin, S100, and smooth muscle actin imm

146 Eye sections were stained with hematoxylin and eosin, Schiff reagent, and fluorescein,

147 The microscopic slides were stained with hematoxylin and eosin, special stains for organisms, and

148 Sections were stained with hematoxylin and eosin, tissue gram stain, and immunostai

149 ions from this tissue were then stained with hematoxylin and eosin, trichrome, and/or tyrosine hydrox

150 n the epithelium) were examined by reviewing hematoxylin and eosin-stained biopsies and by immunohist

151 19 (16%) had morphologic evidence of HCL in hematoxylin and eosin-stained bone marrow sections.

152 Hematoxylin and eosin-stained histologic sections were u

153 rmanent sections were evaluated with up to 4 hematoxylin and eosin-stained levels and cytokeratin imm

154 Hematoxylin and eosin-stained plastic sections were used

155 tmounts and by counting preretinal nuclei of hematoxylin and eosin-stained retinal sections, respecti

156 One hematoxylin and eosin-stained section of the resected pr

157 Full-face hematoxylin and eosin-stained sections of 506 tumors fro

158 Microscopic examination of hematoxylin and eosin-stained sections revealed non-case

159 Hematoxylin and eosin-stained sections were scored for i

160 In addition to the macroscopic analyses, hematoxylin and eosin-stained sections were used to stud

161 und surface and inflammation was assessed on hematoxylin and eosin-stained sections.

162 Morphologic analyses were conducted on hematoxylin and eosin-stained sections.

163 l diagnosis, three pathologists examined the hematoxylin and eosin-stained slides of the known DIF-po

164 Tissue response, indicated by examination of hematoxylin and eosin-stained tissue sections and immuno

165 Demineralized and hematoxylin and eosin-stained tissues at developmental s

166 o neuronal injury in adjacent Nissl-stained, hematoxylin and eosin-stained, and terminal deoxynucleot

167 the alpha-camera and the other stained with hematoxylin and eosin.

168 specimens were decalcified and stained with hematoxylin and eosin.

169 yes, and paraffin sections were stained with hematoxylin and eosin.

170 examined histologically after staining with hematoxylin and eosin.

171 Multiple serial sections were stained with hematoxylin and eosin.

172 examined histologically after staining with hematoxylin and eosin.

173 can be reliably used on tissue stained with hematoxylin and eosin.

174 imaged with autoradiography and stained with hematoxylin and eosin.

175 mage in cardiac tissue sections stained with hematoxylin and eosin.

176 Sections were routinely stained with hematoxylin and eosin.

177 es from each specimen were also stained with hematoxylin and eosin.

178 In parallel, RTDs were stained with hematoxylin and periodic acid Schiff to determine pericy

179 staining methods: Hematoxylin &Eosin, CD31 &Hematoxylin, and Ki-67 and where most of the nuclei were

180 )Cu-NOTA-AE105 was confirmed by alignment of hematoxylin- and eosin-stained and uPAR immunohistochemi

181 or of histopathologic response was scored on hematoxylin- and eosin-stained sections of the surgical

182 , Hoechst fluorescence vascular imaging, and hematoxylin-and-eosin histology-were superimposed, evalu

183 cence assessment was far more sensitive than hematoxylin-and-eosin staining in detecting small MDBs,

184 Hematoxylin-and-eosin staining showed viable grafts in 9

185 MDB formation was compared using hematoxylin-and-eosin staining, or immunofluorescence st

186 mation in scid mice, using immunostained and hematoxylin-and-eosin-stained coronal sections of decalc

187 Decalcified, hematoxylin-and-eosin-stained cross-sections of the defe

188 f an inflammatory infiltrate was measured in hematoxylin-and-eosin-stained sections.

189 ree cohorts with different staining methods: Hematoxylin &Eosin, CD31 &Hematoxylin, and Ki-67 and whe

190 Gross inspection, slicing, and hematoxylin-eosin (10 specimens) and nicotinamide adenin

191 ded temporal arteries were examined first by hematoxylin-eosin (H&E) staining to establish the diagno

192 dye and/or radiotracer and were examined by hematoxylin-eosin (H&E) staining, cytokeratin immunohist

193 riphenyltetrazolium chloride (TTC) staining, hematoxylin-eosin (H&E) staining, the terminal deoxyribo

194 burden, sections were processed for standard hematoxylin-eosin (H&E) staining.

195 oidal thickness and area were measured after hematoxylin-eosin (H&E) staining.

196 uclear layer (ONL) thickness was measured on hematoxylin-eosin (H&E)-stained sections, and apoptosis

197 Sections were scored for TILs on hematoxylin-eosin (H&E)-stained sections, and immunohist

198 block, 3 sequential slides were stained with hematoxylin-eosin (H-E), melanoma antigen (melan-A), and

199 with immunohistochemical analysis, including hematoxylin-eosin (H-E), Von Kossa, and von Willibrand f

200 Hematoxylin-eosin (HE) and immunohistochemical staining

201 ation into hepatic DNA, the mitotic index in hematoxylin-eosin (HE) sections and by immunochemical de

202 e kidneys of 14-16-month-old apoE-null mice, hematoxylin-eosin (HE) staining revealed increased mesan

203 Neuronal damage was subsequently assessed by hematoxylin-eosin and Fluoro-Jade B staining.

204 opsy specimens from all lesions stained with hematoxylin-eosin and immunohistochemical markers (melan

205 upstaged 48 of 161 histopathology-negative (hematoxylin-eosin and immunohistochemistry) SLN specimen

206 The biopsy specimens were stained with hematoxylin-eosin and immunostained for Musashi-1 (Msi-1

207 Brain sections were stained with hematoxylin-eosin and Luxol fast blue.

208 after paraffin embedding, and staining with hematoxylin-eosin and Movat pentachrome.

209 IHC) are visualized as inclusion bodies with hematoxylin-eosin and nucleic acid stains and in methyle

210 HP was performed on hematoxylin-eosin and periodic acid Schiff-stained secti

211 made from all the samples and stained using hematoxylin-eosin and periodic acid-Schiff stains.

212 d at 5 and 10 days post-PHX, as indicated by hematoxylin-eosin and proliferating cell nuclear antigen

213 stological analyses of sections stained with hematoxylin-eosin and tartrate-resistant acid phosphatas

214 At 2 wk, hematoxylin-eosin and terminal deoxynucleotidyl transfer

215 from infected control animals, stained with hematoxylin-eosin and the Gram stain, showed edema and/o

216 multilevel sectioning and were stained with hematoxylin-eosin and the pancytokeratin marker AE1/AE3.

217 Histologic appearance (hematoxylin-eosin and trichrome staining) and presence o

218 Slides stained with hematoxylin-eosin and trichrome were evaluated by two li

219 eth processed for histologic evaluation with hematoxylin-eosin and Verhoeff's stains.

220 imonidazole, sirius red, cytokeratin 14, and hematoxylin-eosin for quantitative assessment of hypoxia

221 samples should be made available for routine hematoxylin-eosin histopathological evaluation until the

222 Sentinel lymph node specimens (hematoxylin-eosin negative) and bone marrow specimens we

223 ed, and alternate sections were stained with hematoxylin-eosin or stained for GFP expression.

224 orrelated with hyperplasia of melanocytes in hematoxylin-eosin sections (kappa = 0.422, P < .001).

225 om 30 laser channels was identified from the hematoxylin-eosin sections.

226 filtrating lymphocytes (TILs) were scored in hematoxylin-eosin slides using current consensus guideli

227 ks of acquired specimens were examined using hematoxylin-eosin stain and double immunostain using HMB

228 Histologic slides (hematoxylin-eosin stain) from three resected rotator cuf

229 formed by using standard light microscopy on hematoxylin-eosin stained specimens; immunohistochemistr

230 reported in the anatomic diagnosis, based on hematoxylin-eosin staining alone, for three (8%) of the

231 The corneal buttons were then evaluated by hematoxylin-eosin staining and by immunostaining with ma

232 Hematoxylin-eosin staining confirmed that all spots with

233 to macromolecule albumin) extravasation, and hematoxylin-eosin staining helped detect only scattered

234 Histologic data from hematoxylin-eosin staining of explanted liver specimens

235 Immunohistochemical and hematoxylin-eosin staining of liver sections was perform

236 ied by frozen section, touch preparation, or hematoxylin-eosin staining on permanent section.

237 stochemically positive or negative [IHC+/-], hematoxylin-eosin staining positive or negative [H & E +

238 Hematoxylin-eosin staining showed that neuronal injury i

239 Histologic examination with hematoxylin-eosin staining showed that results of 36 (67

240 We used hematoxylin-eosin staining to examine cochlear histopath

241 Hematoxylin-eosin staining was also performed.

242 as evaluated and histologic examination with hematoxylin-eosin staining was performed at 4 hours, 24

243 stroduodenoscopy, but histologic findings at hematoxylin-eosin staining were normal.

244 Autoradiography and hematoxylin-eosin staining were performed on the dissect

245 x vivo both for inflammation grade (by using hematoxylin-eosin staining) and for expression of select

246 ivo by means of histologic examination (with hematoxylin-eosin staining) and immunostaining of vascul

247 (reduced alanine transferase) and necrosis (hematoxylin-eosin staining) compared with the HSP27 WT m

248 polymorphonuclear cell (PMN) infiltration by hematoxylin-eosin staining, and for oxygen radical-induc

249 At hematoxylin-eosin staining, coagulation necrosis was obs

250 ses were performed with specific techniques (hematoxylin-eosin staining, terminal deoxynucleotidyl tr

251 e of TF using a similar human-based score on hematoxylin-eosin staining.

252 (98.3%), 3904 (76.3%) were tumor-negative by hematoxylin-eosin staining.

253 sections were taken for autoradiography and hematoxylin-eosin staining.

254 e-mediated dUTP nick end-labeling assay, and hematoxylin-eosin staining.

255 Tumors were assessed for necrosis with hematoxylin-eosin staining.

256 ent to those containing VZV were examined by hematoxylin-eosin staining.

257 At the same time, Gram and hematoxylin-eosin stains of paraffin sections were perfo

258 Finally, coregistration of histologic hematoxylin-eosin stains with autoradiography signals fr

259 ned with isolectin B4, Masson trichrome, and hematoxylin-eosin were used to characterize injured myoc

260 c, major histocompatability complex class I, hematoxylin-eosin).

261 icrom) along the coronal plane, stained with hematoxylin-eosin, and visualized by conventional light

262 GI was quantified on hematoxylin-eosin, CD3, CD20, and CD68 stains on biopsie

263 RPM specimens from 7 eyes were stained with hematoxylin-eosin, cytokeratin 7, cytokeratin AE1/3, smo

264 egration, or regeneration was analyzed using hematoxylin-eosin, immunohistochemical staining, and cel

265 Hematoxylin-eosin, Masson trichrome, and biotinylated is

266 pathologic findings in sections stained with hematoxylin-eosin, periodic acid-Schiff (PAS) reaction,

267 araffin-embedded tissues and correlated with hematoxylin-eosin, periodic acid-Schiff (PAS), and mucic

268 pecimen was examined following staining with hematoxylin-eosin, periodic acid-Schiff, and Gram stain.

269 Sections of the liver were examined with hematoxylin-eosin, periodic acid-Schiff, Masson trichrom

270 tained using a variety of methods, including hematoxylin-eosin, periodic acid-Schiff, methenamine sil

271 anine aminotransferase) and liver histology (hematoxylin-eosin, Sudan III) were determined to monitor

272 Histopathologic slides were evaluated with hematoxylin-eosin, trichrome, and elastin stains.

273 evaluated levels of percentage of TILs using hematoxylin-eosin-stained core biopsy sections taken at

274 luorescence images, NADH-stained images, and hematoxylin-eosin-stained images were compared.

275 Staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr

276 nts using staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr

277 Standard hematoxylin-eosin-stained sections and immunohistochemic

278 re studied by (i) microscopic examination of hematoxylin-eosin-stained sections for inflammation and

279 Hematoxylin-eosin-stained sections of the same transplan

280 After resection, whole-mount hematoxylin-eosin-stained sections were registered to th

281 (1) Review of clinical data and hematoxylin-eosin-stained sections with (2) immunohistoc

282 Review of clinical data, hematoxylin-eosin-stained sections, and immunohistochemi

283 Hematoxylin-eosin-stained slices of mammary tissues were

284 issue sections and/or detection of amebas in hematoxylin-eosin-stained slides.

285 Hematoxylin-eosin-stained tumor slides from patients wit

286 uted tomography (CT) and light microscopy of hematoxylin-eosin-stained tumor tissue were compared.

287 erated and compared with digitized images of hematoxylin-eosin-stained whole-mount histologic slices.

288 ed in each specimen on routine staining with hematoxylin-eosin.

289 Hematoxylin/eosin and toluidine blue staining and atomic

290 Hematoxylin/eosin staining of rd7 tissue shows that the

291 ys in culture was evaluated by staining with hematoxylin/eosin, and by ultrastructural analysis that

292 lso applying a specific DNA probe as well as hematoxylin for electrochemical indicator.

293 d to diagnose LSCD than the conventional PAS-hematoxylin method, although a minimum RNA concentration

294 dium); they were tested with trichrome, iron-hematoxylin, or modified acid-fast stains or the Meridia

295 Histologic analysis was performed by hematoxylin-phloxine-safran staining, followed by immuno

296 et cells in the cornea was determined by PAS-hematoxylin staining, whereas the presence of the MUC5AC

297 ples were also available for comparative PAS-hematoxylin staining.

298 drug uptake and subsequent visualization on hematoxylin staining.

299 preretinal nuclei were quantified by PAS and hematoxylin staining.

300 Nissl and hematoxylin stains provided little information regarding