ライフサイエンスコーパス: frozen section

1 ion, 12 with a paraffin section and 6 with a frozen section.

2 the air spaces between cells when preparing frozen sections.

3 mined in fixed sections and in immunolabeled frozen sections.

4 that were identified in BP whole-mounts and frozen sections.

5 contributes to a high rate of noninformative frozen sections.

6 cells procured by LCM from fixed and stained frozen sections.

7 er capture microdissection (LCM) of adjacent frozen sections.

8 (BrdU) incorporation and immuno-staining of frozen sections.

9 re hybridized to female mouse lacrimal gland frozen sections.

10 re determined by histopathologic analysis on frozen sections.

11 y DO-7 to p53 protein were also performed on frozen sections.

12 y obviating cumbersome oil red O staining of frozen sections.

13 a was measured by fluorescence microscopy on frozen sections.

14 gative margins after positive intraoperative frozen sections.

15 gins after initially positive intraoperative frozen sections.

16 o stain for irreversibly injured myocytes in frozen sections.

17 een fluorescent protein (eGFP) expression in frozen sections.

18 immunofluorescence in either whole mounts or frozen sections.

19 l mucosa by laser capture microdissection on frozen sections.

20 Four or 24 h post-TBI, ten frozen sections (10 microm thick, every 15th section) we

21 Frozen sections (10 microns) were used to reconstruct a

22 (17% v 7%, P < .001), have ITCs detected on frozen section (62% v 8%, P < .001), have lymphovascular

23 Labeling of frozen sections 7 d after a unilateral knife lesion to t

24 re calculated per group (Sens, Spec, AUROC): frozen section = 86%, 96%, 0.96 (n = 9); cytology = 91%,

25 sections was essentially the same as that in frozen sections, although more detail of the subcellular

26 nt-of-procedure pathology protocols, such as frozen section analysis (FSA), are destructive and too t

27 Performing frozen section analysis aimed at the fluorescent spots w

28 Frozen section analysis and touch-preparation cytology h

29 th fine-needle aspiration and intraoperative frozen section analysis had low sensitivities in the det

30 ion of sentinel nodes with touch imprint and frozen section analysis in patients treated with neoadju

31 early GC or patients with comorbidities; (7) frozen section analysis of margins; (8) nonemergent case

32 because metastatic disease was discovered on frozen section analysis of the sentinel node.

33 Yet, intraoperative frozen section analysis of tumor margins is a time-consu

34 overage than destructive and labor-intensive frozen section analysis techniques.

35 rgeons rely on touch preparation cytology or frozen section analysis to assess tumour margin status i

36 Frozen section analysis was again similar with 74% sensi

37 Frozen section analysis was similar with 74% sensitivity

38 models were compared with gross assessment, frozen section analysis, and/or final postoperative path

39 The NeuroSAFE technique, a standardised frozen section analysis, enables accurate real-time dete

40 positive by DESI-MSI/Lasso, but negative by frozen section analysis.

41 Frozen-section analysis rendered a definitive diagnosis

42 l cancer, and given practical limitations of frozen-section analysis, a need exists for real-time, no

43 Pooled data suggest that frozen section and cytology have the greatest diagnostic

44 ulation of breast cancer patients, SLND with frozen section and IHC was a minimally invasive, highly

45 Standard-of-care frozen section and immunohistochemical staining on perma

46 el nodes were examined intraoperatively with frozen section and postoperatively with hematoxylin and

47 group and the NACT group were compared, both frozen section and touch imprint analysis had similar se

48 nuclear density quantification, to physical frozen sectioning and standard microscopy.

49 All lymph nodes underwent frozen sectioning and were examined by hematoxylin and e

50 hat of the macrophage marker sialoadhesin in frozen sections and coincided with that of another macro

51 Normal hiuman corneas were prepared for frozen sections and for culture of corneal keratinocytes

52 rtic root was quantitated by counting serial frozen sections and found to be 143 +/- 17 macrophages p

53 e preclinical feasibility, ex vivo 50 microm frozen sections and fresh intact thick tissue samples ex

54 rods was evaluated by confocal microscopy of frozen sections and immunoelectron microscopy.

55 ing was used to detect sialomucin complex in frozen sections and impression cytology specimens of hum

56 nent role in lymphocyte adhesion to GC in PP frozen sections and participates significantly in bindin

57 -8, and caspase-3 was determined by staining frozen sections and performing Western blot analysis and

58 Frozen sections and/or flat mounts of lens capsules were

59 ion, at which time brains were removed, snap frozen, sectioned and quantitatively analyzed for fluore

60 atrix for spiked drug standards which can be frozen, sectioned and subsequently analyzed for the gene

61 Final pathologic findings were compared with frozen sections, and cost analyses were performed.

62 Immunolocalization of A2aR was performed on frozen sections, and reaction product density was quanti

63 inner or outer retinal surface, processed as frozen sections, and viewed with a fluorescence microsco

64 Tumors were frozen, sectioned, and exposed to phosphor image plates

65 mice bearing HER2 + breast tumors were snap-frozen, sectioned, and imaged using autoradiography.

66 After fixation, frozen sections are immunostained under RNAse-free condi

67 Intraoperative frozen sections are unlikely to abbreviate the LND proce

68 ive cohort study of 3148 cases pertaining to frozen sections associated with the staged excision of N

69 ccurate identification of prostate cancer in frozen sections at the time of surgery can be challengin

70 sion may obviate the need for intraoperative frozen section because excised parathyroid adenomas unif

71 Immunostaining of left ventricular frozen sections before and 8 h after CLP revealed the pr

72 ed criteria features underwent pretransplant frozen section biopsies.

73 We also analyzed the reliability of donor frozen-section biopsies in quantitating microsteatosis.

74 However, known CCA or common duct frozen section biopsy specimen or both showing CCA are a

75 e regression analysis, only common bile duct frozen section biopsy specimen showing CCA was predictiv

76 sociated with female gender, benign tumor on frozen section biopsy, and postoperative intubation (chi

77 We have recently used frozen-section biopsy to distinguish between microvesicu

78 Frozen-section biopsy was reliable for pretransplant dec

79 iNOS protein was detected in biopsy frozen sections by immunofluorescence.

80 ctin and ICAM-1 expression were evaluated on frozen sections by using standard immunohistochemical te

81 nosis of GCA, whereas positive findings from frozen sections can be reliably used to defer a contrala

82 If the DN is positive on intraoperative frozen section, careful evaluation of the central and la

83 more likely to need further resection after frozen section compared to non-aggressive subtypes.

84 Providing intraoperative frozen section control biopsies may offer clarity in cas

85 3%) of 24 of the tumors were resectable with frozen section control of the duct margins (9 pancreatod

86 Use of a frozen section control was associated with statistically

87 ] male), 50% of patients (n = 85) received a frozen section control.

88 h paraffin section control (21.7%), WLE with frozen-section control (19.3%), and excision without mar

89 patients with nondiagnostic margins, use of frozen section controls was associated with statisticall

90 thout a decrease in hormone levels, avoiding frozen-section delay; and correctly identifying the exci

91 ere blinded to the correlating gold standard frozen section diagnoses, independently reviewed the DSC

92 Bulk frozen sections displaying the most extensive but not mi

93 mpts many surgeons to perform intraoperative frozen section during thyroid lobectomy.

94 e alternative to histopathologic analysis of frozen sections during Mohs surgery because large areas

95 eys are discarded, often based on results of frozen section evaluation of a screening biopsy read by

96 The developed method showed agreement with frozen section evaluation of specimen margins in 24 of 3

97 of IIC are similar to that of intraoperative frozen section evaluation.

98 Intraoperative frozen section examination was routinely performed to as

99 veloped a rapid immunostaining procedure for frozen sections followed by laser capture microdissectio

100 tive imprint cytology (IIC) is equivalent to frozen sectioning for rapid SLN evaluation and is advant

101 es closely correspond to those found in Mohs frozen sections for 41 specimens out of 45.

102 Finally, examination of frozen sections from 10 primary brain tumor biopsies by

103 tion was performed on invasive breast cancer frozen sections from 65 patients undergoing resection wi

104 viewed, 60 showed inflammation in histologic frozen sections from an excision specimen that was follo

105 lly selected 1 mm diameter regions of single frozen sections from each tissue.

106 Frozen sections from excised tumors were then evaluated

107 ry acidic protein (GFAP), and factor VIII on frozen sections from eyes of patients with diabetes with

108 ches in these tumor xenografts as well as in frozen sections from primary human breast cancers.

109 Frozen sections from transplanted animals were stained h

110 Frozen section (FS) analysis of sentinel nodes offers po

111 s to test the hypothesis that intraoperative frozen section (FS) and re-resection results to achieve

112 ificity of sentinel lymph node biopsy (SLNB) frozen section (FS) examinations to detect metastatic ly

113 e expression using both whole mount (WM) and frozen section (FS) LacZ staining in 313 unique KOMP mut

114 odenectomy (PD) for ductal adenocarcinoma, a frozen section (FS) neck margin is typically assessed, a

115 Twenty-nine were randomized to the frozen-section group and 32 to the non-frozen-section gr

116 Of the 31 patients in the non-frozen-section group, 3 (10%) showed well-differentiated

117 In the non-frozen-section group, one patient was excluded when gros

118 o the frozen-section group and 32 to the non-frozen-section group.

119 In comparison, bilateral frozen section-guided sequential TABs were performed in

120 Frozen section had a specificity of 99.4% (95% CI, 98.5-

121 -grade or no dysplasia) after intraoperative frozen section had significantly superior OS compared to

122 in cancer (NMSC), inflammation in histologic frozen sections has been found to occasionally presage t

123 dissection of routinely stained or unstained frozen sections has been used successfully to obtain pur

124 CAM-1 in HCL spleen and by the fact that, in frozen sections, HCs adhered (via VCAM-1) to the red pul

125 In 319 patients with both frozen-section hematoxylin and eosin results and BLN Ass

126 From frozen sections, hepatocytes were laser-capture microdis

127 Using frozen-section histologic evaluation in Tanzania (high-t

128 phic surgery of NMSC with the examination of frozen sections, histologic inflammation is modestly pre

129 t delimitation of the tumour and analysed by frozen section histological examination.

130 peration the cyst was proven to be benign by frozen-section histological examination and the transpla

131 section/reconstruction, arterial divestment, frozen section histology of perivascular tissue, extent

132 atients, the initial resection margin on the frozen section histology was not free of tumour cells an

133 amous cell carcinoma, such as intraoperative frozen section histopathology (IFSH) taken from the tumo

134 during Mohs micrographic surgery faster than frozen section histopathology, and one or two orders of

135 islet incubation in 100% human serum before frozen section, human IgG and IgM, C3, C4, and C5b-9 was

136 Significantly, frozen-section immunofluorescence failed to reveal the L

137 ue stained in azure II-methylene blue and on frozen sections immunolabeled for cone, rod, or glial pr

138 on microscopy, and by confocal microscopy in frozen sections immunolabeled for the mouse UV-cone pigm

139 (P < 0.001) and it proved more accurate than frozen section in diagnosing lung adenocarcinomas.

140 Immunohistochemical analysis of frozen sections in human basal cell carcinomas and squam

141 gins, large-scale studies on the accuracy of frozen sections in predicting final surgical margin stat

142 Enzymatic activity, measured either in frozen sections in situ or in the cuvette assay, was pos

143 risk to low-risk margin after intraoperative frozen section is associated with survival benefit and s

144 %) with follicular neoplasms of the thyroid, frozen section is neither informative nor cost-effective

145 chieve a negative neck margin after positive frozen section is not associated with improved OS.

146 s anterior were dissected in their entirety, frozen, sectioned longitudinally, and immunostained for

147 All patients underwent tumor excision with frozen section margin control at the Goldschleger Eye In

148 collaboration based on permanent analysis of frozen section margins, main specimens, and supplemental

149 ssed in 18 whole slide images of donor liver frozen sections (n = 59).

150 nt, routine immunofluorescence analysis of a frozen section of her kidney biopsy with antihuman IgG s

151 s with brain tumors and killed 2 h later for frozen sectioning of brain and film autoradiography.

152 The mice were sacrificed 6 h later for frozen sectioning of the brain and quantitative autoradi

153 antibodies to 27 ECM components was used on frozen sections of 14 normal and 20 PBK/ABK corneas.

154 tyrosine-rich region was detected readily in frozen sections of 5- to 6-month-old mouse corneal strom

155 asionally presage the detection of tumors in frozen sections of adjacent excision specimens.

156 olated by laser-capture microdissection from frozen sections of adjacent regions of arteries affected

157 In contrast, frozen sections of adult human and bovine corneas did no

158 In situ hybridization was performed on frozen sections of albino mouse eyes using riboprobes ge

159 was detected in a subpopulation of cells in frozen sections of aortic valves, suggesting the transdi

160 sue, we performed Stamper-Woodruff assays on frozen sections of biopsy specimens of cutaneous lesions

161 Obtaining frozen sections of bone tissue for intraoperative examin

162 ribution of Kir7.1 protein was determined in frozen sections of bovine retina-RPE-choroid by indirect

163 Frozen sections of capsulated and decapsulated bovine an

164 As was evaluated by in situ hybridization on frozen sections of chick scleras using 33P-labeled RNA p

165 Fresh-frozen sections of corneas from an 18-year-old and a 74-

166 Frozen sections of corneas obtained 6, 18, and 24 hours

167 Frozen sections of EAU eyes were reacted with 3-hydroxy-

168 mmunohistochemical analysis was performed on frozen sections of eight surgically excised ARMD-related

169 Frozen sections of enucleated globes with intact EOMs an

170 es (Lc) or other interstitial nuclei (Li) in frozen sections of extensor digitorum longus.

171 Frozen sections of eyes from naive mice or mice with EAU

172 Frozen sections of gingival specimens from these patient

173 Frozen sections of gray matter from orbitofrontal area 4

174 vestigated by immunofluorescence analysis on frozen sections of human donor eyes.

175 Glands of Wolfring were isolated from frozen sections of human eyelids by laser microdissectio

176 In frozen sections of human skin, FGF-2 binds to keratinocy

177 SKW3 cells added under flow conditions to frozen sections of human tonsil bound and rolled along r

178 complex in ELISA and to tumor endothelium in frozen sections of human tumors, rodent tumors, and huma

179 3G5 stained frozen sections of human, bovine, porcine, rat, and rabb

180 was performed for GLUT1, GLUT2 and GLUT4 in frozen sections of hypothalami from normal rats.

181 performed Stamper-Woodruff binding assays on frozen sections of inflamed and naive brains.

182 Frozen sections of lacrimal glands from five rats were s

183 Frozen sections of lacrimal glands from MRL/+ and MRL/lp

184 Frozen sections of lacrimal glands from MRL/lpr and MRL/

185 Fixed frozen sections of lateral eye were examined with conven

186 hepatocytes that were infected with virus in frozen sections of liver tissue obtained from patients w

187 idermal growth factor receptor in a panel of frozen sections of mammary carcinoma specimens.

188 tured T84 human colon carcinoma cells and in frozen sections of mouse intestine.

189 sing an in vitro autoradiographic technique, frozen sections of New Zealand white rabbit medulla were

190 While frozen sections of normal bowel revealed bright gp180 st

191 detect Fas and Fas ligand proteins in fresh-frozen sections of normal human cornea.

192 Studies were performed on frozen sections of normal human, bovine, porcine, rabbit

193 Frozen sections of postmortem fixed monkey eyes were imm

194 which steatosis is assessed and reported in frozen sections of potential donor livers.

195 Cx26, Cx32, Cx43, and Cx50 was performed on frozen sections of rabbit and rat ciliary body using ind

196 In frozen sections of rat skeletal muscle, antibodies to th

197 = 4), primary breast tumors (n = 8), and the frozen sections of SNs (n = 22) from 22 patients with Am

198 on, we observed increased fak copy number in frozen sections of squamous cell carcinomas.

199 MMP-2 was visualized in frozen sections of the aortic wall by an immunofluoresce

200 Frozen sections of the enucleated eyes were analyzed for

201 ACS and cryptopatch cells were isolated from frozen sections of the intestine by laser-assisted micro

202 When HCII was incubated with frozen sections of the mouse carotid artery, it bound sp

203 Frozen sections of the peripheral retinal margin and par

204 In situ hybridization was carried out on frozen sections of the rat corneas obtained at different

205 e-peptides based on their ability to bind to frozen sections of triple-negative breast cancer, 4T1 tu

206 Frozen sections of two donor eyes obtained at autopsy fr

207 Frozen sections of whole eye, lid margin, and Harderian

208 Frozen sections of whole mount-stained embryonic liver d

209 Archived frozen sections of xeno-kidney grafts over the past 10 y

210 during surgery by pathologic evaluation of (frozen sections of) the tissue at the resected specimen

211 After intraoperative verification (by frozen section) of margin-negative resected periampullar

212 xcised previously with controlled margins by frozen section or Mohs micrographic surgery.

213 Respondents used Mohs surgery, frozen section or multi-stage excision with delayed clos

214 red 2.4 minutes compared to 26.5 minutes for frozen section (P < 0.001) and it proved more accurate t

215 Hybridization was performed on frozen sections, paraffin sections, and sections from JB

216 ccess to histopathology services, especially frozen section pathology during surgery, is limited in r

217 intraoperative decisions surgeons depend on frozen section pathology, a technique developed over 150

218 n-destructive alternative to intra-operative frozen section pathology, using prostate cancer as an in

219 However, frozen sections present challenges for histological scor

220 n after an initially positive intraoperative frozen section (R1 --> R0).

221 elderly donor kidneys was carried out and a frozen section report was obtained.

222 practical utility of routine intraoperative frozen section requires further scrutiny.

223 Tumor content in samples was judged by frozen section review.

224 gh CAP did not correlate with steatosis from frozen sections (rho = 0.08, P = 0.47), it correlated wi

225 ing laser capture microdissection applied to frozen sections, RNA was extracted from the neoplastic e

226 Current guidelines recommend intraoperative frozen section(s) during diagnostic surgery for squamous

227 Although the frozen section seemed to be quite benign, the permanent

228 her sensitivity (95.6%) and NPV (98.2%) than frozen section (sensitivity, 85.6%; NPV, 94.5%).

229 ere excluded due to piecemeal resections, no frozen sections sent during surgery, unknown primaries,

230 mor markers with a fast turnaround time from frozen sections should foster intraoperative histopathol

231 t the hypothesis that negative findings from frozen sections should not be solely relied on to refute

232 In the remaining 28 patients, frozen section showed a "follicular or Hurthle cell neop

233 Frozen sections showed that although the degree of initi

234 Immunohistochemistry of MT-MMP in frozen sections showed that MT-MMP was localized in neop

235 Initial binding studies on frozen sections showed that the integrin-binding domain

236 in digitized histological images of TCGA GBM frozen section slides that were immediately adjacent to

237 nd avoid false-negative findings in fresh or frozen-section SLNs.

238 xpression of mRNA by the RT-PCR assay in the frozen-section SNs (n = 12) without metastases by conven

239 astases by the RT-PCR assay in the blood and frozen-section SNs of patients with breast cancer.

240 Detection of RT-PCR cDNA products in frozen-section SNs was increased with Southern blot anal

241 Additionally, frozen sections stained with Oil Red O were analyzed to

242 Sensitivity and specificity of frozen section TAB for detecting GCA, and discordance ra

243 Immunoperoxidase studies on frozen sections taken from kidneys at 0, 3, 10, 20, and

244 nodes was performed using touch imprint and frozen section techniques.

245 Frozen section temporal artery biopsy (TAB) may prevent

246 cer cells from normal proliferating cells in frozen sections that are typically used as a source of R

247 Frozen sections through the SCN were obtained from fixed

248 Immunohistochemistry was performed on frozen sections to characterize and quantify T-cell subt

249 l markers, with immunoperoxidase staining of frozen sections to confirmed the presence of protein.

250 o 2 SLNs containing metastases identified by frozen section, touch preparation, or hematoxylin-eosin

251 ine phosphatase and dipeptidyl peptidase) of frozen sections, used to discriminate capillary profiles

252 mmunohistochemical studies were performed on frozen sections utilizing anti-CD40L monoclonal antibody

253 charges; however, the charge per informative frozen section was approximately $12,470.

254 was suggestive of malignancy and a directed frozen section was diagnostic of follicular carcinoma.

255 For patients in whom intraoperative frozen section was either negative or not done, the rate

256 Beta-galactosidase staining of frozen sections was used to locate virus in the eyes.

257 Frozen sections were cut, incubated in Graham and Karnov

258 echniques 75-90% of the lymphocytes in these frozen sections were identified as T cells.

259 Frozen sections were immunolabeled for collagenase, insu

260 Frozen sections were immunostained with antibodies to ge

261 The eyes were removed 48 hours later, and frozen sections were prepared for beta-galactosidase his

262 Frozen sections were prepared for immunohistochemistry a

263 Frozen sections were prepared from these tissues and wer

264 eyes were fixed in 4% paraformaldehyde, and frozen sections were prepared.

265 y apparent tumor was removed, intraoperative frozen sections were sent.

266 Frozen sections were stained by two-color immunofluoresc

267 njection (pi), the eyes were enucleated, and frozen sections were stained with antibodies specific fo

268 Frozen sections were stained with oil red O or Sudan bla

269 Therefore, IIC is a viable alternative to frozen sectioning when intraoperative evaluation is requ

270 atients, immunocytochemistry of renal biopsy frozen sections with an anti-H(+)-ATPase monoclonal anti

271 denosine immunolocalization was performed on frozen sections with an antibody against adenosine conju

272 histology typically utilize manually stained frozen sections with imaging on non-clinical grade scann

273 resting limbal and corneal basal cells from frozen sections with minimal tissue processing, thereby

274 103 (86.6%) also had positive results on the frozen section, with 4 false-positives (0.6%) and 20 fal