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

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

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

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

26 Frozen section analysis and touch-preparation cytology h

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

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

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

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

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

32 Frozen section analysis was again similar with 74% sensi

33 Frozen section analysis was similar with 74% sensitivity

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

35 Frozen-section analysis rendered a definitive diagnosis

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 -8, and caspase-3 was determined by staining frozen sections and performing Western blot analysis and

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

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

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

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

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

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

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

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

59 Intraoperative frozen sections are unlikely to abbreviate the LND proce

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

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

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

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

64 ed criteria features underwent pretransplant frozen section biopsies.

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

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

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

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

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

70 Frozen-section biopsy was reliable for pretransplant dec

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

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

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

74 3%) of 24 of the tumors were resectable with frozen section control of the duct margins (9 pancreatod

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

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

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

78 Bulk frozen sections displaying the most extensive but not mi

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

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

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

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

83 Intraoperative frozen section examination was routinely performed to as

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

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

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

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

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

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

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

91 Frozen sections from excised tumors were then evaluated

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

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

94 Frozen sections from transplanted animals were stained h

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

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

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

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

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

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

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

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

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

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

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

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

107 From frozen sections, hepatocytes were laser-capture microdis

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

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

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

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

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

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

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

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

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

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

118 %) with follicular neoplasms of the thyroid, frozen section is neither informative nor cost-effective

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

134 Frozen sections of capsulated and decapsulated bovine an

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

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

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

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

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

140 Frozen sections of enucleated globes with intact EOMs an

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

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

143 Frozen sections of gingival specimens from these patient

144 Frozen sections of gray matter from orbitofrontal area 4

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

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

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

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

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

150 3G5 stained frozen sections of human, bovine, porcine, rat, and rabb

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

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

153 Frozen sections of lacrimal glands from five rats were s

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

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

156 Fixed frozen sections of lateral eye were examined with conven

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

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

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

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

161 While frozen sections of normal bowel revealed bright gp180 st

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

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

164 Frozen sections of postmortem fixed monkey eyes were imm

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

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

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

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

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

170 Frozen sections of the enucleated eyes were analyzed for

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

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

173 Frozen sections of the peripheral retinal margin and par

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

175 Frozen sections of two donor eyes obtained at autopsy fr

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

177 Frozen sections of whole mount-stained embryonic liver d

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

193 Frozen sections showed that although the degree of initi

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

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

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

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

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

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

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

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

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

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

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

205 Frozen sections through the SCN were obtained from fixed

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

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

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

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

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

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

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

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

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

215 Frozen sections were cut, incubated in Graham and Karnov

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

217 Frozen sections were immunolabeled for collagenase, insu

218 Frozen sections were immunostained with antibodies to ge

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

220 Frozen sections were prepared for immunohistochemistry a

221 Frozen sections were prepared from these tissues and wer

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

223 Frozen sections were stained by two-color immunofluoresc

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

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

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

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

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

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