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1 ined, and the liver was fixed for histology (hematoxylin & eosin staining).
2 ent to those containing VZV were examined by hematoxylin-eosin staining.
3 (98.3%), 3904 (76.3%) were tumor-negative by hematoxylin-eosin staining.
4  sections were taken for autoradiography and hematoxylin-eosin staining.
5 e-mediated dUTP nick end-labeling assay, and hematoxylin-eosin staining.
6       Tumors were assessed for necrosis with hematoxylin-eosin staining.
7 e of TF using a similar human-based score on hematoxylin-eosin staining.
8 reported in the anatomic diagnosis, based on hematoxylin-eosin staining alone, for three (8%) of the
9 ks of acquired specimens were examined using hematoxylin-eosin stain and double immunostain using HMB
10 f the NPCE were examined histologically with hematoxylin-eosin stain and immunohistochemical stains i
11   The corneal buttons were then evaluated by hematoxylin-eosin staining and by immunostaining with ma
12 x vivo both for inflammation grade (by using hematoxylin-eosin staining) and for expression of select
13 ivo by means of histologic examination (with hematoxylin-eosin staining) and immunostaining of vascul
14 polymorphonuclear cell (PMN) infiltration by hematoxylin-eosin staining, and for oxygen radical-induc
15 nal tissue was histologically analyzed using hematoxylin-eosin staining, and Ti, aluminum, and vanadi
16 infarction (detected by immunoglobulin G and hematoxylin-eosin staining), as well as increased neuron
17                                           At hematoxylin-eosin staining, coagulation necrosis was obs
18  (reduced alanine transferase) and necrosis (hematoxylin-eosin staining) compared with the HSP27 WT m
19                                              Hematoxylin-eosin staining confirmed that all spots with
20 evaluated levels of percentage of TILs using hematoxylin-eosin-stained core biopsy sections taken at
21         Histology of heart sections included hematoxylin-eosin staining for overt damage, immunofluor
22                           Histologic slides (hematoxylin-eosin stain) from three resected rotator cuf
23 udy used whole-slide images acquired from 98 hematoxylin-eosin-stained frozen and 51 permanent donor
24 to macromolecule albumin) extravasation, and hematoxylin-eosin staining helped detect only scattered
25 ify PDAC molecular subtypes based on routine hematoxylin-eosin-stained histopathologic slides.
26  tumor, stroma, and TIL cells in whole-slide hematoxylin-eosin-stained images of NSCLC tumors.
27 luorescence images, NADH-stained images, and hematoxylin-eosin-stained images were compared.
28 al, is at least as sensitive as conventional hematoxylin-eosin staining in detecting bromobenzene-ind
29 tive histological assessment of liver lipid (hematoxylin-eosin staining), inflammation (galectin-3 im
30                         Histologic data from hematoxylin-eosin staining of explanted liver specimens
31                      Immunohistochemical and hematoxylin-eosin staining of liver sections was perform
32                   At the same time, Gram and hematoxylin-eosin stains of paraffin sections were perfo
33                                              Hematoxylin/eosin staining of rd7 tissue shows that the
34 ied by frozen section, touch preparation, or hematoxylin-eosin staining on permanent section.
35 ogy (aspirate by Wright-Giemse and biopsy by Hematoxylin-Eosin stains) or immunostaining of aspirates
36 -CA1 hippocampal region of the rat brain, in hematoxylin-eosin-stained, paraffin-embedded 6-microm se
37 nts using staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr
38           Staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr
39 stochemically positive or negative [IHC+/-], hematoxylin-eosin staining positive or negative [H & E +
40 s to recognize kidney tissue compartments in hematoxylin & eosin-stained sections from procurement ne
41  The long axis of 304 LNnegs was measured in hematoxylin-eosin stained sections from resection specim
42  image-based automated assessment of TILs on hematoxylin-eosin stained sections in melanoma.
43                                              Hematoxylin-eosin stained sections were reviewed to conf
44 lar mucopolysaccharides which are visible on hematoxylin-eosin-stained sections and highlighted by sp
45                                     Standard hematoxylin-eosin-stained sections and immunohistochemic
46 re studied by (i) microscopic examination of hematoxylin-eosin-stained sections for inflammation and
47                                              Hematoxylin-eosin-stained sections of the same transplan
48                 After resection, whole-mount hematoxylin-eosin-stained sections were registered to th
49              (1) Review of clinical data and hematoxylin-eosin-stained sections with (2) immunohistoc
50               We reviewed the clinical data, hematoxylin-eosin-stained sections, and histochemical st
51                     Review of clinical data, hematoxylin-eosin-stained sections, and immunohistochemi
52 had mucopolysaccharide deposition visible on hematoxylin-eosin-stained sections, which was highlighte
53  the grading of necrosis and inflammation on hematoxylin-eosin-stained sections.
54                                              Hematoxylin-eosin staining showed that neuronal injury i
55                  Histologic examination with hematoxylin-eosin staining showed that results of 36 (67
56                                              Hematoxylin-eosin-stained slices of mammary tissues were
57 and inflammatory cell counts were counted on hematoxylin-eosin-stained slides and osteoclasts were co
58  Stromal TILs were assessed on whole-section hematoxylin-eosin-stained slides using a dichotomized cu
59 ify PDAC molecular subtypes based on routine hematoxylin-eosin-stained slides, potentially leading to
60 issue sections and/or detection of amebas in hematoxylin-eosin-stained slides.
61 formed by using standard light microscopy on hematoxylin-eosin stained specimens; immunohistochemistr
62 ses were performed with specific techniques (hematoxylin-eosin staining, terminal deoxynucleotidyl tr
63 ed skin cancer is microscopic examination of hematoxylin & eosin stained tissue by a pathologist.
64 estigates using the most popular image data, hematoxylin-eosin stained tissue slide images, to find a
65 ned regions of archived, formalin-fixed, and hematoxylin/eosin-stained tissue sections that were diss
66                                      We used hematoxylin-eosin staining to examine cochlear histopath
67                                              Hematoxylin-eosin-stained tumor slides from patients wit
68 uted tomography (CT) and light microscopy of hematoxylin-eosin-stained tumor tissue were compared.
69                                              Hematoxylin-eosin staining was also performed.
70 as evaluated and histologic examination with hematoxylin-eosin staining was performed at 4 hours, 24
71 stroduodenoscopy, but histologic findings at hematoxylin-eosin staining were normal.
72                          Autoradiography and hematoxylin-eosin staining were performed on the dissect
73 on of histopathology features on unannotated hematoxylin-eosin-stained whole slide images (WSIs).
74 and macrovesicular steatosis in the liver on hematoxylin-eosin-stained whole slide images, using the
75 erated and compared with digitized images of hematoxylin-eosin-stained whole-mount histologic slices.
76        Finally, coregistration of histologic hematoxylin-eosin stains with autoradiography signals fr