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1 ined, and the liver was fixed for histology (hematoxylin & eosin staining).
2       Tumors were assessed for necrosis with hematoxylin-eosin staining.
3 ent to those containing VZV were examined by hematoxylin-eosin staining.
4 (98.3%), 3904 (76.3%) were tumor-negative by hematoxylin-eosin staining.
5 e of TF using a similar human-based score on hematoxylin-eosin staining.
6  sections were taken for autoradiography and hematoxylin-eosin staining.
7 e-mediated dUTP nick end-labeling assay, and 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   The corneal buttons were then evaluated by hematoxylin-eosin staining and by immunostaining with ma
11 x vivo both for inflammation grade (by using hematoxylin-eosin staining) and for expression of select
12 ivo by means of histologic examination (with hematoxylin-eosin staining) and immunostaining of vascul
13 polymorphonuclear cell (PMN) infiltration by hematoxylin-eosin staining, and for oxygen radical-induc
14 infarction (detected by immunoglobulin G and hematoxylin-eosin staining), as well as increased neuron
15                                           At hematoxylin-eosin staining, coagulation necrosis was obs
16  (reduced alanine transferase) and necrosis (hematoxylin-eosin staining) compared with the HSP27 WT m
17                                              Hematoxylin-eosin staining confirmed that all spots with
18 evaluated levels of percentage of TILs using hematoxylin-eosin-stained core biopsy sections taken at
19                           Histologic slides (hematoxylin-eosin stain) from three resected rotator cuf
20 to macromolecule albumin) extravasation, and hematoxylin-eosin staining helped detect only scattered
21 luorescence images, NADH-stained images, and hematoxylin-eosin-stained images were compared.
22 al, is at least as sensitive as conventional hematoxylin-eosin staining in detecting bromobenzene-ind
23                         Histologic data from hematoxylin-eosin staining of explanted liver specimens
24                      Immunohistochemical and hematoxylin-eosin staining of liver sections was perform
25                   At the same time, Gram and hematoxylin-eosin stains of paraffin sections were perfo
26                                              Hematoxylin/eosin staining of rd7 tissue shows that the
27 ied by frozen section, touch preparation, or hematoxylin-eosin staining on permanent section.
28 ogy (aspirate by Wright-Giemse and biopsy by Hematoxylin-Eosin stains) or immunostaining of aspirates
29 -CA1 hippocampal region of the rat brain, in hematoxylin-eosin-stained, paraffin-embedded 6-microm se
30           Staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr
31 nts using staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr
32 stochemically positive or negative [IHC+/-], hematoxylin-eosin staining positive or negative [H & E +
33                                              Hematoxylin-eosin stained sections were reviewed to conf
34                                     Standard hematoxylin-eosin-stained sections and immunohistochemic
35 re studied by (i) microscopic examination of hematoxylin-eosin-stained sections for inflammation and
36                                              Hematoxylin-eosin-stained sections of the same transplan
37                 After resection, whole-mount hematoxylin-eosin-stained sections were registered to th
38              (1) Review of clinical data and hematoxylin-eosin-stained sections with (2) immunohistoc
39                     Review of clinical data, hematoxylin-eosin-stained sections, and immunohistochemi
40  the grading of necrosis and inflammation on hematoxylin-eosin-stained sections.
41                                              Hematoxylin-eosin staining showed that neuronal injury i
42                  Histologic examination with hematoxylin-eosin staining showed that results of 36 (67
43                                              Hematoxylin-eosin-stained slices of mammary tissues were
44 issue sections and/or detection of amebas in hematoxylin-eosin-stained slides.
45 formed by using standard light microscopy on hematoxylin-eosin stained specimens; immunohistochemistr
46 ses were performed with specific techniques (hematoxylin-eosin staining, terminal deoxynucleotidyl tr
47 ned regions of archived, formalin-fixed, and hematoxylin/eosin-stained tissue sections that were diss
48                                      We used hematoxylin-eosin staining to examine cochlear histopath
49                                              Hematoxylin-eosin-stained tumor slides from patients wit
50 uted tomography (CT) and light microscopy of hematoxylin-eosin-stained tumor tissue were compared.
51                                              Hematoxylin-eosin staining was also performed.
52 as evaluated and histologic examination with hematoxylin-eosin staining was performed at 4 hours, 24
53 stroduodenoscopy, but histologic findings at hematoxylin-eosin staining were normal.
54                          Autoradiography and hematoxylin-eosin staining were performed on the dissect
55 erated and compared with digitized images of hematoxylin-eosin-stained whole-mount histologic slices.
56        Finally, coregistration of histologic hematoxylin-eosin stains with autoradiography signals fr

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