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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
16 (reduced alanine transferase) and necrosis (hematoxylin-eosin staining) compared with the HSP27 WT m
18 evaluated levels of percentage of TILs using hematoxylin-eosin-stained core biopsy sections taken at
20 to macromolecule albumin) extravasation, and hematoxylin-eosin staining helped detect only scattered
22 al, is at least as sensitive as conventional hematoxylin-eosin staining in detecting bromobenzene-ind
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
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 +
35 re studied by (i) microscopic examination of hematoxylin-eosin-stained sections for inflammation and
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
50 uted tomography (CT) and light microscopy of hematoxylin-eosin-stained tumor tissue were compared.
52 as evaluated and histologic examination with hematoxylin-eosin staining was performed at 4 hours, 24
55 erated and compared with digitized images of hematoxylin-eosin-stained whole-mount histologic slices.
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