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1 ts could not be studied without conventional tissue staining.
2  by PET was 16% smaller than that defined by tissue staining.
3 s were compared with RA and IA determined by tissue staining.
4 tium-99m autoradiography and infarct size on tissue staining.
5 ailable from clinical care records (7.5%) or tissue staining (12.6%).
6                             Using wholemount tissue staining and clearing, or retrograde tracing in a
7 on (LCM) was developed, we modified previous tissue staining and fixation methods so that we could co
8  recommendations for complement component 4d tissue staining and interpretation, staging liver allogr
9    The process of histopathology, comprising tissue staining and morphological pattern recognition, h
10 urons, we examined Slc9a6 knockout mice with tissue staining and related techniques commonly used to
11 -B14, but not RN46A-V1 cells, increased 5-HT tissue staining at L5 in the dorsal white matter as well
12             While phenotypically distinct by tissue staining, both mAbs recognize a 180-kDa epithelia
13 compared with 2-3 d for embryos or dissected tissue stains-but time is saved by eliminating the need
14                                      In situ tissue staining demonstrated that the compounds readily
15 examined RLD profiles in the PGN and dLGN in tissue stained for GABA.
16                                           In tissue stained for gamma amino butyric acid (GABA) using
17  from area 7 at the ultrastructural level in tissue stained for gamma-aminobutyric acid (GABA).
18 ips were found in human subcutaneous adipose tissue stained for the macrophage antigen CD68.
19 owever, diffuse and particulate cellular and tissue staining for CNPS was detected in the brain paren
20 ue of serological testing for anti-PLA2R and tissue staining for the redistributed antigen, and their
21                                  Analysis of tissue stained histochemically for cytochrome oxidase or
22  were delineated on foveal sections of fixed tissue stained in azure II-methylene blue and on frozen
23 ancement, and the blue dye/GFP was used as a tissue stain marker for histology/immunohistochemistry t
24 des comparable results to other conventional tissue staining methods such as H&E.
25  the necessary steps for sample preparation, tissue staining, micro-CT scanning and 3D reconstruction
26                                              Tissue staining of the mouse aorta revealed increased Hu
27 phil degranulation, and four of 10 secretory tissues stained only weakly for eosinophil peroxidase.
28                                      Without tissue staining or clearing, mPAM generates micrometer-r
29 with their corresponding immunohistochemical tissue staining patterns of MET receptors from the same
30 ere stem/progenitor cells are found, and the tissue staining patterns were similar to the established
31 surgical specimens from human prostate tumor tissue stained positive with an antisense riboprobe to a
32                            Ischemic hindlimb tissue stained positively for VEGFR2.
33 port for the tissue sections and MS-friendly tissue staining protocols.
34                                              Tissue staining provides a unique view of virus-induced
35 ess using technetium-99m autoradiography and tissue staining, respectively.
36                                 Periurethral tissue staining revealed a significant increase in colla
37                Histological study of elastic-tissue stained sections disclosed that the leaflet thick
38 uman primary and metastatic pancreatic tumor tissues stained strongly for cancer cell nuclear beta-ca
39 ted in blood vessels of various other normal tissues stained under the same conditions.
40 family history is an ineffective screen, and tissue staining used to type amyloid is unreliable.
41                                              Tissue staining was 7.1+/-2.1 mm in depth and 2.3+/-1.8
42                At the end of the experiment, tissue staining was performed to determine infarct size
43 th radiolabeled microspheres, and postmortem tissue staining was used to determine IS.
44 ally, Western blotting and immunofluorescent tissue staining were used to analyse the PKG isoforms ex
45 as measured by microvessel quantification of tissue stained with antibodies against von Willebrand fa
46 ope to allow intraoperative visualization of tissue stained with Cy3.
47 logic examination of the excised left kidney tissue stained with hematoxylin and eosin and Gomori's m
48 tional organic dyes, can be reliably used on tissue stained with hematoxylin and eosin.
49 uct system, using X-ray micro tomography and tissue staining with phosphotungstic acid.
50 eeding time, and histologic surveys of mouse tissues, stained with an antibody to von Willebrand fact

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