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1 x-y-z resolution ~ 10 x higher than that of paraffin sections.
2 ) alpha and beta expression were assessed in paraffin sections.
3 ptide were performed on 3- to 5-microm thick paraffin sections.
4 sis of archive material of tumor subtypes in paraffin sections.
5 BZLF1 (ZEBRA) protein were also performed in paraffin sections.
6 olyadenylated RNA (EBER)-1 were performed in paraffin sections.
7 by in situ hybridization of adult worm pair paraffin sections.
8 15;19) cancer, we developed a FISH assay for paraffin sections.
9 mmunohistochemical staining was performed on paraffin sections.
10 istochemical analysis of routinely processed paraffin sections.
11 uantitative accuracy, and compatibility with paraffin sections.
12 ch group were determined from cell counts on paraffin sections.
15 ptosis as assessed by both TUNEL labeling in paraffin sections and caspase activity in trypsin-disper
17 studying liver steatosis in mouse models on paraffin sections and, thus, can facilitate reliable qua
18 ntification of chromosomal translocations in paraffin sections, and 3) identification of chromosomal
19 ridization was performed on frozen sections, paraffin sections, and sections from JB-4 plastic-embedd
20 fixed in formalin, decalcified, embedded in paraffin, sectioned, and analyzed via histological metho
21 in Carnoy's fixative, processed, embedded in paraffin, sectioned, and examined by immunohistochemistr
22 Skin was obtained at autopsy, embedded in paraffin, sectioned, and stained with Masson's trichrome
23 anslin in mouse brain has been determined in paraffin sections by immunocytochemistry with an affinit
24 growth factor (TGF) beta1 was quantified in paraffin sections by immunofluorescence and confocal mic
25 ECD independently of its molecular origin in paraffin sections, combining multispectral unmixing of c
26 gery (31.1%), wide local excision (WLE) with paraffin section control (21.7%), WLE with frozen-sectio
27 Immunostaining of myelin basic protein on paraffin sections derived from 18 incompletely resected
28 issue were laser capture-microdissected from paraffin sections, DNA was isolated, and molecular techn
30 budding crypts make it difficult to prepare paraffin sections for conventional histology, resulting
33 ntibody was performed on routinely processed paraffin sections from 189 radical prostatectomy specime
35 ascular tissue sections from the patient and paraffin sections from coronary arteries from six additi
37 out a retrospective study of C4d staining in paraffin sections from renal transplant biopsies to dete
41 l and macrophage populations were studied in paraffin sections from untreated primary lung cancers by
42 cers (NMSCs) are primarily diagnosed through paraffin section histologic analysis of skin biopsy spec
44 vesicular and granular forms was detected in paraffin sections in all invasive tumors, most prominent
45 r HER-2/neu were performed on formalin-fixed paraffin sections of 100 consecutive invasive breast can
48 the size of AQP4 supramolecular clusters in paraffin sections of brain tissue and support AQP4 clust
49 was detected by immunoperoxidase in 2-micron paraffin sections of consecutive biopsies obtained over
54 also detected M. pulmonis in 14 of 20 (70%) paraffin sections of lung and trachea from rats and mice
56 easure AQP4 cluster size in antibody-stained paraffin sections of mouse cerebral cortex and spinal co
60 mmunohistochemical staining was performed on paraffin sections of normal prostate, prostatic intraepi
61 mensional reconstructions, profile counts in paraffin sections of nucleoli within a nucleus were 36%
62 ted immunocytochemically, using anti-PCNA in paraffin sections of the explants; and the total number
64 were also significantly lower than those in paraffin sections of the Matrigel plugs containing contr
69 c antibodies was performed on formalin-fixed paraffin sections of tissue microarray composed of 580 r
71 ransfer system that obviates the need to wet paraffin sections prior to slide mounting significantly
72 oidy for chromosomes 8, 12, and 17 on intact paraffin sections revealed that two tumors were aneuploi
73 lood and bone marrow and immunohistochemical paraffin section staining of bone marrow biopsies in the
74 ures were applied to 25-microm-thick coronal paraffin sections taken at 5-mm intervals throughout the
75 ies, permitting the harvesting of cells from paraffin sections that maintain histological detail.
76 damage, biopsies were taken and prepared for paraffin sections that were stained with a monoclonal an
77 infiltrative tumors and both can be used in paraffin sections, thereby obviating cumbersome oil red
78 areas of anaplasia were microdissected from paraffin sections to determine whether and at what stage
79 ons with (2) immunohistochemical staining of paraffin sections using a polyclonal antibody against th
82 nt membrane proteins (EBV LMP-1) was done on paraffin sections using standard immunohistochemical (IH
84 ified, and hematoxylin and eosin staining of paraffin sections was performed to assess changes in the
85 ining of tuberin, in the cryosections and in paraffin sections, was observed in the small blood vesse
88 otal number of TM cells was determined after paraffin sections were counterstained by hematoxylin.
90 destabilize the medial meniscus, and serial paraffin sections were examined at 2, 4, 8, and 12 weeks
94 e time, Gram and hematoxylin-eosin stains of paraffin sections were performed to monitor the host res
95 es were taken immediately after exposure and paraffin sections were prepared for immunoperoxidase sta
98 lt solution injections into normal eyes, and paraffin sections were stained with hematoxylin and eosi
100 llagen alpha5(IV) and alpha1/2(IV) on kidney paraffin sections with Airyscan confocal microscopy that
101 were studied by immunoperoxidase staining of paraffin sections with monoclonal anti-CK19, anti-viment