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1 ) alpha and beta expression were assessed in paraffin sections.
2 ptide were performed on 3- to 5-microm thick paraffin sections.
3 sis of archive material of tumor subtypes in paraffin sections.
4 BZLF1 (ZEBRA) protein were also performed in paraffin sections.
5 olyadenylated RNA (EBER)-1 were performed in paraffin sections.
6  by in situ hybridization of adult worm pair paraffin sections.
7 15;19) cancer, we developed a FISH assay for paraffin sections.
8 mmunohistochemical staining was performed on paraffin sections.
9 istochemical analysis of routinely processed paraffin sections.
10 uantitative accuracy, and compatibility with paraffin sections.
11 ch group were determined from cell counts on paraffin sections.
12 helial cells of normal brain in conventional paraffin sections after formalin fixation.
13 s underwent a wide local excision, 12 with a paraffin section and 6 with a frozen section.
14 ptosis as assessed by both TUNEL labeling in paraffin sections and caspase activity in trypsin-disper
15      Its ready applicability on conventional paraffin sections and on cytological preparations may br
16 ntification of chromosomal translocations in paraffin sections, and 3) identification of chromosomal
17 ridization was performed on frozen sections, paraffin sections, and sections from JB-4 plastic-embedd
18  fixed in formalin, decalcified, embedded in paraffin, sectioned, and analyzed via histological metho
19 in Carnoy's fixative, processed, embedded in paraffin, sectioned, and examined by immunohistochemistr
20    Skin was obtained at autopsy, embedded in paraffin, sectioned, and stained with Masson's trichrome
21 anslin in mouse brain has been determined in paraffin sections by immunocytochemistry with an affinit
22  growth factor (TGF) beta1 was quantified in paraffin sections by immunofluorescence and confocal mic
23 ECD independently of its molecular origin in paraffin sections, combining multispectral unmixing of c
24 gery (31.1%), wide local excision (WLE) with paraffin section control (21.7%), WLE with frozen-sectio
25    Immunostaining of myelin basic protein on paraffin sections derived from 18 incompletely resected
26 issue were laser capture-microdissected from paraffin sections, DNA was isolated, and molecular techn
27                   DNA was extracted from the paraffin sections followed by PCR amplification of exon
28                          Immunoreactivity of paraffin sections for CRX (cone-rod homebox transcriptio
29 ons for laser-scanning confocal analysis and paraffin sections for immunohistochemistry.
30 ntibody was performed on routinely processed paraffin sections from 189 radical prostatectomy specime
31                             We have analyzed paraffin sections from 190 patients with histologically
32 ascular tissue sections from the patient and paraffin sections from coronary arteries from six additi
33                         Protein extracts and paraffin sections from human eyes were analyzed by Weste
34 out a retrospective study of C4d staining in paraffin sections from renal transplant biopsies to dete
35                                In our study, paraffin sections from scrapie infected (263K and 139H)
36                                              Paraffin sections from the diagnostic specimen were anal
37                                              Paraffin sections from tumor and corresponding normal mu
38 l and macrophage populations were studied in paraffin sections from untreated primary lung cancers by
39 AML), we studied forty-eight cases of AML by paraffin section immunohistochemistry.
40 vesicular and granular forms was detected in paraffin sections in all invasive tumors, most prominent
41 r HER-2/neu were performed on formalin-fixed paraffin sections of 100 consecutive invasive breast can
42                                    Unstained paraffin sections of 35 cases of periocular SC were anal
43                                  H&E stained paraffin sections of all available tissue samples from t
44  the size of AQP4 supramolecular clusters in paraffin sections of brain tissue and support AQP4 clust
45 was detected by immunoperoxidase in 2-micron paraffin sections of consecutive biopsies obtained over
46                                              Paraffin sections of frontal cortices from rhesus macaqu
47 of calponin immunoreactivity was assessed in paraffin sections of human anterior segment tissue.
48                                              Paraffin sections of human ocular tissues obtained after
49                                 Furthermore, paraffin sections of human osteoporotic fractured bone e
50  also detected M. pulmonis in 14 of 20 (70%) paraffin sections of lung and trachea from rats and mice
51 ts was determined by immunohistochemistry on paraffin sections of M21 tumors.
52 easure AQP4 cluster size in antibody-stained paraffin sections of mouse cerebral cortex and spinal co
53                                              Paraffin sections of neuroblastic tumors at various stag
54                                           In paraffin sections of non-small cell lung tumors, ERbeta
55 robes were used for in situ hybridization on paraffin sections of normal human eye tissue.
56 mmunohistochemical staining was performed on paraffin sections of normal prostate, prostatic intraepi
57 mensional reconstructions, profile counts in paraffin sections of nucleoli within a nucleus were 36%
58 ted immunocytochemically, using anti-PCNA in paraffin sections of the explants; and the total number
59  MAC were observed for RPE cells when serial paraffin sections of the laser spots were analyzed.
60  were also significantly lower than those in paraffin sections of the Matrigel plugs containing contr
61                       Blood vessel counts in paraffin sections of the Matrigel plugs containing sRIII
62                                              Paraffin sections of the muscle biopsy sample from the t
63 NEL) method was used to locate nicked DNA in paraffin sections of the retinas.
64  was investigated by immunohistochemistry on paraffin sections of the trigeminal ganglia (TG).
65 c antibodies was performed on formalin-fixed paraffin sections of tissue microarray composed of 580 r
66                                              Paraffin sections of untreated or ischemically treated t
67 ransfer system that obviates the need to wet paraffin sections prior to slide mounting significantly
68 oidy for chromosomes 8, 12, and 17 on intact paraffin sections revealed that two tumors were aneuploi
69 lood and bone marrow and immunohistochemical paraffin section staining of bone marrow biopsies in the
70 ures were applied to 25-microm-thick coronal paraffin sections taken at 5-mm intervals throughout the
71 ies, permitting the harvesting of cells from paraffin sections that maintain histological detail.
72 damage, biopsies were taken and prepared for paraffin sections that were stained with a monoclonal an
73  infiltrative tumors and both can be used in paraffin sections, thereby obviating cumbersome oil red
74  areas of anaplasia were microdissected from paraffin sections to determine whether and at what stage
75 ons with (2) immunohistochemical staining of paraffin sections using a polyclonal antibody against th
76                C4d staining was performed on paraffin sections using a polyclonal rabbit anti-C4d ant
77       In situ hybridization was performed on paraffin sections using a tritium-labeled probe for cath
78 nt membrane proteins (EBV LMP-1) was done on paraffin sections using standard immunohistochemical (IH
79                            Immunostaining in paraffin sections was essentially the same as that in fr
80 ified, and hematoxylin and eosin staining of paraffin sections was performed to assess changes in the
81 ining of tuberin, in the cryosections and in paraffin sections, was observed in the small blood vesse
82             In hematoxylin and eosin-stained paraffin sections, we detect empty lacunae in osteocytes
83                                   Knee joint paraffin sections were analyzed by double and triple imm
84 otal number of TM cells was determined after paraffin sections were counterstained by hematoxylin.
85                 The eyes were then fixed and paraffin sections were cut from each eye.
86  destabilize the medial meniscus, and serial paraffin sections were examined at 2, 4, 8, and 12 weeks
87                      Retinal and optic nerve paraffin sections were examined for fluorescent labeling
88                                         Lung paraffin sections were immunostained and quantitative im
89 e time, Gram and hematoxylin-eosin stains of paraffin sections were performed to monitor the host res
90 es were taken immediately after exposure and paraffin sections were prepared for immunoperoxidase sta
91                                              Paraffin sections were stained with a polyclonal antibod
92                                              Paraffin sections were stained with antibody for a micro
93 lt solution injections into normal eyes, and paraffin sections were stained with hematoxylin and eosi
94 were studied by immunoperoxidase staining of paraffin sections with monoclonal anti-CK19, anti-viment

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