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1 ology of nasal smear by taking with nasal swab and Hansel's staining was performed.
2 nd if the SN was negative with HE, then immunohistochemical staining was performed.
3  animals characterized at G90 and G135, immunohistochemical staining was performed, and 3D structure tensor analyses were
4 evaluated and histologic examination with hematoxylin-eosin staining was performed at 4 hours, 24 hours, and 7 days.
5 tine blood culture bottles newly positive for yeast by Gram staining was performed at five hospitals.
6                                         Corneal fluorescein staining was performed by a masked observer in the different
7                                                         C4d staining was performed by immunohistochemistry and evaluated
8                                                Hepatic iron staining was performed in a central laboratory, and the stain
9                            Morphologic evaluation and PLA2R staining was performed in all cases.
10                                       Hematoxylin and eosin staining was performed in six animals with ICH after 24 hrs t
11                                         Immunohistochemical staining was performed on a tissue microarray representing 54
12                                                         The staining was performed on archival muscle biopsy material, wi
13                                     Immunohistochemical C4d staining was performed on formalin-fixed, paraffin-embedded l
14                               Multilabel immunofluorescence staining was performed on free-floating sections and on 1-mic
15                                              C4d complement staining was performed on frozen biopsy tissue.
16 nges in myelin integrity, aurophosphate (Black Gold) myelin staining was performed on mPFC sections.
17                                    SR-A immunohistochemical staining was performed on paraffin sections of normal prostat
18                                                         C4d staining was performed on paraffin sections using a polyclona
19                                   Double immunofluorescence staining was performed on paraffin-embedded human posterior s
20                                         Immunohistochemical staining was performed on platelet-leukocyte aggregates and p
21 hologic analysis and histochemical iron detection by Perls' staining was performed on retina sections from DKO and contro
22                      In addition, immunohistochemical (IHC) staining was performed on selected tissues to determine the p
23 amples were imaged to quantify total fluorescence, and NADH staining was performed on the same slice.
24                                      In two patients, Perls staining was performed on tissue samples from the LSIR.
25                                                         C4d staining was performed retrospectively on biopsies in patient
26                                             Cytologic quick staining was performed routinely to determine specimen adequa
27                                             Cuprolinic blue staining was performed to analyze stromal proteoglycans (PGs)
28  later, the corneas were processed for histology, and TUNEL staining was performed to assess whether blue-IRIS causes cel
29                                                       TUNEL staining was performed to assess whether IRIS or Na-Fl doping
30                                                       TUNEL staining was performed to detect apoptosis.
31 performed for T-Ag sequences, and immunohistochemical (IHC) staining was performed to detect T-Ag expression.
32                               Hematoxylin and eosin (H & E) staining was performed to detect the pathological changes of
33                                          Immunofluorescence staining was performed to determine expression of cleaved Not
34                        At the end of the experiment, tissue staining was performed to determine infarct size and topograp
35                                         Corneal fluorescein staining was performed to evaluate epithelial regeneration.
36                                         Immunohistochemical staining was performed to evaluate the loss of immune effecto
37                                         Immunohistochemical staining was performed to examine the expression of matrix me
38                                         Immunohistochemical staining was performed to examine the protein expression leve
39 ion, using a gene-trap mouse model for PRCP deletion, X-gal staining was performed to further determine PRCP distribution
40                                         Immunohistochemical staining was performed to identify c-kit and tryptase mast ce
41                                         Immunohistochemical staining was performed to identify the pattern of Dmp1 expres
42                                         Immunohistochemical staining was performed to localize the expression of MT4- and
43                                                   Golgi-Cox staining was performed to measure dendritic spine density.
44 deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining was performed to quantify apoptotic cells in specifi
45                                     Immunofluorescence cell staining was performed to visualize the subcellular localizat
46                                      Affinity-histochemical staining was performed using a HA-specific biotinylated bindi
47 were determined using a spectrophotometric assay, and thiol staining was performed using mercury orange.
48 ure model in BALB/c mice was placed and immunohistochemical staining was performed with CD31/PECAM-1 and LYVE-1 to quanti
49                                         Immunohistochemical staining was performed with polyclonal antibodies against GLA
50 ects without and with diabetes, in combination with insulin staining, was performed to assess beta-cell selectivity of th

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