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1  and changes in HA receptor expression using immunofluorescent microscopy.
2 +) and NG2(+)) were analyzed via whole mount immunofluorescent microscopy.
3 tected in infected cells either by RT-PCR or immunofluorescent microscopy.
4 yuridine, and Hoechst 33342 as visualized by immunofluorescent microscopy.
5 transcriptase polymerase chain reaction, and immunofluorescent microscopy.
6 uten protein structure, using SEM, light and immunofluorescent microscopy.
7 f these proteins with caveolin-1 as shown by immunofluorescent microscopy.
8 at stained for Annexin V [CD146(AnnV+)]) and immunofluorescent microscopy.
9  transcription polymerase chain reaction and immunofluorescent microscopy.
10 t analysis and either immunohistochemical or immunofluorescent microscopy.
11  by electrophoretic mobility shift assay and immunofluorescent microscopy.
12 timates of glomerular IgG deposition seen by immunofluorescent microscopy.
13 anslocation was determined by confocal laser immunofluorescent microscopy.
14 ed macrophages using both immunoblotting and immunofluorescent microscopy.
15 zed to the cytoplasm as detected by indirect immunofluorescent microscopy.
16 ent of compound action potentials (CAPs) and immunofluorescent microscopy.
17                                              Immunofluorescent microscopy also indicated that PTP1(C/
18 calization was experimentally verified using immunofluorescent microscopy and a cell-surface biotinyl
19                                              Immunofluorescent microscopy and FACS analysis demonstra
20              CD14 expression was assessed by immunofluorescent microscopy and flow cytometry.
21 uscle was demonstrated using double labeling immunofluorescent microscopy and immunoelectron microsco
22                        We have used confocal immunofluorescent microscopy and microinjection of affin
23 sessed in denervated mice versus controls by immunofluorescent microscopy and real-time PCR.
24                         Studies using double immunofluorescent microscopy and ultrastructural analysi
25                         Studies using double immunofluorescent microscopy and ultrastructural analysi
26                                              Immunofluorescent microscopy and Western blot analysis d
27                     We found, using confocal immunofluorescent microscopy and Western blot analysis,
28 ion, surface protein biotinylation, confocal immunofluorescent microscopy, and functional measurement
29                            Here, we combined immunofluorescent microscopy, biochemical assays, in sil
30                                              Immunofluorescent microscopy confirmed that MPO added to
31                                 Furthermore, immunofluorescent microscopy data showed that MacMARCKS
32                                              Immunofluorescent microscopy demonstrated basal expressi
33                                              Immunofluorescent microscopy demonstrated that both the
34             Immunohistochemical analysis and immunofluorescent microscopy demonstrated that KSHV infe
35                       Consistently, confocal immunofluorescent microscopy demonstrated that WT RNase
36  Through the use of high-resolution confocal immunofluorescent microscopy for colocalization of these
37                      Immunohistochemical and immunofluorescent microscopy identified basolateral RhBG
38  ( approximately 8,500 dimers per cell), and immunofluorescent microscopy (IFM) located MreCD(Spn) to
39                                              Immunofluorescent microscopy (IFM) showed a change in th
40         We compared three different methods (immunofluorescent microscopy, IFM; flow cytometry, FCM;
41 ult rat CF to myofibroblasts, as assessed by immunofluorescent microscopy, immunoblotting, and collag
42 ogenous Aalpha and Galpha(12) colocalized by immunofluorescent microscopy in Caco-2 cells and in neur
43 t bacterial species was assessed by indirect immunofluorescent microscopy in each participant.
44 detected by immunoblot analysis and confocal immunofluorescent microscopy in fibrotic livers from mic
45                       TRP120 was observed by immunofluorescent microscopy in the nucleus of E. chaffe
46 confirmed by Western blot analysis, confocal immunofluorescent microscopy in vitro, and on cultured o
47 in split-opened collecting ducts followed by immunofluorescent microscopy in WT and intercalated cell
48                Subcellular fractionation and immunofluorescent microscopy indicated that in mutant ce
49                                     Confocal immunofluorescent microscopy indicates that Drm is prese
50                                              Immunofluorescent microscopy localized PcsB mainly to th
51                                              Immunofluorescent microscopy localizes DMN in a stripe-l
52                                              Immunofluorescent microscopy of Chlamydomonas cells conf
53                                     Confocal immunofluorescent microscopy of cultured epidermal kerat
54  incorporation into nascent DNA, followed by immunofluorescent microscopy of DNA fibers.
55                                              Immunofluorescent microscopy of interferon-stimulated CD
56 scence-activated cell sorting (FACS), and by immunofluorescent microscopy of tissue sections and isol
57                                           By immunofluorescent microscopy over-expressed PTP1(C/S) co
58                                     Confocal immunofluorescent microscopy revealed CD73 to be surface
59                                              Immunofluorescent microscopy revealed co-localization of
60 -immunoprecipitated with Cyp60, and confocal immunofluorescent microscopy revealed intracellular co-l
61                        Dual channel confocal immunofluorescent microscopy revealed that the Mr 8,000
62                                              Immunofluorescent microscopy revealed that the treatment
63                                              Immunofluorescent microscopy revealed that VASP localize
64                                              Immunofluorescent microscopy reveals that RuRuPhen cause
65                                              Immunofluorescent microscopy showed that all four isofor
66                                              Immunofluorescent microscopy showed that HBs proteins, i
67                                              Immunofluorescent microscopy shows that anti-Rad51 antib
68 brains sectioned and prepared for dual label immunofluorescent microscopy, single label bright field
69                   Here, we demonstrate using immunofluorescent microscopy that SUR1-TRPM4 expression
70              Using Western blot analysis and immunofluorescent microscopy, the authors determined the
71                                           By immunofluorescent microscopy, this antiserum localizes t
72 uginosa infection, and (iii) high-resolution immunofluorescent microscopy to monitor ExoS translocati
73                                              Immunofluorescent microscopy using a monoclonal antibody
74  existence of this mechanism was provided by immunofluorescent microscopy, using fluorescently labele
75                                              Immunofluorescent microscopy was used to determine nucle
76 iotinylation coupled with immunoblotting and immunofluorescent microscopy, we assessed the kinetics o
77                                         With immunofluorescent microscopy, we demonstrated evidence o
78                                        Using immunofluorescent microscopy, we were able to detect NP(
79             Immunohistochemical analysis and immunofluorescent microscopy were used to localize and i
80                Western immunoblotting and/or immunofluorescent microscopy were used to study beta-cat
81 pression of AP-2 and PAR-1 simultaneously by immunofluorescent microscopy with an automated quantific