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1 lear staining in all cell lines tested using confocal immunofluorescence microscopy.
2 present in SEC based on Western blotting and confocal immunofluorescence microscopy.
3 as detected by membrane subfractionation and confocal immunofluorescence microscopy.
4 pathway, as determined by epifluorescent and confocal immunofluorescence microscopy.
5 lut4 in muscle sections as observed by laser confocal immunofluorescence microscopy.
6 by canine kidney cell lines was studied with confocal immunofluorescence microscopy.
7 were examined using PCR, immunoblotting, and confocal immunofluorescence microscopy.
8  expression of this receptor was verified by confocal immunofluorescence microscopy.
9 criteria, electrophysiological analysis, and confocal immunofluorescence microscopy.
10 ed with wild type by immunoblot analysis and confocal immunofluorescence microscopy.
11 lin and B23 at a frequency of nearly 100% by confocal immunofluorescence microscopy.
12 with human macrophages by immunoelectron and confocal immunofluorescence microscopy.
13 5 relative protein levels were quantified by confocal immunofluorescence microscopy.
14 roteins was determined using immunoblots and confocal immunofluorescence microscopy.
15    IGFBP-3 surface coating was identified by confocal immunofluorescence microscopy.
16 lyzed by using multicolor flow cytometry and confocal immunofluorescence microscopy.
17 mbranes (CNVMs) was analyzed by double-label confocal immunofluorescence microscopy.
18 nd a change in cell shape as demonstrated by confocal immunofluorescence microscopy.
19 mitochondria, as revealed by double-labeling confocal immunofluorescence microscopy.
20 ese methods and conclusions were obtained by confocal immunofluorescence microscopy.
21 ance during the period of study as imaged by confocal immunofluorescence microscopy.
22 tein primarily localized near termini) under confocal immunofluorescence microscopy.
23 n the surface of mast cells as determined by confocal immunofluorescence microscopy, aberrant S1P rec
24 GT) has been studied in human fibroblasts by confocal immunofluorescence microscopy after intranuclea
25 rcellular junction protein distribution with confocal immunofluorescence microscopy and antibodies ag
26                                   Using both confocal immunofluorescence microscopy and biochemical a
27 cdk6 to the nucleus, as demonstrated by both confocal immunofluorescence microscopy and biochemical f
28 two proteins on intact cells was analyzed by confocal immunofluorescence microscopy and by a novel cr
29              In this study, we determined by confocal immunofluorescence microscopy and by immunodete
30 atory responses of TNF, has been analyzed by confocal immunofluorescence microscopy and by Western bl
31 e cellular distribution of phospho-ERK1/2 by confocal immunofluorescence microscopy and cellular frac
32                               Laser scanning confocal immunofluorescence microscopy and domain-select
33 ecame spatially colocalized as determined by confocal immunofluorescence microscopy and fluorescence
34 eta-hydroxylase (DbetaH) was performed using confocal immunofluorescence microscopy and immunoelectro
35                                              Confocal immunofluorescence microscopy and quantitative
36 r replication factories were visualized with confocal immunofluorescence microscopy and single-replic
37                                      We used confocal immunofluorescence microscopy and ts mutant reo
38                                              Confocal immunofluorescence microscopy and virus-specifi
39                                        Using confocal immunofluorescence microscopy and Western blot
40  was demonstrated within cultured neurons by confocal immunofluorescence microscopy and within neuron
41                    Using metabolic labeling, confocal immunofluorescence microscopy, and immunoblot a
42 inases by co-immunoprecipitation studies and confocal immunofluorescence microscopy, and this interac
43 s (ANP-RB, a guanylyl cyclase), we have used confocal immunofluorescence microscopy applied to primar
44 tion, mass spectrometric identification, and confocal immunofluorescence microscopy assays, we found
45                                        Using confocal immunofluorescence microscopy, Ax-II was visual
46                                           By confocal immunofluorescence microscopy, BIG1 was localiz
47 yonic to adult mice by immunohistochemistry, confocal immunofluorescence microscopy, catalyzed report
48                                              Confocal immunofluorescence microscopy confirmed that pr
49                                              Confocal immunofluorescence microscopy confirmed the pre
50                                              Confocal immunofluorescence microscopy demonstrated abno
51 0-kd band in control and TC-grown cells, and confocal immunofluorescence microscopy demonstrated stai
52                                              Confocal immunofluorescence microscopy demonstrated that
53                Both immunohistochemistry and confocal immunofluorescence microscopy demonstrated that
54                       Cell fractionation and confocal immunofluorescence microscopy demonstrated that
55  biopsies (0, 2 and 6 h) were analysed using confocal immunofluorescence microscopy for fibre type-sp
56              We constructed the system using confocal immunofluorescence microscopy images from the H
57 ormation and proteins were analyzed by using confocal immunofluorescence microscopy, immunoblotting,
58 artially colocalized with Rab38 and Rab32 by confocal immunofluorescence microscopy in MNT-1 cells.
59   This P2X4-mCherry expression, confirmed by confocal immunofluorescence microscopy in wild-type (WT)
60                                              Confocal immunofluorescence microscopy indicated that Ca
61                                              Confocal immunofluorescence microscopy indicated that ea
62                                 Quantitative confocal immunofluorescence microscopy indicated that th
63 g retina, RPE, and choroid was processed for confocal immunofluorescence microscopy, laser capture mi
64  (5.4 fold over wild-type), and quantitative confocal immunofluorescence microscopy localized over-ex
65                                              Confocal immunofluorescence microscopy localizes Ecm29 t
66                                           In confocal immunofluorescence microscopy, MINT adopts a re
67                                              Confocal immunofluorescence microscopy of COS cells demo
68                                              Confocal immunofluorescence microscopy of COS-7 cells tr
69 lected deleted Env proteins was confirmed by confocal immunofluorescence microscopy of hemagglutinin-
70                                              Confocal immunofluorescence microscopy of HGF-treated ce
71                                Two-parameter confocal immunofluorescence microscopy of histone and DN
72                                              Confocal immunofluorescence microscopy of live eggs indi
73                                    Moreover, confocal immunofluorescence microscopy of polarized Calu
74                                              Confocal immunofluorescence microscopy of scratch-damage
75                                              Confocal immunofluorescence microscopy of structural and
76                                              Confocal immunofluorescence microscopy of ventricular an
77                         Subfractionation and confocal immunofluorescence microscopy reveal that, in l
78                                              Confocal immunofluorescence microscopy revealed that bot
79 ation of CaMK and GABA immunoreactivity with confocal immunofluorescence microscopy revealed that CaM
80 rikingly, cell fractionation experiments and confocal immunofluorescence microscopy revealed that ET
81 pitated and identified by Western blots, and confocal immunofluorescence microscopy revealed that GPR
82                                     Further, confocal immunofluorescence microscopy revealed that M.
83                                              Confocal immunofluorescence microscopy revealed that the
84                                              Confocal immunofluorescence microscopy revealed that UL5
85                                              Confocal immunofluorescence microscopy revealed that XMA
86                                              Confocal immunofluorescence microscopy revealed the excl
87                                              Confocal immunofluorescence microscopy showed prominent
88 he intracellular neutralization experiments, confocal immunofluorescence microscopy showed prominent
89                                              Confocal immunofluorescence microscopy showed that 11 of
90                                              Confocal immunofluorescence microscopy showed that even
91 reased FYB tyrosine phosphorylation, whereas confocal immunofluorescence microscopy showed that FYB c
92                                              Confocal immunofluorescence microscopy showed that they
93                                              Confocal immunofluorescence microscopy shows 2.5-fold mo
94                Here, we demonstrate by using confocal immunofluorescence microscopy that PECAM-1 is f
95                         Here we show through confocal immunofluorescence microscopy that Pelle functi
96 rol or nocodazole-treated cells was found by confocal immunofluorescence microscopy to be a single ch
97                         We used standard and confocal immunofluorescence microscopy to demonstrate th
98  fully the assembly of the MTOC-TMA, we used confocal immunofluorescence microscopy to examine the lo
99 ved from B-cell-deficient mice were found by confocal immunofluorescence microscopy to express outer
100 ation and immunoblot assay, and were used in confocal immunofluorescence microscopy to reveal low lev
101                                      We used confocal immunofluorescence microscopy to show that Ctr
102                                              Confocal immunofluorescence microscopy using affinity-pu
103 ion were monitored in GH-stimulated cells by confocal immunofluorescence microscopy using an antibody
104 olgi network (TGN) morphology as revealed by confocal immunofluorescence microscopy using antibody to
105  of Cx43 were measured by immunoblotting and confocal immunofluorescence microscopy using isoform-spe
106                                              Confocal immunofluorescence microscopy was used to ident
107                                              Confocal immunofluorescence microscopy was used to ident
108                          At each time point, confocal immunofluorescence microscopy was used to local
109                                        Using confocal immunofluorescence microscopy we also show that
110                                           By confocal immunofluorescence microscopy we find that HMG-
111  Western blotting, immunohistochemistry, and confocal immunofluorescence microscopy, we analyzed the
112 mistry, HIV-1 RNA in situ hybridization, and confocal immunofluorescence microscopy, we demonstrate t
113                                        Using confocal immunofluorescence microscopy, we found that st
114 nventional and immunoelectron microscopy and confocal immunofluorescence microscopy, we show that Gol
115                     Immunohistochemistry and confocal immunofluorescence microscopy were performed on
116 face biotinylation, immobilized lectins, and confocal immunofluorescence microscopy were used to char
117 his study, a murine macrophage cell line and confocal immunofluorescence microscopy were used to more
118  membrane-associated BIG1 and BIG2, which by confocal immunofluorescence microscopy were widely dispe
119                                              Confocal immunofluorescence microscopy with anti-cytoker

 
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