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1 yzed by histology, immunohistochemistry, and immunofluorescence staining.
2 thelium was examined by Western blotting and immunofluorescence staining.
3 ng parallel readout of protein expression by immunofluorescence staining.
4 -time PCR, a viral plaque-forming assay, and immunofluorescence staining.
5 essed by immunoblotting, flow cytometry, and immunofluorescence staining.
6 d their phenotype using Western blotting and immunofluorescence staining.
7 rmally carried out by gel electrophoresis or immunofluorescence staining.
8 zyme-linked immunosorbent assay (ELISA), and immunofluorescence staining.
9 sing fluorescence-activated cell sorting and immunofluorescence staining.
10 te infiltrates in kidneys were visualized by immunofluorescence staining.
11 markers were detected in the ocular tumor by immunofluorescence staining.
12 rophils and macrophages was quantified after immunofluorescence staining.
13 ndard for clinical diagnostics of tissues is immunofluorescence staining.
14 F-2 and actin cytoskeleton was determined by immunofluorescence staining.
15 -time polymerase chain reaction or viewed by immunofluorescence staining.
16 , and Picro-Sirius red staining and collagen immunofluorescence staining.
17  was determined by Western blot analysis and immunofluorescence staining.
18 KCepsilon with Stat3 was confirmed by double immunofluorescence staining.
19 flux, mRNA expression, Western blotting, and immunofluorescence staining.
20 nscription PCR (RT-PCR) and viral antigen by immunofluorescence staining.
21 eta expression were analyzed in BAL cells by immunofluorescence staining.
22 ression in beta-cells was verified by double-immunofluorescence staining.
23 crin was studied in human cornea sections by immunofluorescence staining.
24 ne was determined by using real-time PCR and immunofluorescence staining.
25 key fibrinolytic molecules was determined by immunofluorescence staining.
26 lar matrix interactions (focal adhesions) by immunofluorescence staining.
27 yloric sections and further characterized by immunofluorescence staining.
28 7, P11, P15, P30, and P60 were collected for immunofluorescence staining.
29  lung MC from patients with asthma by double-immunofluorescence staining.
30 PCR and for the nonstructural protein NS3 by immunofluorescence staining.
31  as measured by RT-PCR, western blotting and immunofluorescence staining.
32 us spectroscopic measurements and confirming immunofluorescence staining.
33 s determined using Western blot analysis and immunofluorescence staining.
34 erminal center areas of splenic follicles by immunofluorescence staining.
35  transcription-polymerase chain reaction and immunofluorescence staining.
36 pus was evaluated by immunohistochemistry or immunofluorescence staining.
37 sing real-time polymerase chain reaction and immunofluorescence staining.
38 nd 21, as shown by western blot analysis and immunofluorescence staining.
39 ruses, produce dsRNAs detectable by standard immunofluorescence staining.
40 olute sensitivity when compared to optimized immunofluorescence staining.
41 roduce dsRNA species that can be detected by immunofluorescence staining.
42 titative PCR, SDS-PAGE/Western blotting, and immunofluorescence staining.
43 unts using intercellular adhesion molecule 2 immunofluorescence staining.
44 ctly compared by using enzymatic markers and immunofluorescence stainings.
45 ot express FV, but became positive for FV at immunofluorescence staining after administration of anti
46                                              Immunofluorescence staining against AstA, AT, and TK in
47                       Using Western blot and immunofluorescence staining, all six isoforms of PRX wer
48                                     Specific immunofluorescence staining analyzed by fluorescence-act
49                                 Furthermore, immunofluorescence staining and cell fractionation showe
50 d to nucleus, detected by immunoblotting and immunofluorescence staining and coimmunoprecipitated wit
51 f specific ECM proteins was assessed through immunofluorescence staining and colorimetric assay kits.
52                                       Double immunofluorescence staining and confocal laser scanning
53                                              Immunofluorescence staining and confocal microscopy of c
54                                              Immunofluorescence staining and confocal microscopy were
55                                     By using immunofluorescence staining and confocal microscopy, the
56                                        Using immunofluorescence staining and confocal microscopy, we
57 13 were visualized in glial cells in situ by immunofluorescence staining and confocal microscopy.
58 ation of c-SRC and RARgamma was confirmed by immunofluorescence staining and confocal microscopy.
59  was detected in the DRG and dorsal roots by immunofluorescence staining and confocal microscopy.
60 racellular matrix proteins were evaluated by immunofluorescence staining and confocal microscopy.
61 antibodies (MAbs), as determined by indirect immunofluorescence staining and flow-cytometric analysis
62                                              Immunofluorescence staining and fractionation studies re
63 eptide arrays, and they have been tested for immunofluorescence staining and immunoaffinity purificat
64 ooth muscle actin (alpha-SMA) was studied by immunofluorescence staining and immunoblotting.
65                                         Both immunofluorescence staining and lentiviral vector labeli
66                               As assessed by immunofluorescence staining and membrane biotinylation,
67                                    Data from immunofluorescence staining and protein interaction assa
68                                              Immunofluorescence staining and subcellular fractionatio
69                                      Further immunofluorescence staining and subcellular fractionatio
70                                           By immunofluorescence staining and subcellular fractionatio
71 creased both the level of cell surface Kv1.1 immunofluorescence staining and the proportion of Kv1.1
72                                              Immunofluorescence staining and transmission electron mi
73        We assessed C7 expression by means of immunofluorescence staining and used transmission electr
74 in 1 levels in the stratum corneum (shown by immunofluorescence staining and visualized by confocal m
75            In the present study, we employed immunofluorescence staining and Western blot analysis to
76     Cells treated for 48 hours were used for immunofluorescence staining and Western blot analysis, a
77                           As demonstrated by immunofluorescence staining and Western blot analysis, T
78 nd involucrin protein levels were studied by immunofluorescence staining and Western blot analysis.
79                                     Indirect immunofluorescence staining and western blot techniques
80                                              Immunofluorescence staining and Western blots demonstrat
81                                              Immunofluorescence staining and Western blotting showed
82                           Glucose tolerance, immunofluorescence staining, and examination of islet cu
83       Multiple approaches, including RT-PCR, immunofluorescence staining, and immunoblotting, were us
84 owing BPA exposure using the comet assay and immunofluorescence staining, and used cell counting and
85                        Blocking experiments, immunofluorescence staining, and western blot confirmed
86 ssion of SC markers was analyzed by qRT-PCR, immunofluorescence staining, and Western blot; SC clonal
87 chmarking against in situ hybridizations and immunofluorescence staining, as well as recombinant prot
88                                           Co-immunofluorescence staining assays demonstrate that wild
89                                              Immunofluorescence staining assays demonstrated that hum
90                              In addition, by immunofluorescence staining, both of these antibodies lo
91 vels (r=0.760; P<0.00001).We localized, with immunofluorescence staining, BTNL2 in CD68-positive macr
92                                              Immunofluorescence staining by 14E6 of neonatal rat prim
93                              In double-label immunofluorescence staining, CD11c+, a marker of myeloid
94 oid-monocytic lineage as evaluated by double immunofluorescence staining, cell fate tracking, flow cy
95 LK-FISH patterns were examined in CTCs using immunofluorescence staining combined with filter-adapted
96                                              Immunofluorescence staining confirmed a colocalization o
97                                              Immunofluorescence staining confirmed that the enlarged
98                      Western blot assays and immunofluorescence staining confirmed the nuclear locali
99 rformed using flow cytometry, real-time PCR, immunofluorescence staining, confocal microscopy, and sc
100        Both coimmunoprecipitation and double immunofluorescence staining demonstrate that NAC-1 molec
101                                              Immunofluorescence staining demonstrated accumulation of
102                                              Immunofluorescence staining demonstrated complete disapp
103                              Immunoblots and immunofluorescence staining demonstrated significant inc
104                                              Immunofluorescence staining demonstrated that BAP co-loc
105                                 In addition, immunofluorescence staining demonstrated that endogenous
106                        Furthermore, indirect immunofluorescence staining demonstrated that mature L-S
107                                       Double immunofluorescence staining demonstrated that mu recepto
108       Coimmunoprecipitation and double-color immunofluorescence staining demonstrated that PML physic
109                                 Double-label immunofluorescence staining demonstrated that T cells, m
110  on the ear cartilage surface in sites where immunofluorescence staining detected spirochete antigens
111 V) (Becton Dickinson and Company) and direct immunofluorescence staining (DFA) were compared with cul
112 d by viral culture (405 specimens) or direct immunofluorescence staining (DIF) (65 specimens).
113                   After performing gammaH2AX immunofluorescence staining, DSBs were quantified with a
114   Using a local UV irradiation technique and immunofluorescence staining, E2F1 is shown to accumulate
115                                              Immunofluorescence staining experiments revealed the pre
116 sma membrane localization and function using immunofluorescence staining, flow cytometry, and lucifer
117                               We used triple-immunofluorescence staining followed by multichannel, hi
118                                 We performed immunofluorescence staining for AC(VI) in the AV node of
119 d corneas were excised from BALB/c mice, and immunofluorescence staining for CD11c, CD11b, CD45, CD80
120 olitis patients (n = 67) consistently showed immunofluorescence staining for CD40 in IECs of inflamed
121 re isolated, ethanol-fixed, and subjected to immunofluorescence staining for colocalizing gamma-H2AX/
122                         Western analysis and immunofluorescence staining for cyclins during epithelia
123 target of rapamycin signaling molecules, and immunofluorescence staining for endogenous LC3B, GFP-LC3
124 g wholemounts of wild-type mouse eyes and by immunofluorescence staining for green fluorescent protei
125                       On the basis of double immunofluorescence staining for IAA-RP and calbindin, ma
126 munoblot, electron microscopy, together with immunofluorescence staining for LC3 and p62 indicated an
127                                              Immunofluorescence staining for macrophages in cross-sec
128                                 Using double immunofluorescence staining for markers specific for hep
129                                              Immunofluorescence staining for NCAM and polySia was con
130                                              Immunofluorescence staining for PPARgamma protein also s
131                                       Double-immunofluorescence staining found that tumor-associated
132 , we tested respiratory secretions by direct immunofluorescence staining from December to March.
133                                              Immunofluorescence staining further confirmed the effect
134                                              Immunofluorescence staining further revealed that PMAT p
135  cell sorter analysis, the number of DSBs by immunofluorescence staining gammaH2AX/53BP1-positive rep
136 fluorescence; gammaH2AX, Rad51, and HDAC4 by immunofluorescence staining; HDAC4, Rad51, and ubiquitin
137  presynaptic NKA pump current, combined with immunofluorescence staining, identified the alpha3-NKA i
138  the simultaneous detection of proteins with immunofluorescence staining (IF).
139 olecules carrying pathogenic mutations using immunofluorescence staining, immunogold labeling, and Pr
140 xamined PML protein levels and PML and Sp100 immunofluorescence staining in human embryonic lung cell
141 ortactin by coimmunoprecipitation and double immunofluorescence staining in murine and human hearts a
142         Using surface biotinylation and dual immunofluorescence staining in MYO5B-KD cells expressing
143 iography and histologic markers evaluated by immunofluorescence staining in the same tumor sections.
144                                              Immunofluorescence staining indicated that myosin IIB wa
145                                     However, immunofluorescence staining indicated that the decrease
146                                              Immunofluorescence staining indicated that the HD3alpha
147                     Fluorescence imaging and immunofluorescence staining/laser-scanning confocal micr
148                                              Immunofluorescence staining localized CyRPA at the apex
149 tors and Fc receptors were examined using an immunofluorescence staining method followed by flow cyto
150 ared with ex vivo gamma counting (n = 6) and immunofluorescence staining (n = 6).
151                                     However, immunofluorescence staining of A431DE cells (E-cadherin
152                                              Immunofluorescence staining of AAF-44 and AAF-132 in S p
153                                              Immunofluorescence staining of BacM and MreB shows that
154 ITEGE and DIPEN neoepitopes were detected by immunofluorescence staining of bovine articular cartilag
155                        In this study, we use immunofluorescence staining of BPV1 pseudovirions to sho
156 ull mice were analyzed by immunoblotting and immunofluorescence staining of cell and mouse tissue hom
157 dye labeling through the antennal nerve, and immunofluorescence staining of cell surface markers.
158                                              Immunofluorescence staining of cells using antibodies ag
159 nents whose presence in rods was examined by immunofluorescence staining of cells.
160                                              Immunofluorescence staining of cellular actin showed tha
161 hemangiogenesis) and nerves were observed by immunofluorescence staining of corneal flat mounts.
162                                  Whole-mount immunofluorescence staining of corneas was performed wit
163           Here we demonstrate by whole-mount immunofluorescence staining of ear skin and mesentery th
164                                              Immunofluorescence staining of endplates from the treate
165 urons involving electron microscopy (EM) and immunofluorescence staining of glycoproteins and capsids
166 nce were assessed by immunohistochemical and immunofluorescence staining of hearts and aortas.
167                                     Indirect immunofluorescence staining of HeLa cells using a phosph
168                                              Immunofluorescence staining of human cells with anti-Orc
169                                              Immunofluorescence staining of human primary breast canc
170                                              Immunofluorescence staining of ICP8 in cells infected wi
171                                        Using immunofluorescence staining of intact rat SC tissue, we
172 roduce vIL-6 frequently coexpress XBP-1, and immunofluorescence staining of involved KSHV-MCD lymph n
173   This was further confirmed by differential immunofluorescence staining of lung cells harvested from
174                                              Immunofluorescence staining of lung sections showed that
175                                              Immunofluorescence staining of MB231 cells for V-ATPase
176                                              Immunofluorescence staining of microtubules after 24 h o
177                                 Using double immunofluorescence staining of mouse brain sections, we
178 nses measured by TNF-alpha production, while immunofluorescence staining of murine alveolar macrophag
179 s study, we performed metabolic labeling and immunofluorescence staining of newly synthesized HDV RNA
180 tein kinase B (PKB) activity, as measured by immunofluorescence staining of phospho-PKB, was not alte
181                                              Immunofluorescence staining of platelet glycoprotein GPI
182 localization pattern is further supported by immunofluorescence staining of polytene chromosomes and
183                                              Immunofluorescence staining of precirrhotic HCV livers s
184                                              Immunofluorescence staining of premeablized HeLa cells s
185                                              Immunofluorescence staining of Purkinje cells with anti-
186                                        Using immunofluorescence staining of Rac1 to understand the ce
187                     Electron micrographs and immunofluorescence staining of rat CB sections revealed
188                                              Immunofluorescence staining of regenerating liver identi
189                               Using combined immunofluorescence staining of SGs markers and COX-2 pro
190                                       Double immunofluorescence staining of the cingulate cortex show
191  describes a basic method for dissection and immunofluorescence staining of the Drosophila brain at v
192               Using four-channel whole-mount immunofluorescence staining of the human dermis, we demo
193 l separation of the TJs of adjacent cells in immunofluorescence staining of the TJ molecules occludin
194                                              Immunofluorescence staining of thin sections of lungs fr
195 d genotyping and quantitative analyses after immunofluorescence staining of tissue and cultured cells
196                      Immunohistochemical and immunofluorescence staining of tissue arrays has shown t
197                                              Immunofluorescence staining of tissue sections revealed
198 inucleolar heterochromatin, as identified by immunofluorescence staining of trimethylated H3K9, trime
199                                              Immunofluorescence staining of ventral prostate tissue f
200 ell types expressing PD-1 were identified by immunofluorescence staining of vertical retina sections;
201                                              Immunofluorescence staining of whole larvae showed that
202 sing laser scanning confocal microscopy, and immunofluorescence staining of whole-mount fixed tissue
203         This finding was also validated with immunofluorescence staining on Foxp3(+)CD4(+) and PD-1(+
204                                              Immunofluorescence staining on hepatocyte couplets for b
205 xpression of KCa3.1 in vivo was confirmed by immunofluorescence staining on multinucleated cells at t
206  in the liver with Western blotting and with immunofluorescence staining only in HD-Ad-mVLDLR-treated
207 meter macrosections enables simple and rapid immunofluorescence staining, optical clearing, and confo
208                    This brain dissection and immunofluorescence staining protocol requires approximat
209 rculation and graft by flow cytometry and in immunofluorescence staining, respectively.
210                                              Immunofluorescence staining revealed a decrease in cathe
211 icantly reduced in affected individuals, and immunofluorescence staining revealed a striking decrease
212                                              Immunofluorescence staining revealed an intense nuclear
213                                     Finally, immunofluorescence staining revealed elevated phosphoryl
214                                              Immunofluorescence staining revealed increased AC(VI) ex
215                                              Immunofluorescence staining revealed partial overlap bet
216 d lymphocyte expression of CCR4, and 2-color immunofluorescence staining revealed RA ST CD3+ lymphocy
217                      Immunohistochemical and immunofluorescence staining revealed reactivity with gro
218                                       Double-immunofluorescence staining revealed robust P-selectin e
219                                              Immunofluorescence staining revealed significant RGC-spe
220                                              Immunofluorescence staining revealed that AR8 was primar
221                                         Dual immunofluorescence staining revealed that cleaved caspas
222                     Cellular localization by immunofluorescence staining revealed that p32 is present
223                                              Immunofluorescence staining revealed that regenerating f
224                                              Immunofluorescence staining revealed that sG specificall
225                                              Immunofluorescence staining revealed that subcellular lo
226                                              Immunofluorescence staining revealed the presence of T1L
227  were detected in infected neurons, and dual immunofluorescence staining revealed the presence of VZV
228                   Because flow cytometry and immunofluorescence stainings revealed membranous ST2L ex
229                                              Immunofluorescence staining reveals discrete nuclear foc
230                                              Immunofluorescence staining reveals that CLEC18 are loca
231 as confirmed in all 3 cell types by means of immunofluorescence staining, RT-PCR, and qRT-PCR, and qR
232 I, Ngn1/DAPI, and BMP4/DAPI were measured by immunofluorescence staining; Shh, Gli1, Ngn1, and BMP4 p
233                                     DAPI and immunofluorescence staining showed a single nucleus, kin
234 ut was not present in isolated axonemes, and immunofluorescence staining showed an absence of ODA and
235 t mouse models on nonautoimmune backgrounds, immunofluorescence staining showed extensive linear C3 s
236                                              Immunofluorescence staining showed higher accumulations
237                     Immunohistochemistry and immunofluorescence staining showed NPR-C near the lumina
238                                              Immunofluorescence staining showed that apoE4(1-272) for
239                                              Immunofluorescence staining showed that CD38 was express
240                                              Immunofluorescence staining showed that cyclic MS marked
241                                       Double immunofluorescence staining showed that I (1)(PP2A) and
242                                Intracellular immunofluorescence staining showed that in pattern 2, HB
243                             Western blot and immunofluorescence staining showed that MALAT1 knockdown
244                                              Immunofluorescence staining showed that MCPIP4 was co-lo
245                                              Immunofluorescence staining showed that most N18 cells w
246                       In the former setting, immunofluorescence staining showed that MSCs, after indu
247                                       First, immunofluorescence staining showed that PTC124 treatment
248                                       Double immunofluorescence staining showed that subepithelial gr
249                                              Immunofluorescence staining shows that eIF3j/Hcr1p is lo
250                                              Immunofluorescence staining shows that pS857 is found in
251                Subcellular fractionation and immunofluorescence staining studies revealed that AIFL i
252                                              Immunofluorescence staining studies showed that upon dox
253  Transmission electron microscopy images and immunofluorescence stainings suggested that this effect
254                                              Immunofluorescence staining suggests that the electric s
255                                           In immunofluorescence staining, the number of pNR1-like imm
256 l latent and lytic transcripts and two-color immunofluorescence staining to analyze expression at the
257 otransferase (GalNAc4-ST1), which we show by immunofluorescence staining to be expressed throughout n
258 were imaged in situ and ex vivo, followed by immunofluorescence staining to confirm target labeling.
259 lfate polyacrylamide gel electrophoresis and immunofluorescence staining to confirm the primary targe
260 of galactose-deficient IgG in the fluids and immunofluorescence staining to detect galactose-deficien
261 rther confirmed by coimmunoprecipitation and immunofluorescence staining to occur in FMDV-infected ce
262                                           By immunofluorescence staining using an anti-BrUTP antibody
263 eplication compartments could be detected by immunofluorescence staining using anti-BMRF1 monoclonal
264                                       Double immunofluorescence staining using antibodies against cho
265 ferent nerve fibers was investigated by dual immunofluorescence staining using antibodies targeted fo
266 the mitochondria of RRECs was confirmed with immunofluorescence staining using Cx43 antibody and GFP-
267 zation was confirmed by Western blotting and immunofluorescence staining using polyclonal antibodies
268                                       Triple immunofluorescence stainings using markers against glial
269                                              Immunofluorescence staining was conducted to evaluate ce
270                                              Immunofluorescence staining was employed to identify pro
271                                   Multilabel immunofluorescence staining was performed on free-floati
272                                       Double immunofluorescence staining was performed on paraffin-em
273                                              Immunofluorescence staining was performed to determine e
274 luorescent-labeled lectin perfusion and CD31 immunofluorescence staining) was significantly lower in
275                                 Using triple immunofluorescence staining we tested whether there were
276                                By conducting immunofluorescence staining, we analyzed the expression
277                                        Using immunofluorescence staining, we confirmed the expression
278                                        Using immunofluorescence staining, we demonstrated immunoreact
279                                By using dual-immunofluorescence staining, we demonstrated that increa
280                     Interestingly, by triple-immunofluorescence staining, we detected c-kit (a marker
281                                           By immunofluorescence staining, we found that Oc1 and Oc2 h
282 radient centrifugation, immunoadsorption and immunofluorescence staining, we have shown that Glut4 in
283 egion of MUC1 combined with Western blot and immunofluorescence staining, we identify MUC1 as a direc
284                                        Using immunofluorescence staining, we observed colocalization
285                  Furthermore, using indirect immunofluorescence staining, we showed that the vimentin
286 Assisted Stereology Toolbox morphometry, and immunofluorescence staining were performed at baseline a
287 ddition, caspase 3 enzyme activity assay and immunofluorescence staining were performed to evaluate a
288 sue homogenate fluorescence measurement, and immunofluorescence staining were performed with U87MG tu
289 expression analysis, biochemical assays, and immunofluorescence staining were used to characterize th
290                           Immunoblotting and immunofluorescence staining were used to examine the exp
291 ro and in patients with COPD was assessed by immunofluorescence staining, Western blot analysis, and
292 fections produce dsRNA species detectable by immunofluorescence staining, which may prove useful in v
293 kdown of BRCA1 protein resulted in decreased immunofluorescence staining, which was confirmed by West
294                                              Immunofluorescence staining with an antibody against 5-m
295                                              Immunofluorescence staining with anti-alpha-tubulin anti
296 red using hematoxylin-and-eosin staining, or immunofluorescence staining with antibodies to K8/K18/ub
297                                              Immunofluorescence staining with ICP4 monoclonal antibod
298 nexin V flow cytometry analyses and cellular immunofluorescence staining with propidium iodide, anti-
299   It was confirmed as Balamuthia by indirect immunofluorescence staining with rabbit anti-Balamuthia
300                                              Immunofluorescence staining with the anti-alpha-actinin

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