1 ive vaccine strain with human macrophages by
immunoelectron and confocal immunofluorescence microscop
2 By using
immunoelectron and immunofluorescence microscopy togethe
3 nent at asymmetric synapses as determined by
immunoelectron microcopy.
4 Additionally,
immunoelectron micrographs showed A9 in tubules containi
5 se distances between immunogold particles in
immunoelectron micrographs.
6 Fluorescence and
immunoelectron microscopic analyses document that the su
7 Confocal and
immunoelectron microscopic analyses of transgenic parasi
8 Immunofluorescent and
immunoelectron microscopic analyses showed that the graf
9 was examined by using immunofluorescence and
immunoelectron microscopic analysis of the rat LC and ne
10 Moreover,
immunoelectron microscopic analysis revealed a selective
11 However,
immunoelectron microscopic analysis revealed that in cel
12 Here we provide
immunoelectron microscopic data showing that many asymme
13 d by immunohistochemical and high-resolution
immunoelectron microscopic evaluation of the lesions, wh
14 also assessed using immunohistochemical and
immunoelectron microscopic methods.
15 Immunoelectron microscopic studies of estrogen-stimulate
16 Immunoelectron microscopic studies revealed the colocali
17 Postembedding
immunoelectron microscopic studies were performed with a
18 The present
immunoelectron microscopic study revealed that the basol
19 Immunocytochemical,
immunoelectron microscopic, and biochemical analyses of
20 block its export, as shown by the results of
immunoelectron microscopy (IEM) and antibody adsorption
21 sity gradient centrifugation and analyzed by
immunoelectron microscopy (IEM) and Western blot assays
22 Our
immunoelectron microscopy (IEM) data suggest that mRNA/G
23 vely evaluated the diagnostic performance of
immunoelectron microscopy (IEM) of abdominal fat aspirat
24 aper, we showed by coimmunoprecipitation and
immunoelectron microscopy (IEM) that these Gag-containin
25 ce (IF), immuno-enzymatic staining (IES) and
immunoelectron microscopy (IEM), that have found widespr
26 n as well as healthy and disease controls by
immunoelectron microscopy (IEM), Western blots, and enzy
27 analysis, atomic force microscopy (AFM), and
immunoelectron microscopy (immuno-EM).
28 face could be detected by flow cytometry and
immunoelectron microscopy after expression of the cloned
29 ction, immunoblot analysis, and confocal and
immunoelectron microscopy all indicated increased expres
30 rging from that model by ultrastructural and
immunoelectron microscopy analyses of cores from wild-ty
31 Western blotting and
immunoelectron microscopy analyses suggest that CideB is
32 Electron microscopy/
immunoelectron microscopy analysis and tracking of the e
33 Immunoelectron microscopy analysis provides insight into
34 Immunoelectron microscopy analysis shows that Sac3 local
35 Moreover,
immunoelectron microscopy and analysis of mitochondrial-
36 By using
immunoelectron microscopy and biochemical analysis, we s
37 tissues in Gnptab -/- mice using a combined
immunoelectron microscopy and biochemical approach.
38 addition, we discovered using techniques of
immunoelectron microscopy and biochemical purification o
39 On selected cases,
immunoelectron microscopy and biochemistry were performe
40 Immunoelectron microscopy and cell fractionation reveal
41 Using conventional and
immunoelectron microscopy and confocal immunofluorescenc
42 was concordant with fibril identification by
immunoelectron microscopy and consistent with clinical p
43 cells by immunofluorescence and quantitative
immunoelectron microscopy and developed imaging and traf
44 immunoblots of membrane-associated proteins,
immunoelectron microscopy and flow cytometry assays all
45 Using mass spectrometry,
immunoelectron microscopy and fluorescence lifetime imag
46 used 3,3'diaminobenzidine tetrahydrochloride
immunoelectron microscopy and fluorescence microscopy to
47 We have used
immunoelectron microscopy and gold-labelled antibodies t
48 We show here by
immunoelectron microscopy and immunoblotting that SynCAM
49 ) agonist isoproterenol, consistent with the
immunoelectron microscopy and immunocytochemical data de
50 Immunoelectron microscopy and immunofluorescence analysi
51 Importantly,
immunoelectron microscopy and immunofluorescence studies
52 We show presynaptic expression of TRPV1 by
immunoelectron microscopy and link TRPV1 to Panx1 becaus
53 Based on biochemistry,
immunoelectron microscopy and live cell microscopy, we f
54 trafficking of PfEMP1 was investigated using
immunoelectron microscopy and proteolytic digestion of s
55 Using immunofluorescence and
immunoelectron microscopy and subcellular fractionation
56 the postsynaptic perimeter as determined by
immunoelectron microscopy and super-resolution imaging.
57 we found R6 within RRV virion particles via
immunoelectron microscopy and, furthermore, that virion-
58 sessed DR-5-HT neuronal responses to CRF and
immunoelectron microscopy assessed CRF1 and CRF2 cellula
59 d using tract tracing, light microscopy, and
immunoelectron microscopy at four postnatal ages: P15, P
60 Immunoelectron microscopy co-localized Clag9 and RhopH2
61 Immunoelectron microscopy confirmed D1R colocalization w
62 Confocal and
immunoelectron microscopy confirmed depletion of von Wil
63 Immunoelectron microscopy confirmed that filensin and AQ
64 Immunoelectron microscopy confirmed that neuronal IFs co
65 Immunoelectron microscopy confirmed that PSD95-GFP predo
66 Immunoelectron microscopy confirmed that RANTES is store
67 Immunofluorescence and
immunoelectron microscopy confirmed the colocalization o
68 Double-label
immunoelectron microscopy confirmed the existence of syn
69 Immunoelectron microscopy confirmed the incorporation of
70 Immunoelectron microscopy confirms that binding occurs a
71 brane microdomains, as shown by double-label
immunoelectron microscopy data.
72 Cell fractionation, fluorescence imaging and
immunoelectron microscopy demonstrate that mitosomes con
73 Immunoelectron microscopy demonstrated an increased 3-ni
74 Sucrose gradient fractionation studies and
immunoelectron microscopy demonstrated localization of P
75 Immunoelectron microscopy demonstrated NaV1.6-positive s
76 Double-label
immunoelectron microscopy demonstrated that AT1 and gp91
77 Immunoelectron microscopy demonstrated that betaARs are
78 Here,
immunoelectron microscopy demonstrated that endothelial
79 Quantitative
immunoelectron microscopy demonstrated that the majority
80 Results from
immunoelectron microscopy demonstrated that the protecti
81 Immunoelectron microscopy demonstrated the presence of c
82 Immunoelectron microscopy demonstrates myelination of th
83 Moreover,
immunoelectron microscopy demonstrates the presence of V
84 encoding wheat germ agglutinin (WGA) and by
immunoelectron microscopy determined the presence of VGl
85 Immunofluorescence and
immunoelectron microscopy experiments established that A
86 Immunoelectron microscopy for Als2cr4 verified its expre
87 s investigated in the infragranular PFC with
immunoelectron microscopy for D1R and parvalbumin, a mar
88 Immunoelectron microscopy for GFP indicated that the tra
89 lamo-amygdaloid afferents with postembedding
immunoelectron microscopy for the GluRs in adult rats.
90 Immunoelectron microscopy identified postsynaptic mGluR2
91 GAIP is found by
immunoelectron microscopy in CCPs, and GIPC is found in
92 ritic profiles were measured by quantitative
immunoelectron microscopy in control or stressed rats.
93 avioral pharmacology, electrophysiology, and
immunoelectron microscopy in male and female mice to elu
94 Immunoelectron microscopy in mice with xenograft tumors,
95 Using a combination of electrophysiology and
immunoelectron microscopy in mice, the relationship betw
96 sphorylation states and perform high-quality
immunoelectron microscopy in monkeys is a great advantag
97 Pre-embedding
immunoelectron microscopy in rabbit retina confirmed exp
98 g confocal immunofluorescence microscopy and
immunoelectron microscopy in rat brain.
99 Protease digestion and
immunoelectron microscopy indicate that the alpha-syn am
100 Immunoelectron microscopy indicated that CEP290 is locat
101 Immunoelectron microscopy indicated that CfaE was confin
102 Immunoelectron microscopy indicated that E1 and E2 were
103 Immunoelectron microscopy indicated that this protein wa
104 Confocal microscopy and
immunoelectron microscopy localized ADAMTS10 to fibrilli
105 were employed to test this hypothesis: dual
immunoelectron microscopy localized D1R and HCN channels
106 Immunoelectron microscopy localized ePAD to egg cytoplas
107 Immunoelectron microscopy localized KCNQ isoforms (Kv7.2
108 By use of
immunoelectron microscopy methods, capsids that express
109 Using both biochemical fractionation and
immunoelectron microscopy methods, these vesicles were s
110 nalysis, were examined by immunoconfocal and
immunoelectron microscopy of lens sections.
111 Immunoelectron microscopy of lung endothelium or a cultu
112 Immunoelectron microscopy of neutrophils infected with A
113 Analysis by
immunoelectron microscopy of Sf-9 cells infected with th
114 Immunoelectron microscopy of the adult rat brain showed
115 apsule-like material was readily apparent by
immunoelectron microscopy on bacteria harvested in the p
116 Immunoelectron microscopy pronouncedly detects APH_1235
117 In this study, scanning
immunoelectron microscopy qualitatively demonstrated gre
118 These data, along with
immunoelectron microscopy results, imply that unmyelinat
119 Both immunofluorescence and
immunoelectron microscopy reveal that Sun1 but not Sun2
120 munofluorescence microscopy and quantitative
immunoelectron microscopy reveal that the majority of ne
121 Immunoelectron microscopy revealed a predominant localiz
122 Immunoelectron microscopy revealed a prominent localizat
123 tructural analysis in CA1 interneurons using
immunoelectron microscopy revealed abundant ErbB4 expres
124 Fractionation experiments and
immunoelectron microscopy revealed an association of gam
125 Western blot analysis and quantitative
immunoelectron microscopy revealed an increase in GIRK2
126 Immunoelectron microscopy revealed Bsp22 filaments on th
127 Immunoelectron microscopy revealed excitatory synaptic c
128 te stiffness was increased in the IG KO, and
immunoelectron microscopy revealed increased extension o
129 Immunoelectron microscopy revealed increased strain of t
130 Quantitative
immunoelectron microscopy revealed internalization of GA
131 At postnatal day (P) 7,
immunoelectron microscopy revealed near-equivalent propo
132 Immunoelectron microscopy revealed plasmalemmal OTR at e
133 Ultrastructural analysis by
immunoelectron microscopy revealed that annexin XI assoc
134 Immunoelectron microscopy revealed that ERalpha- and ERb
135 Immunoelectron microscopy revealed that fgl2 was distrib
136 Immunoelectron microscopy revealed that intranodal lymph
137 Furthermore,
immunoelectron microscopy revealed that Kv4.2 and Kv4.3
138 Immunofluorescence and
immunoelectron microscopy revealed that LMO7 localized a
139 Immunoelectron microscopy revealed that nitrated monomer
140 alent to those of unchallenged controls, and
immunoelectron microscopy revealed that NPC-derived myel
141 Immunoelectron microscopy revealed that peripheral affer
142 Immunoelectron microscopy revealed that Pfpmt localizes
143 d analyses on an ultrastructural level using
immunoelectron microscopy revealed that such coating may
144 Immunoelectron microscopy revealed that the loss of pres
145 Immunoelectron microscopy revealed that this sex differe
146 Immunoelectron microscopy revealed the presence of vesic
147 Chemical cross-linking together with
immunoelectron microscopy show that the mitochondrial AP
148 In addition,
immunoelectron microscopy showed AP-1B in coated pits an
149 Dual
immunoelectron microscopy showed coexistence of DYN and
150 Moreover,
immunoelectron microscopy showed ectopic deposition of c
151 Immunoelectron microscopy showed K(ir)6.2 antibodies spe
152 Immunoelectron microscopy showed that a portion of Sindb
153 Fluorescence resonance energy transfer and
immunoelectron microscopy showed that alphaS and parkin
154 of CD4 and G protein in plasma membranes by
immunoelectron microscopy showed that both were organize
155 Consistent with that finding,
immunoelectron microscopy showed that dysbindin-1 is loc
156 Immunoelectron microscopy showed that mAKAP co-localized
157 Immunoelectron microscopy showed that syndecan-1 was exp
158 Immunoelectron microscopy showed that when limited amoun
159 High-resolution
immunoelectron microscopy shows that Cdh8 is concentrate
160 Immunoelectron microscopy shows that FMRP is localized a
161 Immunoelectron microscopy shows that the membrane-bound
162 Furthermore,
immunoelectron microscopy studies revealed an associatio
163 Immunoelectron microscopy studies revealed that this tyr
164 Our
immunoelectron microscopy studies show that phosphorylat
165 Immunoelectron microscopy studies showed that centrin is
166 Immunoelectron microscopy studies suggested a model for
167 ther confirmed by co-immunoprecipitation and
immunoelectron microscopy studies.
168 High resolution
immunoelectron microscopy suggests a remarkable nanoscal
169 ing a postembedding immunogold procedure for
immunoelectron microscopy that included embedding in Uni
170 We now show by
immunoelectron microscopy that VAPB also localizes to th
171 Furthermore, we document by
immunoelectron microscopy the transfer of hER components
172 I mGluRs is altered in parkinsonism, we used
immunoelectron microscopy to analyze the subcellular and
173 nt in B capsids, and bound UL25 was found by
immunoelectron microscopy to be located predominantly at
174 To address this issue, we used
immunoelectron microscopy to compare the subcellular loc
175 Next, we used biochemical analyses and
immunoelectron microscopy to demonstrate that conserved
176 ed high-pressure freezing and serial-section
immunoelectron microscopy to determine the position of M
177 We have now used
immunoelectron microscopy to determine the subcellular s
178 We also used
immunoelectron microscopy to establish the distribution
179 determine whether this is the case, we used
immunoelectron microscopy to examine PR distribution in
180 lective agonists (LY354740 and LY379268) and
immunoelectron microscopy to examine structure-function
181 transgenic mice, brain Abeta42 localized by
immunoelectron microscopy to, and accumulated with aging
182 ed RT-PCR, and immunohisto/cytochemistry and
immunoelectron microscopy using beta-END and mu-opiate r
183 , and immunohistochemistry/cytochemistry and
immunoelectron microscopy using beta-endorphin and mu-op
184 Immunoelectron microscopy using monoclonal antibody (MAb
185 Double pre-embedding
immunoelectron microscopy using substance P and Met-/Leu
186 In support,
immunoelectron microscopy validated the localization of
187 Immunoelectron microscopy was performed on selected case
188 Immunoelectron microscopy was used to detect FSH recepto
189 Dual-labeling
immunoelectron microscopy was used to determine whether
190 e DRN is neurochemically heterogeneous, dual
immunoelectron microscopy was used to examine cellular s
191 Furthermore, doublecortin
immunoelectron microscopy was used to examine the ultras
192 scent protein (YFP) followed by preembedding
immunoelectron microscopy was used to identify RGC axons
193 aser scanning confocal microscopy (LSCM) and
immunoelectron microscopy were used to determine the sub
194 munohistochemistry, electron microscopy, and
immunoelectron microscopy were used to examine corneal i
195 Immunohistochemistry and
immunoelectron microscopy were used to localize IRBP in
196 Using immunofluorescence and
immunoelectron microscopy with an AcCYS1-specific antise
197 Indirect immunofluorescence and
immunoelectron microscopy with antisera to purified reco
198 Immunoelectron microscopy with mAbs to protective antige
199 However, by
immunoelectron microscopy, a small percentage of tau in
200 sence in lamellar-granule-like structures on
immunoelectron microscopy, along with their known struct
201 tubulovesicular organelles, as indicated by
immunoelectron microscopy, and are associated with EEA1
202 g double-immunolabeling confocal microscopy,
immunoelectron microscopy, and biochemistry.
203 ies, as visualized by immunofluorescence and
immunoelectron microscopy, and can be retrieved upon pur
204 in G (VSV-G), was found by video microscopy,
immunoelectron microscopy, and cell fractionation to ent
205 and liver cysts was analyzed by confocal and
immunoelectron microscopy, and ciliary structure and len
206 rse transcriptase-polymerase chain reaction,
immunoelectron microscopy, and immunofluorescence demons
207 parasites, the ultrastructural resolution of
immunoelectron microscopy, and inhibitors of trafficking
208 By immunofluorescence,
immunoelectron microscopy, and mitochondrial subfraction
209 Immunohistochemistry, confocal and
immunoelectron microscopy, and podocyte fractionation lo
210 ed cells for electron microscope tomography,
immunoelectron microscopy, and serial thin section analy
211 munohistochemistry, immunoblot analysis, and
immunoelectron microscopy, and then immunoprecipitation
212 Using genomic analysis,
immunoelectron microscopy, and two-photon microscopy of
213 thin layer 4 was assessed using confocal and
immunoelectron microscopy, as well as optogenetic activa
214 By immunofluorescence and
immunoelectron microscopy, both endogenous as well as ov
215 Upon
immunoelectron microscopy, Cav-3 co-localized with AC5/6
216 By immunofluorescence and
immunoelectron microscopy, dynamin 1 was concentrated at
217 By
immunoelectron microscopy, GIV colocalizes with beta-COP
218 n purified VZV virions were enumerated after
immunoelectron microscopy, gold beads were detected on v
219 Using a combination of
immunoelectron microscopy, immunofluorescence microscopy
220 istopathology, conventional transmission and
immunoelectron microscopy, in situ hybridization, and DN
221 NTPDase1 using confocal immunofluorescence,
immunoelectron microscopy, reverse-transcription polymer
222 Fusion was confirmed by transmission
immunoelectron microscopy, showing immunogold particles
223 By
immunoelectron microscopy, soluble Abeta aggregates typi
224 entary approaches of confocal microscopy and
immunoelectron microscopy, suggest that: (i) OGFr reside
225 ron-dense particles in heat-shocked cells by
immunoelectron microscopy, suggesting that it forms larg
226 Herein, we show, by immunofluorescence and
immunoelectron microscopy, that Nup98 is found on both s
227 By
immunoelectron microscopy, the GP64 and GP(64/F) protein
228 By immunofluorescence/
immunoelectron microscopy, these clusters were associate
229 By
immunoelectron microscopy, this protein was found on the
230 Immunofluorescence and
immunoelectron microscopy, using antisera raised against
231 (vi) By
immunoelectron microscopy, virus-like structures were sp
232 . saprophyticus ATCC 15305 CP, visualized by
immunoelectron microscopy, was extracted and purified us
233 Using
immunoelectron microscopy, we demonstrate the presynapti
234 Finally, using
immunoelectron microscopy, we detected oligomeric-like s
235 sing immunofluorescence light microscopy and
immunoelectron microscopy, we examine the spatial distri
236 Using immunofluorescence microscopy and
immunoelectron microscopy, we find that HIV-1 buds into
237 By both immunofluorescence confocal and
immunoelectron microscopy, we find that Pincher mediates
238 When we examined FV SVPs by
immunoelectron microscopy, we found particles that were
239 Using
immunoelectron microscopy, we found that endogenous neur
240 By
immunoelectron microscopy, we found that ICIS is present
241 By using immunofluorescence and confocal and
immunoelectron microscopy, we found that in interphase,
242 By using colloidal gold
immunoelectron microscopy, we found that synaptobrevin-2
243 Using
immunoelectron microscopy, we found that the Caenorhabdi
244 Using double-label
immunoelectron microscopy, we found that the essential N
245 With confocal and
immunoelectron microscopy, we localize the activated enz
246 ined RGC subtype (OFF-alphaRGCs) with serial
immunoelectron microscopy, we resolved the ultrastructur
247 Using
immunoelectron microscopy, we show that CB(1)Rs and dopa
248 Using
immunoelectron microscopy, we show that FasL and TRAIL a
249 Using double immunofluorescence and
immunoelectron microscopy, we show that pro- and antiang
250 Finally, using
immunoelectron microscopy, we show the presence of HERV-
251 Using immunofluorescence and
immunoelectron microscopy, we showed that translating ri
252 mmunofluorescent staining, confocal imaging,
immunoelectron microscopy, Western blot analysis, histol
253 ed titin extension as a function of SL using
immunoelectron microscopy, which allowed delineation of
254 This suggestion has been corroborated by
immunoelectron microscopy, which revealed cadherin-enric
255 this study, we have combined high-resolution
immunoelectron microscopy, whole-cell patch-clamp record
256 d visualized by using immunofluorescence and
immunoelectron microscopy.
257 he fiber complex lateral to the VMH by using
immunoelectron microscopy.
258 ncidence of EGFR-containing MVBs detected by
immunoelectron microscopy.
259 ximate localization of Beclin-1 was shown by
immunoelectron microscopy.
260 brane compartments, both in live-imaging and
immunoelectron microscopy.
261 blotting, immunofluorescence microscopy, and
immunoelectron microscopy.
262 Mouse Gb(3) localization was confirmed by
immunoelectron microscopy.
263 he NAcb core (NAcbC) and shell (NAcbS) using
immunoelectron microscopy.
264 ther confirmed in co-localization studies by
immunoelectron microscopy.
265 HCLE cells was determined using scanning and
immunoelectron microscopy.
266 in Purkinje cell dendrites was confirmed by
immunoelectron microscopy.
267 zed to the ultrastructural level, as seen by
immunoelectron microscopy.
268 ern blot analysis, immunohistochemistry, and
immunoelectron microscopy.
269 Aergic neurons (GABA-CB1 -RS) was studied by
immunoelectron microscopy.
270 5 in the RPE and CE was further confirmed by
immunoelectron microscopy.
271 th anti-capsular antibodies as visualized by
immunoelectron microscopy.
272 xpression measured by immunofluorescence and
immunoelectron microscopy.
273 ern blot analysis, immunohistochemistry, and
immunoelectron microscopy.
274 endosome-associated tubules as determined by
immunoelectron microscopy.
275 lus contains no SpaABC pilins as detected by
immunoelectron microscopy.
276 ence, and with spore walls, as visualized by
immunoelectron microscopy.
277 thin the loricrin knockout cell envelope via
immunoelectron microscopy.
278 ected on membranes by cell fractionation and
immunoelectron microscopy.
279 in levels was evaluated by real-time PCR and
immunoelectron microscopy.
280 ucleus of the thalamus using high-resolution
immunoelectron microscopy.
281 ion or effectively bind TCP, as evidenced by
immunoelectron microscopy.
282 the fate of these bacteria in the cornea by
immunoelectron microscopy.
283 tion based on cell fractionation studies and
immunoelectron microscopy.
284 nce (EGFP), indirect immunofluorescence, and
immunoelectron microscopy.
285 ffin cells by immunofluorescent confocal and
immunoelectron microscopy.
286 ibrillar components of PtK2 cell nucleoli by
immunoelectron microscopy.
287 rther verified by membrane fractionation and
immunoelectron microscopy.
288 ast and the prevacuolar compartment (PVC) by
immunoelectron microscopy.
289 to be adequately visualized by conventional
immunoelectron microscopy.
290 nd thalamus by using immunocytochemistry and
immunoelectron microscopy.
291 uctures consistent with lamellar granules on
immunoelectron microscopy.
292 observed using both confocal microscopy and
immunoelectron microscopy.
293 tricle using quantitative immunoconfocal and
immunoelectron microscopy.
294 n with tyrosine hydroxylase was confirmed by
immunoelectron microscopy.
295 , as well as filamentous tau, as detected by
immunoelectron microscopy.
296 y to the sporozoite surface as determined by
immunoelectron microscopy.
297 ciliated cells can become goblet cells using
immunoelectron microscopy.
298 ce was observed directly and confirmed using
immunoelectron microscopy.
299 e structures were detected in human cells by
immunoelectron microscopy.
300 observed for endogenously expressed MORs by
immunoelectron microscopy; the acute administration of m