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 Postembedding
immunoelectron microscopic studies were performed with a
19 The present
immunoelectron microscopic study revealed that the basol
20 Immunocytochemical,
immunoelectron microscopic, and biochemical analyses of
21 block its export, as shown by the results of
immunoelectron microscopy (IEM) and antibody adsorption
22 sity gradient centrifugation and analyzed by
immunoelectron microscopy (IEM) and Western blot assays
23 Our
immunoelectron microscopy (IEM) data suggest that mRNA/G
24 vely evaluated the diagnostic performance of
immunoelectron microscopy (IEM) of abdominal fat aspirat
25 aper, we showed by coimmunoprecipitation and
immunoelectron microscopy (IEM) that these Gag-containin
26 ce (IF), immuno-enzymatic staining (IES) and
immunoelectron microscopy (IEM), that have found widespr
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 Immunoelectron microscopy analyses demonstrated a protea
31 rging from that model by ultrastructural and
immunoelectron microscopy analyses of cores from wild-ty
32 Western blotting and
immunoelectron microscopy analyses suggest that CideB is
33 Electron microscopy/
immunoelectron microscopy analysis and tracking of the e
34 Immunoelectron microscopy analysis provides insight into
35 Immunoelectron microscopy analysis shows that Sac3 local
36 Moreover,
immunoelectron microscopy and analysis of mitochondrial-
37 By using
immunoelectron microscopy and biochemical analysis, we s
38 tissues in Gnptab -/- mice using a combined
immunoelectron microscopy and biochemical approach.
39 addition, we discovered using techniques of
immunoelectron microscopy and biochemical purification o
40 On selected cases,
immunoelectron microscopy and biochemistry were performe
41 Immunoelectron microscopy and cell fractionation reveal
42 Using conventional and
immunoelectron microscopy and confocal immunofluorescenc
43 was concordant with fibril identification by
immunoelectron microscopy and consistent with clinical p
44 cells by immunofluorescence and quantitative
immunoelectron microscopy and developed imaging and traf
45 immunoblots of membrane-associated proteins,
immunoelectron microscopy and flow cytometry assays all
46 Using mass spectrometry,
immunoelectron microscopy and fluorescence lifetime imag
47 used 3,3'diaminobenzidine tetrahydrochloride
immunoelectron microscopy and fluorescence microscopy to
48 We have used
immunoelectron microscopy and gold-labelled antibodies t
49 We show here by
immunoelectron microscopy and immunoblotting that SynCAM
50 ) agonist isoproterenol, consistent with the
immunoelectron microscopy and immunocytochemical data de
51 Immunoelectron microscopy and immunofluorescence analysi
52 Importantly,
immunoelectron microscopy and immunofluorescence studies
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 Here,
immunoelectron microscopy demonstrated that endothelial
78 Quantitative
immunoelectron microscopy demonstrated that the majority
79 Results from
immunoelectron microscopy demonstrated that the protecti
80 Immunoelectron microscopy demonstrated the presence of c
81 epithelium isolated from aGVHD animals, and
immunoelectron microscopy demonstrated VCAM-1 reactivity
82 Moreover,
immunoelectron microscopy demonstrates the presence of V
83 encoding wheat germ agglutinin (WGA) and by
immunoelectron microscopy determined the presence of VGl
84 Immunofluorescence and
immunoelectron microscopy experiments established that A
85 Immunoelectron microscopy for Als2cr4 verified its expre
86 s investigated in the infragranular PFC with
immunoelectron microscopy for D1R and parvalbumin, a mar
87 Immunoelectron microscopy for GFP indicated that the tra
88 lamo-amygdaloid afferents with postembedding
immunoelectron microscopy for the GluRs in adult rats.
89 Immunoelectron microscopy has provided a general picture
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 Immunoelectron microscopy in mice with xenograft tumors,
94 Using a combination of electrophysiology and
immunoelectron microscopy in mice, the relationship betw
95 Pre-embedding
immunoelectron microscopy in rabbit retina confirmed exp
96 g confocal immunofluorescence microscopy and
immunoelectron microscopy in rat brain.
97 Protease digestion and
immunoelectron microscopy indicate that the alpha-syn am
98 Immunoelectron microscopy indicated that CEP290 is locat
99 Immunoelectron microscopy indicated that CfaE was confin
100 Immunoelectron microscopy indicated that E1 and E2 were
101 Immunofluorescence and whole-mount
immunoelectron microscopy indicated that GC is on the ou
102 Immunoelectron microscopy indicated that this protein wa
103 sucrose density-gradient centrifugation, and
immunoelectron microscopy indicates that ETR1 is predomi
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 By use of
immunoelectron microscopy methods, capsids that express
108 Using both biochemical fractionation and
immunoelectron microscopy methods, these vesicles were s
109 nalysis, were examined by immunoconfocal and
immunoelectron microscopy of lens sections.
110 Immunoelectron microscopy of lung endothelium or a cultu
111 Immunoelectron microscopy of neutrophils infected with A
112 Analysis by
immunoelectron microscopy of Sf-9 cells infected with th
113 Immunoelectron microscopy of the adult rat brain showed
114 apsule-like material was readily apparent by
immunoelectron microscopy on bacteria harvested in the p
115 Immunoelectron microscopy pronouncedly detects APH_1235
116 In this study, scanning
immunoelectron microscopy qualitatively demonstrated gre
117 These data, along with
immunoelectron microscopy results, imply that unmyelinat
118 Both immunofluorescence and
immunoelectron microscopy reveal that Sun1 but not Sun2
119 munofluorescence microscopy and quantitative
immunoelectron microscopy reveal that the majority of ne
120 Immunoelectron microscopy revealed a predominant localiz
121 Immunoelectron microscopy revealed a prominent localizat
122 Immunoelectron microscopy revealed ABCG5 and ABCG8 on th
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 Dual
immunoelectron microscopy showed coexistence of DYN and
149 Moreover,
immunoelectron microscopy showed ectopic deposition of c
150 Immunoelectron microscopy showed K(ir)6.2 antibodies spe
151 Immunoelectron microscopy showed that a portion of Sindb
152 Fluorescence resonance energy transfer and
immunoelectron microscopy showed that alphaS and parkin
153 of CD4 and G protein in plasma membranes by
immunoelectron microscopy showed that both were organize
154 Consistent with that finding,
immunoelectron microscopy showed that dysbindin-1 is loc
155 Immunoelectron microscopy showed that mAKAP co-localized
156 Immunoelectron microscopy showed that syndecan-1 was exp
157 Immunoelectron microscopy showed that when limited amoun
158 High-resolution
immunoelectron microscopy shows that Cdh8 is concentrate
159 Immunoelectron microscopy shows that FMRP is localized a
160 Immunoelectron microscopy shows that the membrane-bound
161 Furthermore,
immunoelectron microscopy studies revealed an associatio
162 Immunoelectron microscopy studies revealed that this tyr
163 Immunoelectron microscopy studies showed that centrin is
164 Immunoelectron microscopy studies suggested a model for
165 ther confirmed by co-immunoprecipitation and
immunoelectron microscopy studies.
166 orylation of recombinant titin fragments and
immunoelectron microscopy suggest that PKA targets a sub
167 High resolution
immunoelectron microscopy suggests a remarkable nanoscal
168 ing a postembedding immunogold procedure for
immunoelectron microscopy that included embedding in Uni
169 Furthermore, we document by
immunoelectron microscopy the transfer of hER components
170 I mGluRs is altered in parkinsonism, we used
immunoelectron microscopy to analyze the subcellular and
171 nt in B capsids, and bound UL25 was found by
immunoelectron microscopy to be located predominantly at
172 To address this issue, we used
immunoelectron microscopy to compare the subcellular loc
173 Next, we used biochemical analyses and
immunoelectron microscopy to demonstrate that conserved
174 ed high-pressure freezing and serial-section
immunoelectron microscopy to determine the position of M
175 We have now used
immunoelectron microscopy to determine the subcellular s
176 We also used
immunoelectron microscopy to establish the distribution
177 determine whether this is the case, we used
immunoelectron microscopy to examine PR distribution in
178 lective agonists (LY354740 and LY379268) and
immunoelectron microscopy to examine structure-function
179 transgenic mice, brain Abeta42 localized by
immunoelectron microscopy to, and accumulated with aging
180 ed RT-PCR, and immunohisto/cytochemistry and
immunoelectron microscopy using beta-END and mu-opiate r
181 , and immunohistochemistry/cytochemistry and
immunoelectron microscopy using beta-endorphin and mu-op
182 Immunoelectron microscopy using monoclonal antibody (MAb
183 Double pre-embedding
immunoelectron microscopy using substance P and Met-/Leu
184 In support,
immunoelectron microscopy validated the localization of
185 Immunoelectron microscopy was performed on selected case
186 Immunoelectron microscopy was used to detect FSH recepto
187 Dual-labeling
immunoelectron microscopy was used to determine whether
188 e DRN is neurochemically heterogeneous, dual
immunoelectron microscopy was used to examine cellular s
189 Furthermore, doublecortin
immunoelectron microscopy was used to examine the ultras
190 scent protein (YFP) followed by preembedding
immunoelectron microscopy was used to identify RGC axons
191 aser scanning confocal microscopy (LSCM) and
immunoelectron microscopy were used to determine the sub
192 munohistochemistry, electron microscopy, and
immunoelectron microscopy were used to examine corneal i
193 Immunohistochemistry and
immunoelectron microscopy were used to localize IRBP in
194 Using immunofluorescence and
immunoelectron microscopy with an AcCYS1-specific antise
195 Indirect immunofluorescence and
immunoelectron microscopy with antisera to purified reco
196 Immunoelectron microscopy with mAbs to protective antige
197 However, by
immunoelectron microscopy, a small percentage of tau in
198 sence in lamellar-granule-like structures on
immunoelectron microscopy, along with their known struct
199 tubulovesicular organelles, as indicated by
immunoelectron microscopy, and are associated with EEA1
200 g double-immunolabeling confocal microscopy,
immunoelectron microscopy, and biochemistry.
201 ies, as visualized by immunofluorescence and
immunoelectron microscopy, and can be retrieved upon pur
202 in G (VSV-G), was found by video microscopy,
immunoelectron microscopy, and cell fractionation to ent
203 and liver cysts was analyzed by confocal and
immunoelectron microscopy, and ciliary structure and len
204 rse transcriptase-polymerase chain reaction,
immunoelectron microscopy, and immunofluorescence demons
205 parasites, the ultrastructural resolution of
immunoelectron microscopy, and inhibitors of trafficking
206 By immunofluorescence,
immunoelectron microscopy, and mitochondrial subfraction
207 ed cells for electron microscope tomography,
immunoelectron microscopy, and serial thin section analy
208 munohistochemistry, immunoblot analysis, and
immunoelectron microscopy, and then immunoprecipitation
209 Using genomic analysis,
immunoelectron microscopy, and two-photon microscopy of
210 thin layer 4 was assessed using confocal and
immunoelectron microscopy, as well as optogenetic activa
211 By immunofluorescence and
immunoelectron microscopy, both endogenous as well as ov
212 Upon
immunoelectron microscopy, Cav-3 co-localized with AC5/6
213 Immunoelectron microscopy, coimmunoprecipitation, and bl
214 By
immunoelectron microscopy, GIV colocalizes with beta-COP
215 n purified VZV virions were enumerated after
immunoelectron microscopy, gold beads were detected on v
216 Using a combination of
immunoelectron microscopy, immunofluorescence microscopy
217 istopathology, conventional transmission and
immunoelectron microscopy, in situ hybridization, and DN
218 NTPDase1 using confocal immunofluorescence,
immunoelectron microscopy, reverse-transcription polymer
219 Fusion was confirmed by transmission
immunoelectron microscopy, showing immunogold particles
220 By
immunoelectron microscopy, soluble Abeta aggregates typi
221 entary approaches of confocal microscopy and
immunoelectron microscopy, suggest that: (i) OGFr reside
222 ron-dense particles in heat-shocked cells by
immunoelectron microscopy, suggesting that it forms larg
223 Herein, we show, by immunofluorescence and
immunoelectron microscopy, that Nup98 is found on both s
224 By
immunoelectron microscopy, the GP64 and GP(64/F) protein
225 By immunofluorescence/
immunoelectron microscopy, these clusters were associate
226 By
immunoelectron microscopy, this protein was found on the
227 Immunofluorescence and
immunoelectron microscopy, using antisera raised against
228 (vi) By
immunoelectron microscopy, virus-like structures were sp
229 . saprophyticus ATCC 15305 CP, visualized by
immunoelectron microscopy, was extracted and purified us
230 Using
immunoelectron microscopy, we demonstrate the presynapti
231 Finally, using
immunoelectron microscopy, we detected oligomeric-like s
232 sing immunofluorescence light microscopy and
immunoelectron microscopy, we examine the spatial distri
233 Using immunofluorescence microscopy and
immunoelectron microscopy, we find that HIV-1 buds into
234 By both immunofluorescence confocal and
immunoelectron microscopy, we find that Pincher mediates
235 When we examined FV SVPs by
immunoelectron microscopy, we found particles that were
236 Using
immunoelectron microscopy, we found that endogenous neur
237 By
immunoelectron microscopy, we found that ICIS is present
238 By using immunofluorescence and confocal and
immunoelectron microscopy, we found that in interphase,
239 By using colloidal gold
immunoelectron microscopy, we found that synaptobrevin-2
240 Using
immunoelectron microscopy, we found that the Caenorhabdi
241 Using double-label
immunoelectron microscopy, we found that the essential N
242 With confocal and
immunoelectron microscopy, we localize the activated enz
243 ined RGC subtype (OFF-alphaRGCs) with serial
immunoelectron microscopy, we resolved the ultrastructur
244 Using
immunoelectron microscopy, we show that CB(1)Rs and dopa
245 Using
immunoelectron microscopy, we show that FasL and TRAIL a
246 Using double immunofluorescence and
immunoelectron microscopy, we show that pro- and antiang
247 By
immunoelectron microscopy, we show that SOD1 is present
248 Finally, using
immunoelectron microscopy, we show the presence of HERV-
249 Using immunofluorescence and
immunoelectron microscopy, we showed that translating ri
250 mmunofluorescent staining, confocal imaging,
immunoelectron microscopy, Western blot analysis, histol
251 ed titin extension as a function of SL using
immunoelectron microscopy, which allowed delineation of
252 This suggestion has been corroborated by
immunoelectron microscopy, which revealed cadherin-enric
253 this study, we have combined high-resolution
immunoelectron microscopy, whole-cell patch-clamp record
254 blotting, immunofluorescence microscopy, and
immunoelectron microscopy.
255 ncidence of EGFR-containing MVBs detected by
immunoelectron microscopy.
256 ximate localization of Beclin-1 was shown by
immunoelectron microscopy.
257 brane compartments, both in live-imaging and
immunoelectron microscopy.
258 Mouse Gb(3) localization was confirmed by
immunoelectron microscopy.
259 he NAcb core (NAcbC) and shell (NAcbS) using
immunoelectron microscopy.
260 ther confirmed in co-localization studies by
immunoelectron microscopy.
261 HCLE cells was determined using scanning and
immunoelectron microscopy.
262 in Purkinje cell dendrites was confirmed by
immunoelectron microscopy.
263 zed to the ultrastructural level, as seen by
immunoelectron microscopy.
264 ern blot analysis, immunohistochemistry, and
immunoelectron microscopy.
265 5 in the RPE and CE was further confirmed by
immunoelectron microscopy.
266 th anti-capsular antibodies as visualized by
immunoelectron microscopy.
267 ern blot analysis, immunohistochemistry, and
immunoelectron microscopy.
268 endosome-associated tubules as determined by
immunoelectron microscopy.
269 lus contains no SpaABC pilins as detected by
immunoelectron microscopy.
270 ence, and with spore walls, as visualized by
immunoelectron microscopy.
271 ected on membranes by cell fractionation and
immunoelectron microscopy.
272 in levels was evaluated by real-time PCR and
immunoelectron microscopy.
273 ucleus of the thalamus using high-resolution
immunoelectron microscopy.
274 ion or effectively bind TCP, as evidenced by
immunoelectron microscopy.
275 the fate of these bacteria in the cornea by
immunoelectron microscopy.
276 tion based on cell fractionation studies and
immunoelectron microscopy.
277 nce (EGFP), indirect immunofluorescence, and
immunoelectron microscopy.
278 ffin cells by immunofluorescent confocal and
immunoelectron microscopy.
279 ibrillar components of PtK2 cell nucleoli by
immunoelectron microscopy.
280 rther verified by membrane fractionation and
immunoelectron microscopy.
281 ast and the prevacuolar compartment (PVC) by
immunoelectron microscopy.
282 to be adequately visualized by conventional
immunoelectron microscopy.
283 , as well as filamentous tau, as detected by
immunoelectron microscopy.
284 nd thalamus by using immunocytochemistry and
immunoelectron microscopy.
285 uctures consistent with lamellar granules on
immunoelectron microscopy.
286 y to the sporozoite surface as determined by
immunoelectron microscopy.
287 observed using both confocal microscopy and
immunoelectron microscopy.
288 tricle using quantitative immunoconfocal and
immunoelectron microscopy.
289 n with tyrosine hydroxylase was confirmed by
immunoelectron microscopy.
290 membrane localization of LTC(4) synthase by
immunoelectron microscopy.
291 e proteins in resting cells was confirmed by
immunoelectron microscopy.
292 mander retina were compared by postembedding
immunoelectron microscopy.
293 ciliated cells can become goblet cells using
immunoelectron microscopy.
294 Aergic neurons (GABA-CB1 -RS) was studied by
immunoelectron microscopy.
295 xpression measured by immunofluorescence and
immunoelectron microscopy.
296 ce was observed directly and confirmed using
immunoelectron microscopy.
297 e structures were detected in human cells by
immunoelectron microscopy.
298 thin the loricrin knockout cell envelope via
immunoelectron microscopy.
299 he fiber complex lateral to the VMH by using
immunoelectron microscopy.
300 observed for endogenously expressed MORs by
immunoelectron microscopy; the acute administration of m