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1 blotting, immunofluorescence microscopy, and immunoelectron microscopy.
2 ncidence of EGFR-containing MVBs detected by immunoelectron microscopy.
3 ximate localization of Beclin-1 was shown by immunoelectron microscopy.
4 brane compartments, both in live-imaging and immunoelectron microscopy.
5    Mouse Gb(3) localization was confirmed by immunoelectron microscopy.
6 he NAcb core (NAcbC) and shell (NAcbS) using immunoelectron microscopy.
7 ther confirmed in co-localization studies by immunoelectron microscopy.
8 HCLE cells was determined using scanning and immunoelectron microscopy.
9  in Purkinje cell dendrites was confirmed by immunoelectron microscopy.
10 zed to the ultrastructural level, as seen by immunoelectron microscopy.
11 ern blot analysis, immunohistochemistry, and immunoelectron microscopy.
12 5 in the RPE and CE was further confirmed by immunoelectron microscopy.
13 th anti-capsular antibodies as visualized by immunoelectron microscopy.
14 ern blot analysis, immunohistochemistry, and immunoelectron microscopy.
15 endosome-associated tubules as determined by immunoelectron microscopy.
16 lus contains no SpaABC pilins as detected by immunoelectron microscopy.
17 ence, and with spore walls, as visualized by immunoelectron microscopy.
18 ected on membranes by cell fractionation and immunoelectron microscopy.
19 in levels was evaluated by real-time PCR and immunoelectron microscopy.
20 ucleus of the thalamus using high-resolution immunoelectron microscopy.
21 ion or effectively bind TCP, as evidenced by immunoelectron microscopy.
22  the fate of these bacteria in the cornea by immunoelectron microscopy.
23 tion based on cell fractionation studies and immunoelectron microscopy.
24 nce (EGFP), indirect immunofluorescence, and immunoelectron microscopy.
25 ffin cells by immunofluorescent confocal and immunoelectron microscopy.
26 ibrillar components of PtK2 cell nucleoli by immunoelectron microscopy.
27 rther verified by membrane fractionation and immunoelectron microscopy.
28 ast and the prevacuolar compartment (PVC) by immunoelectron microscopy.
29  to be adequately visualized by conventional immunoelectron microscopy.
30 nd thalamus by using immunocytochemistry and immunoelectron microscopy.
31 uctures consistent with lamellar granules on immunoelectron microscopy.
32 , as well as filamentous tau, as detected by immunoelectron microscopy.
33  observed using both confocal microscopy and immunoelectron microscopy.
34 tricle using quantitative immunoconfocal and immunoelectron microscopy.
35 n with tyrosine hydroxylase was confirmed by immunoelectron microscopy.
36 y to the sporozoite surface as determined by immunoelectron microscopy.
37  membrane localization of LTC(4) synthase by immunoelectron microscopy.
38 e proteins in resting cells was confirmed by immunoelectron microscopy.
39 mander retina were compared by postembedding immunoelectron microscopy.
40  electron-dense structures in the nucleus by immunoelectron microscopy.
41 pression of c-Abl in the ER was confirmed by immunoelectron microscopy.
42 ciliated cells can become goblet cells using immunoelectron microscopy.
43 Aergic neurons (GABA-CB1 -RS) was studied by immunoelectron microscopy.
44 ce was observed directly and confirmed using immunoelectron microscopy.
45 xpression measured by immunofluorescence and immunoelectron microscopy.
46 e structures were detected in human cells by immunoelectron microscopy.
47 thin the loricrin knockout cell envelope via immunoelectron microscopy.
48 he fiber complex lateral to the VMH by using immunoelectron microscopy.
49                                  However, by immunoelectron microscopy, a small percentage of tau in
50 face could be detected by flow cytometry and immunoelectron microscopy after expression of the cloned
51 ction, immunoblot analysis, and confocal and immunoelectron microscopy all indicated increased expres
52 sence in lamellar-granule-like structures on immunoelectron microscopy, along with their known struct
53                                              Immunoelectron microscopy analyses demonstrated a protea
54 rging from that model by ultrastructural and immunoelectron microscopy analyses of cores from wild-ty
55                         Western blotting and immunoelectron microscopy analyses suggest that CideB is
56                          Electron microscopy/immunoelectron microscopy analysis and tracking of the e
57                                              Immunoelectron microscopy analysis provides insight into
58                                              Immunoelectron microscopy analysis shows that Sac3 local
59                                    Moreover, immunoelectron microscopy and analysis of mitochondrial-
60                                     By using immunoelectron microscopy and biochemical analysis, we s
61  tissues in Gnptab -/- mice using a combined immunoelectron microscopy and biochemical approach.
62  addition, we discovered using techniques of immunoelectron microscopy and biochemical purification o
63                           On selected cases, immunoelectron microscopy and biochemistry were performe
64                                              Immunoelectron microscopy and cell fractionation reveal
65                       Using conventional and immunoelectron microscopy and confocal immunofluorescenc
66 was concordant with fibril identification by immunoelectron microscopy and consistent with clinical p
67 cells by immunofluorescence and quantitative immunoelectron microscopy and developed imaging and traf
68 immunoblots of membrane-associated proteins, immunoelectron microscopy and flow cytometry assays all
69                     Using mass spectrometry, immunoelectron microscopy and fluorescence lifetime imag
70 used 3,3'diaminobenzidine tetrahydrochloride immunoelectron microscopy and fluorescence microscopy to
71                                 We have used immunoelectron microscopy and gold-labelled antibodies t
72                              We show here by immunoelectron microscopy and immunoblotting that SynCAM
73 ) agonist isoproterenol, consistent with the immunoelectron microscopy and immunocytochemical data de
74                                              Immunoelectron microscopy and immunofluorescence analysi
75                                 Importantly, immunoelectron microscopy and immunofluorescence studies
76                       Based on biochemistry, immunoelectron microscopy and live cell microscopy, we f
77 trafficking of PfEMP1 was investigated using immunoelectron microscopy and proteolytic digestion of s
78                 Using immunofluorescence and immunoelectron microscopy and subcellular fractionation
79  the postsynaptic perimeter as determined by immunoelectron microscopy and super-resolution imaging.
80 zes to the slit diaphragm in podocytes using immunoelectron microscopy and that nephrin and CD2AP co-
81  we found R6 within RRV virion particles via immunoelectron microscopy and, furthermore, that virion-
82  tubulovesicular organelles, as indicated by immunoelectron microscopy, and are associated with EEA1
83 g double-immunolabeling confocal microscopy, immunoelectron microscopy, and biochemistry.
84 ies, as visualized by immunofluorescence and immunoelectron microscopy, and can be retrieved upon pur
85 in G (VSV-G), was found by video microscopy, immunoelectron microscopy, and cell fractionation to ent
86 and liver cysts was analyzed by confocal and immunoelectron microscopy, and ciliary structure and len
87 rse transcriptase-polymerase chain reaction, immunoelectron microscopy, and immunofluorescence demons
88 parasites, the ultrastructural resolution of immunoelectron microscopy, and inhibitors of trafficking
89                       By immunofluorescence, immunoelectron microscopy, and mitochondrial subfraction
90 ed cells for electron microscope tomography, immunoelectron microscopy, and serial thin section analy
91 munohistochemistry, immunoblot analysis, and immunoelectron microscopy, and then immunoprecipitation
92                      Using genomic analysis, immunoelectron microscopy, and two-photon microscopy of
93 thin layer 4 was assessed using confocal and immunoelectron microscopy, as well as optogenetic activa
94 sessed DR-5-HT neuronal responses to CRF and immunoelectron microscopy assessed CRF1 and CRF2 cellula
95 d using tract tracing, light microscopy, and immunoelectron microscopy at four postnatal ages: P15, P
96                    By immunofluorescence and immunoelectron microscopy, both endogenous as well as ov
97                                         Upon immunoelectron microscopy, Cav-3 co-localized with AC5/6
98                                              Immunoelectron microscopy co-localized Clag9 and RhopH2
99                                              Immunoelectron microscopy, coimmunoprecipitation, and bl
100                                              Immunoelectron microscopy confirmed D1R colocalization w
101                                 Confocal and immunoelectron microscopy confirmed depletion of von Wil
102                                              Immunoelectron microscopy confirmed that filensin and AQ
103                                              Immunoelectron microscopy confirmed that neuronal IFs co
104                                              Immunoelectron microscopy confirmed that PSD95-GFP predo
105                                              Immunoelectron microscopy confirmed that RANTES is store
106                       Immunofluorescence and immunoelectron microscopy confirmed the colocalization o
107                                 Double-label immunoelectron microscopy confirmed the existence of syn
108                                              Immunoelectron microscopy confirmed the incorporation of
109                                              Immunoelectron microscopy confirms that binding occurs a
110 brane microdomains, as shown by double-label immunoelectron microscopy data.
111 Cell fractionation, fluorescence imaging and immunoelectron microscopy demonstrate that mitosomes con
112                                              Immunoelectron microscopy demonstrated an increased 3-ni
113   Sucrose gradient fractionation studies and immunoelectron microscopy demonstrated localization of P
114                                              Immunoelectron microscopy demonstrated NaV1.6-positive s
115                                 Double-label immunoelectron microscopy demonstrated that AT1 and gp91
116                                        Here, immunoelectron microscopy demonstrated that endothelial
117                                 Quantitative immunoelectron microscopy demonstrated that the majority
118                                 Results from immunoelectron microscopy demonstrated that the protecti
119                                              Immunoelectron microscopy demonstrated the presence of c
120  epithelium isolated from aGVHD animals, and immunoelectron microscopy demonstrated VCAM-1 reactivity
121                                              Immunoelectron microscopy demonstrates accumulation of P
122                          Further analysis by immunoelectron microscopy demonstrates that LBA-GFP fusi
123                                    Moreover, immunoelectron microscopy demonstrates the presence of V
124  encoding wheat germ agglutinin (WGA) and by immunoelectron microscopy determined the presence of VGl
125                       Immunofluorescence and immunoelectron microscopy experiments established that A
126                                              Immunoelectron microscopy for Als2cr4 verified its expre
127 s investigated in the infragranular PFC with immunoelectron microscopy for D1R and parvalbumin, a mar
128                                              Immunoelectron microscopy for GFP indicated that the tra
129 lamo-amygdaloid afferents with postembedding immunoelectron microscopy for the GluRs in adult rats.
130      Selective membrane permeabilization and immunoelectron microscopy further localized protein A to
131                                           By immunoelectron microscopy, GIV colocalizes with beta-COP
132 n purified VZV virions were enumerated after immunoelectron microscopy, gold beads were detected on v
133                                              Immunoelectron microscopy has provided a general picture
134                                              Immunoelectron microscopy identified postsynaptic mGluR2
135 block its export, as shown by the results of immunoelectron microscopy (IEM) and antibody adsorption
136 sity gradient centrifugation and analyzed by immunoelectron microscopy (IEM) and Western blot assays
137                                          Our immunoelectron microscopy (IEM) data suggest that mRNA/G
138 vely evaluated the diagnostic performance of immunoelectron microscopy (IEM) of abdominal fat aspirat
139 aper, we showed by coimmunoprecipitation and immunoelectron microscopy (IEM) that these Gag-containin
140 ce (IF), immuno-enzymatic staining (IES) and immunoelectron microscopy (IEM), that have found widespr
141 analysis, atomic force microscopy (AFM), and immunoelectron microscopy (immuno-EM).
142                       Using a combination of immunoelectron microscopy, immunofluorescence microscopy
143                             GAIP is found by immunoelectron microscopy in CCPs, and GIPC is found in
144 ritic profiles were measured by quantitative immunoelectron microscopy in control or stressed rats.
145                                              Immunoelectron microscopy in mice with xenograft tumors,
146 Using a combination of electrophysiology and immunoelectron microscopy in mice, the relationship betw
147                                Pre-embedding immunoelectron microscopy in rabbit retina confirmed exp
148 g confocal immunofluorescence microscopy and immunoelectron microscopy in rat brain.
149 istopathology, conventional transmission and immunoelectron microscopy, in situ hybridization, and DN
150                       Protease digestion and immunoelectron microscopy indicate that the alpha-syn am
151                                              Immunoelectron microscopy indicated that CEP290 is locat
152                                              Immunoelectron microscopy indicated that CfaE was confin
153                                              Immunoelectron microscopy indicated that E1 and E2 were
154           Immunofluorescence and whole-mount immunoelectron microscopy indicated that GC is on the ou
155                                              Immunoelectron microscopy indicated that this protein wa
156 sucrose density-gradient centrifugation, and immunoelectron microscopy indicates that ETR1 is predomi
157                                              Immunoelectron microscopy indicates that IFT52 is associ
158                      Confocal microscopy and immunoelectron microscopy localized ADAMTS10 to fibrilli
159  were employed to test this hypothesis: dual immunoelectron microscopy localized D1R and HCN channels
160                                              Immunoelectron microscopy localized ePAD to egg cytoplas
161                                              Immunoelectron microscopy localized NUP-1 to the inner f
162                                    By use of immunoelectron microscopy methods, capsids that express
163     Using both biochemical fractionation and immunoelectron microscopy methods, these vesicles were s
164 n blot analyses of microvillus membranes and immunoelectron microscopy of kidney sections showed that
165 nalysis, were examined by immunoconfocal and immunoelectron microscopy of lens sections.
166                                              Immunoelectron microscopy of lung endothelium or a cultu
167                                 Preembedding immunoelectron microscopy of mouse and rat retinae showe
168                                              Immunoelectron microscopy of neutrophils infected with A
169                                  Analysis by immunoelectron microscopy of Sf-9 cells infected with th
170                                              Immunoelectron microscopy of the adult rat brain showed
171 apsule-like material was readily apparent by immunoelectron microscopy on bacteria harvested in the p
172                                              Immunoelectron microscopy pronouncedly detects APH_1235
173                      In this study, scanning immunoelectron microscopy qualitatively demonstrated gre
174                       These data, along with immunoelectron microscopy results, imply that unmyelinat
175                  Both immunofluorescence and immunoelectron microscopy reveal that Sun1 but not Sun2
176 munofluorescence microscopy and quantitative immunoelectron microscopy reveal that the majority of ne
177                                              Immunoelectron microscopy revealed a predominant localiz
178                                              Immunoelectron microscopy revealed a prominent localizat
179                                              Immunoelectron microscopy revealed ABCG5 and ABCG8 on th
180 tructural analysis in CA1 interneurons using immunoelectron microscopy revealed abundant ErbB4 expres
181                Fractionation experiments and immunoelectron microscopy revealed an association of gam
182       Western blot analysis and quantitative immunoelectron microscopy revealed an increase in GIRK2
183                                              Immunoelectron microscopy revealed Bsp22 filaments on th
184                                              Immunoelectron microscopy revealed excitatory synaptic c
185 te stiffness was increased in the IG KO, and immunoelectron microscopy revealed increased extension o
186                                              Immunoelectron microscopy revealed increased strain of t
187                                 Quantitative immunoelectron microscopy revealed internalization of GA
188                      At postnatal day (P) 7, immunoelectron microscopy revealed near-equivalent propo
189                                              Immunoelectron microscopy revealed plasmalemmal OTR at e
190                  Ultrastructural analysis by immunoelectron microscopy revealed that annexin XI assoc
191                                              Immunoelectron microscopy revealed that ERalpha- and ERb
192                         Western blotting and immunoelectron microscopy revealed that FAP is located n
193                                              Immunoelectron microscopy revealed that fgl2 was distrib
194                                              Immunoelectron microscopy revealed that intranodal lymph
195                                 Furthermore, immunoelectron microscopy revealed that Kv4.2 and Kv4.3
196                       Immunofluorescence and immunoelectron microscopy revealed that LMO7 localized a
197                                              Immunoelectron microscopy revealed that nitrated monomer
198 alent to those of unchallenged controls, and immunoelectron microscopy revealed that NPC-derived myel
199                                              Immunoelectron microscopy revealed that peripheral affer
200                                              Immunoelectron microscopy revealed that Pfpmt localizes
201 d analyses on an ultrastructural level using immunoelectron microscopy revealed that such coating may
202                                    Moreover, immunoelectron microscopy revealed that the alpha-synucl
203                                              Immunoelectron microscopy revealed that the loss of pres
204                                              Immunoelectron microscopy revealed that this sex differe
205                                              Immunoelectron microscopy revealed the presence of vesic
206  NTPDase1 using confocal immunofluorescence, immunoelectron microscopy, reverse-transcription polymer
207         Chemical cross-linking together with immunoelectron microscopy show that the mitochondrial AP
208                                         Dual immunoelectron microscopy showed coexistence of DYN and
209                                    Moreover, immunoelectron microscopy showed ectopic deposition of c
210                                              Immunoelectron microscopy showed K(ir)6.2 antibodies spe
211                                              Immunoelectron microscopy showed that a portion of Sindb
212   Fluorescence resonance energy transfer and immunoelectron microscopy showed that alphaS and parkin
213  of CD4 and G protein in plasma membranes by immunoelectron microscopy showed that both were organize
214                Consistent with that finding, immunoelectron microscopy showed that dysbindin-1 is loc
215                                              Immunoelectron microscopy showed that mAKAP co-localized
216                                              Immunoelectron microscopy showed that Ov-CHI-1 expressio
217                                              Immunoelectron microscopy showed that syndecan-1 was exp
218                                              Immunoelectron microscopy showed that when limited amoun
219         Fusion was confirmed by transmission immunoelectron microscopy, showing immunogold particles
220                              High-resolution immunoelectron microscopy shows that Cdh8 is concentrate
221                                              Immunoelectron microscopy shows that FMRP is localized a
222                                              Immunoelectron microscopy shows that the membrane-bound
223                                           By immunoelectron microscopy, soluble Abeta aggregates typi
224                                 Furthermore, immunoelectron microscopy studies revealed an associatio
225                                              Immunoelectron microscopy studies revealed that this tyr
226                                              Immunoelectron microscopy studies showed that centrin is
227                                              Immunoelectron microscopy studies suggested a model for
228 ther confirmed by co-immunoprecipitation and immunoelectron microscopy studies.
229 orylation of recombinant titin fragments and immunoelectron microscopy suggest that PKA targets a sub
230 entary approaches of confocal microscopy and immunoelectron microscopy, suggest that: (i) OGFr reside
231 ron-dense particles in heat-shocked cells by immunoelectron microscopy, suggesting that it forms larg
232                              High resolution immunoelectron microscopy suggests a remarkable nanoscal
233  by analytical subcellular fractionation and immunoelectron microscopy that HMG-CoA reductase protein
234 ing a postembedding immunogold procedure for immunoelectron microscopy that included embedding in Uni
235   Herein, we show, by immunofluorescence and immunoelectron microscopy, that Nup98 is found on both s
236                             Here we show, by immunoelectron microscopy, that podocin localizes to the
237                  Furthermore, we document by immunoelectron microscopy the transfer of hER components
238                                           By immunoelectron microscopy, the GP64 and GP(64/F) protein
239  observed for endogenously expressed MORs by immunoelectron microscopy; the acute administration of m
240                        By immunofluorescence/immunoelectron microscopy, these clusters were associate
241                                           By immunoelectron microscopy, this protein was found on the
242 I mGluRs is altered in parkinsonism, we used immunoelectron microscopy to analyze the subcellular and
243 nt in B capsids, and bound UL25 was found by immunoelectron microscopy to be located predominantly at
244               To address this issue, we used immunoelectron microscopy to compare the subcellular loc
245       Next, we used biochemical analyses and immunoelectron microscopy to demonstrate that conserved
246 ed high-pressure freezing and serial-section immunoelectron microscopy to determine the position of M
247                             We have now used immunoelectron microscopy to determine the subcellular s
248                                 We also used immunoelectron microscopy to establish the distribution
249  determine whether this is the case, we used immunoelectron microscopy to examine PR distribution in
250 lective agonists (LY354740 and LY379268) and immunoelectron microscopy to examine structure-function
251 ty (GABA-LI) in dorsolateral rat striatum by immunoelectron microscopy to further characterize the po
252  transgenic mice, brain Abeta42 localized by immunoelectron microscopy to, and accumulated with aging
253 ed RT-PCR, and immunohisto/cytochemistry and immunoelectron microscopy using beta-END and mu-opiate r
254 , and immunohistochemistry/cytochemistry and immunoelectron microscopy using beta-endorphin and mu-op
255                                              Immunoelectron microscopy using monoclonal antibody (MAb
256                         Double pre-embedding immunoelectron microscopy using substance P and Met-/Leu
257                            Deconvolution and immunoelectron microscopy using these monospecific antib
258                       Immunofluorescence and immunoelectron microscopy, using antisera raised against
259                                  In support, immunoelectron microscopy validated the localization of
260                                        Using immunoelectron microscopy, VEGF expression by podocytes
261                                      (vi) By immunoelectron microscopy, virus-like structures were sp
262                                        Here, immunoelectron microscopy was conducted in the rat brain
263                                              Immunoelectron microscopy was performed on selected case
264                                              Immunoelectron microscopy was performed to address the s
265                                              Immunoelectron microscopy was used to detect FSH recepto
266                                Dual-labeling immunoelectron microscopy was used to determine whether
267 e DRN is neurochemically heterogeneous, dual immunoelectron microscopy was used to examine cellular s
268                    Furthermore, doublecortin immunoelectron microscopy was used to examine the ultras
269 scent protein (YFP) followed by preembedding immunoelectron microscopy was used to identify RGC axons
270 . saprophyticus ATCC 15305 CP, visualized by immunoelectron microscopy, was extracted and purified us
271                                        Using immunoelectron microscopy, we demonstrate the presynapti
272                               Finally, using immunoelectron microscopy, we detected oligomeric-like s
273 sing immunofluorescence light microscopy and immunoelectron microscopy, we examine the spatial distri
274      Using immunofluorescence microscopy and immunoelectron microscopy, we find that HIV-1 buds into
275      By both immunofluorescence confocal and immunoelectron microscopy, we find that Pincher mediates
276                  When we examined FV SVPs by immunoelectron microscopy, we found particles that were
277                                        Using immunoelectron microscopy, we found that endogenous neur
278                                           By immunoelectron microscopy, we found that ICIS is present
279 By using immunofluorescence and confocal and immunoelectron microscopy, we found that in interphase,
280                      By using colloidal gold immunoelectron microscopy, we found that synaptobrevin-2
281                                        Using immunoelectron microscopy, we found that the Caenorhabdi
282                           Using double-label immunoelectron microscopy, we found that the essential N
283                            With confocal and immunoelectron microscopy, we localize the activated enz
284 ined RGC subtype (OFF-alphaRGCs) with serial immunoelectron microscopy, we resolved the ultrastructur
285                                        Using immunoelectron microscopy, we show that CB(1)Rs and dopa
286                                        Using immunoelectron microscopy, we show that FasL and TRAIL a
287          Using double immunofluorescence and immunoelectron microscopy, we show that pro- and antiang
288                                           By immunoelectron microscopy, we show that SOD1 is present
289                               Finally, using immunoelectron microscopy, we show the presence of HERV-
290                 Using immunofluorescence and immunoelectron microscopy, we showed that translating ri
291 aser scanning confocal microscopy (LSCM) and immunoelectron microscopy were used to determine the sub
292 munohistochemistry, electron microscopy, and immunoelectron microscopy were used to examine corneal i
293                     Immunohistochemistry and immunoelectron microscopy were used to localize IRBP in
294 mmunofluorescent staining, confocal imaging, immunoelectron microscopy, Western blot analysis, histol
295 ed titin extension as a function of SL using immunoelectron microscopy, which allowed delineation of
296     This suggestion has been corroborated by immunoelectron microscopy, which revealed cadherin-enric
297 this study, we have combined high-resolution immunoelectron microscopy, whole-cell patch-clamp record
298                 Using immunofluorescence and immunoelectron microscopy with an AcCYS1-specific antise
299              Indirect immunofluorescence and immunoelectron microscopy with antisera to purified reco
300                                              Immunoelectron microscopy with mAbs to protective antige

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