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1 he IC and auditory cortex did not reveal any double labeling.
2 d JNK proteins were localized by fluorescent double labeling.
3 ionation, immunofluorescence, and immunogold double labeling.
4 method and bisbenzamide/tyrosine hydroxylase double labeling.
5 enalidomide treatment using CD138(+)/IRF4(+) double labeling.
6 ected to both the AI and the LO as judged by double-labeling.
7                                          Our double-labeling analyses of intraneuronal Abeta and CD40
8                               A quantitative double labeling analysis in layers II and III revealed t
9                                     Finally, double-labeling analysis of CTb + Fos showed that contex
10                                    Combining double labeling and confocal microscopy analyses, we fou
11 ergic neurons, we performed BDNF/parvalbumin double labeling and discovered that axons from cortical
12                                              Double labeling and fluorescence-activated cell sorter a
13         Fifteen of these were confirmed with double labeling and microscopy, including the transcript
14 his study, Western blots, immunofluorescence double labeling, and the retrograde tracing method were
15 otope probing (Raman-SIP) using a single and double labeling approach.
16 nstrated by cell lineage tracing and mineral double-labeling approaches that murine PDL progenitor ce
17                          To do this, we used double-labeling combinations of Fos immunocytochemistry
18                               Under the same double-labeling conditions, however, cones in homozygous
19                                              Double labeling confirmed up-regulation of CCL2/CCR2 on
20 tochrome c from mitochondria, as revealed by double-labeling confocal immunofluorescence microscopy.
21 gocytophilum entry into neutrophils by using double-labeling confocal microscopy.
22                                    Extensive double-labeling crossover studies have been conducted.
23 e mechanism was obtained through an isotopic double-labeling crossover study.
24                                              Double labeling demonstrated coexpression of JCV T antig
25                                              Double labeling demonstrated that apoptotic cells includ
26  BrdU staining, providing a valuable tool of double labeling DNA synthesis, e.g., for tracking the tw
27                                   Immunogold double-labeling electron microscopy, using antisera agai
28  abundantly labeled with Fast blue (FB) in a double-labeling experiment in which FB was co-injected i
29                                            A double-labeling experiment with the dimeric model showed
30 ochemical methods to test the feasibility of double labeling experiments during development.
31                                              Double labeling experiments indicate that the neurochemi
32                                              Double labeling experiments revealed that complexes of O
33                                              Double labeling experiments showed that the location of
34       Confocal scanning laser microscopy and double labeling experiments with rhodamine 123 suggested
35                                              Double labeling experiments, by either in situ hybridiza
36 bone formation rates in in vivo fluorochrome double labeling experiments.
37                                              Double-labeling experiments (biocytin backfill x seroton
38                                              Double-labeling experiments colocalizing the bradykinin
39                                              Double-labeling experiments confirm that NADPH-d, the mo
40  cell the "distal Dab1-immunoreactive cell." Double-labeling experiments demonstrate that the distal
41                                              Double-labeling experiments demonstrated that CRN termin
42 ons affected by such lesions, we carried out double-labeling experiments for the inhibitory neurotran
43                                              Double-labeling experiments further demonstrate that V1
44 c gut-associated lymphoid tissue at 14 days; double-labeling experiments indicated that 93.5% of the
45                                              Double-labeling experiments reveal NMB is expressed in a
46                                              Double-labeling experiments revealed several possible li
47                                    Moreover, double-labeling experiments revealed that activation of
48                                              Double-labeling experiments showed striking cellular col
49                                              Double-labeling experiments showed that most of the prin
50 s of vallate papillae and nasoincisor ducts, double-labeling experiments showed that syntaxin-1, SNAP
51                                              Double-labeling experiments showed that the dendritic an
52  of GABA antagonists, uptake inhibitors, and double-labeling experiments showing that Cr-Aint neurons
53  in the control of food intake, we performed double-labeling experiments to evaluate the potential ov
54 tly labeled retinal terminals was counted in double-labeling experiments using confocal microscopy an
55                                              Double-labeling experiments using probes for previously
56                                  Single- and double-labeling experiments were performed to establish
57                                              Double-labeling experiments with a subset of modulators
58                                              Double-labeling experiments with ArINTs and ArINTstBu (T
59 etween caspase activation and NFT formation, double-labeling experiments with fodrin CCP and PHF-1 we
60                When mAb-GlyRbeta was used in double-labeling experiments with GlyRalpha1-, alpha2-, a
61                                           In double-labeling experiments, antibodies to acetylated hi
62                           Also, we performed double-labeling experiments, injecting BDA in the CRNs a
63 in V1 or V2, and, consistently with previous double-labeling experiments, some axons can branch to bo
64 t that we identified as the Golgi complex in double-labeling experiments, while wild type caveolin-3
65 thalamic neurons were compared in retrograde double-labeling experiments.
66                                              Double-labeling FISH showed colocalization of tyrosine h
67 pproach to evaluate this hypothesis, we used double-labeling fluorescence immunohistochemistry to det
68                                              Double-labeling fluorescence immunohistochemistry using
69                                        Using double labeling fluorescent histochemistry with confocal
70 amined using myeloperoxidase (MPO) assay and double-labeling fluorescent immunohistochemical analysis
71                              Combinations of double-labeling fluorescent immunohistochemistry (D-FIHC
72                                 As expected, double labeling for ATF-3, a marker of cell bodies with
73 t macaque monkeys, using immunohistochemical double labeling for bromodeoxyuridine and cell-type-spec
74                                              Double labeling for GAD67 and GHRHR in vitro and in vivo
75 tion of the in situ hybridization signal and double labeling for glial fibrillary acidic protein were
76               The current investigation used double labeling for NADPHd and Fos-like immunoreactivity
77                                              Double labeling for NMDA NR1 and c-fos revealed marked a
78                                              Double labeling for Prox1 and cell-type-specific markers
79 nventional retinal synapses was confirmed by double labeling for synapsin I, a marker for conventiona
80 bserved in dendritic profiles, verified with double labeling for the dendrite-specific marker microtu
81 ze the phenotype of ER-beta-bearing cells by double labeling for the GABAergic-associated calcium-bin
82 al cells were identified as keratinocytes by double labeling for WNV antigen and keratin 10.
83                                        After double-labeling for Cx36 and Cx43 by FRIL, neuronal gap
84                                              Double-labeling for flow cytometric analysis was employe
85                                              Double-labeling for GAD and synaptophysin confirmed that
86                                              Double labeling further reveals that the majority of Cck
87               Light and electron microscopic double labeling further showed that the VGLUT1 subtype o
88                    To address this question, double-labeling histochemical studies were performed for
89                                              Double labeling identified significant co-localization o
90 and protein immunofluorescence (IF)-RNA FISH double labeling (IF/FISH).
91                                              Double labeling immunocytochemical studies confirmed tha
92                                              Double-labeling immunocytochemistry revealed m1 receptor
93                                           By double-labeling immunocytochemistry, alpha-MSH-IR axon v
94 , cat, and monkey was studied by single- and double-labeling immunocytochemistry.
95                                              Double labeling Immunofluorescence was performed using c
96                                        Using double-labeling immunofluorescence analysis of intraneur
97                                              Double-labeling immunofluorescence experiments revealed
98                                              Double-labeling immunofluorescence histochemistry reveal
99                                              Double-labeling immunofluorescence microscopic analyses
100                                              Double-labeling immunofluorescence revealed that approxi
101  from stage 14 (S14) to adulthood by using a double-labeling immunofluorescence technique.
102 mbinant, we have been able to demonstrate by double-labeling immunofluorescence that matrix protein (
103                                           In double-labeling immunofluorescent preparations, 61.1 +/-
104                                         With double-labeling immunogold electron microscopy (EM), we
105                                              Double-labeling immunogold experiments showed that appro
106                                        Using double labeling immunohistochemistry on mouse and rat sp
107                         We demonstrate using double labeling immunohistochemistry that Group II metab
108       Animals were sacrificed for single and double labeling immunohistochemistry to identify which c
109                                              Double labeling immunohistochemistry was used to identif
110                                        Using double-labeling immunohistochemistry and confocal micros
111 ne (BrdU) labeling of newly generated cells, double-labeling immunohistochemistry and TUNEL labeling
112                                              Double-labeling immunohistochemistry indicated that PR-i
113                                     By using double-labeling immunohistochemistry or immunohistochemi
114                                              Double-labeling immunohistochemistry revealed that all o
115                                              Double-labeling immunohistochemistry showed NPY-IR axon
116                                              Double-labeling immunohistochemistry was performed with
117                                              Double-labeling immunohistochemistry was used to determi
118                            Light microscopic double-labeling immunoperoxidase experiments demonstrate
119                                          For double labeling, immunoreactivity was visualized using i
120                                              Double-labeling immunostaining and co-immunoprecipitatio
121 ted into the pylorus of mice and fluorescent double-labeling immunostaining for betaIII-tubulin or PG
122                                      Protein double labeling in aqueous buffer at physiological pH, t
123 lateral lemniscus (VNLL and INLL), with some double labeling in ipsilateral lateral and medial superi
124 ents to clarify the causes of BrdU-gammaH2AX double labeling in mouse and human beta-cells.
125 tion neurons exhibited a higher incidence of double labeling in the superficial dorsal horn.
126                                 Results from double-labeling in situ hybridization suggest that in Tg
127         The purpose of this study was to use double-labeling in situ hybridization to identify nAChR
128                                           By double-labeling in situ hybridization, a subpopulation o
129 e projecting to accumbens shell, with higher double-labeling in the ipsilateral projection than in th
130               In both species, lack of overt double labeling indicated that the ChAT(+) and urocortin
131 verlap of retrograde labeling but negligible double labeling, indicating that ventral striatopallidum
132 oxidase staining and using immunofluorescent double labeling, infrequent TH-immunoreactive, transplan
133                             The advantage of double labeling is revealed in our demonstration of nove
134 d pre-oromotor neurons, but there was sparse double-labeling (<10%).
135 ucleus (XII) motoneurons was studied using a double labeling method of anterogradely biotinylated dex
136 ural level, we develop and apply a "two-tag" double-labeling method to label LT11's dendrites and the
137 eparate populations of synapses, we employed double-labeling methods.
138 a tripeptide tag CIS that allows facile N, S-double labeling of a protein of interest with >90% yield
139                     We hypothesized that the double labeling of an adenovirus with fluorescent protei
140                                              Double labeling of CB2R and glutamine synthetase shows t
141                                              Double labeling of cells with 12-(N-methyl)-N-[(7-nitrob
142 4-5-day hatchling chicks by using single and double labeling of fibers and terminals with biocytin co
143 al surgery activated brain CRF neurons using double labeling of Fos/CRF in naive rats.
144                                          The double labeling of ganglion neurons indicates their site
145                                              Double labeling of JO and ocellar afferents revealed tha
146 a coli OM B(12) transport protein, BtuB, the double labeling of many cysteine pairs is not possible i
147                                      Indeed, double labeling of miR156 showed a meristem-specific pat
148                                              Double labeling of mRNA and beta-galactosidase immunorea
149                                              Double labeling of myocilin with other ECM components wa
150 cally for overlap of retrograde labeling and double labeling of neurons.
151                             Transgenesis and double labeling of NTS and HCRT neurons showed that NTS
152            Double-transgenic mice showed 55% double labeling of periurethral neuroendocrine cells exp
153 ectly in blood and plasma, demonstrating the double labeling of platelet EVs with CD61 and CD9, as we
154 rviving ganglion cells were quantified after double labeling of retinal tissue with TUNEL and Brn3a.
155 incorporated at distinct sites, enabling the double labeling of ScFv with distinct probes, through mu
156                                              Double labeling of sGC with neuronal nitric oxide syntha
157            Moreover, we demonstrate that the double labeling of sites on the periplasmic-facing surfa
158                                   The C-7,19 double labeling of the A-ring enyne was achieved by the
159                                              Double labeling of the HCMV(CR208)-infected HF cells dem
160                                              Double labeling of the N- and C-terminally tagged peripl
161 g context-induced renewal tests by measuring double labeling of the retrograde tracer cholera toxin s
162                                              Double labeling of tissue with two different hair cell m
163                                              Double labeling of TSH4 with the ramosa2, branched silkl
164                                     Although double-labeling of microglia with Iba1 and ED1 revealed
165                                              Double-labeling of neurons in which GFP was driven by C3
166                           First, we measured double-labeling of the neuronal activity marker Fos with
167  process through crossover experiments using double-labeling (oxo and phosphine).
168                                              Double-labeling procedures showed that calretinin-positi
169 ed an iododeoxyuridine and bromodeoxyuridine double labeling protocol for use in the developing embry
170                                              Double labeling revealed that 30.2% of nodose neurons ex
171                                              Double labeling revealed that a large percentage of thes
172                                              Double labeling revealed that GRIP and GluR2 were coloca
173 versely, m2/choline acetyltransferase (ChAT) double labeling revealed that m2-positive neurons corres
174                                              Double labeling revealed that the compartment contained
175                           Immunofluorescence double-labeling revealed a punctate pattern for ENT1 clo
176                                              Double-labeling revealed that only two regions of the mo
177                                              Double labeling reveals that all PV+ cells also contain
178                                  By means of double-labeling RNA in situ hybridization in mice, we sh
179 alitative abnormalities, with bone turnover (double labeling) seen in all specimens.
180                                              Double labeling showed that all protein kinase C-immunor
181                            Immunofluorescent double labeling showed that in aged vessels IL-1beta and
182 in regions (e.g. hypothalamus and amygdala), double labeling showed that most CBP was not co-localize
183                                              Double labeling showed that neuronal nitric oxide syntha
184                                              Double labeling showed that the thalamic valop populatio
185                                              Double labeling showed that type 5b cone bipolar cells e
186                                              Double labeling showed these to be both astrocytes and o
187 r, immunofluorescence of BRCA1 and nucleolin double-labeling showed colocalization in both nucleoli a
188                                              Double labeling shows coincidence of STIM1 and STIM2 wit
189                           Immunofluorescence double labeling shows that approximately 80% of the c-ne
190                                              Double labeling shows that primarily separate population
191                           Immunofluorescence double-labeling staining showed no significant differenc
192                              Here, we used a double-labeling strategy (varying both the distance betw
193                                         This double-labeling strategy provides a simple method to rel
194                            Immunofluorescent double labeling studies additionally reveal the prominen
195                                              Double labeling studies confirmed that the alpha-syn::GF
196                                              Double labeling studies revealed (EGFP)hHsp27 and actin
197                                              Double labeling studies showed that nicotine induced c-f
198                          Immunohistochemical double labeling studies with YFP and serotonin antisera
199                                              Double-labeling studies and examination of preclinical c
200                                              Double-labeling studies demonstrated colocalization of T
201                                              Double-labeling studies demonstrated that NGF mRNA was e
202                                              Double-labeling studies demonstrated the localization of
203                                              Double-labeling studies examining CARTp with tyrosine hy
204                                              Double-labeling studies revealed that approximately 50%
205                                              Double-labeling studies revealed that early OL progenito
206                                          The double-labeling studies revealed that mGluR5 immunoreact
207                                              Double-labeling studies show that lMAN(shell) contains t
208                                              Double-labeling studies showed colocalization of the two
209                                              Double-labeling studies showed that BrdU-labeled cells t
210                                              Double-labeling studies using confocal microscopy showed
211                                           In double-labeling studies using confocal microscopy, fluor
212                                              Double-labeling studies with antibodies to phosphorylate
213 on of all the major septal receptor genes in double-labeling studies.
214 he present results and those from our recent double-labeling study suggest that following spinal cord
215                                      In this double-labeling study, we placed a green axonal tracer i
216 d with the region that showed FluoroGold/Fos double labeling, suggesting reciprocal connections betwe
217 retrogradely labeled neurons and significant double labeling, suggesting that cortical projections sp
218  of markers were correlated, and an antibody double labeling technique was employed.
219                                  Using a new double-labeling technique we have colocalized antibodies
220                          Immunohistochemical double-labeling technique with Fos and markers for norad
221 nd thus the complete covalent structure, the double-labeling technique, along with mass spectrometry,
222 Y-NB (Lucifer yellow-Neurobiotin) retrograde double-labeling technique, in conjunction with specific
223         Immunohistochemistry performed using double labeling techniques with several neuronal markers
224  by employing electron spin and nuclear spin double-labeling techniques did not yield unambiguous cha
225 This was investigated with immunofluorescent double-labeling techniques to coregister PV- and CB-expr
226                    In these studies, we used double-labeling techniques to examine whether Cal conten
227 d that intracellular flora by using the same double-labeling techniques to identify Fusobacterium nuc
228 bers in the IPL, standard immunocytochemical double-labeling techniques were applied, using antibodie
229              Accordingly, immunocytochemical double-labeling techniques were used to identify GABA an
230 BA-type neurons using retrograde marking and double-labeling techniques, are profoundly excited by mu
231                                        Using double-labeling techniques, some presynaptic terminals w
232                                        Using double-labeling techniques, we established that these in
233                                              Double labeling the brainstem sections revealed that irI
234                                              Double labeling the hypothalamic sections with NPB antis
235                                              Double-labeling the hypothalamic sections with guinea-pi
236 ons of the RVM and caudal pons and performed double labeling to evaluate the expression of alpha-7 an
237                                     However, double-labeling uncovered no coexpression of FRU(M) and
238  born neurons using doublecortin, as well as double labeling using an additional antibody to glial fi
239                                  Fluorescent double labeling using antibodies to bNOS and glutamic ac
240                                      En face double labeling using Ki-67 and progenitor markers revea
241 ions were processed for immunohistochemistry/double labeling using patient sera/cerebrospinal fluid a
242 myocilin with ECM components was examined by double labeling, using different-sized gold particles.
243                                              Double labeling was carried out using anti-CD3, anti-CD6
244                                           No double labeling was found when using a fluorescent trace
245 la, and midbrain as CRH neurons, although no double labeling was found.
246                                              Double labeling was observed in the cell bodies of Purki
247 c and any or all of the ipsilateral targets, double labeling was rare, suggesting that contralateral
248                           Immunofluorescence double labeling was used to determine cellular localizat
249                                    Much less double-labeling was associated with injections into eith
250 function (bone formation) after tetracycline double-labeling was performed by fluorescence microscopy
251                          The same pattern of double-labeling was seen from injections at each spinal
252          Commissural divergence, assessed by double labeling, was less than 3% in each area.
253 abeling and with preembedding immunogold for double labeling, was localized in cell bodies with ultra
254                                     By using double labeling, we found no evidence for mGluR1alpha or
255                                              Double labeling with a caveolin antibody indicated that
256                 Cell death was quantified by double labeling with a membrane impermeable dye and 4',6
257 AII amacrine cells, positively identified by double labeling with an antibody against calretinin, wer
258                                              Double labeling with anti-PECAM1 antibody and anti-place
259                                              Double labeling with anti-PECAM1 antibody and one of thr
260      TULP1-positive cells were identified by double labeling with antibodies specific for cones, rods
261                                              Double labeling with antibodies to calretinin and gamma-
262                                              Double labeling with antibodies to each amino acid and t
263 ype of BrdU-positive cells was identified by double labeling with antibodies to neuronal or glial mar
264 transgenic mice were confirmed as neurons by double labeling with antineurofilament antibody.
265                                              Double labeling with BDA and (3)H-leucine signifies that
266                                              Double labeling with BrdU and the cell cycle marker Ki-6
267                                              Double labeling with c-FLIP antibody and terminal deoxyn
268                                           In double labeling with calretinin and parvalbumin, few neu
269                                              Double labeling with ChAT and synapsin antibodies showed
270                                              Double labeling with confocal microscopy of DLB midbrain
271                                      We used double labeling with fluorescent retrograde tracers to i
272                                    Moreover, double labeling with Fluoro-Jade B and glial fibrillary
273                                              Double labeling with glial fibrillary acidic protein (as
274                                              Double labeling with isolectin B4 (IB4) showed that all
275 ricular nucleus of the hypothalamus (PVH) by double labeling with markers expressed in viruses inject
276                                              Double labeling with mGluR4a antibodies and antibodies t
277                                              Double labeling with neuropeptide Y (NPY), a marker for
278                                              Double labeling with OMP and synaptophysin demonstrated
279                                              Double labeling with other molecular markers confirmed t
280                                              Double labeling with parvalbumin antibodies in monkey re
281                                              Double labeling with Plk3 and gamma-tubulin, the latter
282                                           By double labeling with rhodopsin, we demonstrate that earl
283                                              Double labeling with several other markers for amacrine
284                                              Double labeling with SMI-32 and parvalbumin confirmed th
285                                              Double labeling with SNAP25 and calbindin antibodies dem
286              Cone cell death was analyzed by double labeling with TdT-dUTP terminal nick-end labeling
287 al apoptosis was determined by histochemical double labeling with terminal deoxynucleotidyl transfera
288                                              Double labeling with the 275 kD hair cell antigen (HCA)
289                                              Double labeling with the ganglion cell marker RBPMS demo
290 esence of small, clear synaptic vesicles and double labeling with the presynaptic markers synaptophys
291                                              Double labeling with the vesicular glutamate transporter
292 o functional recovery, sequential retrograde double labeling with two fluorescent dextran amines was
293                                              Double labeling with various glutamate receptor subunit
294                                              Double-labeling with a monoclonal antibody against micro
295                                              Double-labeling with anti-CD34 antibodies demonstrated t
296        Immunohistochemistry was performed by double-labeling with anti-human MMP1 and collagen type I
297 rrested in the G2 phase of the cell cycle by double-labeling with BrdU and a mitosis-specific marker;
298                                              Double-labeling with CTB and NPY was observed in the Arc
299                                        Also, double-labeling with synaptotagmin showed that Kv1.2 col
300                                              Double labeling (with NeuN and GFAP) immunohistochemistr

 
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