戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 d JNK proteins were localized by fluorescent double labeling.
2 ionation, immunofluorescence, and immunogold double labeling.
3 method and bisbenzamide/tyrosine hydroxylase double labeling.
4 he IC and auditory cortex did not reveal any 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 nd its alpha5beta1 receptor was confirmed by double labeling and multiple-exposure photomicroscopy.
15 his study, Western blots, immunofluorescence double labeling, and the retrograde tracing method were
16 otope probing (Raman-SIP) using a single and double labeling approach.
17 nstrated by cell lineage tracing and mineral double-labeling approaches that murine PDL progenitor ce
18                          To do this, we used double-labeling combinations of Fos immunocytochemistry
19                               Under the same double-labeling conditions, however, cones in homozygous
20                                              Double labeling confirmed up-regulation of CCL2/CCR2 on
21 tochrome c from mitochondria, as revealed by double-labeling confocal immunofluorescence microscopy.
22 gocytophilum entry into neutrophils by using double-labeling confocal microscopy.
23                                    Extensive double-labeling crossover studies have been conducted.
24 e mechanism was obtained through an isotopic double-labeling crossover study.
25                                              Double labeling demonstrated coexpression of JCV T antig
26                                              Double labeling demonstrated that apoptotic cells includ
27  BrdU staining, providing a valuable tool of double labeling DNA synthesis, e.g., for tracking the tw
28                                   Immunogold double-labeling electron microscopy, using antisera agai
29  abundantly labeled with Fast blue (FB) in a double-labeling experiment in which FB was co-injected i
30                                            A double-labeling experiment with the dimeric model showed
31 ochemical methods to test the feasibility of double labeling experiments during development.
32                                              Double labeling experiments indicate that the neurochemi
33                                              Double labeling experiments revealed that complexes of O
34                                              Double labeling experiments showed that the location of
35       Confocal scanning laser microscopy and double labeling experiments with rhodamine 123 suggested
36                                              Double labeling experiments, by either in situ hybridiza
37 bone formation rates in in vivo fluorochrome double labeling experiments.
38                                              Double-labeling experiments (biocytin backfill x seroton
39                                              Double-labeling experiments colocalizing the bradykinin
40                                              Double-labeling experiments confirm that NADPH-d, the mo
41  cell the "distal Dab1-immunoreactive cell." Double-labeling experiments demonstrate that the distal
42                                              Double-labeling experiments demonstrated that CRN termin
43                However, in immunofluorescent double-labeling experiments for GABA(B)R1 and GAD, we ne
44 ons affected by such lesions, we carried out double-labeling experiments for the inhibitory neurotran
45                                              Double-labeling experiments further demonstrate that V1
46 c gut-associated lymphoid tissue at 14 days; double-labeling experiments indicated that 93.5% of the
47                                              Double-labeling experiments reveal NMB is expressed in a
48                                              Double-labeling experiments revealed several possible li
49                                    Moreover, double-labeling experiments revealed that activation of
50                                              Double-labeling experiments showed striking cellular col
51                                              Double-labeling experiments showed that most of the prin
52 s of vallate papillae and nasoincisor ducts, double-labeling experiments showed that syntaxin-1, SNAP
53                                              Double-labeling experiments showed that the dendritic an
54  of GABA antagonists, uptake inhibitors, and double-labeling experiments showing that Cr-Aint neurons
55  in the control of food intake, we performed double-labeling experiments to evaluate the potential ov
56 tly labeled retinal terminals was counted in double-labeling experiments using confocal microscopy an
57                                              Double-labeling experiments using probes for previously
58                                   Additional double-labeling experiments using the nonspecific neuron
59                                  Single- and double-labeling experiments were performed to establish
60                                              Double-labeling experiments with a subset of modulators
61                                              Double-labeling experiments with ArINTs and ArINTstBu (T
62 etween caspase activation and NFT formation, double-labeling experiments with fodrin CCP and PHF-1 we
63                When mAb-GlyRbeta was used in double-labeling experiments with GlyRalpha1-, alpha2-, a
64                                           In double-labeling experiments, antibodies to acetylated hi
65                           Also, we performed double-labeling experiments, injecting BDA in the CRNs a
66 in V1 or V2, and, consistently with previous double-labeling experiments, some axons can branch to bo
67 t that we identified as the Golgi complex in double-labeling experiments, while wild type caveolin-3
68 thalamic neurons were compared in retrograde double-labeling experiments.
69                        Finally, we performed double-labeling, first by retrograde labeling of HRP inj
70                                              Double-labeling FISH showed colocalization of tyrosine h
71 pproach to evaluate this hypothesis, we used double-labeling fluorescence immunohistochemistry to det
72                                              Double-labeling fluorescence immunohistochemistry using
73                                        Using double labeling fluorescent histochemistry with confocal
74 amined using myeloperoxidase (MPO) assay and double-labeling fluorescent immunohistochemical analysis
75                              Combinations of double-labeling fluorescent immunohistochemistry (D-FIHC
76                                 As expected, double labeling for ATF-3, a marker of cell bodies with
77 t macaque monkeys, using immunohistochemical double labeling for bromodeoxyuridine and cell-type-spec
78                                              Double labeling for GAD67 and GHRHR in vitro and in vivo
79 tion of the in situ hybridization signal and double labeling for glial fibrillary acidic protein were
80               The current investigation used double labeling for NADPHd and Fos-like immunoreactivity
81                                              Double labeling for NMDA NR1 and c-fos revealed marked a
82                                              Double labeling for OMP and MAP2 revealed two distinctiv
83                                              Double labeling for Prox1 and cell-type-specific markers
84 respond to laryngeal afferent stimulation by double labeling for reduced nicotinamide adenine dinucle
85 nventional retinal synapses was confirmed by double labeling for synapsin I, a marker for conventiona
86 bserved in dendritic profiles, verified with double labeling for the dendrite-specific marker microtu
87 ze the phenotype of ER-beta-bearing cells by double labeling for the GABAergic-associated calcium-bin
88 al cells were identified as keratinocytes by double labeling for WNV antigen and keratin 10.
89                                        After double-labeling for Cx36 and Cx43 by FRIL, neuronal gap
90                                              Double-labeling for flow cytometric analysis was employe
91                                              Double-labeling for GAD and synaptophysin confirmed that
92                                              Double labeling further reveals that the majority of Cck
93               Light and electron microscopic double labeling further showed that the VGLUT1 subtype o
94                    To address this question, double-labeling histochemical studies were performed for
95                                              Double labeling identified significant co-localization o
96 and protein immunofluorescence (IF)-RNA FISH double labeling (IF/FISH).
97                                              Double labeling immunocytochemical studies confirmed tha
98                                              Double-labeling immunocytochemistry revealed m1 receptor
99                                           By double-labeling immunocytochemistry, alpha-MSH-IR axon v
100 , cat, and monkey was studied by single- and double-labeling immunocytochemistry.
101                                              Double labeling Immunofluorescence was performed using c
102                                        Using double-labeling immunofluorescence analysis of intraneur
103                                              Double-labeling immunofluorescence experiments revealed
104                                              Double-labeling immunofluorescence histochemistry reveal
105                                              Double-labeling immunofluorescence microscopic analyses
106                                              Double-labeling immunofluorescence revealed that approxi
107  from stage 14 (S14) to adulthood by using a double-labeling immunofluorescence technique.
108 mbinant, we have been able to demonstrate by double-labeling immunofluorescence that matrix protein (
109                                           In double-labeling immunofluorescent preparations, 61.1 +/-
110                                         With double-labeling immunogold electron microscopy (EM), we
111                                              Double-labeling immunogold experiments showed that appro
112                                        Using double labeling immunohistochemistry on mouse and rat sp
113                         We demonstrate using double labeling immunohistochemistry that Group II metab
114       Animals were sacrificed for single and double labeling immunohistochemistry to identify which c
115                                              Double labeling immunohistochemistry was used to identif
116                                        Using double-labeling immunohistochemistry and confocal micros
117 ne (BrdU) labeling of newly generated cells, double-labeling immunohistochemistry and TUNEL labeling
118                                              Double-labeling immunohistochemistry indicated that PR-i
119                                     By using double-labeling immunohistochemistry or immunohistochemi
120                                              Double-labeling immunohistochemistry revealed that all o
121                                              Double-labeling immunohistochemistry showed NPY-IR axon
122                                              Double-labeling immunohistochemistry was performed with
123                                              Double-labeling immunohistochemistry was used to determi
124                            Light microscopic double-labeling immunoperoxidase experiments demonstrate
125                                          For double labeling, immunoreactivity was visualized using i
126                                              Double-labeling immunostaining and co-immunoprecipitatio
127 ted into the pylorus of mice and fluorescent double-labeling immunostaining for betaIII-tubulin or PG
128                                      Protein double labeling in aqueous buffer at physiological pH, t
129 lateral lemniscus (VNLL and INLL), with some double labeling in ipsilateral lateral and medial superi
130 tion neurons exhibited a higher incidence of double labeling in the superficial dorsal horn.
131                                 Results from double-labeling in situ hybridization suggest that in Tg
132         The purpose of this study was to use double-labeling in situ hybridization to identify nAChR
133                                           By double-labeling in situ hybridization, a subpopulation o
134 e projecting to accumbens shell, with higher double-labeling in the ipsilateral projection than in th
135               In both species, lack of overt double labeling indicated that the ChAT(+) and urocortin
136 verlap of retrograde labeling but negligible double labeling, indicating that ventral striatopallidum
137 oxidase staining and using immunofluorescent double labeling, infrequent TH-immunoreactive, transplan
138                             The advantage of double labeling is revealed in our demonstration of nove
139 d pre-oromotor neurons, but there was sparse double-labeling (<10%).
140 ucleus (XII) motoneurons was studied using a double labeling method of anterogradely biotinylated dex
141 ural level, we develop and apply a "two-tag" double-labeling method to label LT11's dendrites and the
142 eparate populations of synapses, we employed double-labeling methods.
143                     We hypothesized that the double labeling of an adenovirus with fluorescent protei
144                                              Double labeling of CB2R and glutamine synthetase shows t
145                                              Double labeling of cells with 12-(N-methyl)-N-[(7-nitrob
146 ent study, this issue was addressed by using double labeling of descending brain neurons.
147 4-5-day hatchling chicks by using single and double labeling of fibers and terminals with biocytin co
148 al surgery activated brain CRF neurons using double labeling of Fos/CRF in naive rats.
149                                          The double labeling of ganglion neurons indicates their site
150                                      Indeed, double labeling of miR156 showed a meristem-specific pat
151                                              Double labeling of mRNA and beta-galactosidase immunorea
152                                              Double labeling of myocilin with other ECM components wa
153 cally for overlap of retrograde labeling and double labeling of neurons.
154                             Transgenesis and double labeling of NTS and HCRT neurons showed that NTS
155            Double-transgenic mice showed 55% double labeling of periurethral neuroendocrine cells exp
156 rviving ganglion cells were quantified after double labeling of retinal tissue with TUNEL and Brn3a.
157                                              Double labeling of sGC with neuronal nitric oxide syntha
158                                              Double labeling of sGC with neuronal nitric oxide syntha
159                                   The C-7,19 double labeling of the A-ring enyne was achieved by the
160                                              Double labeling of the HCMV(CR208)-infected HF cells dem
161                                              Double labeling of the N- and C-terminally tagged peripl
162 g context-induced renewal tests by measuring double labeling of the retrograde tracer cholera toxin s
163                                              Double labeling of tissue with two different hair cell m
164                                              Double labeling of TSH4 with the ramosa2, branched silkl
165                                     Although double-labeling of microglia with Iba1 and ED1 revealed
166                                              Double-labeling of neurons in which GFP was driven by C3
167                           First, we measured double-labeling of the neuronal activity marker Fos with
168  process through crossover experiments using double-labeling (oxo and phosphine).
169                                              Double-labeling procedures showed that calretinin-positi
170 ed an iododeoxyuridine and bromodeoxyuridine double labeling protocol for use in the developing embry
171                                              Double labeling revealed that 30.2% of nodose neurons ex
172                                              Double labeling revealed that a large percentage of thes
173                                              Double labeling revealed that GRIP and GluR2 were coloca
174 versely, m2/choline acetyltransferase (ChAT) double labeling revealed that m2-positive neurons corres
175                                              Double labeling revealed that the compartment contained
176                           Immunofluorescence double-labeling revealed a punctate pattern for ENT1 clo
177                                              Double-labeling revealed that only two regions of the mo
178                                              Double labeling reveals that all PV+ cells also contain
179                                  By means of double-labeling RNA in situ hybridization in mice, we sh
180 alitative abnormalities, with bone turnover (double labeling) seen in all specimens.
181                                              Double labeling showed that all protein kinase C-immunor
182                            Immunofluorescent double labeling showed that in aged vessels IL-1beta and
183 in regions (e.g. hypothalamus and amygdala), double labeling showed that most CBP was not co-localize
184                                              Double labeling showed that neuronal nitric oxide syntha
185                                              Double labeling showed that the thalamic valop populatio
186                                              Double labeling showed that type 5b cone bipolar cells e
187                                              Double labeling showed these to be both astrocytes and o
188 r, immunofluorescence of BRCA1 and nucleolin double-labeling showed colocalization in both nucleoli a
189                                              Double labeling shows coincidence of STIM1 and STIM2 wit
190                           Immunofluorescence double labeling shows that approximately 80% of the c-ne
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                                 Furthermore, double labeling studies for cytochrome c/alpha-synuclein
197                                              Double labeling studies revealed (EGFP)hHsp27 and actin
198                                              Double labeling studies showed that nicotine induced c-f
199                          Immunohistochemical double labeling studies with YFP and serotonin antisera
200                                              Double-labeling studies and examination of preclinical c
201                                              Double-labeling studies combining DAT and tyrosine hydro
202                                              Double-labeling studies demonstrated colocalization of T
203                                              Double-labeling studies demonstrated that NGF mRNA was e
204                                              Double-labeling studies demonstrated the localization of
205                                              Double-labeling studies examining CARTp with tyrosine hy
206                                              Double-labeling studies revealed that approximately 50%
207                                              Double-labeling studies revealed that early OL progenito
208                                          The double-labeling studies revealed that mGluR5 immunoreact
209                                              Double-labeling studies show that lMAN(shell) contains t
210                                              Double-labeling studies showed colocalization of the two
211                                              Double-labeling studies showed that BrdU-labeled cells t
212                                              Double-labeling studies using confocal microscopy showed
213                                           In double-labeling studies using confocal microscopy, fluor
214                                              Double-labeling studies with antibodies to phosphorylate
215 on of all the major septal receptor genes in double-labeling studies.
216 he present results and those from our recent double-labeling study suggest that following spinal cord
217                                      In this double-labeling study, we placed a green axonal tracer i
218 d with the region that showed FluoroGold/Fos double labeling, suggesting reciprocal connections betwe
219 retrogradely labeled neurons and significant double labeling, suggesting that cortical projections sp
220  of markers were correlated, and an antibody double labeling technique was employed.
221                                  Using a new double-labeling technique we have colocalized antibodies
222                          Immunohistochemical double-labeling technique with Fos and markers for norad
223 nd thus the complete covalent structure, the double-labeling technique, along with mass spectrometry,
224 Y-NB (Lucifer yellow-Neurobiotin) retrograde double-labeling technique, in conjunction with specific
225  by employing electron spin and nuclear spin double-labeling techniques did not yield unambiguous cha
226 This was investigated with immunofluorescent double-labeling techniques to coregister PV- and CB-expr
227                    In these studies, we used double-labeling techniques to examine whether Cal conten
228 d that intracellular flora by using the same double-labeling techniques to identify Fusobacterium nuc
229 bers in the IPL, standard immunocytochemical double-labeling techniques were applied, using antibodie
230              Accordingly, immunocytochemical double-labeling techniques were used to identify GABA an
231 BA-type neurons using retrograde marking and double-labeling techniques, are profoundly excited by mu
232                                        Using double-labeling techniques, some presynaptic terminals w
233                                        Using double-labeling techniques, we established that these in
234                                              Double labeling the brainstem sections revealed that irI
235                                              Double labeling the hypothalamic sections with NPB antis
236                                              Double-labeling the hypothalamic sections with guinea-pi
237                                              Double-labeling the sections with PrRP antisera and tyro
238 ons of the RVM and caudal pons and performed double labeling to evaluate the expression of alpha-7 an
239                                     However, double-labeling uncovered no coexpression of FRU(M) and
240  born neurons using doublecortin, as well as double labeling using an additional antibody to glial fi
241                                  Fluorescent double labeling using antibodies to bNOS and glutamic ac
242                                      En face double labeling using Ki-67 and progenitor markers revea
243 ions were processed for immunohistochemistry/double labeling using patient sera/cerebrospinal fluid a
244 myocilin with ECM components was examined by double labeling, using different-sized gold particles.
245                                              Double labeling was carried out using anti-CD3, anti-CD6
246                                           No double labeling was found when using a fluorescent trace
247 la, and midbrain as CRH neurons, although no double labeling was found.
248                                              Double labeling was observed in the cell bodies of Purki
249 c and any or all of the ipsilateral targets, double labeling was rare, suggesting that contralateral
250                           Immunofluorescence double labeling was used to determine cellular localizat
251                                    Much less double-labeling was associated with injections into eith
252 function (bone formation) after tetracycline double-labeling was performed by fluorescence microscopy
253                          The same pattern of double-labeling was seen from injections at each spinal
254          Commissural divergence, assessed by double labeling, was less than 3% in each area.
255 abeling and with preembedding immunogold for double labeling, was localized in cell bodies with ultra
256                                     By using double labeling, we found no evidence for mGluR1alpha or
257                                              Double labeling with a caveolin antibody indicated that
258                 Cell death was quantified by double labeling with a membrane impermeable dye and 4',6
259 AII amacrine cells, positively identified by double labeling with an antibody against calretinin, wer
260                                              Double labeling with anti-PECAM1 antibody and anti-place
261                                              Double labeling with anti-PECAM1 antibody and one of thr
262      TULP1-positive cells were identified by double labeling with antibodies specific for cones, rods
263                                              Double labeling with antibodies to calretinin and gamma-
264                                              Double labeling with antibodies to each amino acid and t
265 ype of BrdU-positive cells was identified by double labeling with antibodies to neuronal or glial mar
266 transgenic mice were confirmed as neurons by double labeling with antineurofilament antibody.
267                                              Double labeling with BDA and (3)H-leucine signifies that
268                                              Double labeling with BrdU and the cell cycle marker Ki-6
269                                              Double labeling with c-FLIP antibody and terminal deoxyn
270                                           In double labeling with calretinin and parvalbumin, few neu
271                                              Double labeling with ChAT and synapsin antibodies showed
272                                              Double labeling with confocal microscopy of DLB midbrain
273                                    Moreover, double labeling with Fluoro-Jade B and glial fibrillary
274                                              Double labeling with glial fibrillary acidic protein (as
275                                              Double labeling with isolectin B4 (IB4) showed that all
276 ricular nucleus of the hypothalamus (PVH) by double labeling with markers expressed in viruses inject
277                                              Double labeling with mGluR4a antibodies and antibodies t
278                                              Double labeling with neuropeptide Y (NPY), a marker for
279                                              Double labeling with OMP and synaptophysin demonstrated
280                                              Double labeling with other molecular markers confirmed t
281                                              Double labeling with parvalbumin antibodies in monkey re
282                                              Double labeling with Plk3 and gamma-tubulin, the latter
283                                           By double labeling with rhodopsin, we demonstrate that earl
284                                              Double labeling with several other markers for amacrine
285                                              Double labeling with SMI-32 and parvalbumin confirmed th
286                                              Double labeling with SNAP25 and calbindin antibodies dem
287              Cone cell death was analyzed by double labeling with TdT-dUTP terminal nick-end labeling
288 al apoptosis was determined by histochemical double labeling with terminal deoxynucleotidyl transfera
289                                              Double labeling with the 275 kD hair cell antigen (HCA)
290                                              Double labeling with the ganglion cell marker RBPMS demo
291 esence of small, clear synaptic vesicles and double labeling with the presynaptic markers synaptophys
292                                              Double labeling with the vesicular glutamate transporter
293 o functional recovery, sequential retrograde double labeling with two fluorescent dextran amines was
294                                              Double labeling with various glutamate receptor subunit
295                                              Double-labeling with a monoclonal antibody against micro
296                                              Double-labeling with anti-CD34 antibodies demonstrated t
297        Immunohistochemistry was performed by double-labeling with anti-human MMP1 and collagen type I
298 rrested in the G2 phase of the cell cycle by double-labeling with BrdU and a mitosis-specific marker;
299                                        Also, double-labeling with synaptotagmin showed that Kv1.2 col
300                                              Double labeling (with NeuN and GFAP) immunohistochemistr

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top