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1 tic specializations of synaptic pairs can be colabeled.
2  suppressed BrdU labeling and BrdU-gammaH2AX colabeling.
3 DCX), which detects neural progenitor cells, colabeled a subset of BrdU-positive cells that extended
4  3-N-methyl group was confirmed by [(11/13)C]colabeling and subsequent carbon-13 NMR spectroscopy.
5 n special equipment, requires immunogold for colabeling, and does not take advantage of the growing n
6 ose, significantly decreased mean numbers of colabeled AVP neurons in each structure in glucoprivic a
7  Specifically in lactating rats, BDA-and NPY-colabeled axonal swellings were in close apposition to c
8      The final step of the protocol involves colabeling by immunohistochemistry for the putative targ
9 tion with deuterated leucine-based metabolic colabeling, candidate proteins can be immediately valida
10                        Each of the Sox2/Pax6-colabeled cell types is at a remove from the birth of ne
11 pression of Fos nor the percentage of TH/Fos colabeled cells was influenced by either mating or mount
12                   Small numbers of BrdU/GFAP-colabeled cells were also consistently observed bilatera
13 cant number of BrdU/NeuN- and BrdU/calbindin-colabeled cells were observed in topographically reorgan
14                       Although no GnRH-tac3a colabeled cells were observed, dense GnRH fibers surroun
15 AM56, a macrophage-specific marker, revealed colabeled cells.
16 e viral tracer (HSV-1) in the dCA3 to reveal colabeled connecting neurons, which were evident only in
17 human genes ("targets") were hybridized with colabeled (Cy3 and biotin) human lung cDNA probes at con
18  a view supported by our immunohistochemical colabeling data.
19                                              Colabeling DRMs and F-actin revealed a correlation betwe
20                                              Colabeling experiments confirmed that the transgenic ICP
21 ic reticulum (ER) retention as determined by colabeling experiments with a specific ER marker.
22                                      Through colabeling experiments, we observed the coalignment and
23                 In both models, BDA- and NPY-colabeled fibers were limited mainly to the hypothalamus
24        Those FIV RNA(+) cells which could be colabeled for a phenotype marker, were labeled for eithe
25                                        Cells colabeled for BrdU and five different neuronal markers w
26 d visualized in DRG and spinal cord sections colabeled for CGRP and SP.
27       Rare islets contained human cells that colabeled for human insulin or PDX-1.
28 brillary acidic protein-immunopositive cells colabeled for IL-12 p40 RNA; indicating that LPS-stimula
29                                              Colabeling for beta-galactosidase and BrdU revealed that
30                                              Colabeling for BrdU and the neural progenitor marker nes
31  4 hours after stimulation, as determined by colabeling for catalase or PMP70.
32 sing nonpyramidal neurons was established by colabeling for EGFP and GAD67 in selected tissue section
33        Apoptotic beta cells were detected by colabeling for insulin and by TUNEL.
34 es and BrdU-positive cells that did not show colabeling for neuronal or glial markers were not influe
35                                              Colabeling for superoxide in the neurons showed a concur
36 nerves that were Sox11 immunopositive showed colabeling for the stress and injury-associated activati
37 ntromission did not affect the percentage of colabeled Fos/ERalpha neurons.
38 us PDGF-alphaR-positive oligodendroglia also colabel heavily with the nuclear cell proliferation mark
39 s from myelinated (Abeta/Adelta) fibers were colabeled in roughly equal proportion with each subunit.
40 ation rather than membrane tension and allow colabeling in the same cells.
41 ubunit B injected into NAc combined with Fos colabeling in vmPFC indicated that vmPFC self-administra
42                               BrdU-gammaH2AX colabeling is neither an age-related phenomenon nor limi
43 used a new antibody to Langerin/CD207, which colabels isolated CD8(+) CD205(+) DCs, to immunolabel sp
44 fferences in patterns of viral infection, we colabeled murine sensory ganglia for evidence of HSV inf
45 present in 26%, 58% and 89% of calbindin-D28-colabeled myenteric neurons.
46 ificant increase in the percentage of TH/Fos colabeled neurons in both A1 and A2 cells compared to mo
47       Fourth, activating only this subset of colabeled neurons is sufficient to elicit sleep homeosta
48 3, and TLR4 post-RT accompanied by increased colabeling of astrocytes and microglia.
49 ficity of the activated neurons, we measured colabeling of Fos with Drd1 and Drd2 in three DS subregi
50          We find distinct differences in the colabeling of molecular markers between the parasubiculu
51 ted protein GAP-43 and the results indicated colabeling of most axons.
52 rdU) administration), as demonstrated by the colabeling of myosin VI and BrdU.
53                                              Colabeling of Purkinje cell dendrites and intersecting p
54 tion to cells identified as Schwann cells by colabeling of S100, a Schwann cell specific protein.
55                                              Colabeling of T cell samples with a fluorescent dye lead
56                           Only minimal (<5%) colabeling of tac3a was observed in kiss2 cells.
57 We used in situ hybridization to measure the colabeling of the activity marker Fos with Drd1 and Drd2
58                                              Colabeling of the cell proliferation marker BrdU with th
59 Ascope in-situ hybridization to quantify the colabeling of the neuronal activity marker Fos, and dopa
60 ence of Vsx1 in mature type 3 bipolar cells, colabeling of Vsx1 and HCN4 was observed at postnatal st
61                            In contrast, ANFs colabeled predominantly with VGLUT1.
62 cy and degree of overlap between clusters of colabeled proteins; and 3) STORM-RLA also calculates the
63           Based on the in situ hybridization colabeling results, we tested the causal role of DMS D1
64 1 hypothalamic neurons were characterized by colabeling select hypothalamic neuropeptides with tdToma
65 e for Ki-67, HGF, and Pax7 was determined by colabeling sets of serial sections with either laminin o
66 eafness leads to increased numbers of VGLUT2-colabeled Sp5 and Cu projections to the ventral and dors
67 in SW1990 pancreatic cancer cells by using a colabeling strategy with light and heavy toluidine.
68                 Here, cD1 or cD2 was seen to colabel subsets of Pax6-expressing radial glial cells (R
69  site on the amino-terminal third of SUR and colabeled the associated K(IR).
70 s; after 24 h of culture, it was possible to colabel these cells with human-specific (154)Sm-tagged a
71                                     In cells colabeled to detect centrosomes and nucleated microtubul
72                              Ligand-receptor colabeling was also common among cortical neurons.
73                                              Colabeling was also high after 24 h separation without r
74 comprised 23% of the total profiles counted; colabeling was most common in dendrites.
75 er numbers were in T cell areas, where CD205 colabeling was noted.
76          Oxytocin labeling and oxytocin/cFos colabeling were higher after interaction with a novel sa
77 xpressed in a subset of sensory neurons that colabel with calcitonin gene-related peptide and TRPV1 s
78 dies of retrogradely labeled neurons did not colabel with EGFP expression in neurons of GAD67-EGFP mi
79 ase 65, but no Per1 : :GFP(+) amacrine cells colabeled with a glycine transporter 1 antibody.
80 also found but no new Cr(+) or GABA(+) cells colabeled with a mature neuron marker, NeuN or chondroit
81  of allogeneic mesenchymal stem cells (MSCs) colabeled with a radiotracer and MR contrast agent to ac
82                                 PNECs can be colabeled with alveolar cells during lung development, a
83 ta, so that any confocal image stack that is colabeled with anti-Brp can be analyzed within standardi
84 , and descending projections to the DCN were colabeled with antibodies against VGluT2, a glutamate tr
85 markers of unmyelinated C-fiber neurons; 68% colabeled with antibodies to TRPV1 (marker of nociceptiv
86                  LacZ was expressed in cells colabeled with antibody against olfactory marker protein
87 rved bilaterally, but these cells were never colabeled with any of the neuronal markers.
88 occlusion, as was the number of neural cells colabeled with both BrdUrd and NeuN.
89 os expression in DMS but not in DLS; Fos was colabeled with both Drd1 and Drd2 DMS injections of SCH3
90  in the NAc core, but not shell, and Fos was colabeled with both Drd1- and Drd2-MSNs.
91                                 Of the cells colabeled with BrdU and a neuronal marker, at least half
92                                        Cells colabeled with BrdU and the astrocytic marker glial fibr
93 amination of TUC-4-positive immature neurons colabeled with BrdU indicated that stage I neurons first
94                              Astrocytes were colabeled with BrdU.
95 re, we identified newly born cells that were colabeled with caspase-3 immunohistochemistry and perfor
96 e specific (52.5 and 39.2% of Fos expression colabeled with Drd1 and Drd2, respectively).
97                      More nNOS-ir cells were colabeled with ERalpha immunoreactivity compared with AR
98 ed in vitro and in vivo within PLB pentamers colabeled with FlAsH and the biarsenical fluorophore ReA
99    The percentage of PNMT-containing neurons colabeled with Fos was not different in C1 and C2 among
100                                    Liposomes colabeled with gadolinium (Gd) and a fluorescent indicat
101 stly GBCs, are heavily stained by GBC-3, and colabeled with GBC-3 and sustentacular cell or HBC marke
102 ough a small percentage ( approximately 10%) colabeled with markers of A-fiber neurons.
103 r TBI, and the number of BrdU-positive cells colabeled with neuron-specific nuclear antigen significa
104             After flicker, phospho-NF-kappaB colabeled with neurons more than microglia.
105 (marker of nociceptive DRG neurons), and <2% colabeled with NF200 (marker of large myelinated neurons
106 vity was detected in larger-sized cells that colabeled with NF200.
107  acidic protein (GFAP) or vimentin, were not colabeled with NR2B.
108 ea, 395.96 +/- 5.6 mum(2)) and predominantly colabeled with peripherin and isolectin B4 markers of un
109 ity was assessed by counting cells in tissue colabeled with PI and Calcein AM.
110 unolabeled for the mouse UV-cone pigment and colabeled with PNA.
111  radial glial cells (RGCs), whereas only cD2 colabeled with Tbr2.
112          At perinatal ages, newly born cells colabeled with the astrocyte marker S100beta in higher n
113  BDNF-, and NT-3-positive neurons in layer V colabeled with their respective high-affinity receptors,
114 colabeled with VGLUT2, but few (2.5% +/- 1%) colabeled with VGLUT1.
115  (47% +/- 3%) of the Sp5 mossy fiber endings colabeled with VGLUT2, but few (2.5% +/- 1%) colabeled w
116 esynaptic release sites were demonstrated by colabeling with antibodies against the synaptic vesicle
117                                              Colabeling with antibodies directed toward AMPARs and/or
118 ents with the lectin peanut agglutinin or by colabeling with antisera to cone photopigments.
119 lement cascade proteins (C1q, C3), TLR4, and colabeling with glia (IBA1, GFAP) were examined using ge
120 easured oxytocin neuron immunoreactivity and colabeling with the immediate early gene product cFos.
121 B(1)) subunit immunoreactivity on Hcrt cells colabelled with antisera to the Hcrt-2 peptide.

 
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