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

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