ライフサイエンスコーパス: colabel

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.