ライフサイエンスコーパス: neurobiotin

1 ercellular spread of the biotinylated tracer Neurobiotin.

2 led extracellularly and juxtacellularly with neurobiotin.

3 h peroxidase, fluorescent dextran amines and neurobiotin.

4 d were labeled by intracellular injection of neurobiotin.

5 ularly filled with horseradish peroxidase or Neurobiotin.

6 nsport of the small molecular weight tracer, Neurobiotin.

7 received a local iontophoretic injection of Neurobiotin.

8 were injected with horseradish peroxidase or neurobiotin.

9 otoneurons were intracellularly stained with Neurobiotin.

10 0, identified by juxtacellular labeling with Neurobiotin.

11 euronal types by juxtacellular labeling with neurobiotin.

12 and label interneurons in laminae I-III with Neurobiotin.

13 iologically and labeled intracellularly with Neurobiotin.

14 als labelled by intracellular injection with neurobiotin.

15 s demonstrated by intracellular injection of Neurobiotin.

16 and stained by intracellular injection with Neurobiotin.

17 ons was studied in single cells labeled with Neurobiotin.

18 unction-permeable tracers Lucifer yellow and Neurobiotin.

19 Iontophoretic injection of Neurobiotin, a low molecular weight compound that passes

20 82) were filled with the intracellular stain Neurobiotin allowing post-fixation morphological reconst

21 s were made by injecting recorded cells with Neurobiotin and analyzing them quantitatively with a com

22 or ciliary neurons were labeled en mass with neurobiotin and biocytin through nerve roots, dye transf

23 these axons in their target ganglia, we used Neurobiotin and dextran-Texas Red microelectrodes to fil

24 verify cell identity, cells were filled with Neurobiotin and examined using confocal microscopy.

25 s with inspiratory activity were filled with Neurobiotin and found to be closely apposed to substance

26 To investigate this possibility, we examined Neurobiotin and glycine diffusion from AIIs to bipolar c

27 , ON-center parasol cells were injected with Neurobiotin and Lucifer yellow in living macaque retinas

28 ic injection of the anterograde tracers BDA, neurobiotin and PHA-L in the host.

29 ntracellular recording before injection with neurobiotin and preparation for electron microscopy.

30 tracellular recording, before injection with neurobiotin and preparation for electron microscopy.

31 afferents were juxtacellularly labeled with Neurobiotin and sections were stained to show filled neu

32 They were injected with neurobiotin and shown by light microscopic immunocytoche

33 upling following injection of alpha-GCs with Neurobiotin and the concerted spike activity of alpha-GC

34 ibution: intracellular filling of cells with neurobiotin and visualization of the cells by using eith

35 urons were then intracellularly labeled with Neurobiotin and visualized with 3,3'diaminobenzidine.

36 tarburst cells injected intracellularly with Neurobiotin, and these AMPA receptor subunits were local

37 umbens projection neurons, the advantages of Neurobiotin are utilised in order to reveal the detailed

38 er yellow (Molecular Probes, Eugene, OR) and neurobiotin at E15.5, Cx43(-/-)/Cx50(-/-) lenses retaine

39 he anatomy of fin motoneurons as revealed by neurobiotin backfills and differential staining using fl

40 abel immunocytochemistry in combination with neurobiotin backfills demonstrated that a single cell ex

41 Neurobiotin backfills of the vocal nerve in combination

42 Neurobiotin backfills were performed on the dorsal cauda

43 ls showed extensive intercellular passage of neurobiotin but little coupling with Lucifer yellow.

44 ional conductances and extensive transfer of neurobiotin, but those expressing CX50R23T did not show

45 ion cells were intracellularly injected with Neurobiotin, cone bipolar cells were immunolabeled, and

46 Intracellular recording and injection of Neurobiotin confirmed that FM1-43 labeled neurons that s

47 Neurones were recorded using neurobiotin-containing whole cell patch electrodes in a

48 dly in some networks than others relative to Neurobiotin controls.

49 Neurobiotin coupling between rods and cones was consiste

50 upported extensive intercellular transfer of Neurobiotin, CX50fs gap junctions were rare, and their s

51 e hundred and one neurons were labelled with neurobiotin during whole-cell recording.

52 g intracellular recording and Lucifer yellow/neurobiotin dye injection methods in the flatmount tiger

53 Micropipette recording with juxtacellular Neurobiotin ejection, linked micropipette-microwire reco

54 Recorded neurons were Neurobiotin filled and identified as RCs or non-RCs usin

55 However, this provides a method to obtain Neurobiotin-filled cone bipolar cells without the necess

56 Neurobiotin-filled dendrites containing GABA received as

57 ogy, we performed whole-cell recordings with Neurobiotin-filled-pipettes in horizontal slices from ad

58 jected with either horseradish peroxidase or Neurobiotin for characterization of its dendrites.

59 erents to be iontophoretically injected with Neurobiotin for subsequent histological analyses.

60 us, when possible, neurons were labeled with neurobiotin for subsequent neurochemical classification

61 ns were confirmed by retrograde transport of neurobiotin from DMN to NSTc.

62 The tracer Neurobiotin has revealed many different networks interco

63 stematically compared the transfer of LY and neurobiotin in embryos containing 16-128 cells.

64 connections, we injected parasol cells with Neurobiotin in lightly fixed baboon retinas.

65 d N-(2-aminoethyl)biotinamide hydrochloride (neurobiotin); in contrast, HeLa-Cx45 and HeLa-Cx43(His)(

66 Furthermore, neurobiotin injected into individual pacemaker or relay

67 drites of type 2 CA cells and examination of neurobiotin-injected DA cells proved that their vitreal

68 A Neurobiotin-injected OFF parasol cell from midperipheral

69 Intracellular neurobiotin injection revealed that AII amacrine cells a

70 This has been used with neurobiotin injection to define the passive and firing p

71 We made focal neurobiotin injections into the midshipman PAG to both m

72 We found that intracellular injection of Neurobiotin into a specific ganglion cell type targeted

73 abeled ganglion cells following injection of Neurobiotin into an amacrine cell.

74 uated by introduction of the tracer molecule Neurobiotin into both neurons (n = 98) and astrocytes (n

75 In contrast, injection of Neurobiotin into ganglion cells almost always resulted i

76 Injection of neurobiotin into the LM and CM confirmed that simultaneo

77 Injection of Neurobiotin into the spinal cord revealed that retrograd

78 Of 57 active, recorded, and neurobiotin-labeled neurons in the lateral hypothalamus,

79 Axons of neurobiotin-labeled subicular pyramidal neurons were vis

80 natal mice to allow intrasomal recording and neurobiotin labeling of individual sensory neurons chara

81 Neurobiotin labeling of the main auditory end organ, the

82 Cellular morphology was identified using Neurobiotin labeling.

83 In contrast, no Neurobiotin-labelled VLM respiratory neurones (n = 19) w

84 Neurobiotin labelling and rapid Golgi techniques were us

85 d by using focal extracellular injections of Neurobiotin (NB) into the spiral ganglion of the basal c

86 Histology was assessed with a combination of neurobiotin (NB) retrograde labeling of retinal ganglion

87 c connections are detected by trans-synaptic Neurobiotin (NB) transfer and by colocalization of Bruch

88 entral projections of CGRP(+) SP(-) neurons, Neurobiotin (NB) was applied to the C7 ventral ramus and

89 ye Lucifer yellow (LY) and the permeable dye neurobiotin (NB) was applied to the optic nerve stump fo

90 Focal injections of Neurobiotin (NB) were made into Rosenthal's canal, label

91 ograde labeling of ganglion cells (GCs) with Neurobiotin (NB, a gap junction permeable dye) and Lucif

92 ed by coinjection of Lucifer yellow (LY) and Neurobiotin (NBN) during whole-cell recordings in cochle

93 oaded with the gap junction-permeable tracer Neurobiotin, only superior coding DSGCs exhibited homolo

94 logically, were stained intracellularly with neurobiotin or biocytin.

95 munication was assessed by microinjection of neurobiotin or by double whole-cell patch-clamp recordin

96 ord of the cat by intracellular injection of Neurobiotin or horseradish peroxidase.

97 sting conductance and are highly coupled via neurobiotin-permeant gap junctions, while midline cells

98 Filling AII amacrine cells with Neurobiotin produces labeling of cone bipolar cells by m

99 Neurobiotin retrograde transport from the spinal cord co

100 previously established LY-NB (Lucifer yellow-Neurobiotin) retrograde double-labeling technique, in co

101 The neurotracer neurobiotin showed that extrinsic axons from the left an

102 In retinal microvessels of control rats, Neurobiotin spread hundreds of micrometers from the trac

103 Under these conditions, Neurobiotin spreads from ON cone bipolar cells into neig

104 Branching patterns and collaterals of 78 Neurobiotin-stained afferents were compared in rats.

105 Neurobiotin that was injected into single rods diffused

106 llow intercellular transfer of microinjected neurobiotin; the alanine mutant allowed transfer, but le

107 neurones were identified after injection of neurobiotin through the recording microelectrode: (i) lo

108 r recording methods followed by filling with Neurobiotin to characterize the morphology and physiolog

109 dy, we used the gap junction-permeant tracer Neurobiotin to compare the coupling pattern of different

110 ere, we use the gap junction-permeant tracer Neurobiotin to determine the architecture and coupling p

111 s then injected with the biotinylated tracer Neurobiotin to determine which of the cells were coupled

112 bulin as well as intracellular injections of Neurobiotin to examine varicosities belonging to heart e

113 tment also rescued intercellular transfer of Neurobiotin to levels similar to those in cells expressi

114 ere intracellularly recorded and filled with neurobiotin to map the distribution of VGLUT1 synapses a

115 transfer of the low molecular weight tracer Neurobiotin to neighbouring motoneurones.

116 them with the gap junction-permanent tracer Neurobiotin to provide, for the first time, a comprehens

117 ollowed by dye-filling these same cells with Neurobiotin, to define their morphology by high-resoluti

118 Photoreceptors showed strong Neurobiotin tracer coupling at night, extensively labeli

119 variability in responses to dim flashes, (2) Neurobiotin tracer coupling, and (3) junctional conducta

120 Our neurobiotin tracing results verified earlier studies sho

121 itive charge substitution (CX50R23K) allowed neurobiotin transfer at levels similar to those of wild-

122 both connexins, but it reduced the extent of neurobiotin transfer only in HeLa-Cx43(His)(6) and HeLa-

123 ap junctions were rare, and their support of Neurobiotin transfer was reduced by >90%.

124 ng a 20-fold lower diffusion coefficient for Neurobiotin transfer.

125 When single rods were injected with Neurobiotin, up to 10 rods were labeled.

126 e study population; these were labelled with Neurobiotin using the juxtacellular method, and visualis

127 Two kinds of amacrine cells were filled with Neurobiotin via gap junctions: a large, polyaxonal cell

128 Whereas LY transfer was never observed, neurobiotin was consistently transferred in both ventral

129 re compartments The retrogradely transported Neurobiotin was found in somata, proximal and distal den

130 icantly fewer Muller cells were labeled when Neurobiotin was injected into astrocytes associated with

131 strocytes associated with arteries than when Neurobiotin was injected into astrocytes that were dista

132 extran amine was injected extracellularly or neurobiotin was injected into physiologically identified

133 Neurobiotin was injected iontophoretically into saccular

134 l coupling the gap junction-permeant tracer, Neurobiotin, was delivered via patch pipettes into peric

135 Neurons labeled with biocytin or neurobiotin were classified on the basis of their dendri

136 ally silent AH-cells that were injected with neurobiotin were found to be multipolar Dogiel type II n

137 anatomical tracer (horseradish peroxidase or neurobiotin) were made in either the caudal medial acces

138 this study, we made restricted injections of Neurobiotin, which labeled small sectors (300-500 microm

139 intracellularly with the biotinylated tracer Neurobiotin, which was then allowed to diffuse across ga