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1 inal cutaneous and muscle branches to HRP or Fluoro-Gold.
2 ce of neurons double-labeled for NADPH-d and Fluoro-Gold.
3 as demonstrated by retrograde labeling with Fluoro-Gold.
4 rograde labeling with the fluorescent tracer Fluoro-Gold.
5 ere investigated by retrograde labeling with Fluoro-Gold.
6 dentin caused increased influx and efflux of Fluoro-Gold.
7 MePO were double-labeled for both FOS-ir and fluoro-gold.
8 the Fos protein and retrograde tracing with Fluoro-Gold.
9 nglion cell loss by retrograde labeling with Fluoro-Gold.
11 In this experiment, the retrograde tracer, Fluoro-Gold (8%, 0.5 microl), was microinjected through
12 tracing procedures using microinjections of Fluoro-Gold (8%, 6 microliters) into the PAG were employ
13 After nerve injury, double labelling with Fluoro-Gold, a marker of retrograde transport from trans
14 mouse, this technique was achieved with only Fluoro-Gold, a neurotoxic fluorescent dye with membrane
15 edial parvocellular subdivisions accumulated Fluoro-Gold after systemic administration, suggesting th
16 group II received a concurrent injection of fluoro-gold along with the pipette lesion, and in group
18 labeled cells following LC iontophoresis of Fluoro-Gold and anterograde LC labeling after forebrain
19 gnificant numbers of neurons containing both Fluoro-Gold and CRH mRNA were seen in the lateral hypoth
21 e of populations of neurons labeled for both Fluoro-Gold and GABA in the ventromedial hypothalamus.
22 abeled, immunopositively labeled, as well as Fluoro-Gold and GABA labeled cells, were identified in t
24 trograde labeling with systemically injected Fluoro-Gold and intracellular injection of neurons in a
25 ic acid, domoic acid, 3-nitropropionic acid, Fluoro-Gold and isoniazid are demonstrated and character
29 ed various tracers (cholera toxin B subunit, Fluoro-Gold, and fluorescent latex microspheres) into th
30 dely labeled from SON-targeted injections of fluoro-gold, and FOS-immunoreactivity (FOS-ir) was used
31 ster) were infused with a retrograde tracer, Fluoro-Gold, and tested for affiliation and aggression t
32 tations, autonomic ganglia were stained with Fluoro-gold, and tissues were examined in whole mounts.
33 that permeabilities of enamel and dentin to Fluoro-Gold are age-related, inter-dependent, and regula
34 phoretic injections of the retrograde tracer Fluoro-Gold at the physiologically characterized sites.
35 and in addition, used the retrograde tracer Fluoro-gold combined with c-Fos to assess the involvemen
42 s employed to localize the retrograde tracer fluoro-gold (FG) in cells expressing tyrosine hydroxylas
43 This region of the VLM was injected with Fluoro-Gold (FG) in eight rats, four of which received P
45 NK1R-ir neurons were retrogradely labeled by Fluoro-Gold (FG) injected in the contralateral pre-BotC
47 s and terminals in cardiac ganglia following Fluoro-Gold (FG) injections to label cardiac ganglia, an
49 After injection of the retrograde tracer Fluoro-Gold (FG) into SNc, the rats received pairings of
51 dorsal column nuclei following injections of Fluoro-Gold (FG) into the thalamus, and a small unilater
54 ry relay neurons; 2) retrograde transport of Fluoro-Gold (FG) or cholera toxin B (CT-B) from NTS-X to
55 projecting to the NAcc were identified with Fluoro-Gold (FG) or cholera toxin B (CTb) retrograde tra
57 ions of GG neurons were labeled by injecting Fluoro-Gold (FG) or True Blue chloride into the anterior
58 parvalbumin (PV), by using a combination of Fluoro-Gold (FG) retrograde labeling and immunohistochem
59 in five male Sprague-Dawley rats by applying Fluoro-Gold (FG) topically to the dorsal root entry zone
60 d in 14 male Sprague-Dawley rats by applying Fluoro-Gold (FG) topically to the dorsal surface of the
61 In double-label control animals, in which Fluoro-Gold (FG) was applied to the spinal cord at 40% b
63 ion of nPGi afferents, the retrograde tracer Fluoro-Gold (FG) was injected into the nPGi of sexually
65 g neuronal markers and the retrograde tracer Fluoro-Gold (FG) were used to identify commissurally pro
67 s were subjected to retrograde labeling with Fluoro-Gold (FG), following which IOP was elevated in on
68 mmunolabeling for a retrograde tract tracer, Fluoro-Gold (FG), with in situ hybridization for VGLUT2
72 trograde labeling with systemically injected Fluoro-Gold, followed by intracellular injection of labe
76 .1% of RVM neurons retrogradely labeled with Fluoro-Gold from the spinal cord were also labeled with
77 ic neurons, identified in rats injected with Fluoro-Gold i.p. prior to PRV inoculation of the spleen,
78 Injections of biotinylated dextran amine and Fluoro-Gold in the ICX retrogradely labelled neurons in
79 radely prelabeled with a fluorescent tracer, Fluoro-Gold, injected in the inferior colliculus were in
80 two-thirds of the cells were ipsilateral to Fluoro-Gold injection sites in both the RVLM and CVLM, a
81 HVC but could not be retrogradely labeled by Fluoro-Gold injections in the robust nucleus of the arch
85 ling procedures following microinjections of Fluoro-Gold into defensive rage sites in the dorsal PAG
86 ne-B into the dorsal raphe nucleus (DRN) and Fluoro-Gold into the lateral geniculate nucleus (LGN) re
88 tion and injections of the retrograde tracer Fluoro-Gold into the medial prefrontal and primary somat
93 in-dextran, Fluoro-Ruby, Fluoro-Emerald, and Fluoro-Gold) into the facial and hypoglossal nuclei of t
96 no effect on the number and distribution of Fluoro-Gold-labeled neuroendocrine neurons in the rat ar
98 motor nucleus of the vagus (DMNV), including Fluoro-gold-labelled parasympathetic preganglionic neuro
100 n amine, Phaseolus vulgaris leucoagglutinin, Fluoro-Gold or tetramethylrhodamine dextran amine into e
104 tia nigra dopaminergic neurons assessed by a Fluoro-gold prelabeling method, a decline in striatal do
106 roscopy and immunocytochemistry to show that Fluoro-Gold rapidly penetrates enamel, the dentin-enamel
108 eritoneal injection of the retrograde tracer Fluoro-Gold resulted in the labeling of 40% of hypophysi
110 th four tracers, cholera toxin-beta subunit, Fluoro-Gold, the Bartha strain of pseudorabies virus, an
112 al activity, Fos, with the retrograde tracer Fluoro-Gold to assess activation in this pathway during
113 beled from both sites and were injected with Fluoro-Gold to determine whether PdPN and lateral MeApd
115 RFRP-3 fibers in the median eminence and of Fluoro-Gold uptake from the periphery imply that the act
116 rent tracers were injected either centrally (Fluoro-Gold: ventral Vi/Vc, or MDH) or peripherally (whe
119 re this study with previous in vivo studies, Fluoro-Gold was injected in vivo into either the olfacto
123 de axonal tract tracing procedures, in which Fluoro-Gold was microinjected into the lateral hypothala
126 ransported tracer, horseradish peroxidase or Fluoro-Gold, was injected into the spinal cord of Platyr
127 is leucoagglutinin and the retrograde tracer Fluoro-Gold, we examined the efferent projections of MO
128 Discrete injections of the retrograde tracer Fluoro-gold were delivered to the PVN, and rats were sub
129 vealed that neurons labeled for both CCK and Fluoro-Gold were located in the dorsolateral aspect of t
130 targets, injections of the retrograde tracer Fluoro-Gold were made into known targets of second-order
132 mmunoreactivity and retrograde labeling with fluoro-gold were used in this study to determine whether
133 cells, identified by retrograde transport of Fluoro-Gold, were found in M1 (57.5 +/- 9.6/median secti
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