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1 d by the immunostaining of fibers for VAChT (vesicular acetylcholine transporter).
2 we used brain sections immunostained for the vesicular acetylcholine transporter.
3 binding of (123)I-iodobenzovesamicol to the vesicular acetylcholine transporter.
4 do not express choline acetyltransferase or vesicular acetylcholine transporter.
5 ng protein toxin, to an antibody against the vesicular acetylcholine transporter.
6 ensities for [3H]vesamicol, which labels the vesicular acetylcholine transporter.
7 zovesamicol (IBVM), an in vivo marker of the vesicular acetylcholine transporter.
8 ning confocal microscopy, colocalized in PnO vesicular acetylcholine transporter, a presynaptic marke
9 of wild-type mice, is immunoreactive for the vesicular acetylcholine transporter, a recently identifi
11 ocytochemically with an antibody against the vesicular acetylcholine transporter and digitally photog
12 tylcholinesterase activities, and binding to vesicular acetylcholine transporter and Na(+)-dependent
14 s encoding choline acetyltransferase and the vesicular acetylcholine transporter and up-regulated ace
15 ons lacked detectable immunoreactivities for vesicular acetylcholine transporter and vasoactive intes
16 was expressed in a minority of SP, VIP, NPY, vesicular acetylcholine transporter, and calcitonin gene
18 ed to calculate [123I]-iodobenzovesamicol to vesicular acetylcholine transporter binding potential va
20 is transported into synaptic vesicles by the vesicular acetylcholine transporter encoded by unc-17.
22 n capture of a vesicle membrane protein, the vesicular acetylcholine transporter, from single vesicle
23 s purpose also carries several copies of the vesicular acetylcholine transporter gene (VAChT), which
24 linergic gene locus, which contains both the vesicular acetylcholine transporter gene and the choline
25 now show that choline acetyltransferase and vesicular acetylcholine transporter homologs are prefere
27 ic terminals in the rat spinal cord by using vesicular acetylcholine transporter immunocytochemistry.
28 tions, a significantly greater proportion of vesicular acetylcholine transporter-immunoreactive (VACh
29 rase [ChAT] activity, the number of ChAT and vesicular acetylcholine transporter-immunoreactive neuro
30 amicol (FBT), which selectively binds to the vesicular acetylcholine transporter in the presynaptic c
33 ur ongoing structure-activity studies of the vesicular acetylcholine transporter ligand 2-(4-phenylpi
34 mpound was more potent than the prototypical vesicular acetylcholine transporter ligand vesamicol.
37 s displayed moderately high affinity for the vesicular acetylcholine transporter, no compound was mor
38 ualized in brain sections stained for either vesicular acetylcholine transporter or choline acetyltra
39 ry motor neurons, labeled with antibodies to vesicular acetylcholine transporter or substance-P, were
40 ized on the same synaptic vesicles as either vesicular acetylcholine transporter or vesicular monoami
41 n addition, dual localization of M2R and the vesicular acetylcholine transporter protein (VAChT), a m
43 y and negatively charged residues of the rat vesicular acetylcholine transporter (rVAChT) were studie
45 antibodies to choline acetyltransferase and vesicular acetylcholine transporter to label cholinergic
46 dobenzovesamicol, a SPECT radiotracer of the vesicular acetylcholine transporter, to evaluate in vivo
47 ampal sections were dually immunolabeled for vesicular acetylcholine transporter (VAChT) and ERalpha
48 ract-tracing and immunocytochemistry for the vesicular acetylcholine transporter (VAChT) and for tyro
49 col derivative that binds selectively to the vesicular acetylcholine transporter (VAChT) and has been
50 ampal sections were dually immunolabeled for vesicular acetylcholine transporter (VAChT) and MOR-1 an
51 reveals that CHT-positive vesicles carry the vesicular acetylcholine transporter (VAChT) and synaptic
52 including choline acetyltransferase (ChAT), vesicular acetylcholine transporter (VAChT) and the high
54 col is a SPECT radioligand selective for the vesicular acetylcholine transporter (VAChT) and used to
56 -12) cells stably transfected with the human vesicular acetylcholine transporter (VAChT) cDNA are des
58 ng with choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT) immunohistoc
59 ed for the visualization of somatostatin and vesicular acetylcholine transporter (VAChT) immunoreacti
61 the NK1 receptor and either 1) SP or 2) the vesicular acetylcholine transporter (VAchT) in rat NAc.
62 cutive function by genetically targeting the vesicular acetylcholine transporter (VAChT) in the mouse
63 roscopic dual immunolabeling of M2Rs and the vesicular acetylcholine transporter (VAchT) in the MPT o
64 cycle had an effect on the expression of the vesicular acetylcholine transporter (VAChT) in the SCN,
67 identifies dopaminergic neurons, whereas the vesicular acetylcholine transporter (VAchT) is present o
71 e cyclase-activating peptide (PACAP) and the vesicular acetylcholine transporter (VAChT) revealed tha
72 study indicated that there was an absence of vesicular acetylcholine transporter (VAChT) staining in
73 tudies with an antiserum that recognizes the vesicular acetylcholine transporter (VAChT) suggest, how
74 of antipeptide antiserum raised against the vesicular acetylcholine transporter (VAchT) that is resp
75 obutyric acid (GABA) transporter (VGAT), and vesicular acetylcholine transporter (VAChT) to determine
76 ructures by cholinergic axons expressing the vesicular acetylcholine transporter (VAChT) was also stu
79 for choline acetyltransferase (ChAT) and the vesicular acetylcholine transporter (VAChT) was used to
80 ell line, A123.7, expressing recombinant rat vesicular acetylcholine transporter (VAChT) with radiola
81 unds having high potency and selectivity for vesicular acetylcholine transporter (VAChT), a heteroaro
82 (SP), vasoactive intestinal peptide (VIP) or vesicular acetylcholine transporter (VAchT), and their n
83 T2 along with three cholinergic markers: the vesicular acetylcholine transporter (VAChT), the high-af
84 fy selective high-affinity inhibitors of the vesicular acetylcholine transporter (VAChT), we have int
85 sion of choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT), which are c
86 activity was localized in significantly more vesicular acetylcholine transporter (VAChT)-IR varicosit
94 ChAT), choline transporter 1 (CHT1, SLC5A7), vesicular acetylcholine transporter (VAChT, SLC18A3), an
95 398 in a three-dimensional homology model of vesicular acetylcholine transporter (VAChT, TC 2.A.1.2.1
96 histochemical markers for cholinergic cells (vesicular acetylcholine transporter [VAChT]), tyrosine h
97 histochemical markers for cholinergic cells (vesicular acetylcholine transporter [VAChT]), tyrosine h
99 bodies to glutamic acid decarboxylase (GAD), vesicular acetylcholine transporter (VAT), or the peptid
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