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1 d by the immunostaining of fibers for VAChT (vesicular acetylcholine transporter).
2 zovesamicol (IBVM), an in vivo marker of the vesicular acetylcholine transporter.
3 we used brain sections immunostained for the vesicular acetylcholine transporter.
4 do not express choline acetyltransferase or vesicular acetylcholine transporter.
5 binding of (123)I-iodobenzovesamicol to the vesicular acetylcholine transporter.
6 ng protein toxin, to an antibody against the vesicular acetylcholine transporter.
7 ensities for [3H]vesamicol, which labels 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 8)F]-VAT, a new radiotracer that targets the vesicular acetylcholine transporter as a proxy measure o
19 ed to calculate [123I]-iodobenzovesamicol to vesicular acetylcholine transporter binding potential va
20 y is a robust predictor of regional cerebral vesicular acetylcholine transporter bindings, especially
22 is transported into synaptic vesicles by the vesicular acetylcholine transporter encoded by unc-17.
24 n capture of a vesicle membrane protein, the vesicular acetylcholine transporter, from single vesicle
25 s purpose also carries several copies of the vesicular acetylcholine transporter gene (VAChT), which
26 linergic gene locus, which contains both the vesicular acetylcholine transporter gene and the choline
27 now show that choline acetyltransferase and vesicular acetylcholine transporter homologs are prefere
29 ic terminals in the rat spinal cord by using vesicular acetylcholine transporter immunocytochemistry.
30 tions, a significantly greater proportion of vesicular acetylcholine transporter-immunoreactive (VACh
31 rase [ChAT] activity, the number of ChAT and vesicular acetylcholine transporter-immunoreactive neuro
32 forebrain morphometry with the topography of vesicular acetylcholine transporter in a large Parkinson
33 herefore examined expression of ChAT and the vesicular acetylcholine transporter in the embryonic and
34 amicol (FBT), which selectively binds to the vesicular acetylcholine transporter in the presynaptic c
39 ur ongoing structure-activity studies of the vesicular acetylcholine transporter ligand 2-(4-phenylpi
40 h de novo and established PD cohorts, we use vesicular acetylcholine transporter ligand [(18)F]FEOBV
41 mpound was more potent than the prototypical vesicular acetylcholine transporter ligand vesamicol.
44 s displayed moderately high affinity for the vesicular acetylcholine transporter, no compound was mor
45 ualized in brain sections stained for either vesicular acetylcholine transporter or choline acetyltra
46 ry motor neurons, labeled with antibodies to vesicular acetylcholine transporter or substance-P, were
47 ized on the same synaptic vesicles as either vesicular acetylcholine transporter or vesicular monoami
50 n addition, dual localization of M2R and the vesicular acetylcholine transporter protein (VAChT), a m
53 y and negatively charged residues of the rat vesicular acetylcholine transporter (rVAChT) were studie
55 on of, and optimize methods to quantify, the vesicular acetylcholine transporter-specific tracer (-)-
56 antibodies to choline acetyltransferase and vesicular acetylcholine transporter to label cholinergic
57 dobenzovesamicol, a SPECT radiotracer of the vesicular acetylcholine transporter, to evaluate in vivo
58 ampal sections were dually immunolabeled for vesicular acetylcholine transporter (VAChT) and ERalpha
59 ract-tracing and immunocytochemistry for the vesicular acetylcholine transporter (VAChT) and for tyro
60 col derivative that binds selectively to the vesicular acetylcholine transporter (VAChT) and has been
61 ampal sections were dually immunolabeled for vesicular acetylcholine transporter (VAChT) and MOR-1 an
62 reveals that CHT-positive vesicles carry the vesicular acetylcholine transporter (VAChT) and synaptic
63 including choline acetyltransferase (ChAT), vesicular acetylcholine transporter (VAChT) and the high
65 col is a SPECT radioligand selective for the vesicular acetylcholine transporter (VAChT) and used to
67 -12) cells stably transfected with the human vesicular acetylcholine transporter (VAChT) cDNA are des
69 ng with choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT) immunohistoc
70 ed for the visualization of somatostatin and vesicular acetylcholine transporter (VAChT) immunoreacti
72 the NK1 receptor and either 1) SP or 2) the vesicular acetylcholine transporter (VAchT) in rat NAc.
73 ncoding choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT) in specific
74 cutive function by genetically targeting the vesicular acetylcholine transporter (VAChT) in the mouse
75 roscopic dual immunolabeling of M2Rs and the vesicular acetylcholine transporter (VAchT) in the MPT o
76 cycle had an effect on the expression of the vesicular acetylcholine transporter (VAChT) in the SCN,
78 melanocortin-1 receptor (MC-1R) agonist and vesicular acetylcholine transporter (VAChT) inhibitor an
80 identifies dopaminergic neurons, whereas the vesicular acetylcholine transporter (VAchT) is present o
85 e cyclase-activating peptide (PACAP) and the vesicular acetylcholine transporter (VAChT) revealed tha
86 study indicated that there was an absence of vesicular acetylcholine transporter (VAChT) staining in
87 tudies with an antiserum that recognizes the vesicular acetylcholine transporter (VAChT) suggest, how
88 of antipeptide antiserum raised against the vesicular acetylcholine transporter (VAchT) that is resp
89 obutyric acid (GABA) transporter (VGAT), and vesicular acetylcholine transporter (VAChT) to determine
90 ructures by cholinergic axons expressing the vesicular acetylcholine transporter (VAChT) was also stu
93 for choline acetyltransferase (ChAT) and the vesicular acetylcholine transporter (VAChT) was used to
94 ell line, A123.7, expressing recombinant rat vesicular acetylcholine transporter (VAChT) with radiola
95 unds having high potency and selectivity for vesicular acetylcholine transporter (VAChT), a heteroaro
96 affold Nemacol and show that it inhibits the vesicular acetylcholine transporter (VAChT), a target re
97 (SP), vasoactive intestinal peptide (VIP) or vesicular acetylcholine transporter (VAchT), and their n
98 T2 along with three cholinergic markers: the vesicular acetylcholine transporter (VAChT), the high-af
99 fy selective high-affinity inhibitors of the vesicular acetylcholine transporter (VAChT), we have int
100 sion of choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT), which are c
101 activity was localized in significantly more vesicular acetylcholine transporter (VAChT)-IR varicosit
110 ChAT), choline transporter 1 (CHT1, SLC5A7), vesicular acetylcholine transporter (VAChT, SLC18A3), an
111 398 in a three-dimensional homology model of vesicular acetylcholine transporter (VAChT, TC 2.A.1.2.1
113 histochemical markers for cholinergic cells (vesicular acetylcholine transporter [VAChT]), tyrosine h
114 histochemical markers for cholinergic cells (vesicular acetylcholine transporter [VAChT]), tyrosine h
116 bodies to glutamic acid decarboxylase (GAD), vesicular acetylcholine transporter (VAT), or the peptid
119 ients with SCZ and explored relationships of vesicular acetylcholine transporter with clinical sympto