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1 still reinforcing even in the absence of the dopamine transporter.
2 ear accumbens without affecting the level of dopamine transporter.
3 ompete with (123)I-FP-CIT for binding to the dopamine transporter.
4 n the transport of AMPH into the cell by the dopamine transporter.
5 ropyl]piperazine), a specific blocker of the dopamine transporter.
6 increases synaptic dopamine by blocking the dopamine transporter.
7 isorder caused by genetic alterations of the dopamine transporter.
8 o cholesterol/CHS in Drosophila melanogaster dopamine transporter.
9 smitter-sodium symporters, such as the human dopamine transporter.
10 ase (COMT), but negligible expression of the dopamine transporter.
11 se of dopamine through reverse activation of dopamine transporters.
12 xcellent selectivity over both serotonin and dopamine transporters.
13 rine transporter over both the serotonin and dopamine transporters.
14 iors by regulating the level and function of dopamine transporters.
15 both total and synaptic membrane-associated dopamine transporters.
16 amics simulations of a complete model of the dopamine transporter, a NSS protein, we observed a parti
18 asurement of functional parameters including dopamine transporter activity and dopamine release at th
20 in this cohort suggests that higher residual dopamine transporter activity is likely to contribute to
23 de dynamic PET scans were performed to image dopamine transporter and D(2)-like receptors, respective
24 imarily regulate striatal dopamine function--dopamine transporter and D2 receptors--was significantly
25 in the striatum, as well as altered striatal dopamine transporter and D2, but not D1, receptor densit
26 and to relate findings to juvenile levels of dopamine transporter and D2-like receptor availabilities
27 models based on the Drosophila melanogaster dopamine transporter and docked paroxetine to these mode
30 show that betaPEA, like Amph, activates the dopamine transporter and the amine-gated chloride channe
31 The tetracyclic compound inhibits both the dopamine transporter and the serotonin transporter, and
32 cient animals in striatal dopamine levels or dopamine transporter and tyrosine hydroxylase expression
33 s well as striatal intensity measurements of dopamine transporter and tyrosine hydroxylase immunoreac
34 appears to be consistently smaller than the dopamine transporter and vesicular monoamine transporter
35 ulant drug used to treat ADHD), which blocks dopamine transporters and norepinephrine transporters, a
36 the expression of the dopamine D2 receptor, dopamine transporter, and adenosine A1 receptor and decr
37 ne uptake, increases dopamine efflux via the dopamine transporter, and affects the excitability of do
38 re scanned with PET tracers for the membrane dopamine transporter, and dopamine synthesis and storage
39 nding phenylalanines 75 and 155 in the human dopamine transporter are the primary determinants of maz
40 tal structure of the Drosophila melanogaster dopamine transporter at 3.0 A resolution bound to the tr
42 e changes in dopamine D(2)/D(3) receptor and dopamine transporter availability (measured by changes i
44 methylphenidate treatment increased striatal dopamine transporter availability in ADHD (caudate, puta
45 he discrepancies in the literature regarding dopamine transporter availability in ADHD participants (
46 ability prior to treatment but showed higher dopamine transporter availability in ADHD participants t
47 dopamine transporter radioligand) to measure dopamine transporter availability in the brains of 18 ne
48 ipants revealed no significant difference in dopamine transporter availability prior to treatment but
50 icantly correlated with juvenile measures of dopamine transporter availability, whereas no significan
52 ed significant group differences in striatal dopamine transporter binding (all age ranges in caudate
53 kinson's disease (n=15) had reduced striatal dopamine transporter binding and (18)F-FDOPA uptake, com
55 )F-FDOPA uptake comparable with controls and dopamine transporter binding lower than in controls.
56 se (n=25) had greater (18)F-FDOPA uptake and dopamine transporter binding than did individuals with s
59 al subregions, whereas both fluoxetine and a dopamine transporter blocker depress reuptake in striatu
62 lar monoamine transporter type 2 (DTBZ), and dopamine transporter (CFT) within 2 months after nigrost
65 PDM blocked the endogenous basal hDAT (human dopamine transporter) current in voltage-clamped (-60 mV
66 pamine activity is normally regulated by the dopamine transporter (DAT) and catechol-O-methyltransfer
67 nterval timing in mice that underexpress the dopamine transporter (DAT) and have chronically higher l
68 l lines expressing the human plasma membrane dopamine transporter (DAT) and human VMAT ortholog, VMAT
69 ized, and evaluated for binding at the SERT, dopamine transporter (DAT) and norepinephrine transporte
70 anges using Western immunoblotting [striatal dopamine transporter (DAT) and tyrosine hydroxylase (TH)
72 addition, PET was used to examine changes in dopamine transporter (DAT) availability after social hie
73 DG PET provides complementary information on dopamine transporter (DAT) availability and overall brai
75 lucinations, and fluctuations) with striatal dopamine transporter (DAT) availability as assessed with
80 g pregnancy, we imaged striatal and midbrain dopamine transporter (DAT) binding by positron emission
82 reduces Parkinsonian symptoms and increases dopamine transporter (DAT) binding in several animal mod
83 tudy was to examine the relationship between dopamine transporter (DAT) binding in the striatum in in
85 related human alpha-synuclein A53T mutant or dopamine transporter (DAT) blockers also differentially
90 yrosine hydroxylase (TH) immunohistology and dopamine transporter (DAT) density with DAT immunohistol
92 que dopamine uptake inhibitor that binds the dopamine transporter (DAT) differently than cocaine and
93 ple aspects of dopamine signaling, including dopamine transporter (DAT) expression and dopamine reupt
94 anes 9-12 were synthesized as ligands of the dopamine transporter (DAT) for use as (18)F-labeled posi
95 in an enriched condition (EC) have decreased dopamine transporter (DAT) function and expression in me
97 cit are unknown, but may include the reduced dopamine transporter (DAT) functioning reported in BD pa
99 rder caused by loss-of-function mutations in dopamine transporter (DAT) gene, leading to severe neuro
101 ed transport reversal at the closely related dopamine transporter (DAT) has been shown previously to
103 of smell identification testing followed by dopamine transporter (DAT) imaging can accurately and ef
105 e top candidate biomarker were measured, and dopamine transporter (DAT) imaging was performed, to eva
107 de antisera against M5R and the plasmalemmal dopamine transporter (DAT) in single sections through th
108 ligand for the in vivo quantification of the dopamine transporter (DAT) in the striatum and substanti
109 effects on [DA]o at high and low doses, one dopamine transporter (DAT) independent and one DAT depen
110 ry for ubiquitination and endocytosis of the dopamine transporter (DAT) induced by the activation of
124 oltammetry in rats, as well as wild-type and dopamine transporter (DAT) knock-out mice, we demonstrat
125 at MPH self-administration in rats increases dopamine transporter (DAT) levels and enhances the poten
126 te of uptake (Vmax), and membrane-associated dopamine transporter (DAT) levels were reduced, and the
127 mission and mania, whilst increased striatal dopamine transporter (DAT) levels would lead to reduced
128 ures reminiscent of ADHD, including elevated dopamine transporter (DAT) levels, hyperactivity, workin
130 sion of rat SNCA, tyrosine hydroxylase (TH), dopamine transporter (DAT) or the vesicular monoamine tr
135 t binds reversibly with high affinity to the dopamine transporter (DaT) protein, a marker for presyna
137 ynamic membrane trafficking of the monoamine dopamine transporter (DAT) regulates dopaminergic signal
141 ives post translational modifications at the dopamine transporter (DAT) to increase the ability of co
142 A53T mice had increased distribution of the dopamine transporter (DAT) to the membrane that was asso
143 uptake and [(3)H]WIN 35428 binding in human dopamine transporter (DAT) wild-type and mutants with al
144 we link tolerance to cocaine effects at the dopamine transporter (DAT) with aberrant cocaine-taking
146 ed dopamine is regulated by the plasmalemmal dopamine transporter (DAT), an integral membrane protein
147 l terminals expressing TH, the high affinity dopamine transporter (DAT), and the vesicular monoamine
148 pamine transients are slower, independent of dopamine transporter (DAT), increasing the lifetime of e
149 can be identified by their expression of the dopamine transporter (DAT), provide the earliest opportu
151 ch as amphetamine and methamphetamine is the dopamine transporter (DAT), the major regulator of extra
152 on extracellular DA-level regulation by the dopamine transporter (DAT), the membrane expression and
153 ic re-uptake of dopamine is dependent on the dopamine transporter (DAT), which is regulated by its di
154 recessive loss-of-function mutations in the dopamine transporter (DAT), which often affects transpor
156 ction, and reduces cocaine inhibition of the dopamine transporter (DAT), which results in tolerance.
157 ryogenesis (EIIa-Cre) or only in DA neurons (dopamine transporter (DAT)-Cre), we developed constituti
171 hat individuals with genetic variants in the dopamine transporter (DAT, SLC6A) have a higher PD risk
172 ed a quantitative autoradiographic survey of dopamine transporter (DAT; [(3)H]mazindol), D1 receptor
173 mulation, and (2) DA reuptake occurs through dopamine transporters (DAT) in a manner consistent with
175 -biotinyl exchange that native and expressed dopamine transporters (DATs) are palmitoylated, and usin
178 al structures of the Drosophila melanogaster dopamine transporter (dDAT) bound to its substrate dopam
181 expands the clinical phenotypic continuum of dopamine transporter deficiency syndrome and indicates t
185 ncluded three adolescent males with atypical dopamine transporter deficiency syndrome of juvenile ons
187 nder-recognized and our data highlights that dopamine transporter deficiency syndrome should be consi
188 ren with a biochemical profile suggestive of dopamine transporter deficiency syndrome were enrolled f
189 a neurotransmitter profile characteristic of dopamine transporter deficiency syndrome were recruited
190 ave identified a new cohort of patients with dopamine transporter deficiency syndrome, including, mos
193 amine concentrations and decreased levels of dopamine transporter density along with increased brain-
194 n with serum urate level to predict striatal dopamine transporter density among all PPMI participants
195 individuals with physiological reductions in dopamine transporter density consistent with prodromal P
197 SPECT and PET studies investigating striatal dopamine transporter density in ADHD patients (N=169) an
198 the PPMI sample, on progression of striatal dopamine transporter density over the 22-month follow-up
200 son's disease and correlated the findings to dopamine transporter density, measured by (123)I-FP-CIT
202 chostimulants was negatively correlated with dopamine transporter density; density was higher in pati
204 neurochemical (ie, developmental changes in dopamine transporter, dopamine D(2) receptor density, an
205 (a drug that increases dopamine by blocking dopamine transporters) during sleep deprivation versus r
206 ice show comparable tyrosine hydroxylase and dopamine transporter expression in the embryonic and adu
208 lular side toward the unoccupied Na2 site of dopamine transporter following the release of the Na2-bo
214 n which Cre- recombinase expression is under dopamine transporter gene (DAT) promoter control to abla
216 ble number tandem repeat polymorphism in the dopamine transporter gene (DAT1/SLC6A3), which has been
217 unctional tandem repeat polymorphisms of the dopamine transporter gene (DAT1; SLC6A3), which are argu
219 ditions have been linked to mutations in the dopamine transporter gene, including hereditary dopamine
221 face transporter, loss of post-translational dopamine transporter glycosylation and failure of amphet
222 imental verifications in both LeuT and human dopamine transporter (hDAT), we apply the novel method t
224 int mutations in the gene encoding the human dopamine transporter (hDAT, SLC6A3) cause a syndrome of
225 between occupancy and plasma concentration, dopamine transporter IC(50) (the plasma concentration of
226 line and assessed annually, including serial dopamine transporter imaging (DAT-SPECT) and ICD assessm
227 nt with in vivo positron emission tomography dopamine transporter imaging data, and with post-mortem
229 ich to assess sensitivity and specificity of dopamine transporter imaging is a limitation, but defini
235 that cocaine self-administration leaves the dopamine transporter in a "primed" state, which allows f
239 D(3)(-/-) mice also display up-regulation of dopamine transporters in the striatum, suggesting a neur
240 important role in regulating the function of dopamine transporters in the striatum.SIGNIFICANCE STATE
241 molecular dynamics trajectories of the human dopamine transporter, in which multiple spontaneous Na(+
242 nistration in rats produced tolerance to the dopamine transporter-inhibiting effects of cocaine in th
244 n of methylphenidate, as well as a selective dopamine transporter inhibitor, facilitated learning-ind
246 etamine (AMPH), cocaine, and other addictive dopamine-transporter inhibitors (DAT-Is) supports transi
249 hetamine enters dopamine neurons through the dopamine transporter, it stimulates endocytosis of an ex
250 me amphetamine-mediated behaviors persist in dopamine transporter knock-out animals, suggesting the e
253 ximately 80% decrease in brain serotonin and dopamine transporter knockout (DAT-KO) mice showing a fi
254 ar depression imaging studies show increased dopamine transporter levels, but changes in other aspect
256 tremor disorders, baseline imaging with the dopamine transporter ligand [(123)I]ioflupane (DaTscan)
257 nsients, suggesting that the activity of the dopamine transporter limits the detection of these event
258 in the NAc, whereas tyrosine hydroxylase and dopamine transporter mRNA levels and tissue dopamine con
260 sally present, and more severely impacted in dopamine transporter mutants causing infantile-onset rat
261 profiling of rationally chosen serotonin and dopamine transporter mutants with respect to a series of
262 ically reduced in early stage, untreated and dopamine transporter neuroimaging-supported Parkinson's
263 ancy) was determined (4.5 ng/mL) and maximum dopamine transporter occupancy was extrapolated (85%); h
264 valuated by determining the effect of mutant dopamine transporter on dopamine uptake, protein express
265 recombinase under the control of either the dopamine transporter or the engrailed-1 promoters, we ge
266 he human serotonin transporter Tyr175 versus dopamine transporter Phe155 is found to be a strong tool
267 rol of the tyrosine hydroxylase, but not the dopamine transporter, promoter exhibit dramatic non-DA c
268 measurement of the binding potential of the dopamine transporter radioligand (123)I-ioflupane in mou
269 tron emission tomography and [(11)C]cocaine (dopamine transporter radioligand) to measure dopamine tr
271 ding the molecular determinants of serotonin/dopamine transporter selectivity and for the development
272 h PTE and genetic susceptibilities including dopamine transporter, serotonergic synaptic function, an
273 nes and barbiturates), and interactions with dopamine transporter, serotonin transporter, and vesicul
274 isms in the genes encoding the serotonin and dopamine transporters (SERT: 5HTTLPR plus rs25531; DAT1
276 ss was smaller than the decrease in striatal dopamine transporter signal measured by dopamine transpo
277 (123)I-FP-CIT scan, the mean total striatal dopamine transporter signal was decreased by 45% and the
278 atal dopamine transporter signal measured by dopamine transporter single photon emission computed tom
279 d loss of dopaminergic neurons assessed with dopamine transporter single photon emission computerized
280 rend was found for the carriers allele 9R of dopamine transporter SLC6A3 40 bp variable tandem repeat
281 genes for dopamine beta-hydroxylase and the dopamine transporter SLC6A3 may play a role in migraine
282 dren with mutations in the gene encoding the dopamine transporter (SLC6A3) with the aim to improve cl
285 paminergic subpopulation using a fluorescent dopamine transporter substrate (ASP(+) [4-(4-diethylamin
286 sponsive FFN probe, FFN102, which as a polar dopamine transporter substrate selectively labels dopami
287 zation, insolubility and complexing with the dopamine transporter, suggesting a physiological mechani
288 nding residue found in the noradrenaline and dopamine transporters, switched the SEC24 isoform prefer
289 ethamphetamine (METH) is a substrate for the dopamine transporter that increases extracellular dopami
290 receptors, an increased translocation of the dopamine transporter to the plasma membrane and a corres
291 SPECT) with technetium 99m ((99m)Tc) tropane dopamine transporter (TRODAT)-1 were performed for furth
292 ed high levels of DOPA decarboxylase and the dopamine transporter, two markers expressed by fully mat
294 , we separated isolated synaptosomes bearing dopamine transporters using immunomagnetic beads and com
295 trast, ubiquitination and endocytosis of the dopamine transporter was dependent on NEDD4-2 in all cel
296 ptor (MOR), preproenkephalin (PENK), and the dopamine transporter was evaluated in the hypothalamus a
297 At the doses evaluated, occupancy of the dopamine transporter was significantly higher than that
298 nal consequences of missense variants on the dopamine transporter were evaluated by determining the e
300 is essential for dopamine synthesis, and the dopamine transporter, which is required for dopamine upt
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