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1 issemination via the mesenteric lymph nodes (indirect pathway).
2 ect pathway) or the lateral globus pallidus (indirect pathway).
3 irect pathway with the functionally opposing indirect pathway.
4 eas motor cortex preferentially targeted the indirect pathway.
5  in humans of the basal ganglia's inhibitory indirect pathway.
6 g the inhibitory output of the basal ganglia indirect pathway.
7 in exponentially growing cells via a second, indirect pathway.
8  motor structures prevents movements via the indirect pathway.
9 h reduced pallidothalamic inhibition via the indirect pathway.
10 t of two enzymes that operate via a separate indirect pathway.
11 sence of the living bacteria and followed an indirect pathway.
12 oduction is dependent on T-cell help via the indirect pathway.
13 o address the functions of the NMDA-R in the indirect pathway.
14 neurons that serves as a simple relay in the indirect pathway.
15  direct pathway without affecting LTP in the indirect pathway.
16 selective inhibition through both direct and indirect pathways.
17 um spiny neurons of the accumbens direct and indirect pathways.
18 f distinct terminal fields via the direct or indirect pathways.
19 ribute cortical input between the direct and indirect pathways.
20 n pressures moving along multiple direct and indirect pathways.
21 the emergence of diseases through direct and indirect pathways.
22 ough complex mechanisms involving direct and indirect pathways.
23 d have functional reciprocal connections via indirect pathways.
24 xert effects through activation of direct or indirect pathways.
25 e motor functions of the striatal direct and indirect pathways.
26 emical and electrical synapses as well as by indirect pathways.
27 m two main efferent pathways, the direct and indirect pathways.
28  monitor striatal output from the direct and indirect pathways.
29 mpact neural clusters in both the direct and indirect pathways.
30 t also in the macroenvironment via direct or indirect pathways.
31 l medium spiny neurons forming the direct or indirect pathways.
32  network tools by distinguishing direct from indirect pathways.
33 he striatopallidal neurons of the so-called 'indirect' pathway.
34                       In the latter two-step indirect pathway, a non-discriminating aspartyl-tRNA syn
35  strengthening of El Nino conditions through indirect pathways, a consistent result in most estuaries
36 ); instead, Gln-tRNA(Gln) is produced via an indirect pathway: a glutamyl-tRNA synthetase (GluRS) fir
37 ation gives rise to stronger activity in the indirect pathway accompanied by decreased dendritic spin
38 striatal input and boosted cortically driven indirect pathway activity.
39                                          The indirect pathway allows an efficient time-based separati
40 way, naive and memory responses, whereas the indirect pathway and 'pure' memory responses are more in
41 ssed recipient alloantigen presented via the indirect pathway and not in response to cross-dressed MH
42 n alters neuronal activity in the direct and indirect pathways and leads to increased synchrony in th
43 n: one going through a CO* intermediate (the indirect pathway) and another that oxidizes methanol dir
44 way) or only as self-restricted allopeptide (indirect pathway) and then assessing the alloantibody re
45 xpression, by increasing excitability in the indirect pathway, and the increased propensity for tic l
46  cluster organization between the direct and indirect pathways, and cluster activities from both path
47 ur findings indicate that the NMDA-Rs of the indirect pathway are essential for habituation, action s
48 in serial order, even though both direct and indirect pathways are active during movement initiation,
49   These observations of competing direct and indirect pathways are consistent with classical predicti
50 spiny neurons (MSNs), in both the direct and indirect pathways are generated in the lateral ganglioni
51 on tuning in MT neurons, suggesting that the indirect pathways are important in the recovery of depth
52                 For instance, the direct and indirect pathways are modulated through dopamine D1 and
53 d midbrain targets similar to the direct and indirect pathways arising from the internal and external
54 fects is consistent with deactivation of the indirect pathway as predicted by preclinical studies; an
55 ration of anti-K(d)-specific T cells via the indirect pathway as well as of non-K(d)-reactive, recipi
56 rs of medium spiny neurons signaling via the indirect pathway, associated with behavioral inhibition.
57 iber-optic cannulae were implanted above the indirect pathway axon terminal field in the dlVP, or the
58 ught to arise from increased efficacy of the indirect pathway basal ganglia circuit, relative to the
59 the gain on signals driving both direct- and indirect-pathway basal ganglia circuits.
60 e changes in synaptic strength of direct and indirect pathways between the cortex and spinal cord in
61 es clearance of HDL cholesteryl ester via an indirect pathway, but has no effect on total plasma chol
62 ies implicate preferential activation of the indirect pathway by host DCs.
63 n-wide effects of stimulating the direct and indirect pathway by optogenetic activation of D1 and D2
64  express FcgammaRs, there is likely to be an indirect pathway by which FcgammaRIII on some other cell
65 her, the results support the existence of an indirect pathway by which iBRB permeability is increased
66                                 However, the indirect pathway can also promote the generation of regu
67       Our results reveal that the direct and indirect pathways can each bidirectionally control movem
68 allograft rejection.Although both direct and indirect pathway CD4 T cells appear active immediately a
69 y after transplantation, it has emerged that indirect pathway CD4 T cells are likely to be the domina
70 ocessed by recipient DCs for presentation to indirect pathway CD4(+) T cells, resulting in abortive a
71                Recipients reconstituted with indirect-pathway CD4 T cells developed long-lasting IgG
72 thway) allows linked help to be delivered by indirect-pathway CD4 T cells for generating destructive
73 hymal cells and suggest a mechanism by which indirect-pathway CD4 T cells provide help for generating
74                               The ability of indirect-pathway CD4 T cells to provide this help remain
75 essed peptide alloantigen for recognition by indirect-pathway CD4 T cells.
76 cause this facilitates linked recognition by indirect-pathway CD4 Th cells.
77 ay performs fast action cancellation and the indirect pathway competitively constrains execution sign
78                      Here, we found that the indirect pathway controls response initiation without af
79 whether by direct "off-target" effects or by indirect "pathway cross-talk" effects.
80    Potentiation of glutamatergic inputs onto indirect pathway D2-MSNs was associated with resilience
81  argue against a protective role of accumbal indirect pathway D2Rs in alcohol consumption but emphasi
82 medium spiny neurons belong to the direct or indirect pathways determines the form of spike timing-de
83 iatonigral direct pathway vs striatopallidal indirect pathway) differ in their input from IT-type and
84            In models of Parkinson's disease, indirect-pathway eCB-LTD is absent but is rescued by a D
85  hyperdirect pathway cortical excitation and indirect pathway external globus pallidus (GPe) inhibiti
86 ion in which co-activation of the direct and indirect pathways facilitate appropriate, while inhibiti
87                    These findings suggest an indirect pathway for Bcl-2 over-expression in PhIP-induc
88 ally, regions consistent with the inhibitory indirect pathway for which there is scant functional evi
89 over time in an imbalance between direct and indirect pathways for properly focusing movement.
90 tal projection systems--so-called direct and indirect pathways--form the functional backbone of the b
91                      Instead, we describe an indirect pathway from Area X to midbrain dopaminergic ne
92                                          The indirect pathway from the amygdala to pOFC via MDmc may
93 ally, we provide evidence consistent with an indirect pathway from the cerebellum to the basal gangli
94 h an imbalanced activation of the direct and indirect pathways, have been linked to the hypokinetic m
95 s) in the striatum--the so-called direct and indirect pathways--have opposing effects on movement: ac
96  and striatopallidal MSNs to the inhibitory, indirect pathway (iMSNs).
97                         The retention of the indirect pathway in B. subtilis and B. halodurans likely
98 ndosomal compartment at least in part via an indirect pathway in which it is internalized from the ce
99 central auditory synapses through direct and indirect pathways in an age-dependent fashion.
100 scribed to imbalances between the direct and indirect pathways in the basal ganglia circuitry.
101 o exocytic sites at the plasma membrane, and indirect pathways in which TCs that are not in proximity
102 ective optogenetic control of the direct and indirect pathways, in combination with single-unit recor
103 agrass seedlings through multiple direct and indirect pathways: increased stress, reduced establishme
104 puts onto individual MSNs of both direct and indirect pathway: individual EGFP-positive structures re
105  facilitates movement and activation of the 'indirect' pathway inhibits movement.
106 basal ganglia, the so-called hyperdirect and indirect pathways, interact within the subthalamic nucle
107 CL-6 and BAZF regulate HPC homeostasis by an indirect pathway involving CD8 T cells.
108 volutionary questions, including whether the indirect pathway is a recent evolutionary invention, as
109                                          The indirect pathway is believed to be longlasting, and is g
110             An improved understanding of the indirect pathway is likely to bring important benefits t
111         It is concluded that activity of the indirect pathway is limited by the nonphotochemical redu
112 r T-cell recognition of antigens through the indirect pathway is necessary for the perpetuation of GV
113                                          The indirect pathway is only evident when GABA(A) receptors
114                                         This indirect pathway is required for hippocampal theta synch
115 strate that activity in either the direct or indirect pathway is sufficient to produce specific and s
116 m spiny neurons (MSNs) in the direct and the indirect pathways is essential for normal striatal funct
117 ential dopamine modulation of the direct and indirect pathways is present in non-mammalian species.
118 ng dopaminergic modulation of the direct and indirect pathways is present in one of the phylogenetica
119 manipulation of the function of the striatal indirect pathway may be a useful therapeutic target for
120                                  This latter indirect pathway may be especially important for evoluti
121 r nuclei upon TT activity through direct and indirect pathways may account for multifunctional roles
122                               Therefore, the indirect pathway measurements reflect a distinct aspect
123 sect the mechanisms underlying BG direct and indirect pathway-mediated control of the mesencephalic l
124                       In contrast, effective indirect pathway-mediated motor suppression was most str
125 e differentially expressed in the direct and indirect pathway medium spiny neurons (dMSNs and iMSNs,
126 the opposing relationship between direct and indirect pathway medium spiny neurons (MSNs), in additio
127 mpanied by decreased dendritic spines on the indirect pathway medium spiny projection neuron, indicat
128 ) receptors, depolarized both the direct and indirect pathway medium spiny projection neurons (MSNs).
129 time that a specific deletion of inhibitory, indirect pathway medium-sized spiny neuron (iMSN) NMDA-R
130 le-cell recordings from striatal direct- and indirect-pathway medium spiny neurons (dMSNs and iMSNs)
131 tive deletion of DA D2 receptors (D2Rs) from indirect-pathway medium spiny neurons (iMSNs) is suffici
132   Here we show that excitatory synapses onto indirect-pathway medium spiny neurons (MSNs) exhibit hig
133 ate their regulation of striatal direct- and indirect-pathway medium spiny neurons (MSNs).
134 tors, which are highly expressed by striatal indirect-pathway medium spiny neurons (MSNs).
135 vo, using optogenetic control of direct- and indirect-pathway medium spiny projection neurons (MSNs),
136 her G-protein or beta-arrestin signaling in 'indirect pathway' medium spiny neurons (iMSNs), because
137 nigral (direct pathway) and striatopallidal (indirect pathway) medium spiny neurons (MSNs) and its re
138 ion markers, suggesting that both direct and indirect pathways might contribute to the observed effec
139 n NAc in vivo and found that direct (but not indirect) pathway MSN expression enhances behavioral res
140 de feedforward inhibition to both direct and indirect pathway MSNs and are important in sculpting the
141   These findings demonstrate that direct and indirect pathway MSNs are similarly innervated by cortic
142 orylation at S563 was significantly lower in indirect pathway MSNs compared with those in the direct
143                     Kv2.1 in both direct and indirect pathway MSNs exhibits markedly lower levels of
144 ine receptor subtypes, markers of direct and indirect pathway MSNs, respectively.
145 t prominent juxtaposed Kv2.1:RyR clusters in indirect pathway MSNs.
146 ut not core, D2 dopamine receptor-expressing indirect pathway MSNs.
147 y of immature spines in D1 direct but not D2 indirect pathway MSNs.
148  for the increased GABA synaptic activity of indirect pathway MSNs.
149 BA synaptic activity impinges principally on indirect pathway MSNs.
150 terminals form synapses with both direct and indirect pathway MSNs.
151 and thalamus was similar for both direct and indirect pathway MSNs.
152 afferents in their innervation of direct and indirect pathway MSNs.
153 ression of GABA release onto both direct and indirect pathway MSNs.
154 ion of collateral transmission from multiple indirect-pathway MSNs (iMSNs) potently inhibits action p
155 ast-spiking (FS) interneurons and direct- or indirect-pathway MSNs after dopamine depletion with 6-OH
156 athways mediating eCB production in striatal indirect-pathway MSNs and found that both pathways were
157                      Bilateral excitation of indirect-pathway MSNs elicited a parkinsonian state, dis
158                   In contrast, deletion from indirect-pathway MSNs had no effect on any measure of be
159                                    Moreover, indirect-pathway MSNs selectively express endocannabinoi
160  striatum may lead to increased synchrony of indirect-pathway MSNs that contributes to pathological n
161 ase and induction of long-term depression at indirect-pathway MSNs, but not direct-pathway MSNs.
162 eferentially target direct-pathway MSNs over indirect-pathway MSNs, suggesting a potential mechanism
163 geted whole-cell recordings from direct- and indirect-pathway MSNs, we demonstrate that A(2A) recepto
164 idual FS cells doubled their connectivity to indirect-pathway MSNs, whereas connections to direct-pat
165  glutamate and DA transmission in direct and indirect pathway MSSNs.
166 nd that coordinated activities of direct and indirect pathway neural clusters are required for normal
167 s rapid production of excitatory synapses on indirect pathway neurons (iSPNs) required the activation
168 d GRK5 are similarly expressed in direct and indirect pathway neurons in the rat striatum.
169 re selectively expressed in either direct or indirect pathway neurons, CNO did not change acute locom
170 tone, via D2 and A2a receptor, in direct and indirect pathway neurons, respectively, to have any sign
171 orally observed synergism between the direct/indirect pathway neurons.
172 ired the functionality of direct-pathway and indirect-pathway neurons and disrupted the behavioral pe
173 e Gq-protein activation in direct-pathway or indirect-pathway neurons produced an enhancement or a de
174 (resulting in longer-lasting deactivation of indirect-pathway neurons).
175 ssion of excitatory synaptic transmission in indirect pathway nucleus accumbens medium spiny neurons.
176 recognize allogeneic MHC class I through the indirect pathway of Ag presentation are rendered toleran
177 irect Ag presentation and thereby favors the indirect pathway of alloreactivity.
178 pacity to present antigen to T cells via the indirect pathway of allorecognition and the generation o
179  activation of anti-donor CD4 T cells by the indirect pathway of allorecognition, a phenomenon that r
180                                          The indirect pathway of allorecognition, in which cells of t
181 ding to the class I MHC mismatch through the indirect pathway of allorecognition.
182  antigens through the direct rather than the indirect pathway of antigen presentation promotes tolera
183 te the consecutive reactions of the two-step indirect pathway of Cys-tRNA(Cys) synthesis (tRNA-depend
184 eurons that occupy a central position in the indirect pathway of the basal ganglia.
185 cells provides a link between the direct and indirect pathways of alloantigen presentation and sugges
186 nderstanding the evolution of the direct and indirect pathways of allorecognition following tissue tr
187 fect of chronic aspiration on the direct and indirect pathways of allorecognition.
188 ncoherent simultaneous use of the direct and indirect pathways of Asn and Asn-tRNA(Asn) formation.
189                                   Direct and indirect pathways of basal ganglia were concomitantly ac
190 input to the striatum between the direct and indirect pathways of the basal ganglia (BG).
191                               The direct and indirect pathways of the basal ganglia have been propose
192 nging to two neural circuits (the direct and indirect pathways of the basal ganglia), subpopulations
193 titive behaviors analogous to the direct and indirect pathways of the basal ganglia.
194  mediators independent, thereby deactivating indirect pathways of the mediators.
195  spiny neurons (MSNs) in both the direct and indirect pathways of the mouse nucleus accumbens (NAc) r
196  is differentially encoded in the direct and indirect pathways of the striatum.
197                                          The indirect pathway operates under normo- or hypercapnic co
198      These findings indicate that direct and indirect pathways originate in the caudal brainstem that
199 to the classic theory emphasizing the direct-indirect pathways, our data suggest that deranged cortic
200 m plasticity capable of sculpting direct and indirect pathway output.
201  directly, we show a previously undescribed, indirect pathway passing through inferior parietal corte
202 me destabilizes TPP1 through both direct and indirect pathways possibly involving TPP1-interacting pr
203 ptogenetic activation of striatal direct and indirect pathway projection neurons produced diverse cel
204 ntingent from axon collaterals of direct and indirect pathway projection neurons.
205 neural activities in the striatal direct and indirect pathways promote and inhibit movement, respecti
206 k to the apical membrane, hepatocytes use an indirect pathway: proteins are delivered to the basolate
207 d phosphorylation between MSNs in direct and indirect pathways provide a cell- and circuit-specific m
208                                       In the indirect pathway, reduced O2 reacts with H(+) and additi
209 stimulator cells, suggesting the presence of indirect pathway regulatory cells whose activity depende
210 activating bitter-sensitive cells versus the indirect pathway represented by the inhibition of sugar
211 se from the NAc, and most likely involves an indirect pathway requiring alpha3beta4 nAChR.
212 e 2 routes are referred to as the direct and indirect pathways, respectively.
213 n be opened or closed by striatal direct and indirect pathways, respectively.
214 ne D1 or D2 receptors, which form direct and indirect pathways, respectively.
215  striatal projection neurons, the direct and indirect pathways, respectively.
216 role of 2-AG signaling in striatal direct or indirect pathways, respectively.
217 ation and suppression through the direct and indirect pathways, respectively.
218                                              Indirect pathway responses were heterogeneous.
219 ast, loss of ERK/MAPK signaling in D2R-MSNs (indirect pathway) resulted in a profound hyperlocomotor
220                                          The indirect pathway results from recipient DCs processing a
221              Cross-sectional analysis of the indirect pathway revealed a spectrum in T-regulatory:T-e
222                 We find no evidence that the indirect pathways selectively target different functiona
223 athway (non-self HLA on donor cells) and the indirect pathway (self-restricted presentation of donor
224 hether these neurons belong to the direct or indirect pathways.SIGNIFICANCE STATEMENT We examined the
225 basal ganglia circuits, affecting direct and indirect pathways simultaneously.
226 1-Cre (direct-pathway-specific) and A2A-Cre (indirect-pathway-specific) mice.
227 ectively increased excitability of NAc shell indirect pathway spiny projection neurons (iSPNs) and al
228 pathway spiny projection neurons (dSPNs) and indirect pathway spiny projection neurons (iSPNs) is dis
229 ns differentially affect striatal direct vs. indirect pathway spiny projection neurons, their reduced
230             Activity in striatal direct- and indirect-pathway spiny projection neurons (SPNs) is crit
231 of D(1) and D(2) DA receptors in direct- and indirect-pathway spiny projection neurons.
232 atially compact, organization of direct- and indirect-pathway SPN activity that maps action space ind
233 o method to specifically measure direct- and indirect-pathway SPN activity, using Cre-dependent viral
234 and synaptic adaptations specifically within indirect pathway SPNs (iSPNs).
235                                              Indirect pathway SPNs, which are more vulnerable in HD,
236 promoting direct pathway SPNs to fire before indirect pathway SPNs.
237 ectively measure the activity of direct- and indirect-pathway SPNs in freely moving animals.
238  to facilitate movement, whereas activity of indirect-pathway SPNs is presumed to inhibit movement.
239 eases in neural activity in both direct- and indirect-pathway SPNs when animals initiated actions, bu
240 ivity was increased similarly in direct- and indirect-pathway SPNs, and action potential-dependent ac
241 ffects on "direct pathway" SPNs (dSPNs) and "indirect pathway" SPNs (iSPNs); their firing rates becam
242 vered that a select population of so-called "indirect pathway" SPNs not only fire at abnormally high
243 /Scgn- interneurons preferentially targeted 'indirect pathway' SPNs.
244 icantly modulated neural coupling within the indirect pathway, strengthening MD thalamus-OFC connecti
245          Contrary to expectation, direct and indirect pathway striatal spiny projection neurons respo
246 s, bidirectionally controlled by direct- and indirect-pathway striatal projection neurons (dSPNs and
247  action potential firing in both direct- and indirect-pathway striatal projection neurons through ves
248 f neurons that form synapses with direct- or indirect-pathway striatal projection neurons.
249  that endocannabinoid-mediated depression of indirect-pathway synapses has a critical role in the con
250    To investigate the role of donor-specific indirect pathway T cells in renal transplant tolerance,
251                                The antidonor indirect pathway T effector response increased across pa
252 ONO < SI < CR; p < 0.0001) whereas antidonor indirect pathway T regulatory response decreased (TOL >
253  intravenously, they decrease the direct and indirect pathway T-cell responses and prolong heart allo
254 rons, respectively, revealed that 47% of the indirect pathway terminals and 36% of the direct pathway
255 n GABAergic terminals), and through a novel, indirect pathway that involved the increased release of
256 ous nodes of the TPN and DMN, and through an indirect pathway that links the TPN and DMN through node
257 site and weaker effects on 2DG uptake in the indirect pathway that were attributed to crossed inhibit
258 n is conveyed to the pallium through complex indirect pathways that originate in the nucleus electros
259 icipate in two parallel circuits, direct and indirect pathways that subserve distinct behavioral func
260 hus, differs markedly from the "direct" and "indirect" pathways that regulate the pallidal (e.g., glo
261                                       In the indirect pathway, the GABA(B) receptor antagonist reduce
262 ogeneous structure in the motor-suppressing "indirect-pathway," the GPe consists of a number of disti
263 urons giving rise to the striatopallidal or "indirect" pathway, they have been implicated in sleep, a
264 ion of D2R-expressing neurons suppresses it (indirect-pathway), this suggests that cocaine's rewardin
265 thway and decreasing the excitability of the indirect pathway, this organization may be conserved as
266 ists reduce excitatory synaptic drive on the indirect pathway through CB(1) receptor signaling, thus
267 rojections to the superior colliculus and an indirect pathway through the basal ganglia.
268 partitions between the direct pathway and an indirect pathway through the early endosome.
269  direct effects through thermoregulation and indirect pathways through trophic interactions.
270 eurons that form the so-called 'direct' and 'indirect' pathways through the basal ganglia.
271 ulation of chromatin structure represents an indirect pathway to downregulate transcription, and thei
272 athway to facilitate intended locomotion and indirect pathway to inhibit unwanted locomotion.
273  MT neurons, which has been attributed to an indirect pathway to MT from the superior colliculus.
274 t that low-value signals are sent by the CDt-indirect pathway to suppress saccades to valueless objec
275 he NAcore and NAcore projections through the indirect pathway to the dlVP as critical for cocaine-plu
276                               Inhibiting the indirect pathway to the dlVP, but not the direct pathway
277 ated cocaine seeking include outputs via the indirect pathway to the dorsolateral subcompartment of t
278       Overall, our findings suggest that the indirect pathways to MT primarily convey modality-specif
279 he selective contributions of the direct and indirect pathways to striatal motor behaviors.
280 ediated predominantly by the hyperdirect and indirect pathways to subthalamic nucleus, respectively,
281  tic learning, by shifting plasticity in the indirect pathway toward long-term potentiation (and poss
282                                          The indirect pathway transporting uncontrolled releases of P
283 rom direct polymerase corruption, or from an indirect pathway triggered by increased protein turnover
284 involve both direct pathways via the Sp5 and indirect pathways via the DR and LC.
285 are 'direct' effects of light on affect, an 'indirect' pathway via altered sleep-wake timing has been
286                                          The indirect pathway was active in all groups except twins b
287 sion, the rate of hydrogen production by the indirect pathway was increased in conditions, such as nu
288 ry items, the connectivity of the direct and indirect pathway was predictive of WMC.
289 tion, such adverse reactions can occur by an indirect pathway when the TCR interacts with self-MHC mo
290 ' HRQoL through a direct pathway, but via an indirect pathway where self-management was a mediator (-
291 by tRNA-dependent mechanism using a two-step indirect pathway, where O-phosphoseryl-tRNA synthetase (
292 ation of the signal-to-baseline ratio in the indirect pathway, which better account of known electrop
293 lamus and forms the origin of the direct and indirect pathways, which are distinct basal ganglia circ
294 , of MLR glutamatergic neurons by direct and indirect pathways, which is required for bidirectional c
295 basal ganglia, in parallel to the direct and indirect pathways, which select actions.
296 ate in a functional analog of the mammalian "indirect" pathway, which may oppose the effects of the d
297  ganglia output nuclei via the "direct" and "indirect" pathways, which can be distinguished by their
298      Here we have reversibly inactivated the indirect pathways while recording from MT neurons and me
299 r, recent evidence convincingly connects the indirect pathway with chronic rejection, including antib
300                                     In COX-1 indirect pathways, women experienced the same or more pl

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