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1 th cortical thinning in regions important in attentional control.
2 e cortical thinning in regions important for attentional control.
3 nother (one or two auditory streams) without attentional control.
4 eas, originating in structures important for attentional control.
5 n regions automatically, largely immune from attentional control.
6 ructures are part of a network for voluntary attentional control.
7 nts, as well as the frontoparietal theory of attentional control.
8 s nor one hitherto thought to be involved in attentional control.
9 d" (MD) system, is involved in cognitive and attentional control.
10 standing of the neural mechanisms underlying attentional control.
11 ining bottom-up sensory inputs with top-down attentional control.
12 d neural mechanisms underlying this flexible attentional control.
13 primates showing how thalamus contributes to attentional control.
14 sence, unreliable predictors of reward usurp attentional control.
15 al networks mediating top-down and bottom-up attentional control.
16  to reward cues also exhibit relatively poor attentional control.
17 motional deficit or is secondary to atypical attentional control.
18 ecruitment of regions implicated in top-down attentional control.
19 the development of treatments of deficits in attentional control.
20 fault mode network, which has been linked to attentional control.
21 erhemispheric competition account of spatial attentional control.
22 sistent with a role for ventrolateral PFC in attentional control.
23 ociated with a much broader dysregulation of attentional control.
24 e task designed to fractionate components of attentional control.
25 anging targets that did not require top-down attentional control.
26 gic projections and plays a critical role in attentional control (AC).
27  distraction depends on the current level of attentional control activity in frontal cortex, but the
28 deo game play may be leveraged for enhancing attentional control, allowing greater cognitive flexibil
29 ly wide transfer may be mediated by enhanced attentional control, allowing increased signal-to-noise
30     Psychosocial stress selectively impaired attentional control and disrupted functional connectivit
31 ietofrontal network previously implicated in attentional control and enhancement is also a locus of c
32 A scores, replicated the correlation between attentional control and FA in left hemisphere anterior c
33 ols reveal a significant correlation between attentional control and FA within a ROI in the left hemi
34 dinal relationships identified between early attentional control and learning in academic settings [9
35 nvestigated the interaction between top-down attentional control and multisensory processing in human
36 hese negative biases result from deficits in attentional control and punishment prediction, respectiv
37 ance is discussed, focusing on the nature of attentional control and the effects of practice.
38 refrontal dopamine has specific functions in attentional control and working memory, mediated mainly
39 ate prefrontal cortex that subserve top-down attentional control and working memory.
40 r understanding the neurobiological basis of attentional control, and highlights the risk of medicati
41 working memory, verbal and motor inhibition, attentional control, and IQ--were assessed at ages 8 and
42 e function, episodic memory, working memory, attentional control, and social cognition.
43     MMFT emphasizes interoceptive awareness, attentional control, and tolerance of present-moment exp
44 ndicating that the neural systems supporting attentional control are transient in nature, tending to
45 sually guided responses to more executive or attentional control areas.
46 mine the effects of distractor expectancy on attentional control as well as target and distractor pro
47 e-back task varied greatly in the demand for attentional control because of differences in trial-to-t
48 sk context interacted with the efficiency of attentional control being present for those trials elici
49                               Despite normal attentional control between levels, LPD patients showed
50 ried behavioral consequences for preparatory attentional control beyond lapses of attentional engagem
51 n which the ACC serves not to exert top-down attentional control but instead to detect and signal the
52 plicated in implementing context-appropriate attentional control, but the learning mechanisms underly
53 ults from a single global deficit or whether attentional control can be fractionated, with some aspec
54 tent as younger adults, and that declines in attentional control can limit word recognition.
55  the place code is under the kind of dynamic attentional control characterized in primates as selecti
56 eous actions, as well as three components of attentional control (conflict resolution, set switching,
57  response features, stimulus categories, and attentional control demands.
58 pothesis that freezing is related to altered attentional control during gait, and suggest that differ
59 ents exhibited no significant dysfunction of attentional control during task performance.
60 task to dissociate brain activity related to attentional control from that related to selective proce
61 elated oscillatory brain activity underlying attentional control function.
62               These findings reveal that the attentional control functions of posterior parietal and
63                 In the light of the proposed attentional control functions of ventrolateral PFC and t
64                          Theories of spatial attentional control have been largely based upon studies
65 d to freezing and may play a role in altered attentional control; however, this relationship has not
66 arkinson's disease (PD) is likely related to attentional control (ie, ability to divide and switch at
67                                   Memory and attentional control impairments are the two most common
68 the implementation of proactive and reactive attentional control in dorsal anterior cingulate and dor
69 wever, the neural pathophysiology of altered attentional control in individuals with PD who freeze is
70  Hence we have shown for the first time that attentional control in PD is critically determined by ge
71 ne nucleus connectivity contribute to poorer attentional control in people with PD who freeze.
72    However, the neural mechanisms underlying attentional control in the intact human brain remain unc
73                                         Weak attentional control increases distractibility and causes
74                  A neural network underlying attentional control involves the anterior cingulate in a
75 processing per se is unchanged, but top-down attentional control is compromised in older adults when
76                                        Human attentional control is unrivaled.
77 as identified deficits in tasks that require attentional control like task-switching, and reward-base
78 affective conflicts engage early dissociable attentional control mechanisms and a later common confli
79  right frontal cortex proactively implements attentional control mechanisms to help filter out any di
80 ed to impoverished recruitment of prefrontal attentional control mechanisms to inhibit distractor pro
81 ht to act through interoceptive salience and attentional control mechanisms, but until now conflictin
82 rial covariations to gain insight into these attentional control mechanisms.
83         Our results suggest that a bilateral attentional control network comprising the intraparietal
84 erred to collectively as the fronto-parietal attentional control network, are engaged during attentio
85 CC) has been proposed as part of the brain's attentional control network, but the exact nature of its
86 odulations may be driven by a frontoparietal attentional control network.
87 specially in emotion regulation, reward, and attentional control neural circuitry in BD versus UD dep
88 onal abnormalities in emotion regulation and attentional control neural circuitry in the two depressi
89                                              Attentional control of executive function declines durin
90 cy interaction mechanistically subserves the attentional control of stimulus selection.SIGNIFICANCE S
91 f task context and transient fluctuations in attentional control on neural processes supporting perfo
92 ict segregation between sources and sites of attentional control on the basis of representational pro
93 an auditory target, suggesting that auditory attentional control operates in part by biasing processi
94 are associated with the timing of a specific attentional control operation that suppresses processing
95 ngle mechanism or separate mechanisms during attentional control or selection is not known.
96 rmation, perhaps because of better executive/attentional control over behavior, which requires fronta
97   Prefrontal cortex can exercise goal-driven attentional control over sensory information via cortica
98 y to moment-by-moment changes in preparatory attentional control over spatial selection.
99  indicate that temporal-parietal areas exert attentional control over the neural transformations occu
100 reconciled with neuropsychological models of attentional control, particularly the Supervisory Attent
101 e imaging response during working memory and attentional control processing, and impaired working mem
102 assume or to respond to a non-action-related attentional control question.
103 sistent with the inhibition of TPJ by dorsal attentional control regions during top-down serial visua
104 g of the systems-level mechanisms underlying attentional control remains limited.
105  (FP) areas underlies the representation and attentional control, respectively, of sensory informatio
106 eflect online, bottom-up priming of top-down attentional control settings.
107 ch the contextual cue was translated into an attentional control signal that facilitated behavior.
108 th ongoing sensory information to provide an attentional control signal to FEF.
109 xtual information and translating it into an attentional control signal.
110 e novel evidence for the organization of the attentional control signals at the level of distributed
111 ed by PFC lesions, other sources of top-down attentional control signals to visual cortex must exist
112 provide the source of at least some forms of attentional control signals.
113 th those of unattended objects, via top-down attentional control signals.
114 l representations of stimulus categories and attentional control states.
115  abstract, "internal" event features such as attentional control states.
116  features, stimulus categories, and internal attentional control states.
117 attention involves dynamic interplay between attentional control systems and sensory brain structures
118 between network communities, particularly in attentional control systems, facilitate the integration
119 osed to be an important component of frontal attentional control systems.
120 plicit emotion regulation (EER) and top-down attentional control (TAC).
121 th reduced performance in working memory and attentional control tasks in healthy humans.
122 o train 11-month-old infants on a battery of attentional control tasks.
123 rtex may underlie the functional deficits in attentional control that are symptomatic of stress-relat
124  amygdala and regions implicated in top-down attentional control (the dorsomedial and lateral frontal
125 al frontoparietal systems are key players in attentional control, their distinct contributions remain
126                 The possibility of enhancing attentional control through targeted interventions, be i
127 motions and memory but is also important for attentional control through unknown synaptic mechanisms.
128  potentials indexed feature-general top-down attentional control to one of several coexisting auditor
129 t demonstration of distal transfer following attentional control training in infancy.
130            Reduced effectiveness of top-down attentional control under SD, especially when conditions
131 ortex (rIFC) is specifically associated with attentional control via the inhibition of behaviorally i
132                        Greater impairment of attentional control was associated with reduced volume i
133       The impairment in flexible shifting of attentional control we observed is distinct from lapses
134 anations that posit limits in the sources of attentional control, we show that mechanisms at the site
135 ferent blocks of trials, and fluctuations of attentional control were considered by examining differe
136 ut little is known about the neural basis of attentional control within and between other sensory mod

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