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1 er the curve (AUC) = 0.87-0.91 for different brain regions).
2 ese devices limit their access to one, small brain region.
3 with an elevated DNA damage response in this brain region.
4 frequency of iES-elicited effects in a given brain region.
5 o both peripheral sensory organs and central brain regions.
6 ehaviors, implying the involvement of higher brain regions.
7 rontal cortex) and subcortical (hippocampus) brain regions.
8 ges and persists throughout adulthood across brain regions.
9 ferences in afferent connectivity with other brain regions.
10 ditioning, as well as c-Fos expression in 14 brain regions.
11 g significantly prevents penetration to deep brain regions.
12 nteractions between cortical and subcortical brain regions.
13 nted both increase and decrease in different brain regions.
14 c tractography (MRtrix 3.0) between pairs of brain regions.
15 nd parameters for a wide range of probes and brain regions.
16 ted with a blast explosion impacts different brain regions.
17 peech comprehension are mediated by the same brain regions.
18 f AMPARs into spines, including in non-motor brain regions.
19 ation in ways that varied with attention and brain regions.
20 Channels were grouped in 30 brain regions.
21 ation of multiple modules can cover extended brain regions.
22 ehavior requires the interaction of multiple brain regions.
23 of the major transcripts in disease-relevant brain regions.
24 alized astrocyte subtypes between and within brain regions.
25 xpression networks constructed from 10 human brain regions.
26 he nervous system, including in the striatal brain regions.
27 ponents that can be mapped onto well-defined brain regions.
28 areas but is also heavily innervated by both brain regions.
29 oid burden and cortical thinning in specific brain regions.
30 ng from within the CeA itself or other input brain regions.
31 independent studies, covering diverse human brain regions.
32 of AMPA-type glutamate receptors in the same brain regions.
33 without large-scale synchronization between brain regions.
34 es revealed this effect to occur in cortical brain regions.
35 identify times of memory reactivation across brain regions.
36 s with exquisite specificity within distinct brain regions.
37 l as their functional diversity in different brain regions.
38 ling of gene expression programs in discrete brain regions.
39 on confidence and involved modality-specific brain regions.
40 ring mode experimentally observed in several brain regions.
41 hat [(11)C]13 accumulated in the mGluR2-rich brain regions.
42 d to compute functional connectivity between brain regions.
43 anges in serotonergic innervation of rostral brain regions.
44 source of dopamine, especially to the limbic brain regions.
45 ext, we used PET/MRI to define uptake in six brain regions.
46 ersist or spontaneously resolve in different brain regions.
47 functional links between auditory and motor brain regions.
48 encoding NPE have been reported in multiple brain regions.
49 ostructure (cellular density) of subcortical brain regions.
50 ross anatomically and functionally connected brain regions.
51 e networks connecting anterior and posterior brain regions.
52 prediction of myelin distribution over large brain regions.
53 odel recovers functional relationships among brain regions.
54 ibuted across multiple, strongly interacting brain regions.
55 performance to HC while utilizing different brain regions.
56 junction in frontal, parietal, and temporal brain regions, a typical localization of CTE tauopathy.
57 n of regional volumes) are reported for each brain region across the sample used to generate the atla
58 ly available expression data from postmortem brain regions across humans, chimpanzees, and rhesus mac
61 etabolism and neurotransmission in different brain regions after SCI, which present evidence for the
63 onger in the hippocampus than in three other brain regions (amygdala, anterior cingulate, and prefron
64 ptional profiles in cortical and subcortical brain regions and brain networks of structural covarianc
67 e the association between intact or lesioned brain regions and cognitive processes or neurological de
69 While associations between individual human brain regions and environmental or genetic factors have
70 ess intracellular tau aggregates in multiple brain regions and exhibit sensorimotor and motor learnin
71 re expressed prenatally in many ASD-relevant brain regions and fall into two categories: broadly expr
72 radiologist blind to the diagnosis scored 12 brain regions and generated a lesion profile for each MR
73 e useful resources for the classification of brain regions and identification of biomarker genes for
74 lasts are transcriptionally distinct between brain regions and identify a regionally localized pial s
80 tein 2 (NPAS2) is enriched in reward-related brain regions and regulates reward, but its role in SU i
81 is known to process information from various brain regions and relay it to other brain regions, servi
82 e loss of inhibitory populations in multiple brain regions and results in neurologic deficits such as
86 sed previously available SDM data from other brain regions and we applied this ratio as a conversion
87 ciated with faster rates of atrophy of other brain regions and whether there is evidence for protein-
88 e number and location of microbleeds in each brain region, and multiple linear regression was used to
89 heterogeneity between cortical measures and brain regions, and 160 genome-wide significant associati
90 SNP-level data found enrichment in multiple brain regions, and eQTL analyses highlighted an inversio
91 human AD cohorts, encompassing six cortical brain regions, and integrate with multi-scale datasets c
93 e of volumetric MRI changes for a variety of brain regions; and (ii) understand the mechanism through
94 d microglia/astrocytes) from three different brain regions (anterior cingulate cortex, dorsolateral p
96 manipulating epigenetic enzymes in specific brain regions are beginning to build causal links betwee
99 ether, our findings indicate that particular brain regions are more vulnerable to TS genetic and horm
100 ion, the patterns of ABS events in different brain regions are similar to each other and are more com
101 f functional interactions across distributed brain regions are suggested to provide a scaffold for th
102 ing among the human, rat, and mouse in these brain regions as well as between the different brain reg
104 ences in connectivity or activity of certain brain regions) as well as extrinsic factors (infections)
105 onal imbalance between frontal and posterior brain regions, as compared to HC: (1) Archetypal MPDs (6
106 flex-PCB cables for recording from multiple brain regions, as well as a facilitated method for coati
107 is prominent within the nucleus accumbens, a brain region associated with mood regulation; however, t
109 , as a formal index of agency, we found that brain regions associated with directed exploration and s
110 that the passage of time was associated with brain regions associated with external attention decreas
111 l early in gestation perturbs development of brain regions associated with motor control in a manner
112 , suggesting impaired neural activity within brain regions associated with the visual processing of m
113 during aging was consistent among different brain regions at the gene level and associated with life
114 fically, functional connectivity patterns of brain regions between and within networks appear to play
116 at) fluorescence in TH-ir neurons across all brain regions, but the most striking colocalization was
117 h volumes of serotonergic axons in all major brain regions can be generalized to map and quantify axo
119 antitative measure of the frequency at which brain regions change their allegiance from one functiona
120 ncer, gliomas may be expected to localize to brain regions characterized by functional hubness, stem-
121 t mode network (DMN) is a distributed set of brain regions coactivated during resting states that is
122 spawning had higher aromatase levels in all brain regions compared to females with lower reproductiv
123 behavioral performance in various tasks and brain regions consistently across 4 monkeys (1 female an
126 e alterations in DS are thought to depend on brain regions critical for learning and memory such as t
128 No stimulation or rTMS on a nonrelevant brain region did not have the same interfering effect on
129 cialized astrocytes, but astrocytes in other brain regions do not generate neurons under physiologica
130 ng perspectives, assessing whether co-active brain regions during task states tend to increase or dec
131 ween the hypothalamus and the reward-related brain regions during water infusion relative to glucose
132 l distribution, appearing more often in some brain regions (e.g. the insula) compared to others (e.g.
134 thin the bilateral dorsal mid-insula, but no brain region exhibited a consistent preference for any i
136 d high-order texture radiomic features in 83 brain regions for the test and evaluation datasets was a
137 n postmortem samples of two frontal cortical brain regions from 214 control subjects aged 20-90 years
138 computational phenotyping method that groups brain regions from MRI and subsets of neuropsychological
140 Analyzing expression data from multiple brain regions from the Genotype-Tissue Expression projec
142 rdinated neuronal ensembles-coupling distant brain regions, gating processing windows, and providing
143 Adult neural stem cells, located in discrete brain regions, generate new neurons throughout life.
144 that spontaneous activations within a given brain region have comparable functional and physiologica
145 t, although its effects on socially relevant brain regions have been extensively studied, OT neuron a
146 s varied as a function of children's age and brain region, highlighting the importance of a developme
147 organization of the vascular network across brain regions, highlighting local adaptations and functi
148 rmation about stimuli-induced changes within brain regions; however, this analysis remains time inten
149 ypothalamus (VPH) is an anatomically complex brain region implicated in arousal, reproduction, energy
152 eory and tools by revealing that activity in brain regions implicated in anticipatory affect at the o
154 ation of serotonergic gene expression across brain regions implicated in emotion regulation revealed
157 focusing on nucleus accumbens (NAc) as a key brain region in developing and reinforcing addiction.
159 ts design, we tested the causal role of this brain region in problem-solving, by applying High Defini
160 the anterior cingulate cortex (ACC) as a key brain region in the mitigation of the competition that a
161 ng marker of intracortical myelination in 68 brain regions in 248 healthy young people (14-25 years o
162 ion profile at different age time points and brain regions in a relevant mouse model of human tauopat
163 ains appropriate synaptic numbers in several brain regions in a time- and circuit-dependent fashion.
166 he results suggest collaboration of multiple brain regions in control of multistep behavior, with MD
171 re probabilistic changes, we discovered that brain regions in the default mode network and somatosens
172 m such injury observed in many, but not all, brain regions in the rhesus macaque model is consistent
173 Partial Least Squares was used to identify brain regions in which intra-cortical myelination (measu
174 died these patients, appeared as well in the brain region (in the temporal lobe) spatially separate f
175 nied by altered activity within a network of brain regions including the amygdala, hypothalamus and d
176 nuanced details are located across numerous brain regions, including some not previously implicated
178 independently on gene expression within many brain regions, including the ventral tegmental area (VTA
184 within those mid-insula regions, as well as brain regions involved in affect and reward, such as the
186 peripheral inflammatory cells and networked brain regions involved in threat and reward processing.
187 gs reveal that the engagement of CAs in some brain regions is essential for providing the brain with
188 l inputs to principle neurons of associative brain regions is established during development is unkno
189 Severe loss of excitatory synapses in key brain regions is thought to be one of the major mechanis
190 ain neural flexibility, were consistent with brain regions known to govern cognitive flexibility in a
191 ons of cannabis, are abundantly expressed in brain regions known to mediate neural processes underlyi
192 d this effect was restricted to D3 selective brain regions (limbic striatum, globus pallidus, and ven
193 erized neural signals in red nucleus (RN), a brain region linked to motor control, as male and female
194 ric and interhemispheric cooperation between brain regions lying outside the damaged area contributes
195 e hippocampal dentate gyrus (DG) is a unique brain region maintaining neural stem cells (NCSs) and ne
197 circuit, providing a potential model for how brain regions may coordinate during the visually guided
198 n via cell death across disparate but linked brain regions may explain how stereotyped patterns of ne
199 ich measures the degree of synchrony between brain regions, may be a useful measure of connectivity p
203 distributed nature of genetic signal across brain regions, multivariate analysis of regional measure
204 g sustained functional communication between brain regions (network stability) by changing their pred
205 erior temporal lobes (ATL) have become a key brain region of interest in cognitive neuroscience found
206 tivity was observed in the blood and several brain regions of a validated animal model for SCZ at bas
207 also assessed ATXN1 CAG repeat expansion in brain regions of an individual with a neurologically and
208 ons with high spatial resolution in specific brain regions of interest, and can be performed using th
209 letion on PV(+) and PV(-) cells within three brain regions of male and female mice: GPe, striatum, an
211 n neuroglia and neurons located in different brain regions on d1, d7, and d28 post Abeta toxicity and
212 ap with the patterns of empirically impaired brain regions on later scans, at both group and individu
213 r, how manganese accumulates in dopaminergic brain regions or how it regulates the activity of dopami
215 tranasal (not intravenous) administration in brain regions (orbitofrontal cortex, striatum, brainstem
216 ce for diurnal variations in the activity of brain regions outside the suprachiasmatic nucleus indica
220 tterns of resting-state connectivity between brain regions predict differential outcome to antidepres
221 nalysis revealed increased activation in the brain regions previously linked with the theory of mind
222 Propagation of signals between neurons and brain regions provides information about the functional
224 cant bilateral B cell diapedesis into remote brain regions regulating motor and cognitive functions a
226 , the stranger elicited activation mainly in brain regions related to visual and motor processing, an
227 changes in mitochondria-associated genes in brain regions relevant to depression symptomatology rema
231 Such cases may provide unique insight into brain regions responsible for mania symptoms and identif
232 ecific GCN edges, we determined how well the brain region samples could be discriminated from each ot
233 found that mid-fusiform cortex is the first brain region sensitive to lexicality, preceding the trad
235 ace-related processing recruits a network of brain regions separate from those recruited in object pr
236 anxiety-like behavior in any of the targeted brain regions, serotonin transporter expression, specifi
237 various brain regions and relay it to other brain regions, serving an essential role in sensory perc
240 DNA binding protein (TDP-43) accumulation in brain regions specifically involved in executive functio
243 and specific binding in GluN2B subunit-rich brain regions such as the cortex, striatum, hypothalamus
244 shown that ACC acts by modulating downstream brain regions such as the dorsal medial striatum (DMS) t
245 ain barrier, delivering oxytocin to specific brain regions, such as the striatum, where oxytocin acts
247 pographical correspondence between DCNNs and brain regions suggests these models are a good approxima
248 period involving substantial changes in the brain regions supporting cognition, learning, and emotio
251 d controllability (less influence over other brain regions), than Parkinson's disease patients withou
252 utput received weaker inputs, from far fewer brain regions, than the overall population of excitatory
254 hippocampus (HPC) has recently emerged as a brain region that integrates feeding-relevant biological
255 ter system was studied in the hippocampus, a brain region that is the principal target of the seroton
256 al prefrontal cortex (rmPFC) is an important brain region that processes stress and regulates immune
257 ffect the central neural circuits within the brain regions that are important for the regulation of c
258 at underlies alcohol use has improved, novel brain regions that are involved in alcohol use and novel
259 s in glutamate and dopamine receptors within brain regions that are known to be critical for decision
263 ped a robust MRI analysis method to identify brain regions that correlate linearly with regional amyl
264 functional specialization in the network of brain regions that directs such preferential processing.
265 simplex virus 1 (HSV-1) can induce damage in brain regions that include the hippocampus and associate
269 kness and white matter integrity in multiple brain regions that were associated with increased polyge
271 ecting differences in perfusion for multiple brain regions thought to be important in MDD, and (2) hi
272 fected rhesus macaques, we analyzed multiple brain regions through acute and chronic infection (90 da
273 ormation and use of a schema in a prefrontal brain region to support a complex cognitive operation.
276 tion, information-laden datasets from entire brain regions to single cells makes it a powerful approa
277 advanced DNA methylation age across several brain regions, to extend work concerning the association
278 asma NfL was associated with PET findings in brain regions typically affected by Alzheimer's disease;
279 tance-based and direction-based responses in brain regions typically involved in spatial navigation:
280 is the most vulnerable region, although all brain regions undergo neuronal degeneration in the disea
281 first to investigate normal ageing in these brain regions using 7T (1)H-MRS and findings indicate th
282 L can activate neurons located in deep mouse brain regions via transcranial optical stimulation and e
283 ubecestat might cause hippocampal (and other brain region) volume loss by assessing its relationship
285 with mania were heterogeneous and no single brain region was lesioned in all, or even most, cases.
288 genes associated with disinhibition-related brain regions were identified, which were significantly
291 ve mostly focused on local CFC in individual brain regions, whereas the presence and functional organ
293 osis and neuroinflammation in reward-related brain regions, which in turn lead to further unhealthy e
294 ical proteins between anatomically connected brain regions, while the latter has been hypothesized to
295 units with central-bias were associated with brain regions with foveal tendencies (e.g. fusiform gyru
298 reatly by cell type and, more moderately, by brain region, with glutamatergic neurons showing the lar
299 nes differentially expressed in at least one brain region, with the greatest number observed in hippo
300 lies on a common network of social-affective brain regions, with the medial prefrontal cortex playing