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1 ices, the subicular complex, and the dorsal, medial thalamus.
2 n involving posterior paramedian pons and/or medial thalamus.
3 i-motor, parietal and cingulate cortices and medial thalamus.
4 P) is an important source of limbic input to medial thalamus.
5 NAS), caudate-putamen (CP), hippocampus, and medial thalamus.
6 l cortex with motor cortex, hippocampus, and medial thalamus.
7 pothalamus 9+/-3%, substantia nigra 10+/-2%, medial thalamus 8+/-2%, and amygdala 9+/-3%.
8     Our data are consistent with the central medial thalamus acting as a key hub through which genera
9 LS) in areas serving the medial pain system (medial thalamus, amygdala, caudate nucleus, anterior cin
10  brain activation, primarily in the anterior medial thalamus and inferior frontal gyrus.
11 ensory and association areas, as well as the medial thalamus and superior colliculus.
12 C FC with the PCC/PCu, retrosplenial cortex, medial thalamus, and periaqueductal/periventricular gray
13 f aIC neurons project to the amygdala or the medial thalamus, and the pathway bidirectionally modulat
14 of activation within the anterior cingulate, medial thalamus, and visual cortex during delay and trac
15 ose utilization in the orbitofrontal cortex, medial thalamus, anterior and posterior cingulate cortic
16 ior hippocampus, ventral tegmental area, and medial thalamus) as well as in areas related to visuospa
17 iting the CER composed of prefrontal cortex, medial thalamus, auditory, and hippocampal regions.
18 easantness and accounted for activity in the medial thalamus, bilateral anterior insula, ventral stri
19 h of neurites from neurons isolated from the medial thalamus but was permissive for the growth of neu
20 rmacologically induced SWDs from the central medial thalamus (CMT) and somatosensory cortex in a Ca(V
21 tex and thalamus, the hippocampus and centro-medial thalamus (CMT).
22 rate in the anterior cingulate, caudate, and medial thalamus compared with controls.
23                                          The medial thalamus contains mu opioid receptors and sends a
24 recordings from the hippocampus, septum, and medial thalamus demonstrated fast poly-spike activity as
25 alamus [DMP] and dorsolateral nucleus of the medial thalamus [DLM]); (3) restricted regions within th
26 these disturbances might have their basis in medial thalamus dysfunction.
27 fically, the anterior, medial, and posterior-medial thalamus exhibit hub-like activity profiles that
28  establishes a critical role for the ventral medial thalamus in the propagation of this exaggerated b
29 togenetically modulated the ventro-posterior-medial thalamus in the vibrissa pathway of the awake mou
30 ation of septal area, but not hippocampus or medial thalamus, in the absence of a seizure resulted in
31                 Within the ventral posterior medial thalamus, membrane currents modulated by norepine
32  this project was to explore the role of the medial thalamus (MT), including the medial dorsal thalam
33 responses of single neurons in the nuclei of medial thalamus (MT), specifically the mediodorsal thala
34                                          The medial thalamus (MThal), anterior cingulate cortex (ACC)
35 se, attributable to an effect in the central medial thalamus, occurs at the point of dexmedetomidine
36 observed in lateral thalamus on day 9 and in medial thalamus on day 10 of PTD treatment, a duration o
37 y ischemia of the posterior paramedian pons, medial thalamus, or cerebellum.
38 ng, while optogenetic stimulation of the aIC-medial thalamus pathway decreased it.
39 mygdala, left anterior orbitofrontal cortex, medial thalamus, pregenual and dorsal anterior cingulate
40 lamic functioning involving the anterior and medial thalamus underlies interindividual variability in
41 SNpr output entrains activity in the ventral medial thalamus (VM) in this frequency range after loss
42 osensory (SI) cortex and the ventroposterior medial thalamus (VPM) before and during the combined adm
43 rges the receptive fields of ventroposterior medial thalamus (VPM) cells, noradrenergic activation de
44 ields of single cells in the ventroposterior medial thalamus (VPM) of urethane-anesthetized rats duri
45 barrel field cortex [BC]), ventral posterior medial thalamus (VPM), and principal nucleus of the trig
46 r effects were observed in ventral posterior medial thalamus (VPm).
47 asal forebrain extending to the anterior and medial thalamus were affected.
48 ctional connectivity (and increased with the medial thalamus), which is implicated in face expression