ライフサイエンスコーパス: anterior thalamus

1 ats and screened for HD cell activity in the anterior thalamus.

2 ssing the ventral striatum, hypothalamus and anterior thalamus.

3 luster of TH-negative neurons in the ventral anterior thalamus.

4 left dorsolateral prefrontal cortex and the anterior thalamus.

5 , anteromesial temporal lobe (amygdala), and anterior thalamus.

6 res include the subiculum, presubiculum, and anterior thalamus.

7 d blood flow in the frontal lobes and in the anterior thalamus.

8 orded from HD cells in the postsubiculum and anterior thalamus.

9 l regions, the ventral striatal complex, and anterior thalamus.

10 d connects to the parahippocampal region and anterior thalamus.

11 in navigation, including the hippocampus and anterior thalamus [9, 10].

12 gated this role by recording HD cells in the anterior thalamus after either neurotoxic or electrolyti

13 The anterior thalamus and dorsal subiculum, sources of spati

14 spatial memory rely on the operation of the anterior thalamus and hippocampus within an integrated n

15 specific mechanisms that govern how the MD, anterior thalamus and pulvinar cortico-thalamocortical i

16 other dorsal thalamic nuclei, including the anterior thalamus and pulvinar, also influence these cog

17 ptors are also present (hippocampus, cortex, anterior thalamus, and cerebellum).

18 prefrontal cortex, supramarginal gyrus, and anterior thalamus; and bilaterally in the hippocampal fo

19 Current evidence shows that the MD (and the anterior thalamus) are crucial for frontotemporal commun

20 rontal gyrus, anterior cingulate cortex, and anterior thalamus, as well as the original stereotactic

21 ed with general symptoms in the right medial anterior thalamus, as well as with disorganization sympt

22 ons damaging hippocampus-related pathways in anterior thalamus (AT) and parahippocampal (PH) cortex o

23 The anterior thalamus (AT) is anatomically interconnected wi

24 We found that in both the anterior thalamus (ATN) and dorsomedial thalamus (DMTN),

25 rom the lateral mammillary nucleus (LMN) and anterior thalamus (ATN) of freely behaving rats and also

26 male rats while bilaterally inactivating the anterior thalamus (ATN), a region critical for expressio

27 brain activity in the prefrontal cortex and anterior thalamus-brain regions associated with emotion

28 , subcortical inputs (such as those from the anterior thalamus) contribute to geometric learning.

29 It persists in the developing anterior thalamus (conventionally termed "ventral" thala

30 y mainly by activating GABA receptors in the anterior thalamus, diagonal band of Broca and RSC.

31 Many cells within the postsubiculum and anterior thalamus discharge as a function of the animal'

32 Neurons within the rat anterior thalamus encode the directional heading of the

33 munoreactivity in the mamillary body and the anterior thalamus following unilateral injections of the

34 Deep brain stimulation of anterior thalamus for partial epilepsy recently was appr

35 motor, and prefrontal cortices [14], whereas anterior thalamus forms a memory network in connection w

36 s involvement of ventrolateral and, notably, anterior thalamus in biasing attention through WM conten

37 is responsible for alpha synchrony, and the anterior thalamus is related to theta synchrony.

38 vity profile suggests that ventrolateral and anterior thalamus may represent a nexus between mnemonic

39 bsence of direction-specific activity in the anterior thalamus of animals with DTN or LMN lesions is

40 a cells from hippocampus, medial septum, and anterior thalamus of freely behaving rats.

41 We report that muscimol injections into the anterior thalamus or diagonal band of Broca provide subs

42 y, and GABA-receptor agonist injections into anterior thalamus prevent injury produced by systemic MK

43 MK801 injections into anterior thalamus reproduce limbic cortex injury, and GA

44 lum, caudate nucleus, centromedian thalamus, anterior thalamus, subthalamus, hippocampus, and neocort

45 nct from the contributions of hippocampus or anterior thalamus to spatial memory.

46 ic site specifically at projections from the anterior thalamus to the ACC caused the tLTD phenotype,

47 nism for spike-timing dependent LTD from the anterior thalamus to the ACC, suggesting that this patho

48 Here we describe neurons in the macaque anterior thalamus tuned to pitch and roll orientation re

49 u-opioid system activation than women in the anterior thalamus, ventral basal ganglia, and amygdala.

50 recorded within the slow-wave cycle was the anterior thalamus, which followed active states of the r

51 ntified increased GBC in dorsal striatum and anterior thalamus, which was reduced in patients on medi

52 and sustained neural correlate of memory in anterior thalamus, whose inhibition substantially disrup