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1 depression (e.g., habenula, dorsal raphe and interpeduncular nucleus).
2 which project IL-18-containing axons to the interpeduncular nucleus.
3 ts of the MHb homolog selectively target the interpeduncular nucleus.
4 medial habenula and its primary target, the interpeduncular nucleus.
5 subunits, which are highly expressed in the interpeduncular nucleus.
6 uctures such as the substantia nigra and the interpeduncular nucleus.
7 N to the adjacent fasciculus retroflexus and interpeduncular nucleus.
8 habenula and a 25% elevation in the related interpeduncular nucleus.
9 nly weakly into the adjacent anterior VTA or interpeduncular nucleus.
10 eral lemniscus, periaqueductal gray, and the interpeduncular nucleus.
11 subiculum, several thalamic regions, and the interpeduncular nucleus.
12 omposing the fasciculus retroflexus, and the interpeduncular nucleus; 2) nuclei and ascending tracts
13 Because the MHb extensively innervates the interpeduncular nucleus, an area critical for both affec
16 ontributing to despair-like behavior (Hb-MOR/interpeduncular nucleus) and anxiety (Hb-MOR/dorsal raph
18 monstrated PP receptors in the brainstem and interpeduncular nucleus, and the PP receptors in the bra
19 a, pineal body, preoptic area, hypothalamus, interpeduncular nucleus, area acusticolateralis, cerebel
21 he subthalamic nucleus, substantia nigra and interpeduncular nucleus as well as in the hippocampus, d
22 he subthalamic nucleus, substantia nigra and interpeduncular nucleus, as well as other areas of the b
24 when microinjected into the habenula or the interpeduncular nucleus, but not into the cortex, ventra
26 c dopamine circuitry and the medial habenula-interpeduncular nucleus complex, which are critical medi
28 ily conserved forebrain to midbrain habenulo-interpeduncular nucleus (Hb-IPN) pathway consists of cho
29 rade tracing showed that, in addition to the interpeduncular nucleus, Hb-MOR neurons project to the d
31 The expression of Gscl is restricted to the interpeduncular nucleus (IP) in the ventral region of th
33 teral habenula (LHb), medial habenula (MHb), interpeduncular nucleus (IP), and median raphe nucleus (
34 y, MHb together with its primary target, the interpeduncular nucleus (IP), have been identified as ma
35 ngly expressed in a subset of neurons in the interpeduncular nucleus (IP), median raphe/paramedian ra
37 ons, which project almost exclusively to the interpeduncular nucleus (IPn) and are known to regulate
38 ons, which project almost exclusively to the interpeduncular nucleus (IPn) and are known to regulate
44 s were designed to determine the role of the interpeduncular nucleus (IPN) in 3 forms of navigation:
45 f Chrna3 gene transcripts in the habenula or interpeduncular nucleus (IPn) increases nicotine intake
46 tic connection from medial habenula (MHb) to interpeduncular nucleus (IPN) is critical for emotion-re
47 rea implicated in nicotine dependence is the interpeduncular nucleus (IPN) located in the ventral mid
48 ACh at synapses of medial habenula (MHN) and interpeduncular nucleus (IPN) neurons in vitro elicited
49 cal substrate for familiarity signaling, the interpeduncular nucleus (IPN) of the midbrain, which is
50 l nAChRs in the medial habenula (MHb) to the interpeduncular nucleus (IPN) pathway are key mediators
51 eptors (nAChRs) in the medial habenula (MHb)-interpeduncular nucleus (IPN) pathway play critical role
52 ated in beta2(-/-) sections, although dorsal interpeduncular nucleus (IPN) retained a faint signal.
53 ors (nAChRs) in the medial habenula (MHb) or interpeduncular nucleus (IPN) triggers withdrawal-like b
54 show that the brainstem circuit linking the interpeduncular nucleus (IPN) with the nucleus incertus
55 conveys motor information may stem from the interpeduncular nucleus (IPN), a brain region that has r
56 related with nicotine-evoked currents in the interpeduncular nucleus (IPN), and that prolonged exposu
57 of beta4 subunits in medial habenula (MHb), interpeduncular nucleus (IPN), and VTA of beta4KO mice r
58 al habenula (MHb) and its unique output, the interpeduncular nucleus (IPN), in mice independently of
59 pha2 and beta4 are transcribed in the target interpeduncular nucleus (IPN), suggesting that the asymm
70 splenial cortex, subiculum, medial habenula, interpeduncular nucleus, locus coeruleus, and brainstem
71 sal tegmental nucleus, dorsal raphe nucleus, interpeduncular nucleus, medial mammillary body, suprama
72 4 also was present in certain neurons of the interpeduncular nucleus, median raphe, superior collicul
74 IRP-LI was most heavily concentrated in the interpeduncular nucleus, nuclei interfascicularis and ro
75 taset by demonstrating that knockdown in the interpeduncular nucleus of a differentially expressed mR
76 l plexiform layer of the olfactory bulb, the interpeduncular nucleus of the midbrain, the ventral and
77 osterior mamilliary nucleus, and dorsomedial interpeduncular nucleus of the rabbit that were not dete
78 the region just dorsal to the posterior VTA, interpeduncular nucleus, or medial mammillary nucleus.
79 ficial layer), arcuate hypothalamic nucleus, interpeduncular nucleus, paratrigeminal nucleus, and lam
80 subnuclei also differentially innervate the interpeduncular nucleus, raphe nuclei, substantia nigra
81 e more active in fish that are not courting: interpeduncular nucleus, red nucleus, and ventrolateral
82 dial amygdala, central gray, pontine nuclei, interpeduncular nucleus, substantia nigra, raphe complex
83 rus semicircularis, mesencephalic tegmentum, interpeduncular nucleus, superior and middle reticular n
84 s of Darkschewitsch, peripeduncular nucleus, interpeduncular nucleus, tegmental nuclei, locus coerule
86 on in neurons clustered above and behind the interpeduncular nucleus that project strongly to the ven
87 m, torus semicircularis, cerebellar nucleus, interpeduncular nucleus, the medial octavolateral nucleu
88 ct projections to midbrain areas such as the interpeduncular nucleus, the median/paramedian nuclei, a
89 antia nigra, the ventral tegmental area, the interpeduncular nucleus, the raphe nuclei, the dorsal te
90 efferent habenular fibers projecting to the interpeduncular nucleus, the rostromedial tegmental area
91 s, the midbrain lateral tegmental field, the interpeduncular nucleus, the ventral pontine reticular f
92 ic input, the habenular nucleus inhibits the interpeduncular nucleus, thereby dis-inhibiting forebrai