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1 r the role of extracellular ATP in mediating habenular activity and reveal how nicotine exposure duri
2 , identification of strategies to manipulate habenular activity may yield approaches to treat nicotin
3 x subunit Med12 impairs the specification of habenular and parapineal neurons and causes a loss of di
4                                          The habenular and thalamic Gpr151 systems displayed both sha
5 51-Cre mouse line, monosynaptic afferents of habenular and thalamic Gpr151-expressing neuronal popula
6 gmental area, and the lateral septal, medial habenular, and interpeduncular nuclei.
7 well as in the Edinger-Westphal, the lateral habenular, and the laterodorsal tegmental nuclei.
8 where the highest levels are observed in the habenular area.
9 mediated ablation of the parapineal disrupts habenular asymmetry and consequently alters the dorsoven
10 ning of the parapineal sets the direction of habenular asymmetry and thereby determines the left-righ
11 the mouse and the zebrafish, we propose that habenular asymmetry formation involves a recurrent devel
12  screen for mutations that result in loss of habenular asymmetry, we identified two mutant alleles of
13  the parapineal organ results in the loss of habenular asymmetry.
14 art by regulating the actions of nicotine on habenular aversion circuits.
15  more limited ventral IPN region where right habenular axons would normally project.
16 Whereas 5-HT and emotional contagion reduced habenular burst firing, limiting 5-HT synthesis prevente
17 h, highlighting the well-conserved nature of habenular cell types across the phylum.
18 e data identify key molecular targets within habenular cell types and provide a critical resource for
19  order drives a persistent depolarization of habenular cells and promotes long-lasting discharges of
20 trains of action potentials, whereas lateral habenular cells are capable of producing action potentia
21                                       Medial habenular cells generate tonic trains of action potentia
22 rphological properties of medial and lateral habenular cells indicate that the two nuclei process and
23                                      Lateral habenular cells produce dendrites that are much longer t
24        However, other data indicate that the habenular cells were labeled by spread of the tracer fro
25                  During recording, we filled habenular cells with biocytin.
26                        We suggest that these habenular cells, by generating persistent action potenti
27 roperty and morphology of medial and lateral habenular cells.
28 es that are much longer than those of medial habenular cells.
29 on of the ATP purinergic receptors increases habenular cholinergic neuronal firing in the adolescent
30                          We suggest that, in habenular cholinergic neurons, the beta3 subunit may be
31 minant striatal input to the macaque pallido-habenular circuit, which is known to function in relatio
32 ition, we found that DCC is expressed in the habenular commissure, the fasciculus retroflexus, and th
33 pose motor bias via a projection through the habenular commissure.
34                                  The lateral habenular complex (LHb) is a bilateral epithalamic brain
35                     In contrast, the lateral habenular complex (LHb), which is known as the center of
36           Here, we tested how lesions of the habenular complex affect the response of optogenetically
37 nicotinic subunits involving the epithalamic habenular complex and its targets.
38    The lateral habenula (LHb) is part of the habenular complex in the dorsal diencephalon.
39                                          The habenular complex in the epithalamus consists of distinc
40                           Traditionally, the habenular complex is divided into the medial nucleus and
41                                          The habenular complex is involved in several estrogen-depend
42                                          The habenular complex of the epithalamus connects the limbic
43                                          The habenular complex of the epithalamus in the mammalian br
44 umber of regions, including the hippocampus, habenular complex, ventral tegmentum, geniculate, and ce
45 ulb, neocortex, hippocampus, and epithalamus/habenular complex.
46 hether estrogen may also act directly on the habenular complex.
47 fact that the subnuclear organization of the habenular complexes in mouse is not known so far.
48 spite their importance, our understanding of habenular development is incomplete.
49 nfluences development of the adjacent dorsal habenular (dHb) nucleus, causing the left and right dHb
50 ent connectivity during subsequent stages of habenular differentiation.
51                                     Severing habenular efferents to the IPN, or only those from the l
52 cular asymmetry extends to protein levels in habenular efferents, providing additional evidence that
53 pecific expression was also seen in efferent habenular fibers projecting to the interpeduncular nucle
54 tive D1 and D2 dopamine receptor agonists on habenular Fos expression.
55 vide a valuable resource for future study of habenular function and dysfunction and demonstrate neuro
56 a identify GPR151 as a critical modulator of habenular function that controls nicotine addiction vuln
57                It has been hypothesized that habenular input to midbrain dopamine neurons is conveyed
58           It is not precisely known, whether habenular input to the aVTA, pVTA, and the newly recogni
59 ered by fr lesions suggesting a role for non-habenular inputs during exposure to highly aversive stim
60  together, we propose that the telencephalic-habenular-interpeduncular pathway plays an important rol
61              Here we demonstrate the role of habenular Kiss1 in alarm substance (AS)-induced fear res
62 ings provide an insight into the role of the habenular kisspeptin system in inhibiting fear.
63           A screen for mutations that affect habenular laterality led to the identification of the se
64 e mice specifically blocks NMDARs in lateral habenular (LHb) neurons, but not in hippocampal pyramida
65                       The medial and lateral habenular (LHb) nuclei play important roles in processin
66  both the medial habenular (MHb) and lateral habenular (LHb) subregions in mammals remain undefined.
67                                       Medial habenular mast cell numbers increase during development,
68 ll populations that comprise both the medial habenular (MHb) and lateral habenular (LHb) subregions i
69 imulation, we show that GLP-1 excites medial habenular (MHb) projections to the interpeduncular nucle
70                      These findings unveil a habenular neurocircuitry devoted to encode external thre
71 conserved, specific for a subdivision of the habenular neurocircuitry, and constitutes a promising no
72 d for a link between melatonin signaling and habenular neurogenesis.
73 to resilience by tuning definite patterns of habenular neuronal activity.
74         In the zebrafish epithalamus, dorsal habenular neurons adopt medial (dHbm) and lateral (dHbl)
75 ified as highly and specifically enriched in habenular neurons by in situ hybridization and translati
76 terminals of cholinergic and non-cholinergic habenular neurons exhibit stereotypic patterns of sponta
77 s retroflexus is directed appropriately, but habenular neurons fail to innervate their targets.
78 tion by antisense morpholinos, prevents left habenular neurons from projecting to the dorsal IPN.
79            In contrast, criteria to classify habenular neurons into distinct groups with potentially
80                                          The habenular neurons primarily received input from basal fo
81 on factor Brn3a/Pou4f1, and Brn3a-expressing habenular neurons project exclusively to the interpedunc
82                  Consequently, disruption of habenular neurons reduces capture performance in prey-ex
83    We find that in wild-type zebrafish, most habenular neurons responding to light are present on the
84  Electrophysiological recordings from medial habenular neurons revealed that GPR139 signaling via G(q
85  essential for lateralized fate selection by habenular neurons that can differentiate along two alter
86 approach, we show that inhibition of cortico-habenular neurons that project to LC, but not to other s
87 Likewise, the genetic pathways acting within habenular neurons to control their asymmetric differenti
88 BA(B) receptors activated in non-cholinergic habenular neurons upon GABA release from the target IPN.
89                         Mice lacking CHAT in habenular neurons were insensitive to nicotine-condition
90  sections, the different retrogradly labeled habenular neurons were quantified and assigned to the co
91 duced the stimulatory effects of nicotine on habenular neurons, and its infusion into the IPn increas
92 duced the stimulatory effects of nicotine on habenular neurons, and its infusion into the IPn increas
93 ymmetry reverse the functional properties of habenular neurons, whereas manipulations that generate e
94 ntral IPN projection pattern typical of left habenular neurons.
95                                          The habenular nuclear (Hb)/dorsal third ventricle (D3 V) and
96                                   The dorsal habenular nuclei (Dh) of the zebrafish are characterized
97 val zebrafish, the bilaterally paired dorsal habenular nuclei (dHb) exhibit prominent left-right diff
98 e neurotransmitter identity of the zebrafish habenular nuclei and reveal functional asymmetry in a ma
99                                          The habenular nuclei are a conserved integrating center in t
100      Left-right asymmetries in the zebrafish habenular nuclei are dependent upon the formation of the
101                           Interestingly, the habenular nuclei are present in all vertebrates, suggest
102 chiasmatic nuclei (SCN), medial amygdala and habenular nuclei in JP17 rats; the rat OT-bNP (rOT-bNP)
103   Previous studies had implicated the dorsal habenular nuclei in regulating fear responses and boldne
104               The connection between the two habenular nuclei is asymmetrical in that only the medial
105 tudy, we investigated the connections of the habenular nuclei of the oriental fire-bellied toad, Bomb
106                                   The medial habenular nuclei of the zebrafish diencephalon, which li
107                                          The habenular nuclei of zebrafish are robustly asymmetric, w
108                Our results indicate that the habenular nuclei provide a common vertebrate circuitry t
109   We examine the formation of neurons in the habenular nuclei, a paired structure found near the dors
110 amic (PVN), paratenial thalamic, and lateral habenular nuclei, and medial substantia nigra, but was i
111  well as the differential innervation by the habenular nuclei, domains gradually comparable to the ma
112 ng of the pineal complex and flanking dorsal habenular nuclei, provides a valuable model for explorin
113 ndary olfactory projections were seen to the habenular nuclei, the rostral pole of the inferior lobe,
114 leus of amygdala, lateral septal and lateral habenular nuclei-brain areas that have been shown to be
115  of the parapineal and the laterality of the habenular nuclei.
116 ling in paraventricular thalamic and lateral habenular nuclei.
117 des the pineal and parapineal organs and the habenular nuclei.
118 ulting in formation of bilaterally symmetric habenular nuclei.
119 and the formation of neural processes in the habenular nuclei.
120 ult in symmetric development of the adjacent habenular nuclei.
121 r research has demonstrated that the lateral habenular nucleus (Lhb) is necessary for the hormonal on
122 RC) nuclei, median eminence (ME), and medial habenular nucleus (MHb), with lower densities in the dor
123 retinal ganglion cells and in neurons of the habenular nucleus and telencephalon, whereas XNIF and NF
124  nucleus of the stria terminalis, and medial habenular nucleus display a greater level in Cape mole-r
125 del, in response to telencephalic input, the habenular nucleus inhibits the interpeduncular nucleus,
126 in neurons of the medial part of the lateral habenular nucleus of the epithalamus.
127 hilar region of the hippocampus, the lateral habenular nucleus of the thalamus, and the suprachiasmat
128 ed nucleus of stria terminalis, hippocampus, habenular nucleus, amygdala, thalamus, hypothalamus, med
129 utamen, geniculate, thalamic nuclei, lateral habenular nucleus, and hippocampal CA3 pyramidal and hil
130 a (NPOmg and NPOpc), entopeduncular nucleus, habenular nucleus, and pretectal nuclei (PSi and PSm).
131 ucleus of the dorsal telencephalic area, the habenular nucleus, and the dorsomedial nucleus of the th
132 s, including the developing pineal gland and habenular nucleus, both implicated in CNS L-R asymmetry
133  gland, superior colliculus, cortex, thymus, habenular nucleus, cornea, liver, tail, and kidney) reve
134  the olfactory bulb, caudate-putamen, medial habenular nucleus, hippocampal granule cells, and superi
135 al habenular nucleus, whereas in the lateral habenular nucleus, intrinsic axons travel largely from m
136 s, thalamic and hypothalamic nuclei, lateral habenular nucleus, locus coeruleus, raphe nuclei, and ce
137 : high densities were detected in the medial habenular nucleus, nucleus paraventricularis thalami, ot
138 f the stria terminalis in the telencephalon; habenular nucleus, paraventricular nucleus of the thalam
139 ory bulb, piriform cortex (layer II), medial habenular nucleus, subregions of the amygdala, specific
140 m cortex, hippocampus, dentate gyrus, medial habenular nucleus, thalamic nucleus and pontine nucleus.
141 tinct intrinsic circuits exist in the medial habenular nucleus, whereas in the lateral habenular nucl
142 , and the nucleus basalis of Meynert, medial habenular nucleus, zona incerta, neurosecretory arcuate
143 h the suprachiasmatic nucleus and the medial habenular nucleus.
144  of the posterior commissure and the lateral habenular nucleus.
145 nucleus of the stria terminalis, and lateral habenular nucleus.
146 amygdala, lateral septal nucleus and lateral habenular nucleus.
147 he shell of the nucleus accumbens and medial habenular nucleus.
148  darkness causes a temporary accumulation of habenular precursor cells, resulting in late differentia
149 anning (from the prefrontal cortex), lateral habenular processing, hippocampal function, and oculomot
150  thereby determines the left-right origin of habenular projections onto the midbrain target, the inte
151 rsely, Sema3D overexpression results in left habenular projections that extend to the dorsal IPN, as
152                                          The habenular region was previously implicated in modulating
153 or double-right-sided brains lead to loss of habenular responsiveness to either odor or light, respec
154 he precise input-output connectivity of each habenular subdivision is essential.
155                                          The habenular subnuclei also differentially innervate the in
156 suggest that the topographic localization of habenular subnuclei is rather similar between mouse and
157 quantified and assigned to the corresponding habenular subnuclei.
158 ng proteins revealed right-left asymmetry of habenular subpopulations and segregation of their interp
159 l size and release frequency of glutamate at habenular synapses, and suggest that the synergistic fun
160 satiety sensors' for nicotine that stimulate habenular systems to promote nicotine avoidance before i

 
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