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1 gic projection neurons that connect with the anterior hypothalamus.
2 abolism and thermoregulation at the level of anterior hypothalamus.
3 s [TNgc]), ventral telencephalon (vTEL), and anterior hypothalamus.
4 to the suprachiasmatic nucleus (SCN) in the anterior hypothalamus.
5 no significant differences were found in the anterior hypothalamus.
6 tly on thermosensitive cells of the preoptic anterior hypothalamus.
7 dinates these processes to build the tuberal/anterior hypothalamus.
8 d into the medial preoptic area (MPA) of the anterior hypothalamus.
9 s in the suprachiasmatic nuclei (SCN) of the anterior hypothalamus.
10 lated, namely the preoptic area (POA) of the anterior hypothalamus.
11 clock in the suprachiasmatic nucleus of the anterior hypothalamus.
12 itored in two brain regions: the caudate and anterior hypothalamus.
13 6) cm2/s and 3.2 +/- 0.6 x 10(-2) s-1 in the anterior hypothalamus.
14 tical function, including lateral septum and anterior hypothalamus.
15 rved in the olfactory area and preoptic area-anterior hypothalamus.
16 lta-2 antagonist naltriben into the preoptic anterior hypothalamus (1 microg, 30 min prior to deltorp
17 r antagonists delivered to the preoptic area-anterior hypothalamus, a primary site for behavioural in
19 0% decrease in vasopressin levels within the anterior hypothalamus, a site involved in the regulation
20 e slices, primarily in the preoptic area and anterior hypothalamus, a thermoregulatory region that in
21 cleus (SON), median preoptic nucleus (MnPO), anterior hypothalamus (AH) and posterior hypothalamus (P
22 the serotonin (5-HT) system innervating the anterior hypothalamus (AH) and the interaction of 5-HT r
23 ion between AVP and 5-HT at the level of the anterior hypothalamus (AH) in the control of offensive a
25 Microinjection of vasopressin (VP) into the anterior hypothalamus (AH) of golden hamsters induces a
27 ogram in 0.5 microliter at 0 + 1 h) into the anterior hypothalamus (AH), paraventricular hypothalamic
28 n this species, the preoptic area (POA), the anterior hypothalamus (AH), septal area (SEP), and ventr
34 within stress neurocircuitry, including the anterior hypothalamus, amygdala, hippocampus, and medial
35 raventricular, supraoptic, circularis in the anterior hypothalamus and fornical in the lateral hypoth
36 tonin-immunoreactive varicosities within the anterior hypothalamus and lateral septum was 20% higher
37 rons in the dorsal raphe that project to the anterior hypothalamus and may mediate the spatiotemporal
39 asing factor output from the amygdala to the anterior hypothalamus and then the lateral septum to mod
40 llular concentrations of ATP increase in the anterior hypothalamus and this has a profound effect on
41 regions of the forebrain (preoptic area and anterior hypothalamus) and of the midbrain (periaqueduct
42 ns between sleep-promoting areas such as the anterior hypothalamus, and arousal systems located in th
43 ricular preoptic area, lateral preoptic area/anterior hypothalamus, and infundibular nucleus/median e
44 the hypothalamus and ventral forebrain (the anterior hypothalamus, arcuate nucleus, anteroventral pe
45 he paraventricular nucleus thalamus, and the anterior hypothalamus, as well as the supraoptic (SON),
46 lamus including the suprachiasmatic nucleus, anterior hypothalamus, bed nucleus stria terminalis, and
47 Kiss1 was not detectable until PND 11 in the anterior hypothalamus, but expression levels were equiva
48 m, basolateral amygdala, paraventricular and anterior hypothalamus, centromedial thalamus, CA1 region
49 europeptides oxytocin and vasopressin in the anterior hypothalamus did not differ among wild-type, he
50 administration into six hypothalamic sites (anterior hypothalamus, dorsomedial hypothalamus, lateral
51 though lower doses were sometimes effective (anterior hypothalamus, dorsomedial hypothalamus, nucleus
52 ained sections from the dorsal preoptic area/anterior hypothalamus (dPOA/AH) of male, but not female,
53 in determining the metabolic capacity in the anterior hypothalamus, external amygdala, dorsal lateral
54 rior hypothalamus (LAH), a sub-region of the anterior hypothalamus, have lasting activation following
56 ventromedial hypothalamus and preoptic area-anterior hypothalamus in normal female whiptail lizards
57 entration of ATP (4.0 +/- 0.7 microm) in the anterior hypothalamus in response to intravenous injecti
60 of the glutamate neural system in the latero-anterior hypothalamus (LAH) in hamsters (Mesocricetus au
61 e whether glutamatergic cells in the lateral anterior hypothalamus (LAH), a sub-region of the anterio
62 aggressive behavior, most notably the latero-anterior hypothalamus (LAH)-an area of convergence for d
63 time-course of AAS-induced changes in latero-anterior hypothalamus (LAH)-VGLUT2 closely paralleled in
64 y higher activity in five regions, including anterior hypothalamus, lateral hypothalamus, somatosenso
65 opulation of parvalbuminergic neurons in the anterior hypothalamus, linking, for the first time, impa
66 dialdehyde to the site of ATP release in the anterior hypothalamus markedly augmented and prolonged t
67 rs, vasopressin (AVP) in the medial preoptic-anterior hypothalamus (MPOA-AH) controls a form of scent
68 croinjection of AVP into the medial preoptic-anterior hypothalamus (MPOA-AH), lateral septal nucleus
69 croinjection of AVP into the medial preoptic-anterior hypothalamus (MPOA-AH), lateral septal nucleus
70 nvolving the medial preoptic area (MPOA) and anterior hypothalamus (n = 5) had no significant effects
71 ytochrome oxidase activity was higher in the anterior hypothalamus of males, in the ventromedial hypo
72 toring the PGE2 synthesizing capacity in the anterior hypothalamus of mice lacking such capacity with
73 ecies, the central amygdalar nucleus (CAmy), anterior hypothalamus, paraventricular nucleus, and post
74 insular area; bed nuclei of terminal stria; anterior hypothalamus; paraventricular, arcuate, and dor
75 us of the stria terminalis, perifornical and anterior hypothalamus, periaqueductal gray, and lateral
76 y were found within the medial preoptic area/anterior hypothalamus, periventricular preoptic area, la
77 ficantly reduced in the medial preoptic area/anterior hypothalamus, periventricular preoptic area, la
78 gulatory neurons in the preoptic area of the anterior hypothalamus (POA) form synaptic networks, whic
80 terize the role of the Pre-Optic Area of the Anterior Hypothalamus (POAH) in the decrease in set poin
81 vagal afferents to the preoptic area of the anterior hypothalamus (POAH), an important thermoregulat
85 d that implantation of progesterone into the anterior hypothalamus preoptic area of castrated, proges
86 show that conditional deletion of Shh in the anterior hypothalamus results in a fully penetrant pheno
88 ypothalamic areas which express ER, e.g. the anterior hypothalamus, showed less dramatic changes.
89 periventricular regions of the thalamus and anterior hypothalamus, stratum periventriculare of the o
90 d in limbic system structures, including the anterior hypothalamus, subgenual anterior cingulate cort
91 ion of excitatory vasopressin neurons in the anterior hypothalamus that may gate corticotropin-releas
92 opulation of parvalbuminergic neurons in the anterior hypothalamus that requires thyroid hormone rece
93 und two types of neurons in the preoptic and anterior hypothalamus that selectively responded to the
94 the bed nucleus of the stria terminalis, the anterior hypothalamus, the lateral hypothalamus, and the
95 al notable aggression regions, including the anterior hypothalamus, the medial and central amygdaloid
96 a, the external nucleus of the amygdala, the anterior hypothalamus, the ventromedial hypothalamus, th
97 ystemic inflammation, ATP is released in the anterior hypothalamus to limit the magnitude and duratio
98 ons of arginine-vasopressin (AVP) within the anterior hypothalamus trigger a stereotyped scent-markin
99 eas of the brain altered by AAS, namely, the anterior hypothalamus, ventrolateral hypothalamus, and m
100 ricular preoptic area, lateral preoptic area/anterior hypothalamus, ventromedial hypothalamus, and la
101 mplex, hippocampus, striatum, preoptic area, anterior hypothalamus, ventromedial hypothalamus, and ve
102 mplex, hippocampus, striatum, preoptic area, anterior hypothalamus, ventromedial hypothalamus, and ve
103 in vocal production (periaqueductal gray and anterior hypothalamus) was significantly higher in the m
104 take rate (k) for choline in the caudate and anterior hypothalamus were calculated using a model for
105 ections through the medial preoptic area and anterior hypothalamus were examined from 18 males and 20
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