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1 om the median preoptic nucleus (MnPO) to the dorsomedial hypothalamus.
2 undefined region which we named intermediate dorsomedial hypothalamus.
3 the lateral septum, medial preoptic area or dorsomedial hypothalamus.
4 djacent hypothalamic nuclei, the arcuate and dorsomedial hypothalamus.
5 rior BNST, the medial preoptic area, and the dorsomedial hypothalamus.
6 ions and their delta 2/delta 1 ratio(s) are: dorsomedial hypothalamus (9.3), ventromedial hypothalamu
8 cell bodies were found scattered within the dorsomedial hypothalamus and the dorsomedial half of the
9 ) special induction of NPY expression in the dorsomedial hypothalamus, and 4) suppression of anorexig
10 teral preoptic area, ventral tegmental area, dorsomedial hypothalamus, and entopeduncular nucleus).
11 sponding to the medial preoptic area and the dorsomedial hypothalamus, and in a site dorsal to the op
12 amus (including the suprachiasmatic nucleus, dorsomedial hypothalamus, and tuberomammillary nucleus r
13 Activation of neurons in the region of the dorsomedial hypothalamus appears to play a key role in t
14 n the A1, nucleus of the solitary tract, and dorsomedial hypothalamus are activated by both chemorece
15 r tubercle nuclei at embryonic stage 26, and dorsomedial hypothalamus at stage 28); then in more caud
16 cardia evoked by chemical stimulation of the dorsomedial hypothalamus can be suppressed by microinjec
19 am leptin-receptor-expressing neurons in the dorsomedial hypothalamus (DMH(LepR)) are tuned to respon
20 r nucleus (MHb), with lower densities in the dorsomedial hypothalamus (DMH) and forebrain regions.
21 in several hypothalamic sites, including the dorsomedial hypothalamus (DMH) and median preoptic area
23 Activation of neurons in the region of the dorsomedial hypothalamus (DMH) appears to generate the s
25 and female mice we show that neurons in the dorsomedial hypothalamus (DMH) are responsible for the m
26 inted GLP-1 receptor (GLP-1R) neurons in the dorsomedial hypothalamus (DMH) as candidates for encodin
27 nals satiety, whereas GABAergic cells in the dorsomedial hypothalamus (DMH) can increase food consump
28 ed this behavior in rats with lesions in the dorsomedial hypothalamus (DMH) challenged with a shock-i
29 ween excitatory and inhibitory inputs to the dorsomedial hypothalamus (DMH) determines the level of a
30 tly enhanced glutamatergic excitation in the dorsomedial hypothalamus (DMH) develop panic-like respon
31 ections from OB to medial amygdala (MeA) and dorsomedial hypothalamus (DMH) exhibit female-specific c
32 rs responsible for responses evoked from the dorsomedial hypothalamus (DMH) from which similar cardio
34 duced, a novel expression of NPY mRNA in the dorsomedial hypothalamus (DMH) has been observed, sugges
36 te nucleus of the hypothalamus (ARH) and the dorsomedial hypothalamus (DMH) have been implicated in f
37 ity in humans, and expression of TrkB in the dorsomedial hypothalamus (DMH) is critical for maintaini
38 ly, activation of glutamate receptors in the dorsomedial hypothalamus (DMH) is required for COX-indep
39 that mWAKE/ANKFN1 labels a subpopulation of dorsomedial hypothalamus (DMH) neurons involved in rhyth
40 ulation of leptin receptor (Lepr)-containing dorsomedial hypothalamus (DMH) neurons marked by the exp
41 o an up-regulation of RFRP expression in the dorsomedial hypothalamus (DMH) of adult male rats and th
42 selective knock-down of BDNF in the VMH and dorsomedial hypothalamus (DMH) of adult mice, we were ab
43 the virus was injected unilaterally into the dorsomedial hypothalamus (DMH) of mice that express Cre
44 ve populations, we found that neurons in the dorsomedial hypothalamus (DMH) of ob/ob mice expressing
45 vealed an elevation of Ttr expression in the dorsomedial hypothalamus (DMH) of rats with exercise-ind
46 shown that: (1) activation of neurons in the dorsomedial hypothalamus (DMH) of the rat by blockade of
47 Studies in intact rats have shown that the dorsomedial hypothalamus (DMH) plays a key role in gener
48 howed that large electrolytic lesions of the dorsomedial hypothalamus (DMH) promoted hypothermia in c
49 e report that TrkB-expressing neurons in the dorsomedial hypothalamus (DMH) regulate food intake.
50 e suggested that neuropeptide Y (NPY) in the dorsomedial hypothalamus (DMH) serves as an important si
51 asmatic nucleus (SCN) and relays through the dorsomedial hypothalamus (DMH) to LC; this circuit input
53 roxytryptamine (5-HT)] concentrations in the dorsomedial hypothalamus (DMH), a midline hypothalamic s
54 isruption of GABA-mediated inhibition in the dorsomedial hypothalamus (DMH), achieved by chronic micr
55 via the subparaventricular zone (SPZ) to the dorsomedial hypothalamus (DMH), and thence to ventrolate
56 dentified Fgf15, expressed in neurons of the dorsomedial hypothalamus (DMH), as a negative regulator
57 BP are mediated by neuronal circuits in the dorsomedial hypothalamus (DMH), as blocking leptin with
58 jections to effector control areas, like the dorsomedial hypothalamus (DMH), require labeling in live
65 luded the ventrolateral periaqueductal gray, dorsomedial hypothalamus, dorsolateral lateral hypothala
66 ave identified a dynorphinergic input to the dorsomedial hypothalamus from the dorsolateral parabrach
67 t a projection from the preoptic area to the dorsomedial hypothalamus has recently been implicated.
68 sed in the hippocampus, central amygdala and dorsomedial hypothalamus in pups tested early in the SHR
69 ot analysis was significantly reduced in the dorsomedial hypothalamus (including the paraventricular
71 x hypothalamic sites (anterior hypothalamus, dorsomedial hypothalamus, lateral hypothalamus, paravent
72 ng during scheduled feeding, we identified a dorsomedial hypothalamus leptin receptor-expressing (DMH
73 sometimes effective (anterior hypothalamus, dorsomedial hypothalamus, nucleus tractus solitarius), t
74 drugs, whereas those in the perifornical and dorsomedial hypothalamus regulate arousal and response t