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1 tide and pro-opiomelanocortin neurons in the hypothalamic arcuate nucleus.
2 in and particularly strong expression in the hypothalamic arcuate nucleus.
3 ituitary gland, also release GABA within the hypothalamic arcuate nucleus.
4 are mainly located in the medial part of the hypothalamic arcuate nucleus.
5 bular dopamine (TIDA) neurons located in the hypothalamic arcuate nucleus.
6 uced ERK1/2 activation was restricted to the hypothalamic arcuate nucleus.
7 ic proopiomelanocortin (POMC) neurons of the hypothalamic arcuate nucleus.
8 ide Y and proopiomelanocortin neurons in the hypothalamic arcuate nucleus.
9 derived from POMC-containing neurons of the hypothalamic arcuate nucleus.
10 responses in neuroendocrine neurons from the hypothalamic arcuate nucleus.
11 n tyrosine hydroxylase-positive cells in the hypothalamic arcuate nucleus.
12 iPSCs) to model the development of the human hypothalamic arcuate nucleus.
13 we observed that activation of 5-HT(DRN) to hypothalamic arcuate nucleus (5-HT(DRN) ARH) projections
14 nd transcriptomes from male and female mouse hypothalamic arcuate nucleus, a key site for energy bala
15 iomelanocortin (POMC) neurons located in the hypothalamic arcuate nucleus and downstream neurons cont
16 We report that, in fasted rats, an intact hypothalamic arcuate nucleus and hepatic sympathetic inn
17 adipose tissue, liver, skeletal muscle, and hypothalamic arcuate nucleus and PTP1B protein 2-fold in
18 3 is expressed in Kiss1 neurons of the mouse hypothalamic arcuate nucleus and that MKRN3 repressed pr
19 penditure (e.g., melanocortin neurons in the hypothalamic arcuate nucleus) and are stimulated by inpu
21 exigenic peptide neuropeptide Y (NPY) in the hypothalamic arcuate nucleus, and reduced expression of
23 surprisingly high tdTomato expression in the hypothalamic arcuate nucleus (Arc) (i.e., within parts o
26 e, high fat diet containing sucrose (HPD) on hypothalamic arcuate nucleus (ARC) gene expression for n
27 ng activated reporter gene expression in the hypothalamic arcuate nucleus (Arc) in a small subset of
29 eptin in the medial preoptic area (mPOA) and hypothalamic arcuate nucleus (ARC) may operate downstrea
30 uin 1 (SIRT1)/FoxO1 signaling pathway in the hypothalamic arcuate nucleus (ARC) mediates MCH-induced
31 re, we show that the great majority of mouse hypothalamic arcuate nucleus (ARC) neurons that synthesi
32 indolol) were significantly increased in the hypothalamic arcuate nucleus (ARC) of DiO rats (58%; P<0
33 ti-related peptide (AgRP) mRNA levels in the hypothalamic arcuate nucleus (ARC) of Npy(--/--) and Npy
34 is mediated primarily through activation of hypothalamic arcuate nucleus (ARC) pro-opiomelanocortin
35 GABA(DVC) circuitry identified GABA(DVC) -> hypothalamic arcuate nucleus (ARC) projections as appeti
37 a unique class of excitatory neurons in the hypothalamic arcuate nucleus (ARC) that utilizes glutama
38 endocrine dopaminergic (NEDA) neurons in the hypothalamic arcuate nucleus (ARC) to maintain low level
44 logical processes governed by neurons in the hypothalamic arcuate nucleus (ARC), such as growth, repr
45 glutamate neurons are sparse in the rostral hypothalamic arcuate nucleus (ARC), the subregion that h
52 lar responses to chemical stimulation of the hypothalamic arcuate nucleus (ARCN) was studied in ureth
53 Proopiomelanocortin (POMC) neurons of the hypothalamic arcuate nucleus are essential to regulate f
59 e and immune function, and regulation of the hypothalamic arcuate nucleus, but demonstrated modest im
60 1% (P < 0.05), and levels of NPY mRNA in the hypothalamic arcuate nucleus by 42.3% (P < 0.05) as comp
61 do not show elevated NPY mRNA levels in the hypothalamic arcuate nucleus compared to wild-type/heter
65 notype, VGF mRNA levels are regulated in the hypothalamic arcuate nucleus in response to fasting.
67 amic-retrochiasmatic area and the mediobasal hypothalamic arcuate nucleus independently generate ultr
68 ermined that glucokinase activity within the hypothalamic arcuate nucleus is involved in regulation o
71 f the hypothalamic feeding center, such that hypothalamic arcuate nucleus neurons exhibit reduced sen
73 gestive of neuron injury were evident in the hypothalamic arcuate nucleus of rats and mice within the
74 sm and pancreatic beta-cell function, to the hypothalamic arcuate nucleus of rodents results in a los
75 orphin and neurokinin B (NKB) neurons in the hypothalamic arcuate nucleus participate in the sex-ster
77 ed by pro-opiomelanocortin (POMC) neurons of hypothalamic arcuate nucleus regulate food intake, energ
80 te and ultimately body weight.Neurons in the hypothalamic arcuate nucleus, the ventromedial hypothala
81 tection of leptin adiposity signaling is the hypothalamic arcuate nucleus, where leptin inhibits expr