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1 in and particularly strong expression in the hypothalamic arcuate nucleus.
2 are mainly located in the medial part of the hypothalamic arcuate nucleus.
3 bular dopamine (TIDA) neurons located in the hypothalamic arcuate nucleus.
4 uced ERK1/2 activation was restricted to the hypothalamic arcuate nucleus.
5 ic proopiomelanocortin (POMC) neurons of the hypothalamic arcuate nucleus.
6 ide Y and proopiomelanocortin neurons in the hypothalamic arcuate nucleus.
7 derived from POMC-containing neurons of the hypothalamic arcuate nucleus.
8 responses in neuroendocrine neurons from the hypothalamic arcuate nucleus.
9 ituitary gland, also release GABA within the hypothalamic arcuate nucleus.
10 We report that, in fasted rats, an intact hypothalamic arcuate nucleus and hepatic sympathetic inn
11 adipose tissue, liver, skeletal muscle, and hypothalamic arcuate nucleus and PTP1B protein 2-fold in
12 penditure (e.g., melanocortin neurons in the hypothalamic arcuate nucleus) and are stimulated by inpu
14 exigenic peptide neuropeptide Y (NPY) in the hypothalamic arcuate nucleus, and reduced expression of
16 surprisingly high tdTomato expression in the hypothalamic arcuate nucleus (Arc) (i.e., within parts o
19 e, high fat diet containing sucrose (HPD) on hypothalamic arcuate nucleus (ARC) gene expression for n
20 ng activated reporter gene expression in the hypothalamic arcuate nucleus (Arc) in a small subset of
22 eptin in the medial preoptic area (mPOA) and hypothalamic arcuate nucleus (ARC) may operate downstrea
23 re, we show that the great majority of mouse hypothalamic arcuate nucleus (ARC) neurons that synthesi
24 indolol) were significantly increased in the hypothalamic arcuate nucleus (ARC) of DiO rats (58%; P<0
25 ti-related peptide (AgRP) mRNA levels in the hypothalamic arcuate nucleus (ARC) of Npy(--/--) and Npy
26 is mediated primarily through activation of hypothalamic arcuate nucleus (ARC) pro-opiomelanocortin
27 endocrine dopaminergic (NEDA) neurons in the hypothalamic arcuate nucleus (ARC) to maintain low level
37 lar responses to chemical stimulation of the hypothalamic arcuate nucleus (ARCN) was studied in ureth
42 e and immune function, and regulation of the hypothalamic arcuate nucleus, but demonstrated modest im
43 1% (P < 0.05), and levels of NPY mRNA in the hypothalamic arcuate nucleus by 42.3% (P < 0.05) as comp
44 do not show elevated NPY mRNA levels in the hypothalamic arcuate nucleus compared to wild-type/heter
47 notype, VGF mRNA levels are regulated in the hypothalamic arcuate nucleus in response to fasting.
49 amic-retrochiasmatic area and the mediobasal hypothalamic arcuate nucleus independently generate ultr
50 ermined that glucokinase activity within the hypothalamic arcuate nucleus is involved in regulation o
53 gestive of neuron injury were evident in the hypothalamic arcuate nucleus of rats and mice within the
54 sm and pancreatic beta-cell function, to the hypothalamic arcuate nucleus of rodents results in a los
55 orphin and neurokinin B (NKB) neurons in the hypothalamic arcuate nucleus participate in the sex-ster
57 ed by pro-opiomelanocortin (POMC) neurons of hypothalamic arcuate nucleus regulate food intake, energ
59 te and ultimately body weight.Neurons in the hypothalamic arcuate nucleus, the ventromedial hypothala
60 tection of leptin adiposity signaling is the hypothalamic arcuate nucleus, where leptin inhibits expr
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