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1 in mature males and females, in the rostral mediobasal hypothalamus.
2 uated outside the blood-brain barrier in the mediobasal hypothalamus.
3 tion and gliosis returned permanently to the mediobasal hypothalamus.
4 fusion of either insulin or vehicle into the mediobasal hypothalamus.
5 as associated with autophagic decline in the mediobasal hypothalamus.
6 y increased GnRH secretion from the preoptic-mediobasal hypothalamus.
7 hibits cyclic AMP (cAMP) accumulation in the mediobasal hypothalamus.
8 determining the distribution of cells in the mediobasal hypothalamus.
9 out the brain as well as in tanycytes in the mediobasal hypothalamus.
10 lso been observed among cells located in the mediobasal hypothalamus, a brain area that exerts centra
11 e of long-chain fatty acyl-coenzyme A in the mediobasal hypothalamus and blunted the hypothalamic res
12 euromedin B, which are found in axons in the mediobasal hypothalamus and may also be released from th
13 e Y (NPY) gene and protein expression in the mediobasal hypothalamus and that central administration
15 he hindbrain, including the hippocampus, the mediobasal hypothalamus, and the circumventricular organ
16 minent in the lateral septum, preoptic area, mediobasal hypothalamus, and tuberomammillary nucleus, w
17 tivity of beta-endorphinergic neurons in the mediobasal hypothalamus, as measured by Fos immunoreacti
18 livery of constitutively active FoxO1 to the mediobasal hypothalamus, but not to the suprachiasmatic
19 ther showed that NF-kappaB inhibition in the mediobasal hypothalamus counteracted obesity-related hyp
21 beta-endorphinergic neuronal activity in the mediobasal hypothalamus during pregnancy in the rat.
22 D61A)-expressing adeno-associated virus into mediobasal hypothalamus elicited a similar antiobese eff
23 sults show activation of POMC neurons in the mediobasal hypothalamus following general arousal but no
24 genetic inhibition of HDAC5 activity in the mediobasal hypothalamus increases food intake and modula
26 ling in WAT, but it abolished the ability of mediobasal hypothalamus insulin to suppress WAT lipolysi
27 sensitive potassium (K(ATP)) channels in the mediobasal hypothalamus is sufficient to lower blood glu
28 sensing of circulating nutrients within the mediobasal hypothalamus may be critical for energy homeo
29 f thyrotropin-releasing hormone (TRH) in the mediobasal hypothalamus (MBH) and thyroid-stimulating ho
32 diet stimulates microglial reactivity in the mediobasal hypothalamus (MBH) in association with decrea
33 receptors located more ventrally within the mediobasal hypothalamus (MBH) may inhibit the behavior o
35 xamine extracellular serotonin (5-HT) in the mediobasal hypothalamus (MBH) of male and female Fischer
36 Here we show that leptin infused into the mediobasal hypothalamus (MBH) of rats inhibits white adi
39 we demonstrate that Socs3 deficiency in the mediobasal hypothalamus (MBH) reduces food intake, prote
40 The metabolism of lactate to pyruvate in the mediobasal hypothalamus (MBH) regulates hepatic glucose
43 n in forebrain neurons, dominantly targeting mediobasal hypothalamus (MBH), display impaired fasting-
49 ith specialized neurons within nuclei of the mediobasal hypothalamus, namely the arcuate (ARC) and ve
52 e found evidence of increased gliosis in the mediobasal hypothalamus of obese humans, as assessed by
54 ts of either surgical deafferentation of the mediobasal hypothalamus or administration of a kappa opi
55 oadly across the brain or locally within the mediobasal hypothalamus, or specifically in hypothalamic
56 the infusion of a K(ATP) blocker within the mediobasal hypothalamus, or the surgical resection of th
57 activation of IKK-beta and NF-kappaB in the mediobasal hypothalamus--particularly in the hypothalami
58 ene expression patterns in the preoptic area/mediobasal hypothalamus (POA/MBH) of male rat brain 7 h
59 s accumbens; surgical deafferentation of the mediobasal hypothalamus prevented the effect of quinelor
60 ase-beta (IKK-beta, encoded by Ikbkb) in the mediobasal hypothalamus rapidly elevated blood pressure
62 Our results indicate that astrocytes in the mediobasal hypothalamus respond rapidly and robustly to
64 expressed in nutrient-sensing neurons of the mediobasal hypothalamus, responds to hormonal and nutrie
65 hroughout the CNS but highly enriched in the mediobasal hypothalamus, sense hormonal, nutrient and ne
66 the third cerebral ventricle (icv) or in the mediobasal hypothalamus stimulated GP independent of cha
67 that most kiss1 mRNA-containing cells of the mediobasal hypothalamus strongly express ERalpha and sli
68 he ventromedial nucleus (VMN), a part of the mediobasal hypothalamus that regulates sexual behavior i
69 an adipose-derived hormone, acts within the mediobasal hypothalamus to control food intake and energ
70 ulations of leptin-responsive neurons in the mediobasal hypothalamus to MCH and ORX cells in the LHA
71 developed with autophagic inhibition in the mediobasal hypothalamus using site-specific delivery of
72 talk" between leptin and insulin within the mediobasal hypothalamus via the intracellular enzyme, ph
74 e (GnIH-ir) cell bodies are clustered in the mediobasal hypothalamus with pronounced projections and
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