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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         Adult-onset ablation of Sh2b1 in the mediobasal hypothalamus also impairs the SNS/BAT/thermog
12 e of long-chain fatty acyl-coenzyme A in the mediobasal hypothalamus and blunted the hypothalamic res
13 euromedin B, which are found in axons in the mediobasal hypothalamus and may also be released from th
14 e Y (NPY) gene and protein expression in the mediobasal hypothalamus and that central administration
15 A expression of Cav3.1 alpha1 subunit in the mediobasal hypothalamus and the pituitary.
16  that attenuation of IGF-1R signaling in the mediobasal hypothalamus, and specifically in AgRP neuron
17 he hindbrain, including the hippocampus, the mediobasal hypothalamus, and the circumventricular organ
18 minent in the lateral septum, preoptic area, mediobasal hypothalamus, and tuberomammillary nucleus, w
19 tivity of beta-endorphinergic neurons in the mediobasal hypothalamus, as measured by Fos immunoreacti
20 livery of constitutively active FoxO1 to the mediobasal hypothalamus, but not to the suprachiasmatic
21 ed higher elevation of Luc expression in the mediobasal hypothalamus compared to the cortex, and stud
22 ther showed that NF-kappaB inhibition in the mediobasal hypothalamus counteracted obesity-related hyp
23                                       In the mediobasal hypothalamus, DEPTOR was expressed in neurons
24    Prostaglandin PGE2 levels increase in the mediobasal hypothalamus during high-fat-diet (HFD) feedi
25 beta-endorphinergic neuronal activity in the mediobasal hypothalamus during pregnancy in the rat.
26 D61A)-expressing adeno-associated virus into mediobasal hypothalamus elicited a similar antiobese eff
27 sults show activation of POMC neurons in the mediobasal hypothalamus following general arousal but no
28  genetic inhibition of HDAC5 activity in the mediobasal hypothalamus increases food intake and modula
29 s that activation of 5-HT1A receptors in the mediobasal hypothalamus inhibits lordosis behavior.
30 ling in WAT, but it abolished the ability of mediobasal hypothalamus insulin to suppress WAT lipolysi
31 ation initiation factor eIF2alpha within the mediobasal hypothalamus is known to suppress food intake
32 sensitive potassium (K(ATP)) channels in the mediobasal hypothalamus is sufficient to lower blood glu
33  sensing of circulating nutrients within the mediobasal hypothalamus may be critical for energy homeo
34 f thyrotropin-releasing hormone (TRH) in the mediobasal hypothalamus (MBH) and thyroid-stimulating ho
35                    Kisspeptin neurons in the mediobasal hypothalamus (MBH) are critical targets of ov
36                                          The mediobasal hypothalamus (MBH) contains neurons capable o
37         In response to nutrient stimuli, the mediobasal hypothalamus (MBH) drives multiple neuroendoc
38 diet stimulates microglial reactivity in the mediobasal hypothalamus (MBH) in association with decrea
39                                          The mediobasal hypothalamus (MBH) is involved in energy home
40  receptors located more ventrally within the mediobasal hypothalamus (MBH) may inhibit the behavior o
41        In the current study, we examined the mediobasal hypothalamus (MBH) of 57 obese human subjects
42 xamine extracellular serotonin (5-HT) in the mediobasal hypothalamus (MBH) of male and female Fischer
43    Here we show that leptin infused into the mediobasal hypothalamus (MBH) of rats inhibits white adi
44                      Previous studies on the mediobasal hypothalamus (MBH) of rats, rhesus monkeys an
45           Because the arcuate nucleus in the mediobasal hypothalamus (MBH) plays a pivotal role in in
46                     We hypothesized that the mediobasal hypothalamus (MBH) provides the neuroendocrin
47  we demonstrate that Socs3 deficiency in the mediobasal hypothalamus (MBH) reduces food intake, prote
48 -1 receptor (CB1R) expressing neurons in the mediobasal hypothalamus (MBH) regulate increased appetit
49 The metabolism of lactate to pyruvate in the mediobasal hypothalamus (MBH) regulates hepatic glucose
50                   Opioid activity within the mediobasal hypothalamus (MBH) regulates suckling-induced
51 f fibroblast growth factor 1 (FGF1), and the mediobasal hypothalamus (MBH) was recently implicated as
52        Here, we investigated the role of the mediobasal hypothalamus (MBH), a key center involved in
53 n in forebrain neurons, dominantly targeting mediobasal hypothalamus (MBH), display impaired fasting-
54 ose and long-chain fatty acids (LCFA) by the mediobasal hypothalamus (MBH).
55 h clocks in energy regulatory centers of the mediobasal hypothalamus (MBH).
56 actions that include nutrient sensing in the mediobasal hypothalamus (MBH).
57 sulin signaling and activation of S6K in the mediobasal hypothalamus (MBH).
58 ty in the third cerebral ventricle or in the mediobasal hypothalamus (MBH).
59 odothyronine deiodinase (D2) activity in the mediobasal hypothalamus (MBH).
60  tanycytes lining the 3(rd) ventricle of the mediobasal hypothalamus (MBH).(8)(,)(9)(,)(10) Here we u
61 ically delete beta-catenin expression in the mediobasal hypothalamus (MBH-beta-cat KO).
62 ith specialized neurons within nuclei of the mediobasal hypothalamus, namely the arcuate (ARC) and ve
63  (Pomc) in a group of neurons located in the mediobasal hypothalamus of all vertebrates.
64                                       In the mediobasal hypothalamus of B2KO mice, expression of gene
65 owed that autophagy was highly active in the mediobasal hypothalamus of normal mice.
66 e found evidence of increased gliosis in the mediobasal hypothalamus of obese humans, as assessed by
67 enzyme A) were injected bilaterally into the mediobasal hypothalamus of rats.
68 ts of either surgical deafferentation of the mediobasal hypothalamus or administration of a kappa opi
69 nucleus of the solitary tract (NTS), but not mediobasal hypothalamus or area postrema, resulted in de
70 on, AAV-mediated Dusp8 overexpression in the mediobasal hypothalamus, or metyrapone-induced chemical
71 oadly across the brain or locally within the mediobasal hypothalamus, or specifically in hypothalamic
72  the infusion of a K(ATP) blocker within the mediobasal hypothalamus, or the surgical resection of th
73  activation of IKK-beta and NF-kappaB in the mediobasal hypothalamus--particularly in the hypothalami
74 ene expression patterns in the preoptic area/mediobasal hypothalamus (POA/MBH) of male rat brain 7 h
75 s accumbens; surgical deafferentation of the mediobasal hypothalamus prevented the effect of quinelor
76 ase-beta (IKK-beta, encoded by Ikbkb) in the mediobasal hypothalamus rapidly elevated blood pressure
77                                          The mediobasal hypothalamus regulates functions necessary fo
78  Our results indicate that astrocytes in the mediobasal hypothalamus respond rapidly and robustly to
79       Here, we report that astrocytes in the mediobasal hypothalamus respond robustly and rapidly to
80 expressed in nutrient-sensing neurons of the mediobasal hypothalamus, responds to hormonal and nutrie
81 hroughout the CNS but highly enriched in the mediobasal hypothalamus, sense hormonal, nutrient and ne
82 the third cerebral ventricle (icv) or in the mediobasal hypothalamus stimulated GP independent of cha
83 that most kiss1 mRNA-containing cells of the mediobasal hypothalamus strongly express ERalpha and sli
84 he ventromedial nucleus (VMN), a part of the mediobasal hypothalamus that regulates sexual behavior i
85  an adipose-derived hormone, acts within the mediobasal hypothalamus to control food intake and energ
86 ulations of leptin-responsive neurons in the mediobasal hypothalamus to MCH and ORX cells in the LHA
87  developed with autophagic inhibition in the mediobasal hypothalamus using site-specific delivery of
88  talk" between leptin and insulin within the mediobasal hypothalamus via the intracellular enzyme, ph
89               Hypocretin cells innervate the mediobasal hypothalamus where they can potentially influ
90 e (GnIH-ir) cell bodies are clustered in the mediobasal hypothalamus with pronounced projections and