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1                                          The mediobasal hypothalami from adult male rats were incubat
2 xin neurons correlates with place preference Mediobasal hypothalamic Agrp neurons inhibit orexin neur
3 or hypothalamic-retrochiasmatic area and the mediobasal hypothalamic arcuate nucleus independently ge
4 /x-deficient tanycytes give rise to multiple mediobasal hypothalamic neuronal subtypes that can matur
5 alamus, estradiol increases spine density in mediobasal hypothalamic nuclei that regulate reproductio
6 e PERIOD2::LUCIFERASE (PER2::LUC) rhythms in mediobasal hypothalamic nuclei, which influence these be
7 nar thalamic nuclei, the supramammillary and mediobasal hypothalamic nuclei.
8               Ex vivo biochemical studies of mediobasal hypothalamic tissue revealed that insulin sti
9  obesity and diabetes, and downregulation of mediobasal hypothalamic TXNIP expression prevents diet-i
10                                        Thus, mediobasal hypothalamic TXNIP plays a critical role in n
11 f thyrotropin-releasing hormone (TRH) in the mediobasal hypothalamus (MBH) and thyroid-stimulating ho
12                    Kisspeptin neurons in the mediobasal hypothalamus (MBH) are critical targets of ov
13                                          The mediobasal hypothalamus (MBH) contains neurons capable o
14         In response to nutrient stimuli, the mediobasal hypothalamus (MBH) drives multiple neuroendoc
15 diet stimulates microglial reactivity in the mediobasal hypothalamus (MBH) in association with decrea
16                                          The mediobasal hypothalamus (MBH) is involved in energy home
17  receptors located more ventrally within the mediobasal hypothalamus (MBH) may inhibit the behavior o
18        In the current study, we examined the mediobasal hypothalamus (MBH) of 57 obese human subjects
19 xamine extracellular serotonin (5-HT) in the mediobasal hypothalamus (MBH) of male and female Fischer
20    Here we show that leptin infused into the mediobasal hypothalamus (MBH) of rats inhibits white adi
21                      Previous studies on the mediobasal hypothalamus (MBH) of rats, rhesus monkeys an
22           Because the arcuate nucleus in the mediobasal hypothalamus (MBH) plays a pivotal role in in
23                     We hypothesized that the mediobasal hypothalamus (MBH) provides the neuroendocrin
24  we demonstrate that Socs3 deficiency in the mediobasal hypothalamus (MBH) reduces food intake, prote
25 -1 receptor (CB1R) expressing neurons in the mediobasal hypothalamus (MBH) regulate increased appetit
26 The metabolism of lactate to pyruvate in the mediobasal hypothalamus (MBH) regulates hepatic glucose
27                   Opioid activity within the mediobasal hypothalamus (MBH) regulates suckling-induced
28 f fibroblast growth factor 1 (FGF1), and the mediobasal hypothalamus (MBH) was recently implicated as
29        Here, we investigated the role of the mediobasal hypothalamus (MBH), a key center involved in
30 n in forebrain neurons, dominantly targeting mediobasal hypothalamus (MBH), display impaired fasting-
31 ose and long-chain fatty acids (LCFA) by the mediobasal hypothalamus (MBH).
32 actions that include nutrient sensing in the mediobasal hypothalamus (MBH).
33 h clocks in energy regulatory centers of the mediobasal hypothalamus (MBH).
34 sulin signaling and activation of S6K in the mediobasal hypothalamus (MBH).
35 ty in the third cerebral ventricle or in the mediobasal hypothalamus (MBH).
36 odothyronine deiodinase (D2) activity in the mediobasal hypothalamus (MBH).
37  tanycytes lining the 3(rd) ventricle of the mediobasal hypothalamus (MBH).(8)(,)(9)(,)(10) Here we u
38 ically delete beta-catenin expression in the mediobasal hypothalamus (MBH-beta-cat KO).
39 ene expression patterns in the preoptic area/mediobasal hypothalamus (POA/MBH) of male rat brain 7 h
40         Adult-onset ablation of Sh2b1 in the mediobasal hypothalamus also impairs the SNS/BAT/thermog
41 e of long-chain fatty acyl-coenzyme A in the mediobasal hypothalamus and blunted the hypothalamic res
42 euromedin B, which are found in axons in the mediobasal hypothalamus and may also be released from th
43 e Y (NPY) gene and protein expression in the mediobasal hypothalamus and that central administration
44 A expression of Cav3.1 alpha1 subunit in the mediobasal hypothalamus and the pituitary.
45 ed higher elevation of Luc expression in the mediobasal hypothalamus compared to the cortex, and stud
46 ther showed that NF-kappaB inhibition in the mediobasal hypothalamus counteracted obesity-related hyp
47    Prostaglandin PGE2 levels increase in the mediobasal hypothalamus during high-fat-diet (HFD) feedi
48 beta-endorphinergic neuronal activity in the mediobasal hypothalamus during pregnancy in the rat.
49 D61A)-expressing adeno-associated virus into mediobasal hypothalamus elicited a similar antiobese eff
50 sults show activation of POMC neurons in the mediobasal hypothalamus following general arousal but no
51  genetic inhibition of HDAC5 activity in the mediobasal hypothalamus increases food intake and modula
52 s that activation of 5-HT1A receptors in the mediobasal hypothalamus inhibits lordosis behavior.
53 ling in WAT, but it abolished the ability of mediobasal hypothalamus insulin to suppress WAT lipolysi
54 ation initiation factor eIF2alpha within the mediobasal hypothalamus is known to suppress food intake
55 sensitive potassium (K(ATP)) channels in the mediobasal hypothalamus is sufficient to lower blood glu
56  sensing of circulating nutrients within the mediobasal hypothalamus may be critical for energy homeo
57  (Pomc) in a group of neurons located in the mediobasal hypothalamus of all vertebrates.
58                                       In the mediobasal hypothalamus of B2KO mice, expression of gene
59 owed that autophagy was highly active in the mediobasal hypothalamus of normal mice.
60 e found evidence of increased gliosis in the mediobasal hypothalamus of obese humans, as assessed by
61 enzyme A) were injected bilaterally into the mediobasal hypothalamus of rats.
62 ts of either surgical deafferentation of the mediobasal hypothalamus or administration of a kappa opi
63 nucleus of the solitary tract (NTS), but not mediobasal hypothalamus or area postrema, resulted in de
64 s accumbens; surgical deafferentation of the mediobasal hypothalamus prevented the effect of quinelor
65 ase-beta (IKK-beta, encoded by Ikbkb) in the mediobasal hypothalamus rapidly elevated blood pressure
66                                          The mediobasal hypothalamus regulates functions necessary fo
67  Our results indicate that astrocytes in the mediobasal hypothalamus respond rapidly and robustly to
68       Here, we report that astrocytes in the mediobasal hypothalamus respond robustly and rapidly to
69 the third cerebral ventricle (icv) or in the mediobasal hypothalamus stimulated GP independent of cha
70 that most kiss1 mRNA-containing cells of the mediobasal hypothalamus strongly express ERalpha and sli
71 he ventromedial nucleus (VMN), a part of the mediobasal hypothalamus that regulates sexual behavior i
72  an adipose-derived hormone, acts within the mediobasal hypothalamus to control food intake and energ
73 ulations of leptin-responsive neurons in the mediobasal hypothalamus to MCH and ORX cells in the LHA
74  developed with autophagic inhibition in the mediobasal hypothalamus using site-specific delivery of
75  talk" between leptin and insulin within the mediobasal hypothalamus via the intracellular enzyme, ph
76               Hypocretin cells innervate the mediobasal hypothalamus where they can potentially influ
77 e (GnIH-ir) cell bodies are clustered in the mediobasal hypothalamus with pronounced projections and
78 lso been observed among cells located in the mediobasal hypothalamus, a brain area that exerts centra
79  that attenuation of IGF-1R signaling in the mediobasal hypothalamus, and specifically in AgRP neuron
80 he hindbrain, including the hippocampus, the mediobasal hypothalamus, and the circumventricular organ
81 minent in the lateral septum, preoptic area, mediobasal hypothalamus, and tuberomammillary nucleus, w
82 tivity of beta-endorphinergic neurons in the mediobasal hypothalamus, as measured by Fos immunoreacti
83 livery of constitutively active FoxO1 to the mediobasal hypothalamus, but not to the suprachiasmatic
84                                       In the mediobasal hypothalamus, DEPTOR was expressed in neurons
85 ith specialized neurons within nuclei of the mediobasal hypothalamus, namely the arcuate (ARC) and ve
86 on, AAV-mediated Dusp8 overexpression in the mediobasal hypothalamus, or metyrapone-induced chemical
87 oadly across the brain or locally within the mediobasal hypothalamus, or specifically in hypothalamic
88  the infusion of a K(ATP) blocker within the mediobasal hypothalamus, or the surgical resection of th
89 expressed in nutrient-sensing neurons of the mediobasal hypothalamus, responds to hormonal and nutrie
90 hroughout the CNS but highly enriched in the mediobasal hypothalamus, sense hormonal, nutrient and ne
91  activation of IKK-beta and NF-kappaB in the mediobasal hypothalamus--particularly in the hypothalami
92  in mature males and females, in the rostral mediobasal hypothalamus.
93 uated outside the blood-brain barrier in the mediobasal hypothalamus.
94 tion and gliosis returned permanently to the mediobasal hypothalamus.
95 fusion of either insulin or vehicle into the mediobasal hypothalamus.
96 as associated with autophagic decline in the mediobasal hypothalamus.
97 y increased GnRH secretion from the preoptic-mediobasal hypothalamus.
98 hibits cyclic AMP (cAMP) accumulation in the mediobasal hypothalamus.
99 determining the distribution of cells in the mediobasal hypothalamus.
100 out the brain as well as in tanycytes in the mediobasal hypothalamus.