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1 antially more abundant than those containing melanin-concentrating hormone.
2 cells were distinct from those that express melanin-concentrating hormone.
3 escribed neuropeptides hypocretin/orexin and melanin-concentrating hormone.
4 wly generated neurons expressing ENK, OX, or melanin-concentrating hormone.
7 related peptide, melanocortins, orexins, and melanin concentrating hormone, among other mediators.
8 e mice, C75 markedly increased expression of melanin-concentrating hormone and its receptor in the hy
9 st, direct projections to the MOB arise from melanin-concentrating hormone and orexin neurons in the
10 particular interest: pattern A, hypothalamic melanin-concentrating hormone and proopiomelanocortin bu
11 o be present, eliminated some neurons (Hcrt, melanin-concentrating hormone, and adenosine deaminase-c
12 in the brain, including neurons that secrete melanin-concentrating hormone, and culminates in the rel
13 er of hypothalamic neurons producing orexin, melanin-concentrating hormone, and histamine in 7 narcol
14 These cells included those producing orexin, melanin-concentrating hormone, and luteinizing hormone-r
15 vitro, but not in inhibiting cannabinoid-1, melanin-concentrating hormone, and melanin-concentrating
17 opiomelanocortin, thyroid-releasing hormone, melanin-concentrating hormone, and orexin expression.
18 proopiomelanocortin in the arcuate nucleus, melanin-concentrating hormone, and orexin in the lateral
19 duces excitatory synaptic strength onto both melanin-concentrating hormone- and orexin-expressing neu
20 Y (NPY), agouti-related protein (AgRP), and melanin-concentrating hormone] and anorexigenic [pro-opi
21 orexigenic peptides, enkephalin, orexin and melanin-concentrating hormone, as revealed using real-ti
22 nic neuropeptides Agouti-related peptide and melanin-concentrating hormone but surprisingly has no ef
23 with optogenetic activation of hypothalamic melanin-concentrating hormone containing cells to increa
24 citatory synaptic inputs to both orexin- and melanin-concentrating hormone expressing LHA neurons pro
25 ly implicated in this disorder: hypothalamic melanin-concentrating hormone-expressing neurons (MNs).
30 n the paraventricular nucleus and orexin and melanin-concentrating hormone in the perifornical latera
31 mygdala, OX, and another orexigenic peptide, melanin-concentrating hormone, in the perifornical later
32 xpression, increased hypothalamic Orexin and melanin-concentrating hormone, increased food intake, re
33 A, and genetic disruption of kappaOR reduced melanin concentrating hormone-induced liver steatosis.
37 pus, lateral hypothalamic neurons containing melanin concentrating hormone (MCH) and GABA send long a
39 e a selective association of these INRs with melanin concentrating hormone (MCH) and tyrosine hydroxy
47 for body weight, mice with selective loss of melanin concentrating hormone (MCH) neurons were generat
49 two hypothalamic neuropeptides oxytocin and melanin concentrating hormone (MCH) share several physio
50 ropeptide systems NPY, AGRP, orexin (OX) and melanin concentrating hormone (MCH), 3) special inductio
52 s in the LH, expressing hypocretin/orexin or melanin concentrating hormone (MCH), have been shown to
53 in hypothalamus of neuropeptide Y (NPY) and melanin concentrating hormone (MCH), two neuropeptides t
56 the number of hypocretin (29.7% reduction), melanin concentrating hormone (MCH; 24.7% reduction), an
58 in the LHA and in the posterior Pe coexpress melanin-concentrating hormone (MCH) and glutamic acid de
59 wn classes of LHA projection neurons, namely melanin-concentrating hormone (MCH) and hypocretin/orexi
64 ropeptide Y (NPY) in the arcuate nucleus and melanin-concentrating hormone (MCH) and orexins/hypocret
66 mic neurons that synthesize the neuropeptide melanin-concentrating hormone (MCH) are claimed to be ac
67 Here we show that LHA neurons that produce melanin-concentrating hormone (MCH) are dynamically resp
68 orexigenic peptides hypocretin (orexin) and melanin-concentrating hormone (MCH) are involved in the
72 the use of Eu3+ chelate-labeled analogues of melanin-concentrating hormone (MCH) as ligands for both
86 s of evidence indicate that the neuropeptide melanin-concentrating hormone (MCH) is an important comp
95 spontaneous behavioral acts and activity of melanin-concentrating hormone (MCH) neurons (MNs) in beh
98 lateral hypothalamic (LH) circuits involving melanin-concentrating hormone (MCH) neurons are subject
99 tudy, we show that optogenetic activation of melanin-concentrating hormone (MCH) neurons during intak
100 During encounters with objects, hypothalamic melanin-concentrating hormone (MCH) neurons emit brief s
102 esity (DIO) by activating appetite-promoting melanin-concentrating hormone (MCH) neurons in the hypot
106 creased the activity of lateral hypothalamic melanin-concentrating hormone (MCH) neurons selectively
107 in-releasing peptide (PrRP) cells innervated melanin-concentrating hormone (MCH) neurons that are cru
108 (mGluR1 and mGluR5) activation on identified melanin-concentrating hormone (MCH) neurons was studied
112 s expression in orexinergic but not adjacent melanin-concentrating hormone (MCH) neurons; suggesting
113 amic neurons including those that synthesize melanin-concentrating hormone (MCH) or hypocretin/orexin
117 s that both PrRP and PrRP-NA cells innervate melanin-concentrating hormone (MCH) producing neurons in
119 n suggest that the hypothalamic neuropeptide melanin-concentrating hormone (MCH) regulates body weigh
123 t fertility also upregulate the hypothalamic melanin-concentrating hormone (MCH) system that promotes
128 e AcbSh contains high levels of receptor for melanin-concentrating hormone (MCH), a lateral hypothala
130 ntibodies against tyrosine hydroxylase (TH), melanin-concentrating hormone (MCH), and hypocretin (Hcr
131 ontaining the feeding-related neuropeptides, melanin-concentrating hormone (MCH), and orexin (Orx).
132 ressin (AVP), histidine decarboxylase (HDC), melanin-concentrating hormone (MCH), and orexin/hypocret
133 rected to rWAT and iWAT expressed orexin and melanin-concentrating hormone (MCH), but male rats had a
134 eurons, and not nearby LH neurons expressing melanin-concentrating hormone (MCH), have mu-opioid rece
136 LHAad did not express significant amounts of melanin-concentrating hormone (MCH), orexin, or galanin;
137 oopiomelanocortin (POMC), orexin/hypocretin, melanin-concentrating hormone (MCH), thyrotropin-releasi
139 e distinct from neighboring leptin-regulated melanin-concentrating hormone (MCH)- or orexin (OX)-expr
141 ing impulsivity involving communication from melanin-concentrating hormone (MCH)-expressing lateral h
151 ortin (POMC), agouti-related peptide (AgRP), melanin-concentrating-hormone (MCH) and orexin (ORX) neu
155 hypothalamic neuropeptides, hypocretin-1 and melanin-concentrating hormone, measured in the human amy
157 ght to moderate inputs arose from orexin and melanin concentrating hormone neurons, but cholinergic o
159 Glut4 neuron ablation affects orexigenic melanin-concentrating hormone neurons but has limited ef
160 in gene transfer into the striatum or in the melanin-concentrating hormone neurons in the ZI or LH ha
161 excitatory current with repeated coexposure (melanin-concentrating hormone neurons), synergistic dire
162 Neither rPP nor NPY stimulated c-Fos in melanin-concentrating hormone neurons, but both activate
164 rons and/or fibers in this area positive for melanin concentrating hormone, oxytocin, arginine vasopr
165 ons and contain dopamine, histamine, orexin, melanin-concentrating hormone, oxytocin, and vasopressin
166 , agouti-related peptide, hypocretin/orexin, melanin-concentrating hormone, oxytocin, arginine vasopr
167 Expression of transcripts for human pro-melanin concentrating hormone (pMCH) were studied in the
172 -2-o ne (7) is a potent, orally bioavailable melanin concentrating hormone receptor 1 (MCHr1) antagon
174 mitogen-activated protein kinase 7 (MAPK7), melanin concentrating hormone receptor 1 (MCHR1), and sp
175 of multiple structurally distinct series of melanin concentrating hormone receptor 1 antagonists in
176 ormation but disrupts normal localization of melanin concentrating hormone receptor 1 to ciliary memb
177 ioselective synthesis of SNAP-7941, a potent melanin concentrating hormone receptor antagonist, was a
179 We identified the consensus sequence in melanin-concentrating hormone receptor 1 (Mchr1) and con
180 screening mode to triage multiple classes of melanin-concentrating hormone receptor 1 (MCHr1) antagon
181 DNA phage-display library, we identified the melanin-concentrating hormone receptor 1 (MCHR1) as a no
182 of somatostatin receptor type 3 (Sstr3) and melanin-concentrating hormone receptor 1 (Mchr1) in neur
184 n of a high-throughput screening hit against melanin-concentrating hormone receptor 1 (MCHr1) led to
187 ts exhibited autoantibodies to more than one melanin-concentrating hormone receptor 1 epitope indicat
188 identification of autoantibodies against the melanin-concentrating hormone receptor 1 in patients wit
189 ediction of the potential B cell epitopes on melanin-concentrating hormone receptor 1 revealed that t
191 stence of multiple antibody binding sites on melanin-concentrating hormone receptor 1, including regi
193 ) and found that the distribution of ciliary melanin-concentrating hormone receptor-1 (MchR1) was sig
194 s for the G-protein-coupled receptor (GPCR), melanin-concentrating hormone receptor-1 (MCHR1), with a
195 are potent but nonspecific ligands for human melanin-concentrating hormone receptors 1 and 2 (hMCH-1R
196 s a potent but nonselective agonist at human melanin-concentrating hormone receptors 1 and 2 (hMCH-1R
198 a nonselective natural ligand for the human melanin-concentrating hormone receptors: hMCH-1R and hMC
201 altered mRNA expression levels of orexin and melanin-concentrating hormone, two peptides that are imp