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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 wly generated neurons expressing ENK, OX, or melanin-concentrating hormone.
4 escribed neuropeptides hypocretin/orexin and melanin-concentrating hormone.
6 related peptide, melanocortins, orexins, and melanin concentrating hormone, among other mediators.
7 e mice, C75 markedly increased expression of melanin-concentrating hormone and its receptor in the hy
8 particular interest: pattern A, hypothalamic melanin-concentrating hormone and proopiomelanocortin bu
9 o be present, eliminated some neurons (Hcrt, melanin-concentrating hormone, and adenosine deaminase-c
10 in the brain, including neurons that secrete melanin-concentrating hormone, and culminates in the rel
11 er of hypothalamic neurons producing orexin, melanin-concentrating hormone, and histamine in 7 narcol
12 These cells included those producing orexin, melanin-concentrating hormone, and luteinizing hormone-r
13 vitro, but not in inhibiting cannabinoid-1, melanin-concentrating hormone, and melanin-concentrating
15 opiomelanocortin, thyroid-releasing hormone, melanin-concentrating hormone, and orexin expression.
16 proopiomelanocortin in the arcuate nucleus, melanin-concentrating hormone, and orexin in the lateral
17 duces excitatory synaptic strength onto both melanin-concentrating hormone- and orexin-expressing neu
18 Y (NPY), agouti-related protein (AgRP), and melanin-concentrating hormone] and anorexigenic [pro-opi
19 orexigenic peptides, enkephalin, orexin and melanin-concentrating hormone, as revealed using real-ti
20 nic neuropeptides Agouti-related peptide and melanin-concentrating hormone but surprisingly has no ef
21 citatory synaptic inputs to both orexin- and melanin-concentrating hormone expressing LHA neurons pro
26 n the paraventricular nucleus and orexin and melanin-concentrating hormone in the perifornical latera
27 mygdala, OX, and another orexigenic peptide, melanin-concentrating hormone, in the perifornical later
28 xpression, increased hypothalamic Orexin and melanin-concentrating hormone, increased food intake, re
29 A, and genetic disruption of kappaOR reduced melanin concentrating hormone-induced liver steatosis.
33 pus, lateral hypothalamic neurons containing melanin concentrating hormone (MCH) and GABA send long a
35 e a selective association of these INRs with melanin concentrating hormone (MCH) and tyrosine hydroxy
43 for body weight, mice with selective loss of melanin concentrating hormone (MCH) neurons were generat
44 ropeptide systems NPY, AGRP, orexin (OX) and melanin concentrating hormone (MCH), 3) special inductio
46 s in the LH, expressing hypocretin/orexin or melanin concentrating hormone (MCH), have been shown to
47 in hypothalamus of neuropeptide Y (NPY) and melanin concentrating hormone (MCH), two neuropeptides t
50 the number of hypocretin (29.7% reduction), melanin concentrating hormone (MCH; 24.7% reduction), an
51 in the LHA and in the posterior Pe coexpress melanin-concentrating hormone (MCH) and glutamic acid de
52 wn classes of LHA projection neurons, namely melanin-concentrating hormone (MCH) and hypocretin/orexi
57 ropeptide Y (NPY) in the arcuate nucleus and melanin-concentrating hormone (MCH) and orexins/hypocret
59 orexigenic peptides hypocretin (orexin) and melanin-concentrating hormone (MCH) are involved in the
62 the use of Eu3+ chelate-labeled analogues of melanin-concentrating hormone (MCH) as ligands for both
74 s of evidence indicate that the neuropeptide melanin-concentrating hormone (MCH) is an important comp
83 lateral hypothalamic (LH) circuits involving melanin-concentrating hormone (MCH) neurons are subject
84 tudy, we show that optogenetic activation of melanin-concentrating hormone (MCH) neurons during intak
85 (mGluR1 and mGluR5) activation on identified melanin-concentrating hormone (MCH) neurons was studied
88 s expression in orexinergic but not adjacent melanin-concentrating hormone (MCH) neurons; suggesting
89 amic neurons including those that synthesize melanin-concentrating hormone (MCH) or hypocretin/orexin
92 n suggest that the hypothalamic neuropeptide melanin-concentrating hormone (MCH) regulates body weigh
96 t fertility also upregulate the hypothalamic melanin-concentrating hormone (MCH) system that promotes
101 e AcbSh contains high levels of receptor for melanin-concentrating hormone (MCH), a lateral hypothala
103 ntibodies against tyrosine hydroxylase (TH), melanin-concentrating hormone (MCH), and hypocretin (Hcr
104 ontaining the feeding-related neuropeptides, melanin-concentrating hormone (MCH), and orexin (Orx).
105 ressin (AVP), histidine decarboxylase (HDC), melanin-concentrating hormone (MCH), and orexin/hypocret
106 rected to rWAT and iWAT expressed orexin and melanin-concentrating hormone (MCH), but male rats had a
107 eurons, and not nearby LH neurons expressing melanin-concentrating hormone (MCH), have mu-opioid rece
109 oopiomelanocortin (POMC), orexin/hypocretin, melanin-concentrating hormone (MCH), thyrotropin-releasi
110 e distinct from neighboring leptin-regulated melanin-concentrating hormone (MCH)- or orexin (OX)-expr
124 hypothalamic neuropeptides, hypocretin-1 and melanin-concentrating hormone, measured in the human amy
126 ght to moderate inputs arose from orexin and melanin concentrating hormone neurons, but cholinergic o
128 Glut4 neuron ablation affects orexigenic melanin-concentrating hormone neurons but has limited ef
129 in gene transfer into the striatum or in the melanin-concentrating hormone neurons in the ZI or LH ha
130 excitatory current with repeated coexposure (melanin-concentrating hormone neurons), synergistic dire
131 Neither rPP nor NPY stimulated c-Fos in melanin-concentrating hormone neurons, but both activate
133 rons and/or fibers in this area positive for melanin concentrating hormone, oxytocin, arginine vasopr
134 ons and contain dopamine, histamine, orexin, melanin-concentrating hormone, oxytocin, and vasopressin
135 , agouti-related peptide, hypocretin/orexin, melanin-concentrating hormone, oxytocin, arginine vasopr
136 Expression of transcripts for human pro-melanin concentrating hormone (pMCH) were studied in the
141 -2-o ne (7) is a potent, orally bioavailable melanin concentrating hormone receptor 1 (MCHr1) antagon
142 mitogen-activated protein kinase 7 (MAPK7), melanin concentrating hormone receptor 1 (MCHR1), and sp
143 of multiple structurally distinct series of melanin concentrating hormone receptor 1 antagonists in
144 ormation but disrupts normal localization of melanin concentrating hormone receptor 1 to ciliary memb
145 ioselective synthesis of SNAP-7941, a potent melanin concentrating hormone receptor antagonist, was a
147 We identified the consensus sequence in melanin-concentrating hormone receptor 1 (Mchr1) and con
148 screening mode to triage multiple classes of melanin-concentrating hormone receptor 1 (MCHr1) antagon
149 DNA phage-display library, we identified the melanin-concentrating hormone receptor 1 (MCHR1) as a no
150 of somatostatin receptor type 3 (Sstr3) and melanin-concentrating hormone receptor 1 (Mchr1) in neur
152 n of a high-throughput screening hit against melanin-concentrating hormone receptor 1 (MCHr1) led to
155 ts exhibited autoantibodies to more than one melanin-concentrating hormone receptor 1 epitope indicat
156 identification of autoantibodies against the melanin-concentrating hormone receptor 1 in patients wit
157 ediction of the potential B cell epitopes on melanin-concentrating hormone receptor 1 revealed that t
159 stence of multiple antibody binding sites on melanin-concentrating hormone receptor 1, including regi
161 are potent but nonspecific ligands for human melanin-concentrating hormone receptors 1 and 2 (hMCH-1R
162 s a potent but nonselective agonist at human melanin-concentrating hormone receptors 1 and 2 (hMCH-1R
164 a nonselective natural ligand for the human melanin-concentrating hormone receptors: hMCH-1R and hMC
166 altered mRNA expression levels of orexin and melanin-concentrating hormone, two peptides that are imp
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