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1 ortin with an increase in neuropeptide Y and agouti-related protein.
2 dullin (hazard ratio per log increase 2.53), agouti-related protein; (1.48), chitinase-3-like protein
3 ed expression of the orexigenic neuropeptide agouti related protein (AgRP) in the BMPR1A-deficient AR
6 ssing the endogenous melanocortin antagonist agouti-related protein (AgRP) also exhibit obesity, incr
9 w that changes in hypothalamic expression of agouti-related protein (Agrp) and neuropeptide Y (Npy) c
10 e expression of the orexigenic neuropeptides agouti-related protein (AgRP) and neuropeptide Y (NPY).
11 ) whether food deprivation (FD) co-increases agouti-related protein (AgRP) and PPARgamma mRNA express
12 we examined the role of insulin signaling in agouti-related protein (AgRP) and pro-opiomelanocortin (
14 t, the endogenous antagonists Agouti and the Agouti-related protein (AGRP) and signals through the in
17 eurons that express neuropeptide Y (NPY) and agouti-related protein (AgRP) are thought to be critical
19 imulating hormone (alpha-MSH) and orexigenic Agouti-related protein (AgRP) from discrete hypothalamic
20 the ability of proopiomelanocortin (POMC) or agouti-related protein (Agrp) hypothalamic neurons to se
21 ablation of hypothalamic neurons expressing agouti-related protein (AgRP) in adult mice leads to ano
24 C), reduce food intake, whereas hypothalamic agouti-related protein (AgRP) is a MC-4 receptor antagon
38 olves targeting the human DT receptor to the agouti-related protein (Agrp) locus so that systemic adm
40 examine the importance of GABA release from agouti-related protein (AgRP) neurons (which also releas
41 examine the importance of GABA release from agouti-related protein (AgRP) neurons (which also releas
43 crease but their size increase in orexigenic agouti-related protein (Agrp) neurons during the transit
46 used targeted knock-ins to express InsRs in agouti-related protein (AgRP) or proopiomelanocortin (PO
47 ther, CTRP13 and the orexigenic neuropeptide agouti-related protein (AgRP) reciprocally regulate each
49 ithin the hypothalamus, neurons that express agouti-related protein (AgRP) sense orexigenic factors a
50 ortin sequence-based MC4R antagonists vs the agouti-related protein (AGRP) sequence-based antagonists
57 ion of key orexigenic [neuropeptide Y (NPY), agouti-related protein (AgRP), and melanin-concentrating
58 pically express either agouti (Ay/a mice) or agouti-related protein (Agrp), antagonists of melanocort
59 (A(y)) mice, and causes obesity by mimicking agouti-related protein (Agrp), found primarily in the hy
60 re, the endogenous MC3R and MC4R antagonist, agouti-related protein (AgRP), hyperpolarizes POMC and R
61 ortin receptor (MC3-R and MC4-R) antagonist, agouti-related protein (AGRP), is a potent stimulant of
63 e (alpha-MSH) and its endogenous antagonist, agouti-related protein (AgRP), is fundamental for the ce
66 A expression levels of neuropeptide Y (NPY), agouti-related protein (AGRP), proopiomelanocortin (POMC
67 luding those producing neuropeptide Y (NPY), Agouti-related protein (AGRP), proopiomelanocortin (POMC
68 othalamic GHS-R1a, neuropeptide Y (NPY), and agouti-related protein (AgRP), suggesting that prolonged
69 are absent in mice lacking the gene encoding agouti-related protein (Agrp), suggesting that this func
71 gonists, agouti signaling protein (ASIP) and agouti-related protein (AGRP), were assessed by studying
72 neurons containing neuropeptide Y (NPY) and agouti-related protein (AgRP), which are conditional pac
73 eceptors are antagonized by agouti (ASP) and agouti-related protein (AGRP), which are the only known
82 ture-activity relationship study of chimeric agouti-related protein (AGRP)/[Nle4,DPhe7]alpha-melanocy
83 enic neuropeptides [neuropeptide Y (NPY) and agouti-related protein (AgRP)] and activates expression
84 lpha-MSH(4-10)-NH(2) (SHU9119)] and natural [agouti-related protein (AGRP)] MC3R antagonists but not
85 e appetite-stimulating (neuropeptide Y, NPY; agouti-related protein, AGRP) and appetite-inhibiting (c
86 gen, decreases AMPK activity in PVH, whereas agouti-related protein, an orexigen, increases AMPK acti
87 S chains, syndecans potentiate the action of agouti-related protein and agouti signaling protein, end
88 ing hormone, oxytocin, arginine vasopressin, agouti-related protein and alpha-melanocyte stimulating
89 orexigenic neuropeptides neuropeptide Y and agouti-related protein and down-regulation of expression
91 ons but has limited effect on neuropeptide Y/agouti-related protein and proopiomelanocortin neurons.
92 be mediated by leptin action on arcuate NPY/agouti-related protein and proopiomelanocortin neurons.
93 ession of key orexigenic (neuropeptide Y and agouti-related protein) and anorexigenic (pro-opiomelano
96 howed that in the DMH abundant alpha-MSH and agouti-related protein fibers are in close apposition to
97 er evaluated using the endogenous antagonist agouti-related protein fragment hAGRP(83-132) and hAGRP(
100 adrenocorticotropin (ACTH)], the antagonist agouti-related protein hAGRP(87-132), and synthetic agon
102 rons were stained for a second neuropeptide, agouti-related protein, immunoreactivity was found in th
108 1, which caused increased neuropeptide Y and agouti-related protein mRNAs in the hypothalamus, stimul
109 sm in proopiomelanocortin and neuropeptide Y/agouti-related protein neurons and links hypothalamic AM
110 ate nucleus, specifically the neuropeptide Y/agouti-related protein neurons and the dorsal medial nuc
111 CK1 in either pro-opiomelanocortin (POMC) or agouti-related protein neurons, mediators of leptin acti
113 ivation of ARC glia enhances the activity of agouti-related protein/neuropeptide Y (AgRP/NPY)-express
114 RNAs in the hypothalamus, stimulation of the agouti-related protein/neuropeptide Y neurons, and activ
117 sed sequence tag was identified that encodes Agouti-related protein, whose RNA is normally expressed
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