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1 1) was identified as a specific receptor for neuromedin U.
2 obilize intracellular calcium in response to neuromedin U.
3 dentified as receptors for the neuropeptide, neuromedin U.
6 ptide Y, corticotropin-releasing factor, and neuromedin U) and peripheral (eg, gastrin, histamine, ac
7 haracterized in this report are activated by neuromedin U at nanomolar potency in heterologous expres
9 enes, as well as the 3' partial locus of the Neuromedin U gene; sequence analysis also suggests the p
13 ion of perikarya and nerve fibers containing neuromedin U-like immunoreactivity in the brain of Rana
16 ron (PSN) subset producing the neuropeptides neuromedin U (NMU) and calcitonin gene-related peptide b
18 nverse correlation between tumor RhoGDI2 and Neuromedin U (NMU) expression, suggesting that NMU might
19 revealed that IL-2, IL-4, IL-27, IL-10, and neuromedin U (NMU) increased IL-10 production in activat
26 n of type 2 innate lymphoid cells (ILC2s) by neuromedin U (NMU) is highly selective and key in contro
31 e also modulate physical activity, including neuromedin U (NMU), a peptide found in the gut and brain
32 utionarily related to the vertebrate peptide neuromedin U (NMU), or are related to arginine vasopress
36 neuronal termini expressing the neuropeptide neuromedin U (NMU), which stimulates type 2 (T2) cytokin
41 namely pyrokinins, as well as the vertebrate neuromedin U peptide also induced a calcium response.
42 the generation of a mouse model based on the neuromedin U receptor 1 (Nmur1) promoter as a driver for
43 receptor 1-dependent, highlighting the ILC2-neuromedin U receptor 1 axis as a novel therapeutic targ
44 The renoprotective effects of LIMM102 were neuromedin U receptor 1-dependent, highlighting the ILC2
46 ese data, we conclude that NmU-R2 is a novel neuromedin U receptor subtype that is likely to mediate
50 leasing Capa hormones, homologs of mammalian neuromedin U, which activate the Capa receptor (CapaR) i
51 peptide is highly related to neurotensin and neuromedin U, which are involved in blood pressure regul
52 S2, bone-morphogenetic protein 2A, MT1G, and neuromedin U, which showed frequent promoter hypermethyl