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1 the GH secretagogue receptor 1a (GHSR1a, ie, ghrelin receptor).
2 growth hormone secretagogue receptor (GHSR; ghrelin receptor).
3 p with the high constitutive activity of the ghrelin receptor.
4 one (GH), a major downstream effector of the ghrelin receptor.
5 he functional and structural behavior of the ghrelin receptor.
6 nverse agonist K-(d-1-Nal)-FwLL-NH(2) at the ghrelin receptor.
7 ing that the GHSR is a biologically relevant ghrelin receptor.
8 that the GHSR is a physiologically relevant ghrelin receptor.
9 sepsis by vagus nerve activation via central ghrelin receptors.
10 uced gut barrier dysfunction through central ghrelin receptors.
11 the growth hormone secretagogue receptor 1a (ghrelin receptor), a peptidic G-protein-coupled receptor
18 hormone secretagogues act as agonists at the ghrelin receptor and have been described as "ago-alloste
20 s prepared from cells coexpressing the human ghrelin receptor and the G protein Galpha(o1), N-[1(R)-1
21 ents of the ghrelin system, including native ghrelin, receptors and the recently discovered splicing
23 ventricular (LV) ghrelin increased, while LV ghrelin receptor antagonism suppressed the magnitude of
24 and improved glucose tolerance, whereas the ghrelin receptor antagonist D-Lys GHRP-6 reduced plasma
26 programs aimed at delivering small molecule ghrelin receptor antagonists and inverse agonists to the
27 t cells containing both leptin receptors and ghrelin receptors are mainly located in the medial part
29 ce for the high constitutive activity of the ghrelin receptor being an intrinsic property of the prot
30 st- and signaling protein-induced changes in ghrelin receptor conformation, thus preventing it from a
31 ly on distinct neuronal populations and that ghrelin receptor deficiency does not affect sensitivity
32 red fasting blood glucose levels observed in ghrelin receptor-deficient mice were returned to wild-ty
34 et-derived growth factor by inhibiting, in a ghrelin-receptor-dependent manner, Rac1 activation and c
35 Surprisingly, we found that deletion of the ghrelin receptor did not affect the sensitivity to exoge
37 memories, and pharmacological agonism of the ghrelin receptor during the memory consolidation period
38 ly occurring truncated splice variant of the ghrelin receptor exerts a dominant negative effect on gh
39 ould allow localization and visualization of ghrelin receptor expressing carcinomas using PET imaging
40 stingly, both leptin receptor expression and ghrelin receptor expression have been observed within ma
44 histological mapping of leptin receptor and ghrelin receptor expression, we found that cells contain
50 Despite being unable to activate the cognate ghrelin receptor (GHS-R), unacylated ghrelin (UAG) posse
51 of food intake, and inverse agonists of the ghrelin receptor (GHS-R1a) are widely considered to offe
52 otein-coupled receptors (GPCRs), such as the ghrelin receptor (GHS-R1a), the melanocortin 3 receptor
53 The mechanism must accommodate noncanonical ghrelin receptor (GHS-R1a)-G-protein coupling to Galpha(
55 hrelin action, we have examined the roles of ghrelin receptor (GHSR) expression in the mouse hindbrai
58 hippocampal neurogenesis in depression-prone ghrelin receptor (Ghsr)-null mice to that in wild-type l
62 tive and/or agonist-induced signaling of the ghrelin receptor, GPR119, the beta(2)-adrenergic recepto
63 -acyl ghrelin, although devoid of binding to ghrelin receptor (GRLN), exerts many biological effects,
66 are guided largely by the expression of the ghrelin receptor growth hormone secretagogue type 1a (GH
69 reproghrelin gene, but not those lacking the ghrelin receptor, have impaired abilities to manifest an
71 phobic pocket between TM-III and TM-V in the ghrelin receptor in four of five positions impaired rece
73 Furthermore, to confirm the role of central ghrelin receptors in ghrelin's effect, ghrelin (1 nmol)
77 o somatostatin receptors (sst2 and sst5) and ghrelin receptor, induction of cAMP and p38-mitogen-acti
79 d that the high constitutive activity of the ghrelin receptor is dependent upon flexibility in the C-
80 n function (r = 0.99) for both wild-type and ghrelin receptor knockout animals, with the latter havin
81 of cell proliferation via the mediation of a ghrelin receptor, likely a novel unidentified subtype.
82 a provide direct evidence of a mechanism for ghrelin receptor-mediated Gq signaling in which transiti
84 elin promotes food intake, an action lost in ghrelin receptor null mice and also helps maintain fasti
85 in overnight-fasted, streptozotocin-treated ghrelin receptor-null mice that were administered GcgR m
87 onstituted system, we show that the isolated ghrelin receptor per se activates G(q) in the absence of
88 growth hormone secretagogue receptor (GHSR) (ghrelin receptor) plays an important role in the regulat
89 pite its inability to activate the classical ghrelin receptor, preclinical studies suggest that UAG m
91 ass A G protein-coupled receptor (GPCR), the ghrelin receptor, reconstituted as a monomer into lipid
92 e the authors show that MRAP2 also regulates ghrelin receptor signalling in the hypothalamus and star
96 lin (a pentapeptide-selective agonist of the ghrelin receptor that speeds gastric emptying in patient
97 d rats, ghrelin activation of a postsynaptic ghrelin receptor, the growth hormone secretagogue recept
98 s occur mainly via binding to the only known ghrelin receptor, the growth hormone secretagogue recept
99 on of the high constitutive signaling of the ghrelin receptor, this loop was subjected to a detailed
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