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1 based model of the recently identified human MCH receptor.
2 tors (melanocortin receptors) and one or two MCH receptors.
3 nd functional assays on cells expressing the MCH receptors.
4 ue to lack of identification of hypothalamic MCH receptors.
5 tic manipulation studies in mice at both the MCH receptor 1 (MCHR1) as well as the MCH peptide levels
7 ic neuropeptide that acts in rodents via the MCH receptor 1 (MCHR1) to regulate a wide variety of phy
10 We conclude that both Asp(123)(3.32) in the MCH receptor and Arg(11) in the MCH peptide are required
11 have analysed the tissue localization of the MCH receptor and find that it is expressed in several br
12 es sleep, drug abuse behavior, and mood, and MCH receptor antagonists are currently being developed a
15 sing non-neuronal cells transfected with the MCH receptor gene; these cells exhibited an increase in
18 ude that MCH1R is a physiologically relevant MCH receptor in mice that plays a role in energy homeost
19 fied the full complement of melanocortin and MCH receptors in both zebrafish and the pufferfish, Fugu
31 eurons send numerous projections to multiple MCH receptor-rich targets with presumed roles in sensory
32 sms, indicating that therapies targeting the MCH receptor should act on the neuronal regulation of fo
36 report the identification of a second human MCH receptor termed MCH-2R, which shares about 38% amino
37 colonic epithelial cells express functional MCH receptors, the activation of which induces IL-8 expr
38 se monocytic cells, which express endogenous MCH receptor, we found that treatment with MCH enhanced
39 bility to bind to and activate the wild-type MCH receptor, whereas [Ala(11)]-MCH displayed a 3000-fol
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