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1 in the SAT and very little expression of the beta3-adrenoceptor.
2 a-antagonists have agonist properties at the beta3-adrenoceptor.
3 e of two active conformational states of the beta3-adrenoceptor.
4 ative beta4-adrenoceptor) that resembles the beta3-adrenoceptor.
5 tive beta4-adrenoceptor is distinct from the beta3-adrenoceptor.
6 drenoceptor is genetically distinct from the beta3-adrenoceptor.
9 he beta1-adrenoceptor agonist dobutamine and beta3-adrenoceptor agonist BRL 37344A had little effect
10 ater by intra-BAT injections of the specific beta3-adrenoceptor agonist CL316,243 in one pad and the
14 s, but with limited clinical experience, are beta3 adrenoceptor agonists and phosphodiesterase type 5
16 ker that causes agonist effects through both beta3-adrenoceptors and cardiac putative beta4-adrenocep
17 for future studies to better understand the beta3-adrenoceptor as a novel pharmacological target.
18 ased after activation of adipocyte-expressed beta3 adrenoceptors by catecholamines, and identified eo
20 First, the ligand-recognition profile of beta3-adrenoceptors differs considerably from that of th
21 er, these experiments suggest that the human beta3-adrenoceptor exists in at least two different agon
25 ypothesis that postmenopausal women with the beta3-adrenoceptor gene variant (Trp64Arg) have reduced
26 ion, older obese women carrying the Trp64Arg beta3-adrenoceptor gene variant have an impaired capacit
28 tagonist affinity measurements varied at the beta3-adrenoceptor in a manner similar to those observed
36 efore examined the pharmacology of the human beta3-adrenoceptor stably expressed in Chinese hamster o
38 pamycin (mTOR) complex 2 has a novel role in beta3-adrenoceptor-stimulated glucose uptake in brown ad
41 onfounding factor in previous studies of the beta3-adrenoceptor Trp64Arg variant and energy expenditu
43 arently differs between the human and rodent beta3-adrenoceptor, yielding considerable species differ
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