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1 tain interacting partners such as Lfc or the parathyroid hormone receptor.
2 within the rheumatoid lesion do not express parathyroid hormone receptor.
3 d receptors, closely related to secretin and parathyroid hormone receptors.
7 inferences are surprising in the case of the parathyroid hormone receptor, a receptor that contains s
8 receptor, the kappa-opioid receptor, and the parathyroid hormone receptor, as well as growth factor t
9 otein-coupled receptors (GPCRs), such as the parathyroid hormone receptor, can increase bone mass; ho
10 HrP(-/-)), and a constitutively active PTHrP/Parathyroid hormone Receptor expressed under the control
13 A catalytic and regulatory subunits, and the parathyroid hormone receptor in opossum kidney cells.
15 ormonal responses were not due to changes in parathyroid hormone receptor number or binding kinetics
16 receptors, the beta2-adrenoreceptor and the parathyroid hormone receptor; occupancy of the metal-bin
20 seven transmembrane-spanning receptors, the parathyroid hormone receptor (PTH1R) and frizzled (FZD),
21 f the first extracellular loop (ECL1) of the parathyroid hormone receptor (PTH1R) in the presence of
23 Agonist-mediated activation of the type 1 parathyroid hormone receptor (PTH1R) results in several
25 receptor (beta(2)AR; a type A receptor), the parathyroid hormone receptor (PTH1R; type B), and the ca
30 ement is similar to that of the ECD-1 of the parathyroid hormone receptor (PTHR), suggesting a conser
33 s and intracellular trafficking of the human parathyroid hormone receptor subtype 1 (hPTH1-Rc) and it
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