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1 hormone activation and the allostery of the ANP receptor.
2 e with selective deletion of the endothelial ANP receptor.
3 le because these cells only express a single ANP receptor.
4 ytic) domains of atrial natriuretic peptide (ANP) receptor-A (Npra) in postbinding events and metabol
5 cytes exists within caveolae bound to type B ANP receptors (ANP-RB, a guanylyl cyclase), we have used
6 (5 muM) that was inhibited completely by the ANP receptor antagonist anantin and a 60% increase in ne
11 ences in either density or affinity of renal ANP receptors, but was abolished when accumulation of cG
12 ng domain of the atrial natriuretic peptide (ANP) receptor contains two possible dimer pairs, the hea
13 Endoglycosidase treatment of the full-length ANP receptor expressed in COS-1 cells also had no detect
14 isruption of the atrial natriuretic peptide (ANP) receptor [guanylyl cyclase-A (GC-A)] gene yields mi
16 suggest that transmembrane signaling by the ANP receptor is initiated via a hormone-induced rotation
18 ylation sites in the extracellular domain of ANP receptor (NPR-ECD) from rat expressed in COS-1 cells
20 the dimerized hormone binding domain of the ANP receptor provides a first three-dimensional view of
23 ed by hormone binding extracellularly to the ANP receptor, thereby activating its intracellular guany
24 lding and transport of the newly synthesized ANP receptor to the cell surface, the oligosaccharide mo
25 GMP-dependent signaling cascade leading from ANP receptors to nuclear accumulation of both molecules.
26 ed member is the atrial natriuretic peptide (ANP) receptor, which is involved in blood pressure regul
27 use of a beta-cell-specific knockout of the ANP receptor with guanylate cyclase activity (betaGC-A-K
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