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1 have a high affinity and selectivity for the sigma(2)-receptor.
2 acterization of sigma-2 receptor ligands and sigma-2 receptors.
3 fold selectivity for VAChT over sigma(1) and sigma(2) receptors.
4 liver and guinea pig liver membranes and the sigma-2 receptor (18 kDa) in rat liver membranes with hi
5 l metabolite II (sigma-1 receptor antagonist/sigma-2 receptor agonist ligand) obtained by conjugation
8 emonstrated high affinities for sigma(1) and sigma(2) receptors and thus failed to show significantly
9 hemical compounds with high affinity for the sigma-2 receptor and showed rapid internalization of the
15 sed to study the subcellular localization of sigma-2 receptors by two-photon and confocal microscopy.
16 t 66 P cells had approximately 10 times more sigma 2 receptors/cell than the 66 Q cells from 10-day c
18 onradioactive) glucose in blood, sigma-1 and sigma-2 receptor expression in the tumor, animal weight,
22 itting radionuclides, which selectively bind sigma 2 receptors, have the potential to noninvasively a
24 rs have demonstrated increased expression of sigma-2 receptors in rapidly proliferating tumors and th
25 in isothiocyanate group, irreversibly labels sigma-2 receptors in rat liver; the membrane-bound prote
28 ls that both PGRMC1 and SW120, a fluorescent sigma-2 receptor ligand, colocalize with molecular marke
30 clusions of previous studies suggesting that sigma-2 receptor ligands should be evaluated as potentia
32 ontrast, caspase inhibitors had no effect on sigma-2 receptor-mediated (CB-64D and CB-184) cytotoxici
39 their binding affinities to the sigma-1 and sigma-2 receptors, we show that both photoaffinity label
42 aspase-independent apoptotic pathway used by sigma-2 receptors, which is distinct from mechanisms use
44 yield and specific activity that target the sigma(2) receptor with high affinity and selectivity.
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