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1 ceptor and discuss the recent cloning of the sigma(2) receptor.
2 opy, demonstrating their specificity for the sigma(2) receptor.
3 known about the mechanisms activated by the sigma(2) receptor.
4 have a high affinity and selectivity for the sigma(2)-receptor.
5 and predicted regulators of the sigma-1 and sigma-2 receptors.
6 acterization of sigma-2 receptor ligands and sigma-2 receptors.
7 fold selectivity for VAChT over sigma(1) and sigma(2) receptors.
8 binding affinity and subtype selectivity for sigma(2) receptors.
9 liver and guinea pig liver membranes and the sigma-2 receptor (18 kDa) in rat liver membranes with hi
11 l metabolite II (sigma-1 receptor antagonist/sigma-2 receptor agonist ligand) obtained by conjugation
14 emonstrated high affinities for sigma(1) and sigma(2) receptors and thus failed to show significantly
15 hemical compounds with high affinity for the sigma-2 receptor and showed rapid internalization of the
16 (K(i) = 1.2 nM), excellent selectivity over sigma(2) receptors, and promising logD(7.4) (3.05) and l
26 sed to study the subcellular localization of sigma-2 receptors by two-photon and confocal microscopy.
27 t 66 P cells had approximately 10 times more sigma 2 receptors/cell than the 66 Q cells from 10-day c
29 onradioactive) glucose in blood, sigma-1 and sigma-2 receptor expression in the tumor, animal weight,
33 itting radionuclides, which selectively bind sigma 2 receptors, have the potential to noninvasively a
36 PET radiotracer for imaging the function of sigma(2) receptors in central nervous system disorders.
37 rs have demonstrated increased expression of sigma-2 receptors in rapidly proliferating tumors and th
38 in isothiocyanate group, irreversibly labels sigma-2 receptors in rat liver; the membrane-bound prote
40 h ligands displayed strong interactions with sigma(2) receptors indicating poor selectivity towards t
44 ls that both PGRMC1 and SW120, a fluorescent sigma-2 receptor ligand, colocalize with molecular marke
46 clusions of previous studies suggesting that sigma-2 receptor ligands should be evaluated as potentia
48 ontrast, caspase inhibitors had no effect on sigma-2 receptor-mediated (CB-64D and CB-184) cytotoxici
62 validated as powerful tools for the study of sigma(2) receptors via fluorescence-based techniques.
63 their binding affinities to the sigma-1 and sigma-2 receptors, we show that both photoaffinity label
66 aspase-independent apoptotic pathway used by sigma-2 receptors, which is distinct from mechanisms use
68 yield and specific activity that target the sigma(2) receptor with high affinity and selectivity.