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1  transporters were collaterally sensitive to tiopronin.
2                     Here we demonstrate that tiopronin (1), a thiol-substituted N-propanoylglycine de
3 alogs revealed two additional LPAs, PX12 and tiopronin, and suggest a potential LPA family, within wh
4 e-coated gold MPCs with aqueous solutions of tiopronin-coated gold MPCs yields toluene-phase MPCs tha
5 te-coated gold MPCs and aqueous solutions of tiopronin-coated silver MPCs, in which tiopronin ligands
6      Synthesis and screening of analogues of tiopronin demonstrated that the thiol functional group w
7 despite functional assays demonstrating that tiopronin does not interact with P-gp.
8                                          The tiopronin/ethidium MPC binding to DNA was imaged by AFM.
9  were either N-(2-mercaptopropionyl)glycine (tiopronin/ethidium MPC) or trimethyl(mercaptoundecyl)amm
10                       The negatively charged tiopronin/ethidium MPC, in contrast, exhibits slow inter
11                                     The drug tiopronin has been previously shown to elicit CS.
12 culty in exploiting this hypersensitivity to tiopronin in the clinic.
13 p studies, we discovered that sensitivity to tiopronin in the original study was mediated by infectio
14   We have determined that the CS activity of tiopronin is mediated by the generation of reactive oxyg
15 (GPx), and the mode of inhibition of GPx1 by tiopronin is shown in this report.
16  Treatment of MRP1-overexpressing cells with tiopronin led to a significant reduction in MRP1 protein
17 PCs yields toluene-phase MPCs that have some tiopronin ligands and aqueous-phase MPCs that have some
18 ns of tiopronin-coated silver MPCs, in which tiopronin ligands are transferred to the former and gold
19  by monolayers of N-acetyl-l-cysteine and of tiopronin ligands.
20 e used to study the synthesis of a series of tiopronin monolayer-protected gold nanoclusters (MPCs) a
21 tionation of N-(2-mercaptopropionyl)glycine (tiopronin) monolayer protected gold clusters into monodi
22              N-(2-mercaptopropionyl)glycine (tiopronin) monolayer-protected silver particles were par
23 trophotometry verified the separation of the tiopronin MPCs through the inspection of surface plasmon
24              CFE separation of water-soluble tiopronin MPCs yielded fractions that varied in color, U
25 abundance (with respect to disulfide bridged tiopronin species) before dramatically increasing in abu
26          Specifically, selective toxicity of tiopronin toward MDR cells is achieved by inhibition of
27 ed here are p-mercaptobenzoic acid ( p-MBA), tiopronin (TP), and thiolated PEG(7) (S-PEG(7)).
28 of tri(ethylene glycol) thiol (EG(3)-SH) and tiopronin (Tp), which was prepared by a one-step synthes