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1 DMPS was an effective mercury chelator in this system, s
2 DMPS with saturated acyl chains was found to be a much m
5 with 2,3-dimercapto-1-propanesulfonic acid (DMPS) or meso-2,3-dimercaptosuccinic acid (DMSA) caused
6 inefficient packing between cholesterol and DMPS occurs probably because of the strong interactions
7 FTIR spectroscopy, using analogs of DMPC and DMPS with perdeuterated acyl chains, showed that the mel
9 nhibited by NAC (K(i) of 2.0 +/- 0.3 mM) and DMPS (K(i) of 0.10 +/- 0.02 mM), providing further evide
10 lts indicate that the MeHg antidotes NAC and DMPS and their mercaptide complexes are transported by O
15 ubated with an equimolar mixture of DMPC-d54/DMPS or DMPC/DMPS-d54 remained mostly discocytic whereas
16 ncubated with equimolar mixtures of DMPC-d54/DMPS or DMPC/DMPS-d54, the deuterated species exhibited
18 steine (NAC) and dimercaptopropanesulfonate (DMPS) are sulfhydryl-containing compounds that produce a
19 ithiol ligand 2,3-dimercaptopropanesulfonic (DMPS) acid has been employed to synthesize dithiol-prote
20 to penetrate dimyristoylphosphatidylcholine/DMPS monolayers, and at an initial surface pressure of 3
22 ne (DMPC) and dimyristoylphosphatidylserine (DMPS), utilizing the nixtroxide-labeled cholesterol anal
23 DMPC-d54) and dimyristoylphosphatidylserine (DMPS-d54) were incorporated by incubation into human ery
25 holine (DMPC)/dimyristoylphosphatidylserine (DMPS)/dioleoylglycerol (DO) vesicles was compared with t
26 holine (DMPC)/dimyristoylphosphatidylserine (DMPS)/dioleoylglycerol (DO), DMPC/DMPS/1-palmitoyl-2-ole
28 (DMPC-d54) and dimyristoyphosphatidylserine (DMPS-d54) were incorporated into human erythrocytes.
29 , at 20 degrees C, the 14-carbon disaturated DMPS in the gel phase has an area of 40.8 A(2) vs. 48.1
31 /1-palmitoyl-2-oleoylglycerol (PO), and DMPC/DMPS/dimyristoylglycerol (DM) was analyzed and compared
32 DO (chi(DO)) in DMPC/DO, DMPS/DO, and [DMPC/DMPS (1:1, mol/mol)]/DO multilamellar vesicles (MLVs).
33 dylserine (DMPS)/dioleoylglycerol (DO), DMPC/DMPS/1-palmitoyl-2-oleoylglycerol (PO), and DMPC/DMPS/di
34 ximately 0.10 and approximately 0.3 for DMPC/DMPS/DO, chiPO = approximately 0.05 and approximately 0.
35 ximately 0.05 and approximately 0.4 for DMPC/DMPS/PO, and chiDM = approximately 0.025 and approximate
36 O (chiDO), PO (chiPO), or DM (chiDM) in DMPC/DMPS (1:1) multilamellar vesicles (MLVs) and of chiDO in
37 files of all three lipid components in [DMPC/DMPS (1:1, mol/mol)]/DO MLVs virtually overlay when chi(
38 n equimolar mixture of DMPC-d54/DMPS or DMPC/DMPS-d54 remained mostly discocytic whereas cells incuba
39 equimolar mixtures of DMPC-d54/DMPS or DMPC/DMPS-d54, the deuterated species exhibited no thermotrop
41 on of mole fraction DO (chi(DO)) in DMPC/DO, DMPS/DO, and [DMPC/DMPS (1:1, mol/mol)]/DO multilamellar
44 ed uptake of [(14)C]MeHg-NAC and [(14)C]MeHg-DMPS was inhibited by prototypical substrates for Oat1,
45 roM for MeHg-NAC and 9 +/- 2 microM for MeHg-DMPS, indicating that these are relatively high-affinity
46 by glutarate, PAH, NAC, DMPS, MeHg-NAC, MeHg-DMPS, and a mercapturic acid, indicating that these are
49 was trans-stimulated by glutarate, PAH, NAC, DMPS, MeHg-NAC, MeHg-DMPS, and a mercapturic acid, indic
50 y was further enhanced by the combination of DMPS with either chlorothiazide or furosemide (P < 0.000
53 transport process involving the movement of DMPS from the bathing compartment to the luminal compart
54 reas cells incubated with either DMPC-d54 or DMPS-d54 alone became echinocytic or stomatocytic, respe
55 (14)C]MeHg when complexed with either NAC or DMPS but not when complexed with L-cysteine, glutathione
57 ng agent 2, 3-dimercaptopropane-1-sulfonate (DMPS) significantly alters the renal tubular transport,
58 helator, 2,3-dimercaptopropane-1-sulphonate (DMPS), but was blocked by the metal chelator, calcium di
61 h that of the ternary mixtures suggests that DMPS/DO interactions may be more favorable than DMPC/DO
64 ferentially into the outer monolayer whereas DMPS-d54 was selectively incorporated into the inner mon
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