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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
3 these vesicles was varied between 1% and 10% DMPS.
4 maximal at 4 mN m(-1) in the presence of 10% DMPS).
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
8 ges were detected when inorganic mercury and DMPS were added to the bath.
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
11                                      NAC and DMPS are themselves excreted in urine in high concentrat
12 on (P = 0.003), which was further reduced by DMPS treatment (P < 0.0001).
13                                 In contrast, DMPS-d54 incorporated into red cells exhibited no phase
14                                 In contrast, DMPS-d54 incorporated into the outer leaflet of echinocy
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
17                             Fully deuterated DMPS or DMPG is ordered in a way similar to that of DMPC
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
21               Dimyristoylphosphatidylserine (DMPS), phosphatidylserine from bovine brain (brain-PS),
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
24 atidylcholine/dimyristoylphosphatidylserine (DMPS) vesicles.
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
27 )O) of either dimyristoylphosphatidylserine (DMPS) or dimyristoylphosphatidylglycerol (DMPG).
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
30 ly 0.025 and approximately 0.5-0.6 for DMPC/ DMPS/DM.
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
40        PKC activity was measured using [DMPC/DMPS (1:1, mol/mol)]/DO MLVs as the lipid activator.
41 on of mole fraction DO (chi(DO)) in DMPC/DO, DMPS/DO, and [DMPC/DMPS (1:1, mol/mol)]/DO multilamellar
42            Anionic phospholipids, especially DMPS, were located at the center of the LTRs and spanned
43  0.0001) in the renal 213Bi uptake; however, DMPS was more effective than DMSA (P < 0.001).
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
47                       Addition of 200 microM DMPS to the bath provided complete protection from the t
48                   In the presence of 1 mg/ml DMPS in the transport milieu, the flux of FITC-Dextran-4
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
51 port is linked to the therapeutic effects of DMPS.
52 d component grows in as the mole fraction of DMPS increases.
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
56                                    Saturated DMPS was also more effective in delaying resistance reco
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
59           We also tested the hypothesis that DMPS can extract cellular mercury while being transporte
60        We also obtained data indicating that DMPS is transported by the organic anion transport syste
61 h that of the ternary mixtures suggests that DMPS/DO interactions may be more favorable than DMPC/DO
62         Additional data indicated that, when DMPS and inorganic mercury were coperfused through the l
63               Our findings showed that, when DMPS was applied to the basolateral membranes of S2 segm
64 ferentially into the outer monolayer whereas DMPS-d54 was selectively incorporated into the inner mon
65 ists in domains in the outer monolayer while DMPS-d54 is dispersed in the inner monolayer.
66 ecame echinocytic while those incubated with DMPS-d54 became stomatocytic.
67 bited became echinocytic when incubated with DMPS-d54.
68                             The results with DMPS were also confirmed in a monkey model.

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