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1 d organic carbon) of SRFA passed through the dialysis membrane.
2 ble species across the lipid bilayer and the dialysis membrane.
3 lly separated from the seeds and plants by a dialysis membrane.
4 sues, and was finally eliminated through the dialysis membrane.
5 branes increases the biocompatibility of the dialysis membranes.
6 s a relevant feature for characterization of dialysis membranes.
7 liver support or treatment with conventional dialysis membranes.
8       Bisphenol A (BPA), a component of some dialysis membranes, accumulates in CKD.
9 e analyte diffusive driving force across the dialysis membrane and a subsequent increase in the relat
10 riving force for analyte to pass through the dialysis membrane and thus increases the RR.
11  relative recovery of the analyte across the dialysis membrane and yielded for the first time quantit
12  due to the development of new materials for dialysis membranes and commercial availability of smalle
13  taxane that otherwise bound irreversibly to dialysis membranes and which exhibited distinctive lipop
14                The effects of dialysis dose, dialysis membrane, and other clinical parameters on infe
15 ed through a 100-500 molecular weight cutoff dialysis membrane, and the dialysate and retentate were
16 f desalting methods, including spin columns, dialysis membranes, and filters.
17 sed attention on the biocompatibility of the dialysis membrane as a possible factor influencing patie
18 sing single Sephadex beads as osmometers and dialysis membranes as protein filters.
19 ive ELISA performed in tubes or wells with a dialysis membrane attached to their bottoms.
20    In this article, we review the concept of dialysis membrane biocompatibility and highlight the dif
21 bound solutes than do conventional high-flux dialysis membranes but at the cost of some albumin loss
22 s are catalytically reduced to NO within the dialysis membrane by the immobilized organoselenium spec
23 this regard, several studies have utilized a dialysis membrane chamber (DMC) cultivation system to ge
24  that although widely dissimilar, the UT and dialysis membrane chamber growth conditions promote more
25 nd host adaptation of lp25-B. burgdorferi in dialysis membrane chambers (DMCs) implanted in rats.
26 hanced upon growth of the spirochetes within dialysis membrane chambers (DMCs) implanted intraperiton
27 ian host-adapted organisms cultivated within dialysis membrane chambers (DMCs) implanted within the p
28 rotein was expressed by spirochetes grown in dialysis membrane chambers (DMCs).
29  were able to survive within intraperitoneal dialysis membrane chambers at a level equivalent to that
30  strain 297 cultivated either in vitro or in dialysis membrane chambers implanted in rat peritoneal c
31 , or during mammalian host adaptation (Bb in dialysis membrane chambers implanted in rats).
32 with "host-adapted" spirochetes grown within dialysis membrane chambers implanted into the peritoneal
33 ort, we cultivated B. burgdorferi 297 within dialysis membrane chambers implanted into the peritoneal
34 ities of B. burgdorferi grown in vitro or in dialysis membrane chambers implanted intraperitoneally i
35  relatively immune-privileged environment of dialysis membrane chambers implanted within the peritone
36 were able to survive as well as wild type in dialysis membrane chambers in the rat peritoneum.
37 g the complete set of plasmids were grown in dialysis membrane chambers that were implanted into rat
38 RpoS regulon was uniquely upregulated within dialysis membrane chambers, further underscoring the imp
39 ations after cultivation in vitro and within dialysis membrane chambers, mimicking a mammalian host-a
40 mmalian host-adapted organisms cultivated in dialysis membrane chambers.
41     When nanoblends and MC were separated by dialysis membrane colorimetric response (CR) was similar
42                             State-of-the-art dialysis membranes comprise a relatively thick polymer l
43 de a sealed, small segment of a hollow fiber dialysis membrane (diameter 0.5 mm, length 0.5 cm, molec
44 e necessary electrical connection across the dialysis membrane for defining the electric fields neede
45               Commercial ultrafiltration and dialysis membranes have broad pore size distributions an
46                         These methods employ dialysis membranes in 96-well format or spin filters.
47 bile salt and complete porcine bile across a dialysis membrane, in the presence and absence of two ce
48 e beta2m with transition metal cation at the dialysis membrane interface is causal to dialysis relate
49        A key component of its apparatus is a dialysis membrane interface that eliminates electrolysis
50 passively diffuse from the brain through the dialysis membrane into an infusion solution which is the
51 that, for a 15 kDa polyelectrolyte, a 50 kDa dialysis membrane is not sufficient to remove all PAH po
52  when a 1000 MWCO (molecular weight cut off) dialysis membrane is placed in the front of the diffusiv
53                                            A dialysis membrane is sandwiched between the disks to for
54 s sensor with a thin organoselenium modified dialysis membrane mounted at the distal sensing tip.
55 e conditions of the event, cellulose acetate dialysis membranes of various ages were retrieved from o
56 study investigates the potential role of the dialysis membrane on patient outcome in a prospective mu
57 ral clinical studies analyzing the impact of dialysis membranes on the course and outcome of acute re
58 trode consisted of nitrate reductase held by dialysis membrane onto a Nafion-coated glassy carbon ele
59 ally reduced upon elimination of copper from dialysis membranes, our results provide a molecular unde
60                         In this study, a rat dialysis membrane peritoneal model was used to evaluate
61 s concluded that the biocompatibility of the dialysis membrane plays a role in the outcome of patient
62                                              Dialysis membranes ranging from 3 kD to 100 kD were used
63 rganisms and the electrodes was prevented by dialysis membrane, suggesting that soluble electron carr
64 se and 6-phosphogluconate dehydrogenase by a dialysis membrane, there was no apparent channeling.
65 iffusion performance of anthocyanins along a dialysis membrane was determined in the presence and abs
66 n performance of nine anthocyanins through a dialysis membrane was evaluated in the presence and abse
67    Using molecular weight cutoff filters and dialysis membranes, we found that the molecular weight o
68 m the antibiotic-resistant mutant by using a dialysis membrane were carried out.
69 monium chloride (PDA) aqueous solution and a dialysis membrane were used as a binding phase and a dif
70                                Treating AN69 dialysis membrane, which bears negative charge due to in
71 s of complement and neutrophil activation by dialysis membranes, which may prolong the recovery from
72 n escape from 25,000 molecular weight cutoff dialysis membranes with velocity constants of 5.1 x 10(-

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