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1 effects of (in)Abeta depended on changes in oncotic pressure.
2 RPF), blood pressure, hematocrit, and plasma oncotic pressure.
3 der basal conditions to result in changes in oncotic pressure.
4 icantly faster in groups 2 to 4, and colloid oncotic pressure after resuscitation was greater in grou
7 tic pressure (piGC) from knowledge of plasma oncotic pressure and the filtration fraction revealed th
11 e to hemodilution caused by its high colloid oncotic pressure, but may facilitate diffusive oxygen tr
12 vestigate this further, Lp and the effective oncotic pressure difference (f3DeltaPi) acting across th
14 hese results support our hypothesis that the oncotic pressure difference across the tumor microvascul
15 otic pressure alone, not the plasma-to-lymph oncotic pressure difference, modulates pulmonary transva
17 c pressures were estimated as the sum of the oncotic pressure due to HA alone plus the oncotic pressu
18 ficients to HA and A, there was an effective oncotic pressure (E pi) of between 3.46 and 6.0 cm H2O o
20 e circulation and the resulting reduction in oncotic pressure exerted by the plasma, although the fat
23 Starling's equation indicates that reduced oncotic pressure gradients will favor edema formation, a
24 4.5 and 17.7 +/- 2.2 mm Hg; plasma-to-lymph oncotic pressure gradients, respectively, were 4.4 +/- 0
27 ecies is known, no data are available on the oncotic pressure in the interstitial space of tumors.
28 ecause of the leaky nature of tumor vessels, oncotic pressure in tumor interstitium should be close t
30 ability to expand plasma volume and improve oncotic pressure in various clinical settings, such as i
31 aised left atrial pressure elevation, plasma oncotic pressures in dextran and control sheep, respecti
33 ic wick method for the direct measurement of oncotic pressures in the interstitial fluid of tumors gr
36 ross the endothelial glycocalyx and that the oncotic pressure of interstitial fluid does not directly
37 cromolecules was assessed from the effective oncotic pressure (omega delta pi) exerted by the perfusa
39 Computation of glomerular intracapillary oncotic pressure (piGC) from knowledge of plasma oncotic
40 min (HSA) serves not only as a physiological oncotic pressure regulator and a ligand carrier but also
41 ntial contribution of medullary interstitial oncotic pressure to the net balance of forces influencin
42 ents in serum albumin, immunoglobulin G, and oncotic pressure values were 31, 32, and 26%, respective
43 glomerular filtration during HPP, perfusate oncotic pressure was reduced by lowering the concentrati
45 ack triangle down pi was near 70% of luminal oncotic pressure when the tissue concentration equalled