ライフサイエンスコーパス: heparinize

1 sulin (40 mU. kg(-1). min(-1)), and Liposyn (heparinized 10% lipid emulsion) infusions were initiated

2 of hyperacute rejection of porcine by fresh, heparinized (6 microM/ml) human blood with or without 1

3 the direct detection of calcium in undiluted heparinized and citrated blood.

4 Twelve mongrel dogs were intubated, heparinized and euthanized by pentothal injection and ve

5 mption was significantly reduced in both the heparinized and nonheparinized NO test groups when compa

6 s were imaged for up to 4 h after injection, heparinized, and sacrificed.

7 Perfusion with heparinized autologous blood (n=3) was compared with hum

8 and raised, forming a cradle superfused with heparinized blood (activated clotting time >350 seconds)

9 summary, the decay of HIV-1 RNA measured in heparinized blood after 6 h was small (-0.05 to -0.12 lo

10 and normal arterial segments were exposed to heparinized blood at flow conditions modeling medium-gra

11 nonatherosclerotic segments) were exposed to heparinized blood at high shear rate conditions in the B

12 us gold electrodes when immersed in serum or heparinized blood containing potassium ferricyanide show

13 amponade, produced by injection of saline or heparinized blood into the pericardial space through thi

14 In a separate study, trapping whole-heparinized blood mimicked the ability of trapped platel

15 Native or heparinized blood obtained from normal volunteers was pr

16 Whole heparinized blood was incubated overnight in separate we

17 within 2 h, the loss (decay) of HIV-1 RNA in heparinized blood was significant (P < 0.05) but small a

18 Twenty milliliters of whole heparinized blood was used for in vitro studies includin

19 y stimulate cytokine/chemokine production in heparinized blood.

20 The ACTs of the heparinized, but not native samples were significantly p

21 the thigh muscle was exposed and bathed with heparinized canine blood.

22 Four groups were studied: systemically heparinized control circuits, systemically heparinized N

23 HSPCs harvested from the bone marrow (BM) of heparinized deceased organ donors (HDODs).

24 animals were reanesthetized and systemically heparinized for cannulation of the left carotid and comm

25 ex vivo xenoperfused for 12 hours with whole heparinized human blood.

26 Porcine forelimbs were perfused with whole, heparinized human or autologous pig blood.

27 ci by polymorphonuclear leukocytes (PMNs) in heparinized human peripheral whole blood.

28 y heparinized control circuits, systemically heparinized NO test circuits, nonheparinized control cir

29 lar subcutaneous region of anaesthetized and heparinized nondiabetic Sprague-Dawley rats, in which ra

30 ation (clotting) times (ACTs) were longer in heparinized patients treated with c7E3 Fab than in those

31 e of the frequency of thrombocytopenia among heparinized patients, the limited specificity of widely

32 es and venules were perfused with oxygenated/heparinized physiological salt solution at 37 degrees C.

33 Of the plasma types evaluated, heparinized plasma introduced the lowest relative bias f

34 Heparinized plasma samples, which were pretreated with h

35 In heparinized plasma, the radioactivity shifted from a 30-

36 nderwent 6 hours of end-ischemic NMP using a heparinized plasma-based perfusion fluid.

37 complex formation between the serum and the heparinized plasma.

38 trations were required for citrated than for heparinized plasmas due to competition of citrate with H

39 ition of L- and D-SNC to NO upon addition to heparinized rat blood or upon direct application to cult

40 e implanted in jugular veins of systemically heparinized rats and used in 4-h experiments, during whi

41 ere randomly assigned to one of five groups: heparinized saline (n = 6), epinephrine infusions only (

42 plantation, freshly aspirated ABM (n = 7) or heparinized saline (n = 7) was injected transendocardial

43 The remaining 13 fetuses were infused with heparinized saline at the same rate (controls).

44 en at all sampling intervals if small-volume heparinized saline was given through the intraosseous si

45 ted the in vitro persistence of P. putida in heparinized saline: even under refrigerated conditions,

46 vein catheters before and after gavage with heparinized, warmed blood from donor rats, air, standard

47 Using heparinized whole blood and flow conditions, it was show

48 Heparinized whole blood containing mepacrine-labeled pla

49 Heparinized whole blood from healthy volunteers was circ

50 SECC was established by recirculating heparinized whole blood from human volunteers on a membr

51 (baseline) and lipopolysaccharide-activated heparinized whole blood of healthy subjects (n=15) and s

52 Heparinized whole blood samples were obtained from pedia

53 ght be used, human monocytic THP-1 cells and heparinized whole human blood were stimulated with lipop

54 litter mates (hDAF(-/-)) were perfused with heparinized whole human blood.