ライフサイエンスコーパス: microperfusion

1 examined by confocal microscopy during IBDU microperfusion.

2 erve as an intraoperative quality control of microperfusion.

3 re and during application of these agents by microperfusion.

4 or 4 to 13 d before isolation of the CCD for microperfusion.

5 hetized rats previously prepared for in vivo microperfusion.

6 revealed a 49% reduction of kidney allograft microperfusion 2 hr after the intake of CsA, which might

7 l nephron net HCO(3) reabsorption by in vivo microperfusion (37.8 +/- 3.2 versus 16.6 +/- 1.5 pmol/mm

8 ydroxyethyl starches and saline on pulmonary microperfusion and gas exchange during systemic inflamma

9 Ex vivo microperfusion and in vitro experiments with NEFA-bound

10 al tubule function, in vitro proximal tubule microperfusion and in vivo micropuncture measurements we

11 ith limited spatial access, we have designed microperfusion and in-bore oxygenation systems capable o

12 A dual microperfusion apparatus was used to expose guinea-pig o

13 igher distal nephron H+ secretion by in vivo microperfusion as shown previously.

14 nses to AMPA (1 or 5 microM applied by brief microperfusion) as measured using the nystatin patch met

15 The use of the microperfusion chamber has the following major advantage

16 A novel microperfusion chamber was developed to measure kinetic

17 Using the microperfusion chamber, water and dimethylsulfoxide (DMS

18 s the first distinct image with quantitative microperfusion data from gated human foot microvasculatu

19 re whether acute changes of kidney allograft microperfusion due to the administration of cyclosporine

20 ws intraoperative quantitative assessment of microperfusion during kidney transplantation.

21 Further, microperfusion experiments showed that HOE694-sensitive

22 Stationary in vivo microperfusion experiments showed that luminal perfusion

23 er, REM sleep was not reduced by scopolamine microperfusion in this same region, at a concentration c

24 Yohimbine (an alpha 2 antagonist) microperfusion into the urinary space produced opposite

25 In the present study, during in vivo microperfusion, lanthanum was used as an extracellular m

26 Stationary in vivo microperfusion measured PT NHE3 activity.

27 We used microperfusion, micropuncture, and renal clearance of FI

28 An extra microperfusion needle filled with a high-ionic strength

29 Contrary to the prevailing model, bilateral microperfusion of 8-OH-DPAT into the PPTn (n = 23 rats)

30 Microperfusion of agmatine into renal interstitium and i

31 ithelial NH3 transport, examined by in vitro microperfusion of cortical and outer medullary collectin

32 As measured by in vitro microperfusion of cortical TAL, CaSR inhibitors increase

33 As predicted, combined microperfusion of D-AP5 (glutamate receptor antagonist)

34 In contrast, microperfusion of etomidate (10 and 30 muM) into the ven

35 In SHR on the basal diet, microperfusion of exogenous ANP into the AHA elicited a

36 ter, bile acid, and HCO(3)(-) transport: the microperfusion of intrahepatic bile duct units (IBDUs) i

37 Microperfusion of isolated cortical TALs revealed no bas

38 response to different flow rates during the microperfusion of isolated S2 proximal tubules from mous

39 In vitro microperfusion of isolated TAL showed no significant dif

40 A set of sophisticated techniques including microperfusion of juxtaglomerular apparatus in vitro, mi

41 We used sophisticated techniques, including microperfusion of juxtaglomerular apparatus in vitro, mi

42 Microperfusion of L-arginine (10[-3] M) into the peritub

43 Microperfusion of live renal distal tubules reveals that

44 During in vivo microperfusion of proximal tubules, the extracellular tr

45 In vivo microperfusion of rat distal tubules suggests that a sig

46 y ISS and CSS were therefore recorded during microperfusion of strychnine to block the short latency

47 We test this hypothesis using bilateral microperfusion of the 5-HT(1A) receptor agonist 8-hydrox

48 lem after kidney transplantation; sufficient microperfusion of the allograft is crucial for postopera

49 Microperfusion of the deltaGABAAR-preferring agonist 4,5

50 Microperfusion of urinary space with BU-224 (microM), a

51 resents a novel approach combining open flow microperfusion (OFM) technology in a porcine model with

52 s evidence that FET analysis performed under microperfusion opens a brand new alternative for inexpen

53 re applied from micropipettes by brief (1 s) microperfusion pulses.

54 In situ microperfusion revealed that fluid absorptive rate (Jv)

55 Such attributes will ensure the microperfusion rig's continued utility as it may be used

56 d including renal clearance studies, in situ microperfusion, RT-PCR and whole-cell patch clamping.

57 e discretization scheme for blood and oxygen microperfusion simulations does not require expensive me

58 Microperfusion studies demonstrated that transepithelial

59 A voltage-controlled microperfusion system for delivering drugs and simultane

60 A double-barreled microperfusion system was used to apply solutions of wea

61 ated using a development of the single bolus microperfusion technique at chosen flow velocities (U) i

62 ated using a development of the single bolus microperfusion technique at chosen flow velocities in th

63 Therefore, we applied the open flow microperfusion technique to extract interstitial fluid f

64 A novel microperfusion technique was used to identify elevated l

65 With the stationary microperfusion technique, PAH secretion by both normal a

66 mega delta pi were estimated by the red cell microperfusion technique.

67 Net fluid absorption was determined using microperfusion techniques and methoxy[(3)H]inulin with i

68 MTALs from rats were studied by in vitro microperfusion to identify the mechanism underlying cros

69 In contrast, kidney allograft microperfusion was neither significantly reduced in pati

70 Intraoperative assessment of the allograft microperfusion was performed by near-infrared fluorescen

71 -fluid glucose concentrations, and open-flow microperfusion was used to determine the concentrations

72 In vivo luminal microperfusion was used to examine iron transport by the

73 Second, in vivo micropuncture and microperfusion were employed to measure the concentratio

74 biochemical evaluation, and in vitro tubule microperfusion were performed in both sexes.