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1 The IFP and tumor volumes were followed for up to 10 days after a single dose of 10, 20, or 30 G

2 IL-2 was detected in tumor ascites for up to 10 days after a single i.p. injection of IL-2

3 enetrated into the vessel wall and persisted for up to 14 days after a short, single intraluminal inf

4 methasone was present in the treated segment for up to 14 days after a single infusion, with no plasm

5 The animals were monitored for up to 15 days after acid aspiration.

6 stitial glucose concentrations were measured for up to 7 days after birth.

7 , even when serum administration was delayed for up to 4 days after challenge.

8 a fluvoxamine levels were performed serially for up to 10 days after drug withdrawal.

9 oncentrations in plasma collected once daily for up to 5 days after enrollment.

10 STAT proteins were activated for up to 8 days after explantation of SCG in vitro.

11 n (33.8+/-2.3 versus 4.1+/-1.5 tablets/week) for up to 360 days after GTx; reduced ischemia by electr

12 ardial perfusion by SPECT-sestamibi scanning for up to 90 days after GTx when compared with images ob

13 ent, most remained mixed donor/host chimeras for up to 180 days after HCT.

14 and P-selectin on the pulmonary vasculature for up to 7 days after I.T.-SRBC challenge.

15 In addition, STAT1 remains nuclear for up to 7 days after IFN-gamma removal.

16 1/CFA immunization inhibits clinical disease for up to 100 days after immunization.

17 FR mRNA levels detectable at 24 h and stable for up to 10 days after infection.

18 rom 0% to 75%, even when therapy was delayed for up to 5 days after infection with influenza virus.

19 II-deficient Abo mice had high virus titers for up to 90 days after infection (4.30 log10 PFU per g

20 urine and by cocultivation of kidney tissue for up to 247 days after initial infection.

21 GFP expression was observed for up to 14 days after injection.

22 the beta-galactosidase protein were followed for up to 21 days after injection.

23 Rhinoviruses induced IL-8 release for up to 7 days after inoculation onto PBMC.

24 Animals were evaluated daily for up to 8 days after inoculation.

25 ) of islets achieved sustained normoglycemia for up to 60 days after islet transplantation.

26 elevated as early as 2 days and continuously for up to 7 days after pressure overload.

27 ring sperm have evolved to remain motionless for up to several days after spawning, yet are still cap

28 6 post-C. rodentium challenge, and persisted for up to 19 days after stressor termination.

29 mals were monitored electrocardiographically for up to 7 days after surgery, at which time they were

30 te depletion of circulating CD2+CD3+ T cells for up to 10 days after the last dose; T cells recovered

31 od, while bilirubin levels continued to drop for up to 20 days after the initiation of treatment (P <

32 ool samples were found to be positive by EIA for up to 24 days after the peak elevation of liver enzy

33 onses during a subsequent dehydration stress for up to 5 days after the initial stress.

34 by PCR-ETBr for up to 34 days and by PCR-NA for up to 54 days after the peak elevation of liver enzy

35 40 days but remaining, to a smaller extent, for up to 75 days after the headache event.

36 e receptive to IL-4-mediated differentiation for up to 3 days after their initial priming.

37 italized for CAP were prospectively followed for up to 30 days after their hospitalization for this i

38 d plain SCID xenografted with PI was similar for up to 14 days after transplantation, after which the

39 sity within the tumor on T2*-weighted images for up to 5 days after treatment and was related to the

40 and antiviral T-cell responses were analyzed for up to 30 days after vaccination.

41 d a strong selective pressure that persisted for up to 10 days, after which the importance of stochas

42 % of ova were able to retain their viability for up to 16 days, after which the rate of inactivation

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