ライフサイエンスコーパス: fresh blood

1 50 and 2000 basophil granulocytes in <0.1 ml fresh blood.

2 onfidence interval: 86, 100) of the yield of fresh blood.

3 its stored for more than 35 days, but not in fresh blood.

4 ting parasites by microscopic examination of fresh blood.

5 pothesis that transfusion of stored, but not fresh blood, adversely affects liver outcome in vivo fol

6 reated human dentin surfaces were exposed to fresh blood allowed to clot and were then rinsed before

7 e subpopulations of blood dendritic cells in fresh blood and will be of great value for their further

8 ned independently with lymphocyte subsets in fresh blood, apoptosis was negatively correlated with th

9 Subarachnoid infusion of 1-2 ml of fresh blood at 200 microl/min over cortical sulci caused

10 election was then used to isolate cells from fresh blood based on EBNA1-induced cytokine production.

11 ic and blood resuscitation groups (BR) (with fresh blood [BR-d0], blood stored for 4 [BR-d4] or 7 [BR

12 to the 9-mer epitopes were visualized within fresh blood by ELISPOT using free peptide or by binding

13 nificant improvement in liver perfusion with fresh blood (% change in functional MRI signal intensity

14 The consecutive fresh blood cultures received in the laboratory were ana

15 r CNVs present in lymphoblasts but absent in fresh blood DNA suggest that these represent clonal outg

16 e proteome of platelets highly purified from fresh blood donations, using elaborate protocols to ensu

17 bility genes in 100% of parental exomes from fresh blood draw, compared with only 82% of autopsy-sour

18 hole-exome sequencing coverage than DNA from fresh blood draw.

19 In experiments with fresh blood drawn from filaria-infected patients, we fou

20 Fresh blood from each subject was screened ex vivo using

21 ach blood culture bottle was inoculated with fresh blood from healthy donors.

22 g 156 mer nucleotide, was prepared using the fresh blood from patients with allergic disease.

23 For ex vivo studies, fresh blood from patients with atopic dermatitis and hea

24 At 90 days, 448 patients (37.0%) in the fresh-blood group and 430 patients (35.3%) in the standa

25 ored a mean (+/-SD) of 6.1+/-4.9 days in the fresh-blood group as compared with 22.0+/-8.4 days in th

26 ts were assigned to receive fresh red cells (fresh-blood group) and 1219 patients were assigned to re

27 analysis, the hazard ratio for death in the fresh-blood group, as compared with the standard-blood g

28 5-20 months earlier showed that most CEC in fresh blood had recipient genotype.

29 Only about 1.5% of spectrin isolated from fresh blood is unphosphorylated, about 9% has more than

30 soon after collection, suggesting that even "fresh" blood may have developed adverse biological chara

31 al T cell-activating cells can express TL1A, fresh blood monocytes and monocyte-derived dendritic cel

32 n, buffy coat, and residual blood cells from fresh blood (n = 10 volunteers) and from both fresh and

33 Further, in consecutive samples of fresh blood obtained from patients with B-CLL cells, the

34 to determine the frequency and phenotype in fresh blood of CD8+ T cells specific for two A*0201-rest

35 These data suggest that most CEC in fresh blood originate from vessel walls and have limited

36 gher among patients who received "older" vs "fresh" blood (P < 0.001).

37 gher among patients who received "older" vs "fresh" blood (P < 0.001).

38 dition, the same species were subcultured to fresh blood plates daily and DNA was extracted from the

39 sed to assess the "NO-generating" ability of fresh blood samples by effectively detecting the total l

40 Direct analysis of fresh blood samples has also been achieved with improved

41 In fresh blood samples Hb(III)NO accounts for 75% of the re

42 d compared with fresh blood, suggesting that fresh blood should be used for assessing the T cell immu

43 Our data suggest that fresh blood should not be washed routinely because, in a

44 antly lower in 1-day-old blood compared with fresh blood, suggesting that fresh blood should be used

45 p36) or VP1(p100) epitopes, as determined by fresh blood tetramer staining (FBTS), ranged from 1/6,00

46 We recently demonstrated that transfusion of fresh blood to 100 g/L hemoglobin in anemic animals offe

47 ly improved in the anemic animals undergoing fresh blood transfusion compared to control anemic anima

48 e of blood negates the beneficial effects of fresh blood transfusion, which include reductions in inf

49 with 100% O2, and reperfused for 90 min with fresh blood via a cannula in the pulmonary artery.

50 that had been stored for less than 35 days ("fresh" blood), whereas 429 (31.4%) patients received at

51 that had been stored for less than 35 days ("fresh" blood), whereas 429 (31.4%) patients received at

52 Our data indicate that transfusion of fresh blood, which results in less hemolysis, CFH, and i

53 Anemic animals were randomized to receive fresh blood (within 4 hrs), stored blood (7 days), or no

54 In contrast, washing fresh blood worsened all these same clinical parameters