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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 Xpert HIV-1 Qual for PoC-EID testing, using fresh blood and dried blood spots (DBS) samples at obste
8 e subpopulations of blood dendritic cells in fresh blood and will be of great value for their further
10 ned independently with lymphocyte subsets in fresh blood, apoptosis was negatively correlated with th
13 election was then used to isolate cells from fresh blood based on EBNA1-induced cytokine production.
14 ic and blood resuscitation groups (BR) (with fresh blood [BR-d0], blood stored for 4 [BR-d4] or 7 [BR
15 to the 9-mer epitopes were visualized within fresh blood by ELISPOT using free peptide or by binding
16 nificant improvement in liver perfusion with fresh blood (% change in functional MRI signal intensity
18 r CNVs present in lymphoblasts but absent in fresh blood DNA suggest that these represent clonal outg
19 e proteome of platelets highly purified from fresh blood donations, using elaborate protocols to ensu
20 bility genes in 100% of parental exomes from fresh blood draw, compared with only 82% of autopsy-sour
30 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
31 ts were assigned to receive fresh red cells (fresh-blood group) and 1219 patients were assigned to re
32 analysis, the hazard ratio for death in the fresh-blood group, as compared with the standard-blood g
34 Only about 1.5% of spectrin isolated from fresh blood is unphosphorylated, about 9% has more than
35 red at the point-of-care within 26 min using fresh blood, it can be easily delivered using clinical c
36 soon after collection, suggesting that even "fresh" blood may have developed adverse biological chara
37 al T cell-activating cells can express TL1A, fresh blood monocytes and monocyte-derived dendritic cel
38 n, buffy coat, and residual blood cells from fresh blood (n = 10 volunteers) and from both fresh and
40 to determine the frequency and phenotype in fresh blood of CD8+ T cells specific for two A*0201-rest
41 ipheral blood mononuclear cells derived from fresh blood of healthy donors and patients with CLN3 dis
42 cells and circulating cytotoxic molecules in fresh blood of patients with early-to-mid iPD, especiall
45 dition, the same species were subcultured to fresh blood plates daily and DNA was extracted from the
46 tion from severe HS after TBI in rats, using fresh blood, polymerized human hemoglobin (PolyhHb), and
49 e infectious nature of SARS-CoV-2, patients' fresh blood samples are limited to access for in vitro e
50 sed to assess the "NO-generating" ability of fresh blood samples by effectively detecting the total l
54 e control selection, the need for processing fresh blood samples, and the existence of non-releasing
55 d compared with fresh blood, suggesting that fresh blood should be used for assessing the T cell immu
57 antly lower in 1-day-old blood compared with fresh blood, suggesting that fresh blood should be used
58 p36) or VP1(p100) epitopes, as determined by fresh blood tetramer staining (FBTS), ranged from 1/6,00
59 We recently demonstrated that transfusion of fresh blood to 100 g/L hemoglobin in anemic animals offe
60 ly improved in the anemic animals undergoing fresh blood transfusion compared to control anemic anima
61 e of blood negates the beneficial effects of fresh blood transfusion, which include reductions in inf
63 that had been stored for less than 35 days ("fresh" blood), whereas 429 (31.4%) patients received at
65 Anemic animals were randomized to receive fresh blood (within 4 hrs), stored blood (7 days), or no