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1 nsposon-site hybridization (TraSH) screen in whole human blood.
2 ion of CD34+ and Flk1+ cells from untreated, whole human blood.
3 que to separate white blood cells (WBC) from whole human blood.
4 s (hDAF(-/-)) were perfused with heparinized whole human blood.
5 S-induced up-regulation of TNF-alpha mRNA in whole human blood.
6 obtained without purification directly from whole human blood.
7 h CHC, and incubated with non-anticoagulated whole human blood.
8 stability of the analyte and metabolites in whole human blood and in DBS samples; effect of the volu
9 bulins in various clinical samples including whole human blood and plasma is a particular scientific
11 es 4 also exhibited significant stability in whole human blood, attributed to its interaction with HS
12 us buffer, little work has been performed in whole human blood because it contains numerous inhibitin
13 tly depleted lymphoma and myeloma cells from whole human blood but also exhibited some toxicity to B
14 fluidic device for separation of plasma from whole human blood by size exclusion in a cross-flow.
16 lpha-induced interleukin (IL)-8 by p75-Fc in whole human blood exhibited a U-shaped inhibition curve,
18 positive bacteria, fungi and endotoxins from whole human blood flowing through a single biospleen uni
19 ntroduction of red blood cell (RBC) depleted whole human blood followed by controlled washing led to
20 ithout surface treatment with MHA mixed with whole human blood; group 6 (G6) implant samples were tre
21 oietic stem cells are directly isolated from whole human blood in a rapid and efficient fashion (>96%
22 re coenzymes and antioxidants in extracts of whole human blood, in addition to the nearly 70 metaboli
23 ficantly decreased survival of the mutant in whole human blood, increased phagocytosis by human leuko
25 phoresis-based purification of 16S rRNA from whole human blood infected with Pseudomonas putida .
26 netium-99m-P483H was incubated with citrated whole human blood, layered onto WBC isolation media and
28 ion of lymphoma cells and depletes them from whole human blood more potently than the combination of
29 ivated cell sorter analysis was performed on whole human blood (n=2) and isolated neutrophils (n= 4)
30 tafruB mutants to survive in the presence of whole human blood or neutrophils was impaired, the pheno
34 eliminary studies with chlorofumarate 24a in whole human blood revealed that mixed-onium thiazolidine
36 ut not precursor IL-18 induces IFN-gamma; in whole human blood stimulated with endotoxin, inhibition
38 O is bound to the ferrous hemoglobin heme in whole human blood under basal and stimulated conditions
40 human monocytic THP-1 cells and heparinized whole human blood were stimulated with lipopolysaccharid
41 e survival of wild-type and SCV S. aureus in whole human blood, which contains high numbers of neutro
42 e, the developed PCT assay can be applied in whole human blood with an adequate sensitivity (LOD=0.02
43 of vCJD prion-infected brain homogenate into whole human blood, with a baseline control of normal hum
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