ライフサイエンスコーパス: whole human blood

1 erial types with and without the presence of whole human blood.

2 ere administered into a reservoir containing whole human blood.

3 ion of CD34+ and Flk1+ cells from untreated, whole human blood.

4 que to separate white blood cells (WBC) from whole human blood.

5 s (hDAF(-/-)) were perfused with heparinized whole human blood.

6 S-induced up-regulation of TNF-alpha mRNA in whole human blood.

7 nsposon-site hybridization (TraSH) screen in whole human blood.

8 obtained without purification directly from whole human blood.

9 in) and a limit of detection of 0.18 U/ml in whole human blood.

10 sis by neutrophils or killing of bacteria by whole human blood.

11 h CHC, and incubated with non-anticoagulated whole human blood.

12 s approach was validated with heparin-spiked whole human blood and had a linear correlation with the

13 stability of the analyte and metabolites in whole human blood and in DBS samples; effect of the volu

14 bulins in various clinical samples including whole human blood and plasma is a particular scientific

15 When tested in whole human blood and unstimulated human saliva maximum

16 e (PBS), (2) spiked human plasma, (3) spiked whole human blood, and (4) clinical samples from patient

17 es 4 also exhibited significant stability in whole human blood, attributed to its interaction with HS

18 us buffer, little work has been performed in whole human blood because it contains numerous inhibitin

19 tly depleted lymphoma and myeloma cells from whole human blood but also exhibited some toxicity to B

20 fluidic device for separation of plasma from whole human blood by size exclusion in a cross-flow.

21 mutant also exhibited decreased survival in whole human blood due to phagocytosis.

22 lpha-induced interleukin (IL)-8 by p75-Fc in whole human blood exhibited a U-shaped inhibition curve,

23 essful in the determination of H2S spiked in whole human blood, fetal bovine serum, and E. coli.

24 positive bacteria, fungi and endotoxins from whole human blood flowing through a single biospleen uni

25 ntroduction of red blood cell (RBC) depleted whole human blood followed by controlled washing led to

26 ithout surface treatment with MHA mixed with whole human blood; group 6 (G6) implant samples were tre

27 oietic stem cells are directly isolated from whole human blood in a rapid and efficient fashion (>96%

28 re coenzymes and antioxidants in extracts of whole human blood, in addition to the nearly 70 metaboli

29 ficantly decreased survival of the mutant in whole human blood, increased phagocytosis by human leuko

30 Cytokine production in whole human blood indicated that anti-CD14 failed to blo

31 phoresis-based purification of 16S rRNA from whole human blood infected with Pseudomonas putida .

32 netium-99m-P483H was incubated with citrated whole human blood, layered onto WBC isolation media and

33 by interferon-alpha induction activities in whole human blood models.

34 ion of lymphoma cells and depletes them from whole human blood more potently than the combination of

35 ivated cell sorter analysis was performed on whole human blood (n=2) and isolated neutrophils (n= 4)

36 tafruB mutants to survive in the presence of whole human blood or neutrophils was impaired, the pheno

37 The methods are exemplified using whole human blood plasma, and it is shown that it is pos

38 The sulfur K-edge spectra for whole human blood, plasma, and erythrocytes are shown.

39 elevance of this inhibition was borne out in whole human blood platelet aggregation assays.

40 eliminary studies with chlorofumarate 24a in whole human blood revealed that mixed-onium thiazolidine

41 Cs in 30 anonymized, random and disease-free whole human blood samples.

42 ut not precursor IL-18 induces IFN-gamma; in whole human blood stimulated with endotoxin, inhibition

43 In tests with whole human blood, the device is shown to reduce the con

44 O is bound to the ferrous hemoglobin heme in whole human blood under basal and stimulated conditions

45 Using whole human blood under flow at low and high shear rates

46 human monocytic THP-1 cells and heparinized whole human blood were stimulated with lipopolysaccharid

47 e survival of wild-type and SCV S. aureus in whole human blood, which contains high numbers of neutro

48 e, the developed PCT assay can be applied in whole human blood with an adequate sensitivity (LOD=0.02

49 of vCJD prion-infected brain homogenate into whole human blood, with a baseline control of normal hum