ライフサイエンスコーパス: peritoneal lavage

1 gates but were recovered from the spleen and peritoneal lavage.

2 The number of intact mast cells in the peritoneal lavages after eotaxin injection was significa

3 s, 101 were assigned to undergo laparoscopic peritoneal lavage and 98 were assigned to colon resectio

4 llate-elicited macrophages were collected by peritoneal lavage and bone marrow was harvested.

5 FAST, invasive procedures such as diagnostic peritoneal lavage and exploratory laparotomy were common

6 Peritoneal lavage and plasma samples were analyzed for p

7 levels of proinflammatory cytokines in both peritoneal lavage and serum.

8 phages obtained from thioglycollate-elicited peritoneal lavages and differentiated bone marrow cells

9 al cavity of mice, incubation, retrieval via peritoneal lavage, and observation of the number of cell

10 our methods: computed tomography, diagnostic peritoneal lavage, celiotomy, or serial clinical evaluat

11 Immunoprecipitation of lumican from peritoneal lavage co-precipitates CD14, a cell surface l

12 In contrast to peritoneal lavage eosinophils, dispersed granuloma cells

13 ons during Escherichia coli pneumonia, or in peritoneal lavage fluid after 4 h of S. pneumoniae perit

14 of TNF-alpha and IFN-gamma in the spleen and peritoneal lavage fluid as compared to values determined

15 phage inflammatory protein (MIP)-2 levels in peritoneal lavage fluid as well as induced RNA expressio

16 Peritoneal lavage fluid concentrations of IL-10 were con

17 NK cells and significantly reduced levels of peritoneal lavage fluid IL-5, whereas the number of IL-5

18 e significantly increased in both plasma and peritoneal lavage fluid in CpG ODN-treated versus non-Cp

19 lso determined that cells collected from the peritoneal lavage fluid of E. faecalis-infected mice sho

20 rophils and macrophages were concentrated in peritoneal lavage fluid of experimental animals (p < 0.0

21 ), but did not significantly affect IL-10 in peritoneal lavage fluid or in lysates of peritoneal cell

22 tric analysis of cytokine-producing cells in peritoneal lavage fluid revealed increased numbers of IL

23 Additionally, VEGF levels measured in peritoneal lavage fluid were 300-fold lower compared to

24 ontrast, microbial burdens in the organs and peritoneal lavage fluid were similar between mono- and c

25 enzyme-linked immunosorbent assay) in serum, peritoneal lavage fluid, and liver and lung samples at 4

26 ostaglandin levels were measured from serum, peritoneal lavage fluid, and muscularis culture media.

27 P augmented cytokine levels in the blood and peritoneal lavage fluid.

28 hanges in protein levels in cell lysates and peritoneal lavage fluid.

29 ignificant increase in the levels of CCL4 in peritoneal lavage fluid.

30 the peritoneum and showed lower IL-1beta in peritoneal lavage fluid.

31 In vitro, mouse eosinophils from peritoneal lavage fluids did not produce superoxide anio

32 Peritoneal lavage fluids from CREB-inhibited tumor-beari

33 Peritoneal lavage fluids from these mice also contained

34 were performed on their kidneys, livers, and peritoneal lavage fluids.

35 CT has virtually replaced diagnostic peritoneal lavage for the detection of important injurie

36 Chemotaxis assays using peritoneal lavage from pristane-injected Irf5(+/+) and I

37 e and lower IL-1beta levels were detected in peritoneal lavages from Cd44(-/-) mice (p < 0.01).

38 peritonitis (15 patients in the laparoscopic peritoneal lavage group vs 13 in the colon resection gro

39 nd P2X(7)R(-/-) animals display increases in peritoneal lavage IL-6 levels but no detectable IL-1.

40 in-6, and interleukin-10 levels in serum and peritoneal lavage in G6PD-deficient mice compared with w

41 Diagnostic peritoneal lavage is rarely performed, and CT is used wh

42 of abdominal computed tomography, diagnostic peritoneal lavage, laparotomy, autopsy, and/or clinical

43 arious sources, including cell culture (CC), peritoneal lavage (Lav) from the tumor microenvironment,

44 tients were assigned to undergo laparoscopic peritoneal lavage (n = 101) or colon resection (n = 98)

45 rate that peritoneal macrophages isolated by peritoneal lavage of unchallenged mice express P-selecti

46 cytometric analysis of cells recovered from peritoneal lavages of anti-CR3-treated T. gondii-infecte

47 Reduced monocyte recruitment in peritoneal lavages of Fpr2/3(-/-) animals was reflected

48 tients were assigned to undergo laparoscopic peritoneal lavage or colon resection based on computer-g

49 Parallel analyses of peritoneal lavage proteins for protein dityrosine and ni

50 ts were compared with findings of diagnostic peritoneal lavage, repeat US, computed tomography (CT),

51 Microarrays of infected peritoneal lavage revealed >10-fold up-regulation of neu

52 bacterial densities in kidneys, livers, and peritoneal lavage samples than mice immunized with stand

53 er LPS injection for collection of serum and peritoneal lavage samples that were used to assay IL-10

54 abdominal sonography for trauma, diagnostic peritoneal lavage, spiral computed tomography (CT) scan,

55 In the in vivo peritoneal lavage study, animals received injections of

56 mputed tomographic, repeat US, cystographic, peritoneal lavage, surgical, and/or autopsy findings in

57 icacy of hypothermia induced by an automated peritoneal lavage system in patients with ST-segment-ele

58 Automated peritoneal lavage system is a safe and ultrarapid method

59 cooling technology, the Velomedix Automated Peritoneal Lavage System using ice-cold fluids continuou

60 nts to detect hemopericardium and diagnostic peritoneal lavage to detect hemoperitoneum.

61 In the late period, diagnostic peritoneal lavage was phased out in favor of torso ultra

62 n, peritonitis was induced by SEB injection; peritoneal lavages were collected after 48 h and analyze