ライフサイエンスコーパス: parenchymal tissue

1 (larynx, trachea and bronchus) and the lung parenchymal tissue.

2 pes, without substantial delivery into brain parenchymal tissue.

3 f antigen-responsive T cells across all lung parenchymal tissues.

4 matory cytokines systemically and within the parenchymal tissues.

5 d found predominantly in the bone marrow; in parenchymal tissues.

6 ion leading to migration of lymphocytes into parenchymal tissues.

7 nsported across the capillary endothelium to parenchymal tissues.

8 red mainly by their counterparts residing in parenchymal tissues.

9 atched, paired NSCLC tumor and non-malignant parenchymal tissues.

10 ed a marked accumulation of iron in affected parenchymal tissues, a finding consistent with early wor

11 days before such T cells can enter the lung parenchymal tissue and airway.

12 pillary beds, efferent vein, and surrounding parenchymal tissue are explanted and maintained for 24 h

13 FN-gamma expression in cognate Ag-expressing parenchymal tissues as well as death via a mechanism tha

14 ve been implicated in the repair of inflamed parenchymal tissue, but the signals that regulate their

15 l dysfunction by day 15 and little remaining parenchymal tissue by day 20.

16 Clara cell of the airway protect surrounding parenchymal tissue by inducing apoptosis of Fas(+) immun

17 Although kidney parenchymal tissue can be generated in vitro, reconstruc

18 However, in parenchymal tissue, CBFv oscillated with peaks at both a

19 ompensation for loss of IP-10 in lymphoid vs parenchymal tissue compartments.

20 reased apoptosis of lymphoid organs and some parenchymal tissues contributes to this immune suppressi

21 hat neutrophil infiltration was required for parenchymal tissue damage in the brain.

22 nges, with increasing cavitary formation and parenchymal tissue destruction.

23 Renal parenchymal tissues express a limited repertoire of rece

24 apid response mechanism that is operative in parenchymal tissues for effective defense against tissue

25 onstitutively in phagocytes and inducibly in parenchymal, tissue-forming cells.

26 regarding the cellular origin of human liver parenchymal tissue generation during embryonic developme

27 etabolic rate of the vessel wall relative to parenchymal tissue in the rat mesentery suggests that in

28 or restore expression of B7-H1 expression by parenchymal tissues in the recipient could prevent or am

29 lobase message was present in multiple human parenchymal tissues including heart, skeletal muscle, pl

30 way hyperresponsiveness to methacholine, and parenchymal tissue inflammation were also dramatically r

31 tion of host hematopoietic cells but minimal parenchymal tissue injury.

32 ective barrier to movement of pathogens from parenchymal tissues into the blood circulation.

33 contrast, infiltration of immune cells into parenchymal tissue is significantly delayed.

34 In chronic disease, failure to regenerate parenchymal tissue leads to the replacement of lost cell

35 Microglia, the parenchymal tissue macrophages in the brain, surround am

36 The results suggest that parenchymal tissues may retain the capacity to directly

37 ant tumors could "reawaken" after changes in parenchymal tissue mechanical properties, as may arise d

38 ng enzyme (ACE) in pulmonary artery and lung parenchymal tissues (obtained at the time of resection f

39 ome fibroblasts in various organs, including parenchymal tissue of the gut, lung, skin, and liver.

40 ted KT inhibitor associated with the gut and parenchymal tissues of the infective juvenile stage of F

41 the lung, unable to populate either the lung parenchymal tissue or the airway under homeostatic condi

42 lorative single-center clinical trial, renal parenchymal tissue perfusion of 32 stable kidney allogra

43 8(+) effector cells, and PD-L1 expression on parenchymal tissues protected against effector OT-I T ce

44 histologic evidence of ongoing vascular and parenchymal tissue remodeling, including interstitial fi

45 ivo, and the impact of cannabis use on HIV-1 parenchymal tissue reservoirs is unexplored.

46 (TNF) superfamily is a conserved response of parenchymal tissues to injury and inflammation that comm

47 ve immunity, dendritic cells (DCs) move from parenchymal tissues to lymphoid organs by migrating alon

48 ater (H(2)(17)O), which has direct access to parenchymal tissues via aquaporin-4 water channels, exhi

49 recipient vs donor) and localization (eg, in parenchymal tissue vs lymphoid organs) of these response

50 origin was from the vasculature rather than parenchymal tissue, while interindividual variability in

51 s represents the uncontrolled replacement of parenchymal tissue with extracellular matrix (ECM) produ