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1  with the initial influx of chMMP-9-positive heterophils.
2 ripheral blood mononuclear cells but not for heterophils.
3 ronger, up-regulated gene expression of line heterophils A than line B, and these genes include sever
4 in vivo a further infiltration of endogenous heterophils and monocytes and dramatically rescued the i
5 properties; transferases cloned from chicken heterophils and red cells have signal peptides and may b
6             To dissect the interplay between heterophils and SE infection, we utilized large-scale ge
7 trated in vascular endothelium, macrophages, heterophils, and cardiac myocytes.
8 mplants of activated fibroblasts, monocytes, heterophils, and endothelial cells.
9 phil-like inflammatory cells, namely chicken heterophils, and the development of new blood vessels.
10                                   This early heterophil arrival was followed by the infiltration of m
11                                 Sex-specific heterophil concentrations, heterophil/lymphocyte ratios
12 us stents induced significantly more luminal heterophils/eosinophils and fibrin deposition than Cyphe
13 greater fibrin deposition, medial cell loss, heterophils/eosinophils, and late neointimal hyperplasia
14                             Large numbers of heterophils, equivalent to neutrophils in mammals, and i
15 ntributed to the dominance of the neutrophil/heterophil in modern-day mammals and birds.
16                           Moreover, purified heterophils incorporated into onplants lacking growth fa
17                        The exogenously added heterophils induced in vivo a further infiltration of en
18                                  Previously, heterophils isolated from broilers with different geneti
19 lammatory response and similar values of the heterophil/lymphocyte (H/L) ratio than those that were n
20             Duration of tonic immobility and heterophil/lymphocyte (H/L) ratios were also not respons
21      Sex-specific heterophil concentrations, heterophil/lymphocyte ratios and PHA responses differed
22                         In vivo, a decreased heterophil (neutrophil-like cell) migration was observed
23 d the MIL4 Ab, which detects both guinea pig heterophils (neutrophils) and eosinophils, to provide th
24                A direct addition of isolated heterophils or purified chMMP-9 into the HT-1080 onplant
25 se of the rabbit skeletal muscle and chicken heterophil, respectively.
26 osis and multiple immune cell types, notably heterophils (the avian equivalent of neutrophils).
27        Birds with microfilariae had elevated heterophil to lymphocyte ratios and were all co-infected
28 atinase B (chMMP-9) as a specific marker for heterophils, we now show that the onset and extent of an