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1  of the microglia in allografts displayed an ameboid (activated) configuration, with retracted proces
2 contrast, microglia in the optic tectum were ameboid and clustered around neurogenic zones.
3 ed on increased staining with OX42), with an ameboid appearance.
4 ROS expression and increased the fraction of ameboid BV-2 microglia cells in an NF-kB dependent manne
5 s between twelve hours and one day, appeared ameboid by three days, and assumed a ramified morphology
6     In this article a mathematical model for ameboid cell movement is developed using a spring-dashpo
7 cells with Trap-14 induced rapid rounding of ameboid cells adherent to fibronectin-coated slides, whe
8                                    Round and ameboid cells became predominant in the ischemic core le
9                                    Round and ameboid cells were localized to the inner boundary of th
10                                    Round and ameboid cells were present throughout the entire ischemi
11 ced significant rounding and inactivation of ameboid cells within 20 min except for arterial endothel
12                               In chemotaxing ameboid cells, a complex leading-edge signaling circuit
13         In this time, the leukocyte moves in ameboid fashion across the endothelial borders, which re
14 udies suggest that leukocytes locomote in an ameboid fashion independently of pericellular proteolysi
15 apedesis, in which the leukocyte moves in an ameboid fashion through tightly apposed endothelial bord
16  transglutaminase nor LAV1-2 is found in the ameboid form of the organism.
17 elination is evident, many GFP(+) cells with ameboid form were detected in the white matter of the sp
18 rounding of spontaneously activated (mobile) ameboid human monocytes, granulocytes, or arterial endot
19                                     However, ameboid-like microglia were evident in an adjacent area
20                               Rod, round and ameboid-like microglia were present in the ischemic lesi
21  POE and maternal HCV infection exhibited an ameboid-like phenotype, characterized by smaller area/pe
22 ltered their morphology towards reactive and ameboid-like phenotypes in a thermal dose-dependent mann
23 garding microglial morphology, LPS caused an ameboid-like shape while poly(I:C) induced a bushy shape
24 by inference myosin II, are required for the ameboid locomotion of these cells.
25 lace of an actin cytoskeleton to drive their ameboid locomotion.
26 in, iron was detected in reactive microglia, ameboid microglia and macrophages in MS brains.
27             Neonatal males had twice as many ameboid microglia as females and a more activated morpho
28                           CD200R(+) /Iba1(+) ameboid microglia in the cingulum at P1-P5 were the only
29  was a significant increase in the number of ameboid microglia in the D7 group.
30                                         Only ameboid microglia present in the cultures responded to I
31 , we quantified ramified, hypertrophied, and ameboid microglia using unbiased stereological technique
32                               No evidence of ameboid microglia was found.
33 ssion is key for SCLC cells to acquire rapid ameboid migration and high metastatic potential.
34 usly unrecognized role of YAP in suppressing ameboid migration and tumor metastasis, and the mechanis
35 h its target genes CCN1/CCN2 to inhibit SCLC ameboid migration.
36  cells and parenchymal microglia with a more ameboid morphology expressed HLA-DR, indicating immune a
37 r their swift transformation to an activated ameboid morphology in response to pathological insults.
38 her signals, microglia assume an activated, "ameboid" morphology and release matrix metalloproteinase
39 ulated to measure the degree of ramified vs. ameboid morphotypes as an indicator of activation state.
40 because of its ability to mediate actin-like ameboid motility in nematode sperm, despite a lack of se
41 choroiditis included (1) choroiditis with an ameboid or serpentine shape; (2) characteristic imaging
42 ology in the dentate gyrus identified a more ameboid phenotype in LPS-exposed offspring, predominantl
43  through collagen-lined pores by adopting an ameboid phenotype.
44 results add to the evidence implicating soil ameboid predators as important factors for the maintenan
45         CD200R(+) cells were a population of ameboid/pseudopodic Iba1(+) microglia/macrophages observ
46 nomenon occurs during differentiation of the ameboid sperm of Caenorhabditis elegans as they activate
47 mation of spontaneously activated cells from ameboid to round.
48 rasites was typical of P. vivax, with highly ameboid trophozoites evident; however, infected erythroc