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1 rat basophilic leukemia cells (as a model of nonadherent cell).
2 out a cell viability assay with adherent and nonadherent cells.
3 FN before stimulation with IL-6, relative to nonadherent cells.
4 ls adherent to those ECM proteins but not in nonadherent cells.
5 embrane targeting and effector activation in nonadherent cells.
6 astic modulus, and intracellular pressure of nonadherent cells.
7  up-regulation of mediator release by FYB in nonadherent cells.
8 se in PLL-adherent and FN-nonadherent or PLL-nonadherent cells.
9 han in poly-L-lysine (PLL)-adherent or (PLL)-nonadherent cells.
10 cell shape mediates increased collagenase in nonadherent cells.
11 n caused an increase in C3 production by the nonadherent cells.
12 nors, and required HCMV interaction with the nonadherent cells.
13 p-regulation of plasminogen receptors in the nonadherent cells.
14 ed plate enclosed, was centrifuged to remove nonadherent cells.
15                                              Nonadherent cells accumulate in the nadir of the well an
16                                              Nonadherent cells also fail to activate the cyclin E-ass
17 ding AFM mechanical property measurements to nonadherent cells and characterizes properties of human
18  yeast, our techniques are suitable for most nonadherent cells and subcellular particles to character
19 an increase in LMP2A phosphorylation both in nonadherent cells and upon cell adhesion.
20                                              Nonadherent cells are captured in an array of 2,048 micr
21                                Because these nonadherent cells are depleted of mature NK cells and T
22 a wide variety of adherent cell types, while nonadherent cells are found to be refractory.
23 anges in the phosphorylation state of PAK in nonadherent cells, as evidenced by electrophoretic mobil
24        Furthermore, when we activated ERK in nonadherent cells by expression of active components of
25 th this novel method, receptor clustering on nonadherent cells can easily be monitored by high-throug
26   Natural killer (NK) cells develop from the nonadherent cell component of NK long-term bone marrow (
27 c analysis, sorting, and quantitation of the nonadherent cell component of NK-LTBMC showed that NK pr
28 row stroma, while reducing the production of nonadherent cells, did not increase apoptosis and cell d
29 S2 (i.e., CAS2A and CAS2B isoforms), whereas nonadherent cells (e.g., B cells, T cells, and myeloid c
30 ogical compounds in hundreds of adherent and nonadherent cells, enabling measurements of previously u
31                                              Nonadherent cells fail to phosphorylate the retinoblasto
32 tmentalize small populations of adherent and nonadherent cells in controlled microenvironments that c
33 re for a further 5 weeks, before plating the nonadherent cells in semisolid media.
34 were maintained by a significant fraction of nonadherent cells in the third passage, although these s
35 assay was used to count various adherent and nonadherent cells, including human tumors, L6, and HT-2
36 onolayers for 7 days and the total number of nonadherent cells increased 47- and 295-fold, respective
37                                   Killing of nonadherent cells is increased by treatment with antiint
38 spection of many isolated single adherent or nonadherent cells is required.
39  of paracrine signaling in both adherent and nonadherent cell lines.
40                                 In contrast, nonadherent cells (NAC) from purified protein derivative
41      This method is tested with adherent and nonadherent cells (NIH 3T3 fibroblasts, PANC-1 pancreati
42                                              Nonadherent cells of purified-protein-derivative-positiv
43 isphenol A, as well as the capture of living nonadherent cells on electrode surfaces by DNA hybridiza
44 gnificantly higher in FN-adherent than in FN-nonadherent cells, or than in poly-L-lysine (PLL)-adhere
45      PCR positivity was detected only in the nonadherent cell population among this group of individu
46  up-regulation of receptor expression in the nonadherent cell population was: 1) induced rapidly and
47 required an interaction between adherent and nonadherent cell populations, and 4) associated with an
48 rivation due to changes in both adherent and nonadherent cell populations.
49 ovudine enhanced apoptosis and cell death in nonadherent cells produced by both HIV-infected and cont
50                                   Thus, like nonadherent cells, size homeostasis requires feedback co
51 e techniques are not appropriate for probing nonadherent cells, such as passive human leukocytes, due
52 ring chamber has been optimized for use with nonadherent cells, such as Saccharomyces cerevisiae, and
53 stein was shown to decrease the viability of nonadherent cells, suggesting a lack of dependence on ce
54 t in the plasminogen binding capacity of the nonadherent cells, suggesting that the increase in bindi
55 ntegrated a high-density cell trap array for nonadherent cells that are challenging to handle under f
56 Studies that rely on fluorescence imaging of nonadherent cells that are cultured in suspension, such
57 t and eliminates the washing steps to remove nonadherent cells that can cause well-to-well and plate-
58 rphonuclear neutrophils (PMN) are quiescent, nonadherent cells that rapidly activate at sites of infl
59    Although T lymphocytes are constitutively nonadherent cells, they undergo facultative polarity dur
60 abrupt transition of hemocytes from resting, nonadherent cells to activated, adherent cells during th
61 the ability of pairs of related adherent and nonadherent cells to bind a recombinant Ebola virus rece
62  suppressed the mitogenic response of normal nonadherent cells to concanavalin A and IL-2.
63 weeks, but granulocytes were the predominant nonadherent cell type.
64     The loss of viability of M. smegmatis in nonadherent cells was correlated with an increase in non
65            Raf-R89L-CAAX activity was low in nonadherent cells, was rapidly stimulated to wild-type l
66 stein's effects on growth in adherent versus nonadherent cells were identified.
67 ays, 73% +/- 1% (mean +/- SEM; n = 6) of the nonadherent cells were mononuclear eosinophils, 13% +/-
68                   After 7 days of coculture, nonadherent cells were removed and cultured in the absen
69                              After 24 hours, nonadherent cells were removed and replated on fibronect
70  Here we present a method for characterizing nonadherent cells with AFM by mechanically immobilizing
71 o a culture surface, a method to encapsulate nonadherent cells within a gelatin plug on the concave m

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