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1 nfection at nanomolar concentrations without mitogenicity.
2 GroEL as a participant in the observed HUVEC mitogenicity.
3 effect of Acvr2a/b signaling on support cell mitogenicity.
4 ost immune responses, including B-lymphocyte mitogenicity, adjuvanticity and macrophage activation.
5  fragment-nonbinding) CD3 antibody has lower mitogenicity and a precise therapeutic window for diseas
6 lfate fragments that markedly activate FGF-2 mitogenicity and are found in wound fluids.
7 short interfering RNA blocked strain-induced mitogenicity and attenuated ERK phosphorylation but not
8 ere was an inverse correlation between serum mitogenicity and CFI (r=-0.61, P<0.01).
9                                              Mitogenicity and chemotaxis induced by PDGF-BB were enha
10 h ETA exhibits activities such as lymphocyte mitogenicity and epidermolytic activity.
11 d to demonstrate a correlation between HUVEC mitogenicity and GroEL levels in the lysate (r(2) = 0.85
12 ted responses both in vitro (transformation, mitogenicity and invasion), and in vivo (tumorigenicity
13 However, EDG-1 appears to be dispensable for mitogenicity and survival effects, even those induced by
14 thway, which plays an important role in cell mitogenicity and transformation.
15 uding regulation of cell volume, chemotaxis, mitogenicity, and inhibition of natural killer cell acti
16 imerin inhibited HRG-induced ERK activation, mitogenicity, and migration in breast cancer cells.
17 th inhibition concomitant with a decrease in mitogenicity, as measured by thymidine incorporation and
18   In contrast, when tested in the human cell mitogenicity assay, these mutant toxins were active.
19 ain potently inhibits heparin-mediated FGF-2 mitogenicity because of the poorly sulfated domains in i
20 on-FcR-binding antibodies have shown reduced mitogenicity compared to OKT3.
21 gh SEA-D227A exhibited substantially reduced mitogenicity compared with SEA wild type, it expanded th
22 any responses in eukaryotic cells, including mitogenicity, cytokine production, epithelial cell invas
23 B. henselae, although possessing significant mitogenicity for HUVECs, resulted in only about a twofol
24           Importantly, FGF-21 did not induce mitogenicity, hypoglycemia, or weight gain at any dose t
25 ptor PTKs and a moderate inhibition of their mitogenicity in monolayer.
26 h VEGF165R and modulating KDR/Flk-1-mediated mitogenicity indirectly and that exon 7-derived peptides
27  and glycocluster assays reveal that loss of mitogenicity is strongly correlated with loss of pi-pi s
28 expression of Fyn, but not Lck, restored the mitogenicity of FcR nonbinding anti-CD3 in primary T cel
29 velopment of lectins has been stalled by the mitogenicity of many of these proteins, which is the abi
30                                              Mitogenicity of PDGF-D and -B for mesangial cells was co
31 esidue Asn-23, Phe-44, or Cys-93 reduced the mitogenicity of SEB by a degree that depended upon the a
32   Antiserum to GroEL significantly inhibited mitogenicity of the lysate.
33  largely eliminating the potentially harmful mitogenicity of the parent compound.
34                                              Mitogenicity of the primary tumor was associated with mo
35 84 from histidine to threonine minimizes the mitogenicity of the wild-type lectin while maintaining a
36 vivo tumorigenicity, an effect for which the mitogenicity of this signalling pathway is likely to pla
37 colin (Hordeum vulgare lectin), seen to lack mitogenicity owing to the divergence in the residues at
38 nfluenza virus in vivo, and that the loss of mitogenicity seen previously in tissue culture is also s
39                                    Decreased mitogenicity was associated with disruption of pi-pi sta
40                                              Mitogenicity was tested by 3H-thymidine uptake.
41  cyclin D1 expression has been linked to its mitogenicity, we characterized the ability of estrogen t
42  with a threonine, significantly reduces its mitogenicity, while preserving its broad-spectrum antivi