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1             The lack of cell-cycle arrest in postconfluent A7r5-N3IC was associated with an attenuate
2                                              Postconfluent Caco-2 cells were used in all experiments.
3 and initiator caspases in high cell density, postconfluent CD44 knock-out (CD44KO), and CD31KO cultur
4 soluble and latent TGF-beta 1 was highest in postconfluent cells (280 +/- 74 and 4320 +/- 610 pg/mg p
5 o-2 cells, and elevated SOCS-2 expression in postconfluent cells is associated with reduced prolifera
6  wounds as dissociated single cells, whereas postconfluent cells moved as contiguous sheets, retainin
7  with subconfluent cells using NF-kappaB and postconfluent cells using EGFR, MEK1/2, and p38.
8  PTHrP resulted in reduced cell viability in postconfluent cells, which was also dependent on cAMP ac
9 ptional rate of eNOS in proliferating versus postconfluent cells.
10 ch can be induced by PKC-alpha, increased in postconfluent cells.
11 f p21waf1, were examined in preconfluent and postconfluent cells.
12 endent inhibition of growth predominantly in postconfluent cells.
13 2 mM), from the cytosol into the membrane in postconfluent cells.
14 tylation of NF-YA and Bcl6 were increased in postconfluent cells.
15 ferating cells, and ELK1 is most abundant in postconfluent cells; during MC3T3-E1 osteoblast differen
16 lpha-sm-actin expression in preconfluent and postconfluent ciliary muscle cell cultures by immunocyto
17 ith cultures in early-confluence (2-3 days), postconfluent cultures (weeks) had more mature adherens
18                                              Postconfluent cultures also had fewer Ki-67-positive cel
19 pothesized that KGF increased cell number in postconfluent cultures by affecting the ability of norma
20                                              Postconfluent cultures can be used to examine the molecu
21 hat nucleosomal fragmentation was reduced in postconfluent cultures of KGF-treated keratinocytes.
22                                           In postconfluent cultures, treatment with KGF promoted tigh
23 iven to whether the behavior of RPE cells in postconfluent cultures, where intercellular adhesions ar
24                                      In some postconfluent cultures,the activity of the lysosomal enz
25 ler and fainter when growth was reinduced in postconfluent cultures.
26 y increased after repropagation of long-term postconfluent cultures.
27                                          The postconfluent dividing cells share features with cells t
28 genous TSP on the movement of albumin across postconfluent EC monolayers.
29                                           In postconfluent ECs, CD31 was desialylated compared with s
30 ecreased activation of effector caspase 3 in postconfluent EOMA cell cultures.
31 l-molecule inhibitor HNMPA-(AM(3)) inhibited postconfluent growth.
32 cetylation, but not for serum starvation nor postconfluent growth.
33                       PTPmu was expressed in postconfluent human pulmonary artery and lung microvascu
34 o were examined by analysis of confluent and postconfluent human RPE cultures, using the methods of r
35                                           In postconfluent monolayers of I-7 keratinocytes, an increa
36 to the particulate fraction in confluent and postconfluent NHEK cultures, suggesting that this isozym
37 tiation was critical for these responses, as postconfluent NHK yielded mRNA and protein levels an ord
38 NA levels are increased 4-fold compared with postconfluent, nonproliferating cells.
39                                    Over long postconfluent periods, cultured RPE cells became more gr
40 human and bovine RPE cultures after extended postconfluent periods.
41 imately 7 days postplating) and during their postconfluent phase (up to 20 days postplating), both to
42 ted in a biphasic manner with high levels in postconfluent preadipocytes and terminally differentiate
43  adipocyte differentiation, growth-arrested, postconfluent preadipocytes are required to reenter the
44 not other cathepsins, inhibited KSHV-induced postconfluent proliferation and the formation of spindle
45 challenge with photoreceptor outer segments, postconfluent RPE cultures accumulate heterogeneous mate
46                                              Postconfluent spheroids exhibit a necrotic core cemented
47                                       In the postconfluent state, when CD31 ectodomains are homophili
48  human vascular calcification model in which postconfluent vascular smooth muscle cell (VSMC) culture

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