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1 cultures and to inappropriate conidiation in submerged culture.
2 degrees, and induced stalk cell formation in submerged culture.
3 I-4) mixtures and grown at clonal density in submerged culture.
4 bon sources does not suppress conidiation in submerged culture.
5 ium and exhibit inappropriate sporulation in submerged cultures.
6 owth phenotypes and develop conidiophores in submerged cultures.
7 ual fruiting and during carbon starvation in submerged cultures.
8 P mutation in PHKs grown in undifferentiated submerged cultures.
9  the corneal, epithelium in airlift, but not submerged, cultures.
10 sion of fluG activates sporulation in liquid-submerged culture, a condition that does not normally su
11 ere compared using three exposure platforms: submerged culture, air-liquid-interface (ALI) exposure i
12                               As compared to submerged cultures, air-lifting significantly promoted e
13 lock normally imposed on vegetative cells in submerged culture and leads to the formation of complex
14 ssion of flbA can also induce sporulation in submerged culture and this flbA activity requires fluG.
15 man bronchial epithelial cells were grown in submerged cultures and exposed to three occupationally-r
16 tinocytes (HCEKs) impairs differentiation in submerged cultures and in a "three-dimensional" organoty
17 n occurs only when beta-d-allose is added to submerged cultures before 12 h of development.
18                                           In submerged culture, concentrations of 0.001-1 microg/ml T
19                                              Submerged-culture conidiation is refractory to cAMP but
20 rhbA strain underwent asexual development in submerged cultures, even under ammonium-excess condition
21                      In addition, Deltagna-3 submerged cultures express the glucose-repressible gene,
22                                           In submerged cultures, FvVE1 deletion caused alterations in
23 C mutants elaborated conidiophores in liquid submerged culture, indicating that loss of either of the
24                                              Submerged cultures of primary human corneal epithelial k
25  cell lines and primary epithelial cells, in submerged cultures or grown in air-liquid interface cond
26 0 mRNA and protein when maintained in either submerged cultures or in organotypic cultures.
27                                  Exposure of submerged cultured PBEC (primarily consisting of basal c
28                                  In ALI (vs. submerged) cultures, pIgR expression was strongly induce
29 ncreased AfubrlA mRNA accumulation in liquid submerged culture, suggesting that they act as repressor
30 A caused inappropriate conidiation in liquid submerged culture, supporting the idea that GanB signall
31            One of these failed to develop in submerged culture, though it developed normally on agar.
32       BEAS-2B cells were exposed to WS-23 in submerged culture to validate the main results from prot
33 e human tracheobronchial epithelial cells in submerged culture were measured simultaneously using vid
34  previously isolated that could conidiate in submerged culture without imposing nutrient limitation a
35                    Compared with traditional submerged cultures without VIP, VIP-assisted ALI culture