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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 ual fruiting and during carbon starvation in submerged cultures.
6 ium and exhibit inappropriate sporulation in submerged cultures.
7 owth phenotypes and develop conidiophores 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
12 lock normally imposed on vegetative cells in submerged culture and leads to the formation of complex
13 ssion of flbA can also induce sporulation in submerged culture and this flbA activity requires fluG.
14 tinocytes (HCEKs) impairs differentiation in submerged cultures and in a "three-dimensional" organoty
18 rhbA strain underwent asexual development in submerged cultures, even under ammonium-excess condition
21 C mutants elaborated conidiophores in liquid submerged culture, indicating that loss of either of the
23 cell lines and primary epithelial cells, in submerged cultures or grown in air-liquid interface cond
27 ncreased AfubrlA mRNA accumulation in liquid submerged culture, suggesting that they act as repressor
28 A caused inappropriate conidiation in liquid submerged culture, supporting the idea that GanB signall
30 e human tracheobronchial epithelial cells in submerged culture were measured simultaneously using vid
31 previously isolated that could conidiate in submerged culture without imposing nutrient limitation a
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