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1 d upstream of rpoE1, suggesting the gene may be autoregulated.
2 we have demonstrated that sigU transcription is autoregulated.
3 ns tested, indicating that frp transcription is autoregulated.
4 , and we demonstrated that expression of cmr is autoregulated.
5 on of SUF14 mRNA, suggesting that expression is autoregulated.
6 ionally regulated by DNA damage and p53, and is autoregulated.
7 in this report suggest that SarA expression is autoregulated.
8 It also depended on sigN, thus sigN was autoregulated.
9 ly that transcription from the INO2 promoter is autoregulated 12-fold in a manner identical to that o
10 To determine if the TrcR response regulator is autoregulated, a trcR-lacZ fusion plasmid and a TrcR
12 regulation and further suggest that TPBF may be autoregulated and may participate in the regulation o
13 se genes, suggesting that agr-like genes may be autoregulated and that they regulate gelE and sprE ex
14 Further, we demonstrate that vfr expression is autoregulated and cAMP dependent and involves Vfr bin
18 fsr locus, fsrA, fsrB, and fsrC, appears to be autoregulated, and we have shown that mutants with in
19 Characteristic of other TA modules, shpAB is autoregulated, and high persistence depends on the Lo
20 s demonstrate that the transcription of rdgA is autoregulated, and strongly support the idea that pro
21 nase; phoP, indicative that the phoPQ operon is autoregulated; and an open reading frame encoding a p
22 s studies demonstrated that the parDE operon is autoregulated as a result of the binding of the ParD
25 e observations suggest that Grp1 family GEFs are autoregulated by mechanisms that depend on plasma me
32 central domain of ARHGEF17 with Mps1, which is autoregulated by the activity of Mps1 kinase, for whi
33 vitro, repressed by the addition of zinc and is autoregulated by the copper-responsive CopY repressor
34 IL-10 by THP-1 cells stimulated with L-OspA was autoregulated by a negative feedback mechanism invol
39 ecting the likelihood that PNPase expression is autoregulated in an RNase III-dependent manner in S.
40 P promoter, raising the likelihood that tylP is autoregulated in its native host, Streptomyces fradia
43 the Drosophila homolog of hoxc-4, Deformed, is autoregulated, mutation of the hoxc-4 gene does not a
44 ly, our data suggest that ainS transcription is autoregulated, resulting in an over 2,000-fold increa
45 These data demonstrate that B-Raf activity is autoregulated, that constitutive phosphorylation of S
48 imary initiator of its own expression, which is autoregulated through a novel FGF2-PI3K-Akt loop.
51 tational analyses of PknK revealed that PknK is autoregulated via intramolecular interactions with it
52 d flow than their axons; ganglion blood flow is autoregulated within the range of blood pressure test
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