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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
11                       The Nmp4/CIZ promoters are autoregulated and deletion analysis identified regio
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
15                                         CRT1 is autoregulated and is itself induced by DNA damage, in
16             The results indicate that AF1298 is autoregulated and is part of an operon with two downs
17                                The arsR gene is autoregulated and is typically part of an operon that
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
23                     The B. subtilis rho gene was autoregulated at the level of transcription; autoreg
24  during growth with tryptophan and that they are autoregulated by kynurenine.
25 e observations suggest that Grp1 family GEFs are autoregulated by mechanisms that depend on plasma me
26 of two main promoters (P0 and P1), and these are autoregulated by Pax6.
27                    We further show that nusA is autoregulated by a transcription attenuation mechanis
28                     Thus, IRF7 transcription is autoregulated by binding of the IRF7-containing VAF t
29 at exhibited by mammalian family members and is autoregulated by cisacting inhibitory domains.
30 eviously demonstrated that Plk4 accumulation is autoregulated by its own kinase activity.
31 and provide information on how this promoter is autoregulated by proteins within the locus.
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
35 d that lozenge-lacZ reporter-gene expression was autoregulated by Serpent and Lozenge.
36        Transcription of the three TA operons was autoregulated by the antitoxins.
37 gene named rctBp was identified and found to be autoregulated in Escherichia coli.
38                              CE2 is shown to be autoregulated in the diencephalon, responding to abse
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
41                              ABI5 expression is autoregulated in transgenic plants and yeast (Sacchar
42                       The expression of dnaA is autoregulated, in that transcription of the gene incr
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
46                                 Because DnaA is autoregulated, these results might be due to the inhi
47                                   Polyamines are autoregulated through induction of antizyme, which r
48 imary initiator of its own expression, which is autoregulated through a novel FGF2-PI3K-Akt loop.
49                              In addition, Zp is autoregulated through two sites that bind the BZLF1 g
50                     Expression of Ire1p mRNA was autoregulated through a process that required a func
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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