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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 on of SUF14 mRNA, suggesting that expression is autoregulated.
5 ionally regulated by DNA damage and p53, and is autoregulated.
6  in this report suggest that SarA expression is autoregulated.
7 , and we demonstrated that expression of cmr is autoregulated.
8 own diversity of how the HigB-HigA TA family is autoregulated.
9          It also depended on sigN, thus sigN was autoregulated.
10 ly that transcription from the INO2 promoter is autoregulated 12-fold in a manner identical to that o
11  To determine if the TrcR response regulator is autoregulated, a trcR-lacZ fusion plasmid and a TrcR
12                       The Nmp4/CIZ promoters are autoregulated and deletion analysis identified regio
13 regulation and further suggest that TPBF may be autoregulated and may participate in the regulation o
14 se genes, suggesting that agr-like genes may be autoregulated and that they regulate gelE and sprE ex
15  Further, we demonstrate that vfr expression is autoregulated and cAMP dependent and involves Vfr bin
16                                         CRT1 is autoregulated and is itself induced by DNA damage, in
17             The results indicate that AF1298 is autoregulated and is part of an operon with two downs
18                                The arsR gene is autoregulated and is typically part of an operon that
19  fsr locus, fsrA, fsrB, and fsrC, appears to be autoregulated, and we have shown that mutants with in
20    Characteristic of other TA modules, shpAB is autoregulated, and high persistence depends on the Lo
21 s demonstrate that the transcription of rdgA is autoregulated, and strongly support the idea that pro
22 nase; phoP, indicative that the phoPQ operon is autoregulated; and an open reading frame encoding a p
23 s studies demonstrated that the parDE operon is autoregulated as a result of the binding of the ParD
24                     The B. subtilis rho gene was autoregulated at the level of transcription; autoreg
25                                   FUS levels are autoregulated by a mechanism in which human FUS down
26  during growth with tryptophan and that they are autoregulated by kynurenine.
27 e observations suggest that Grp1 family GEFs are autoregulated by mechanisms that depend on plasma me
28 of two main promoters (P0 and P1), and these are autoregulated by Pax6.
29                    We further show that nusA is autoregulated by a transcription attenuation mechanis
30                     Thus, IRF7 transcription is autoregulated by binding of the IRF7-containing VAF t
31 at exhibited by mammalian family members and is autoregulated by cisacting inhibitory domains.
32                        Tubulin concentration is autoregulated by feedback control of messenger RNA (m
33           Yeast ribosomal protein gene RPL7B is autoregulated by inhibition of splicing.
34 eviously demonstrated that Plk4 accumulation is autoregulated by its own kinase activity.
35 and provide information on how this promoter is autoregulated by proteins within the locus.
36  central domain of ARHGEF17 with Mps1, which is autoregulated by the activity of Mps1 kinase, for whi
37 vitro, repressed by the addition of zinc and is autoregulated by the copper-responsive CopY repressor
38  IL-10 by THP-1 cells stimulated with L-OspA was autoregulated by a negative feedback mechanism invol
39 d that lozenge-lacZ reporter-gene expression was autoregulated by Serpent and Lozenge.
40        Transcription of the three TA operons was autoregulated by the antitoxins.
41 gene named rctBp was identified and found to be autoregulated in Escherichia coli.
42                              CE2 is shown to be autoregulated in the diencephalon, responding to abse
43 ecting the likelihood that PNPase expression is autoregulated in an RNase III-dependent manner in S.
44 P promoter, raising the likelihood that tylP is autoregulated in its native host, Streptomyces fradia
45                              ABI5 expression is autoregulated in transgenic plants and yeast (Sacchar
46                       The expression of dnaA is autoregulated, in that transcription of the gene incr
47  the Drosophila homolog of hoxc-4, Deformed, is autoregulated, mutation of the hoxc-4 gene does not a
48 ly, our data suggest that ainS transcription is autoregulated, resulting in an over 2,000-fold increa
49   These data demonstrate that B-Raf activity is autoregulated, that constitutive phosphorylation of S
50                                 Because DnaA is autoregulated, these results might be due to the inhi
51                                   Polyamines are autoregulated through induction of antizyme, which r
52 imary initiator of its own expression, which is autoregulated through a novel FGF2-PI3K-Akt loop.
53                         Transcription of rho is autoregulated through a Rho-dependent attenuation in
54                              In addition, Zp is autoregulated through two sites that bind the BZLF1 g
55                     Expression of Ire1p mRNA was autoregulated through a process that required a func
56 tational analyses of PknK revealed that PknK is autoregulated via intramolecular interactions with it
57 d flow than their axons; ganglion blood flow is autoregulated within the range of blood pressure test