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1 ed FFAs impaired the ability of the liver to autoregulate.
2 onstrate that yefM-yoeB is transcriptionally autoregulated.
3 tested, indicating that frp transcription is autoregulated.
4 ed if mutated and so appear to be negatively autoregulated.
5 of SUF14 mRNA, suggesting that expression is autoregulated.
6 ally regulated by DNA damage and p53, and is autoregulated.
7 rolled in a Pdr1p/Pdr3p-dependent manner and autoregulated.
8 ied a specific transcript that is positively autoregulated.
9 this report suggest that SarA expression is autoregulated.
10 e operons might be negatively and positively autoregulated.
11 g that the expression of sigM was positively autoregulated.
12 of the group A streptococcus, is positively autoregulated.
13 ia coli transcription factors are negatively autoregulated.
14 that this transcription factor is positively autoregulated.
15 in vitro, indicating that sigR is positively autoregulated.
16 milar, we conclude that the sde locus is not autoregulated.
17 pstream of rpoE1, suggesting the gene may be autoregulated.
18 ity in the full-length protein is negatively autoregulated.
19 o report that E. coli fabR expression is not autoregulated.
20 nd we demonstrated that expression of cmr is autoregulated.
21 from two promoters, one constitutive and one autoregulated.
22 nsive promoters; only promoter P(A4) is PhoP autoregulated.
23 have demonstrated that sigU transcription is autoregulated.
24 It also depended on sigN, thus sigN was autoregulated.
25 The otx gene also autoregulates.
26 that transcription from the INO2 promoter is autoregulated 12-fold in a manner identical to that of t
27 determine if the TrcR response regulator is autoregulated, a trcR-lacZ fusion plasmid and a TrcR exp
30 mRNAs from the exuperantia and att genes and autoregulates alternative splicing of its own pre-mRNA.
31 riptional activity such that sc is unable to autoregulate, an essential function for the segregation
32 hila homologs of mammalian SRp20, negatively autoregulate and crossregulate at the level of alternati
34 rther, we demonstrate that vfr expression is autoregulated and cAMP dependent and involves Vfr bindin
35 ested that both BlxR and VjbR are positively autoregulated and cross-regulate the expression of each
40 ulation and further suggest that TPBF may be autoregulated and may participate in the regulation of t
41 genes, suggesting that agr-like genes may be autoregulated and that they regulate gelE and sprE expre
42 Characteristic of other TA modules, shpAB is autoregulated, and high persistence depends on the Lon p
43 emonstrate that the transcription of rdgA is autoregulated, and strongly support the idea that proteo
44 r locus, fsrA, fsrB, and fsrC, appears to be autoregulated, and we have shown that mutants with inser
45 e; phoP, indicative that the phoPQ operon is autoregulated; and an open reading frame encoding a prot
46 tudies demonstrated that the parDE operon is autoregulated as a result of the binding of the ParD pro
48 operon (rnc operon) expression is negatively autoregulated at the level of message stability by ribon
49 nce master regulator ComK is also positively autoregulated at the level of transcription and negative
50 ma-proteobacteria, E. coli Sxy is positively autoregulated at the level of transcription by a mechani
54 and suggest that ApxR not only is positively autoregulated but also acts as a transcriptional regulat
55 ystem whereas the ytbRI system is positively autoregulated but only at the level of ytbI expression.
57 nt manner, and cinI expression is positively autoregulated by 3OH,C14:1-HSL, the only identified N-ac
58 10 by THP-1 cells stimulated with L-OspA was autoregulated by a negative feedback mechanism involving
64 Transcription of the rpoE gene is positively autoregulated by Esigma(E) and by unknown mechanisms tha
65 also found that INO4 gene expression is not autoregulated by Ino2p and Ino4p, despite the presence o
68 servations suggest that Grp1 family GEFs are autoregulated by mechanisms that depend on plasma membra
74 ntral domain of ARHGEF17 with Mps1, which is autoregulated by the activity of Mps1 kinase, for which
77 ro, repressed by the addition of zinc and is autoregulated by the copper-responsive CopY repressor pr
79 ur inducing (Ti) plasmids is both negatively autoregulated by the RepA and RepB proteins, and positiv
82 liloti, and it is expressed similarly to the autoregulated C. crescentus ctrA in that both genes have
83 hat CCt, a proteolytic fragment of Ca(V)1.2, autoregulates Ca(V)1.2 expression in cardiac myocytes.
85 mal anxiety-related behaviors through direct autoregulated control of serotonergic gene expression.
86 olecular Cell, Badis et al. demonstrate that autoregulated destabilization of the RPS28B mRNA is medi
87 flow to CP of the fourth ventricle does not autoregulate during nonpharmacological increases in AP.
88 ood flow to the CP of the lateral ventricles autoregulates during nonpharmacological or pharmacologic
92 coli ribonuclease III (RNase III) negatively autoregulates expression of its own gene (rnc) approxima
94 reas hipB encodes a DNA-binding protein that autoregulates expression of the hip operon and binds to
97 tmitotic neurons by the sustained, and often autoregulated, expression of the same transcription fact
99 , our data demonstrate that homodimerization autoregulates FGF9 and FGF20's receptor binding and conc
100 due to an inhibition of transcription of the autoregulated G1 cyclins, CLN1 and CLN2; the transcripti
101 ed the behaviour of an inducible, negatively autoregulated gene circuit arranged in different transcr
102 or of the dynamics and the noise behavior of autoregulated gene circuits, and this T-based technique
109 define a novel transcriptional mechanism of autoregulated homeostasis of BRCA1 that selectively titr
112 ing the likelihood that PNPase expression is autoregulated in an RNase III-dependent manner in S. coe
114 lls and tissues, GR expression is positively autoregulated in human leukemic T cells and in other cel
115 romoter, raising the likelihood that tylP is autoregulated in its native host, Streptomyces fradiae.
116 t BMP4-dependent transcription is negatively autoregulated in part by SIN3B alternative splicing, and
122 start points, shown that CarR is positively autoregulated in the presence of OHHL, and have demonstr
124 e show that the cdk-inhibitor p21(Waf1/Cip1) autoregulates in a positive fashion transcription throug
125 cistronic operons that are cotranscribed and autoregulated, in a manner unlike typical TA modules.
130 a mechanism to explain how bFGF functions to autoregulate its expression and demonstrate that Egr-1 i
131 wn transcripts, and one of these is known to autoregulate its expression by coupling alternative spli
134 present study, we show that PTEN is able to autoregulate its expression through the stabilization of
136 consistent with wild-type p53 being able to autoregulate its levels by down-regulating expression of
138 HJ50 and acts as the extracellular signal to autoregulate its own biosynthesis through BovK/R two-com
139 es within the ZTA promoter and to positively autoregulate its own expression in transient cotransfect
142 inhibitor SOCS-3 acts in a negative loop to autoregulate its own gene expression, thus limiting its
144 These results indicate that QseB may act to autoregulate its own transcription through binding to lo
146 a phytopathogenic bacterium that appears to autoregulate its virulence genes, produces compounds tha
149 We present evidence that TBP negatively autoregulates its accessibility to promoter DNA in yeast
150 liferation/differentiation through STAT6 and autoregulates its effects on Th2 growth and effector fun
153 kinase-dead mutant, we established that Mnk1 autoregulates its interaction with eIF4G, releasing itse
155 described role as a splicing activator, Nova autoregulates its own expression by acting as a splicing
156 ccharomyces cerevisiae ribosomal protein L30 autoregulates its own expression by binding to a purine-
157 how that RstR both positively and negatively autoregulates its own expression from this promoter.
159 d previously published data that blimp1/krox autoregulates its own expression, but discovered, surpri
164 l-fusion reporter assays indicated that CovR autoregulates its own expression; this was verified by t
166 The human U1 snRNP-specific U1A protein autoregulates its own production by binding to and inhib
167 -kDa alternative sigma factor (sigma22) that autoregulates its own promoter (PalgT) as well as the pr
168 lR protein is a transcription activator that autoregulates its own promoter by repressing transcripti
170 onas aeruginosa toxA regulatory protein PtxS autoregulates its own synthesis by binding to a 52-bp fr
171 the accumulation of the SPT protein, and SPT autoregulates its own transcript abundance in conjunctio
172 sion, ChIP, and co-IP studies show that SCL3 autoregulates its own transcription by directly interact
173 ore, we provide evidence that GIV positively autoregulates its own transcription by enhancing STAT3 a
174 rR expression and found that SgrR negatively autoregulates its own transcription in the presence and
181 iated from the Qa promoter in prgQ, and PrgX autoregulates its transcription either by mediating tran
182 co transcription unit, suggesting that Disco autoregulates its transcription in the optic lobe primor
186 ts upstream cre were not required for normal autoregulated mga expression from Pmga P2 as long as Mga
187 ive Pmga resulted in a dramatic reduction in autoregulated mga expression in both mutant strains.
188 in G may play a central role in the p53-Mdm2 autoregulated module, but the precise function of cyclin
190 e Drosophila homolog of hoxc-4, Deformed, is autoregulated, mutation of the hoxc-4 gene does not affe
192 ression of Pax3 itself (suggesting that Pax3 autoregulates), neuronal differentiation and delaminatio
193 mational plasticity provides a mechanism for autoregulating NS1 functions, depending on its temporal
200 We programmed protein expression cycles, autoregulated protein levels, and a signaling expression
201 ber bacterial plasmids, typically encode two autoregulated proteins and an adjacent cis-acting centro
202 our data suggest that ainS transcription is autoregulated, resulting in an over 2,000-fold increase
203 tivate the transcription of two operons: the autoregulated sigV-rsiV-oatA-yrhK operon and dltABCDE.
204 lular level of wild-type PrrA was negatively autoregulated so that less PrrA was present in the absen
205 that are mechanistically distinct; and it is autoregulating so as to maintain intracellular iron home
207 affected by the growth substrate and was not autoregulated, suggesting that binding of SusR to maltos
208 hese data demonstrate that B-Raf activity is autoregulated, that constitutive phosphorylation of Ser(
215 longed membrane depolarization, inactivation autoregulates the activity of voltage-gated ion channels
217 ults suggest that B. pertussis is capable of autoregulating the activity of the bvg regulon through i
218 ls to adapt to the hyperosmotic milieu while autoregulating the expression of molecules that generate
219 isite intrinsic mechanisms the heart has for autoregulating the force of contraction to maintain card
220 assembly and disassembly processes, thereby autoregulating the interaction of MDA5 with dsRNA, and p
221 h of the mammary epithelial cell line and in autoregulating the powerful internal growth-inhibiting d
224 h GAG and aggrecan synthesis, disc cells can autoregulate their osmotic environment and accommodate m
232 egulatory elements and that it is negatively autoregulated through two EBNA-1 binding sites downstrea
236 7A mutant IE86 protein is able to negatively autoregulate transcription from the major immediate-earl
239 t bFGF leads to its own synthesis through an autoregulated transcriptional response that requires the
240 hrough the exact stochastic simulation of an autoregulated two-gene cascade operating near instabilit
242 ional analyses of PknK revealed that PknK is autoregulated via intramolecular interactions with its C
244 hat different classes of viral ncRNAs act to autoregulate viral gene expression and evade host antivi
245 ugh specific viral miRNAs have been shown to autoregulate viral mRNAs or downregulate cellular mRNAs,
246 ting that it is an intercellular signal that autoregulates virulence gene expression in wild-type R.
247 ly, the codY gene was shown to be negatively autoregulated, with its protein binding directly to the
248 low than their axons; ganglion blood flow is autoregulated within the range of blood pressure tested.
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