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1 , suggesting that the Cgi system operates by transcription attenuation.
2  concentration higher than that required for transcription attenuation.
3 of the Bacillus subtilis trpEDCFBA operon by transcription attenuation.
4  rplJL operon of B. subtilis is regulated by transcription attenuation and antitermination mechanisms
5  TRAP regulates expression of these genes by transcription attenuation and translation control mechan
6 of the Bacillus subtilis trpEDCFBA operon by transcription attenuation and translation control mechan
7  operon of Bacillus subtilis is regulated by transcription attenuation and translation control mechan
8 of the Bacillus subtilis trpEDCFBA operon by transcription attenuation and translation control mechan
9 s that use short-range mechanisms to control transcription attenuation and translation initiation and
10 EDCFBA operon is regulated by TRAP-dependent transcription attenuation and translation repression mec
11 Pausing at U107 and U144 participates in the transcription attenuation and translational control mech
12 se two regulatory pause sites participate in transcription attenuation and translational control mech
13 of the Bacillus subtilis trpEDCFBA operon by transcription attenuation and translational control mech
14     Pausing at U107 and U144 participates in transcription attenuation and trpE translation control m
15 the tryptophan biosynthetic genes includes a transcription attenuation and two distinct translation c
16            Translation of pheL mRNA controls transcription attenuation and, consequently, expression
17 operon by promoting premature termination of transcription (attenuation) at a specific site within th
18 e 5' ends of pyrG transcripts act to prevent transcription attenuation by base pairing with the seque
19 sm of binding is important for TRAP-mediated transcription attenuation control of the trp operon.
20 ogical role for intragenic enhancer-mediated transcription attenuation in cell fate determination.
21 ic AMP receptor protein, riboswitch-mediated transcription attenuation in response to cyclic di-AMP,
22 usly shown to be mediated by a novel form of transcription attenuation in which low levels of intrace
23    These studies demonstrate that release of transcription attenuation is a mechanism used to induce
24  subtilis trpEDCFBA operon is regulated by a transcription attenuation mechanism controlled by the tr
25 lJL expression is regulated by an autogenous transcription attenuation mechanism in which L10(L12)4 b
26 further show that nusA is autoregulated by a transcription attenuation mechanism that does not rely o
27  of pyrimidine biosynthetic (pyr) genes by a transcription attenuation mechanism that is mediated by
28  of the plasmid pT181 antisense-RNA-mediated transcription attenuation mechanism.
29 e of the rate of TRAP binding to RNA for the transcription attenuation mechanism.
30 acillus subtilis trpEDCFBA operon by a novel transcription attenuation mechanism.
31 p leader transcript also plays a role in the transcription attenuation mechanism.
32 of nasF operon expression is determined by a transcription attenuation mechanism.
33  molecules and regulate gene expression by a transcription attenuation mechanism.
34 ncing evidence that epigenetic silencing and transcription attenuation play important roles.
35 anking sequences and supports a mechanism of transcription attenuation that is regulated in part by a
36  some evidence suggests that it operates via transcription attenuation, the components of this pathwa
37 as shown previously to occur at the level of transcription attenuation via structural rearrangements
38            An elaborate regulatory strategy, transcription attenuation, was discovered that is often

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