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1 re-like sequences identified in the promoter-operator region.
2 low binding efficiency compared with the bio operator region.
3 shed by deletion of the 105-bp alcA promoter-operator region.
4 for a repressor gene, adjacent to a putative operator region.
5 number of half-site sequences present in the operator region.
6 nsmission organization or independent system operator region.
7 specifically to cbb(I) and cbb(II) promoter-operator regions.
8 odel to examine whether known differences in operator regions and binding affinities between Stx phag
9 h iron concentrations, IdeR binds to several operator regions and represses transcription of target g
10 to bind to DNA fragments carrying the 19-bp operator regions, and transcriptional analysis of putati
11 en symmetry and half-site spacing within the operator region are altered, whereas binding by the redu
12 inding of gonococcal Fur to its own promoter/operator region, as well as to the opa family of genes t
13 anscriptional repressor, as well as the MbdR operator regions (ATACN10GTAT) have been characterized.
14 933W has only two binding sites in its left operator region (compared to three in phage lambda), but
15 rotein and analyzed its interaction with the operator region controlling the expression of the dihydr
16 e YafQ-(DinJ)2-YafQ complexes binding to the operator region do not appear to amplify the extent of r
19 Southern blots probed with the vlsE promoter/operator region indicated that part or all of this seque
21 oligomerization of CI bound to two distinct operator regions (O(L) and O(R)), increases repression o
22 coccal Fur was found to bind to the promoter/operator region of a gene encoding the previously identi
24 ted MNase-hypersensitive sites in the alpha2 operator region of MFA2 in alpha cells but not in a cell
28 e distinctive features, we characterized the operator regions of H-19B, a lambdoid phage carrying stx
30 dentified a hexameric (G/T)ATAAT unit in the operator regions of these genes similar to that observed
31 onococcal Fur, we demonstrate binding to the operator regions of tonB, fur, recN, secY, sodB, hemO, h
32 hich have three operator repeats in the left operator region (OL), 933W only has two operator repeats
33 ells, confirming its specific binding to lac operator regions on the chromosome; we also showed that
34 933W has three operator repeats in the right operator region (OR), but unlike lambda and all other st
35 imer at in vivo concentrations, binds to the operator regions preferentially as a monomeric protein,
37 c binding to a DNA fragment encoding the lac operator region; the K(d) for the protein-DNA binding is
39 sis mutant in which the 105-bp alcA promoter-operator region was deleted by allelic exchange was unab
40 ter/operator region, we determined that this operator region was functional during N. gonorrhoeae inf
42 ur binding sequences within the fur promoter/operator region, we determined that this operator region
43 s, lytic for L. lactis NCK203, have a common operator region which can be targeted by a truncated der