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1 mRNA stem-loop structure, the selenocysteine insertion sequence element.
2 cal to that in O157:H7 is bounded by the IS1 insertion sequence element.
3 egion of the cDNA contains a canonical Secys insertion sequence element.
4 and >204 nucleotides from the selenocysteine insertion sequence element.
5  accounted for by the presence or absence of insertion sequence elements.
6 vealed the presence of one or two classes of insertion sequence elements.
7 n to those previously known in dnaX and nine insertion sequence elements.
8 ariable deletion events between the flanking insertion-sequence elements, all resulting in eliminatio
9  frame is homologous to a family of putative insertion sequence elements, although our evidence shows
10 eatures of the cDNA include a selenocysteine insertion sequence element approximately 4.8 kb 3' to th
11      A total of 80 copies of three different insertion sequence elements are interspersed throughout
12  parent strain using all known P. gingivalis insertion sequence elements as probes suggested that no
13 on of mooV by the joining of the ends of the insertion sequence element at the circle junction.
14 idence that homologous recombination between insertion sequence elements can be a primary determinant
15                    Discrepancies between the insertion sequence element distribution patterns, the di
16 vel program that searches for selenocysteine insertion sequence elements, followed by selenoprotein g
17 A-binding protein B binds the selenocysteine insertion sequence elements from the GPX1 and type I iod
18 including phage-derived genes, plasmids, and insertion-sequence elements, highlighting its dynamic na
19                                     A common insertion sequence element in Escherichia coli, IS5, has
20 g protein that recognizes the selenocysteine insertion sequence element in human cellular glutathione
21 g from stop to Sec involves a cis-acting Sec insertion sequence element in the 3' untranslated region
22 ) and its insertion was dependent on the Sec insertion sequence element in the 3'UTR of TR1 mRNA.
23  rs713041 is located near the selenocysteine insertion sequence element in the GPX4 3' untranslated r
24 hia coli K-12 strain MG1655 contained an IS1 insertion sequence element in the regulatory region of t
25                 Among these are 85 predicted insertion sequence elements in eight different families.
26                                          The insertion sequence elements in the composite transposon-
27 ct key regulatory sites in the udp promoter, insertion sequence element insertions that activated cry
28                                          The insertion sequence element is located on the plasmid bet
29                               Several likely insertion sequence elements (IS100, IS630, and IS911) an
30 lis: (i) the transposition of the endogenous insertion sequence element IS1126 and (ii) the modulatio
31 determined that the endogenous P. gingivalis insertion sequence element IS1126 is capable of transpos
32                                          The insertion sequence element IS1358, found in both O1 and
33                   We describe the use of two insertion sequence elements (ISFtu1 and ISFtu2) in Franc
34                                 A 155-159 bp insertion sequence element known as the Correia element,
35  depends on the nature of the selenocysteine insertion sequence element located in the 3' UTR of sele
36 lication and maintenance regions, with seven insertion sequence elements, located mostly at the bound
37   PXO99A contains numerous copies of diverse insertion sequence elements, members of which are associ
38 conversion and several other loci containing insertion sequence elements or phage-related gene insert
39                                       Three "insertion" sequence elements present in POLQ are not fou
40  gingivalis was a concerted up-regulation of insertion sequence elements related to IS1 transposases.
41 se genes, conjugative functions and multiple insertion sequence elements suggests that the PAI, or se
42  the presence of a functional selenocysteine insertion sequence element that is highly active but onl
43                 The genome contains numerous insertion sequence elements that have mediated extensive
44       Here, we performed RFLP analyses using Insertion Sequence elements to resolve the phylogenetic
45 gly, however, we also observed that a 1.8-kb insertion sequence element was positioned between ccmB a
46 expressed when the Drosophila selenocysteine insertion sequence element was used, whereas the corresp
47 em-loop structures resembling selenocysteine insertion sequence elements were identified in the 3'-un
48                      Although many phage and insertion sequence elements were missing from the core c

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