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1 matic myogenesis in Drosophila relies on the reiterative activity of the basic helix-loop-helix trans
2 which low levels of intracellular CTP induce reiterative addition of G residues at position +4 in the
3 ide that can, among other things, be used in reiterative alkyne coupling and iodocyclization to give
5 ther follow-up of 87 months, we examined, in reiterative analyses, the effect of increasing time inte
6 ion may have the opposite effect, leading to reiterative and cumulative strengthening of memory over
12 to enrich for utricle-specific genes, using reiterative cDNA subtraction and demonstrate enrichment
13 woody developmental program results from the reiterative coactivation of pathways that are largely in
14 riminate dG addition by telomerase occurs by reiterative copying of C residues in the telomerase RNA
15 s whereby PV RNA functions as a template for reiterative CRE-dependent VPg uridylylation before and d
21 ation of innate lymphoid cells have revealed reiterative developmental programs that result in cells
23 complementarity to the RNA template induced reiterative dG incorporation, indicating that the reacti
24 enhancements in specificity and activity by reiterative DNA shuffling and screening, even for an enz
25 noacyl-tRNA and for translocation during the reiterative elongation reactions of protein synthesis.
28 ization, possibly related to the presence of reiterative Ikaros binding sites in the intergenic eleme
29 that can be visualized on the same cells via reiterative in situ labeling and erasing of markers on c
33 DNA sequence determinants for TSS selection, reiterative initiation ("slippage synthesis"), and trans
34 p IES inside the larger IES, suggesting that reiterative integration of these elements can occur.
35 ensus sequence mutation and the evidence for reiterative integration support the theory that Parameci
40 the annelid Platynereis dumerilii exhibits a reiterative, nearly universal embryonic pattern of nucle
42 ustering is induced in a highly specific and reiterative pattern, independent of receptor activation,
44 are generated by branching morphogenesis, a reiterative process of branch initiation and invasion fr
45 The airways of the lung develop through a reiterative process of branching morphogenesis that give
48 genesis appears to be a serially homologous, reiterative process, we find that there are differences
49 itecture of the pancreas is established by a reiterative program of progenitor cell expansion and mig
51 tion in conjunction with recyclable markers, Reiterative Recombination provides a highly efficient, t
52 ibe the design and construction of the first Reiterative Recombination system in Saccharomyces cerevi
57 tation genes partition the early embryo into reiterative segments along the anterior-posterior axis,
58 quent encounters with a pathogen would evoke reiterative, self-renewing, asymmetric division by memor
59 molecular organization; it is arranged as a reiterative series of arcuate territories arrayed bilate
65 eving temporal precision during formation of reiterative structures at the SAM, thus indicating an or
67 in both the initial de novo folding and the reiterative support of p56lck structure in rabbit reticu
68 ditis elegans development as a Wnt-dependent reiterative switch to generate nonequivalent sister cell
70 late at low temperatures and are amenable to reiterative synthesis strategies, as demonstrated by the
72 cordant for Crohn's disease, shared the same reiterative TCR-beta chain sequences in their CD4+ perip
73 Crohn's disease, and diverticulitis revealed reiterative TCR-beta chain sequences that were not found
74 llus subtilis The structure reveals that the reiterative transcript detours from the dedicated RNA ex
75 through a mechanism involving UTP-sensitive reiterative transcription (i.e., repetitive addition of
76 er, the resulting transcripts are subject to reiterative transcription (i.e., repetitive nucleotide a
77 er, the resulting transcripts are subject to reiterative transcription (i.e., repetitive UMP addition
79 G6- and A7-initiated transcripts that avoid reiterative transcription and are elongated normally.
80 ons in the native pyrG template that altered reiterative transcription and attenuation in vivo result
81 ults in transcripts that can, in part, avoid reiterative transcription and be elongated normally.
82 pyrG initially transcribed region abolished reiterative transcription and caused constitutive expres
85 transcripts that generally do not engage in reiterative transcription and thus can be normally elong
86 hat the incorporation of extra G residues by reiterative transcription at the wild-type promoter occu
87 AUAC tetranucleotide affected the process of reiterative transcription by analyzing the nucleotide se
88 enzyme from Thermus thermophilus, engaged in reiterative transcription during transcription initiatio
89 operons regulated (in part) by UTP-sensitive reiterative transcription in E. coli is the carAB operon
90 as well as the general use of UTP-dependent reiterative transcription in gene regulation, are discus
91 ol mechanisms, including mechanisms based on reiterative transcription in which nucleotides are repet
96 ed data consistent with a template-dependent reiterative transcription mechanism for polyadenylation.
97 NA-dependent RNA polymerase (3D(pol)) uses a reiterative transcription mechanism while replicating th
98 lso prevented the polymerase from performing reiterative transcription necessary for generation of th
100 upport a model of PV RNA replication wherein reiterative transcription of homopolymeric templates ens
103 ich high intracellular levels of UTP promote reiterative transcription that adds extra U residues to
105 thought to result from polymerase slippage (reiterative transcription) by the VSV polymerase on the
106 t determinants in establishing the extent of reiterative transcription, levels of productive transcri
107 in Bacillus subtilis involves CTP-sensitive reiterative transcription, which introduces up to 11 ext
108 ncreased intracellular levels of UTP promote reiterative transcription, which results in the synthesi
112 strong experimental support for the proposed reiterative transcription/antitermination mechanism and
113 vestigate the mechanism(s) of Dim1 function, reiterative two-hybrid screening was performed to identi
115 ng mitotic spindle positioning, as well as a reiterative use of spindle orientation in the skin to bu
117 cation of primary pigment cells requires the reiterative use of the sequential integration between th
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