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1          UV-induced reversion of the arg4-17 ochre allele in Saccharomyces cerevisiae is largely depe
2        Escherichia coli WP2 bacteria with an ochre amino acid auxotrophy show no evidence of growth d
3 ete set of orthogonal 21st synthetase-amber, ochre and opal suppressor tRNA pairs including the first
4                                       Amber, ochre and opal suppressor tRNAs with a wide range of act
5                          We show that amber, ochre and opal suppressor tRNAs, derived from Escherichi
6  and for the regulated suppression of amber, ochre and opal termination codons in mammalian cells.
7 the beta-gal gene as a reporter, that amber, ochre, and opal suppressors derived from the serine and
8 ere assayed for the ability to complement an ochre B mutant and defects in the morphogenetic pathway
9 dere finds as hematite pushes the use of red ochre by (early) Neandertals back in time significantly,
10 onstitute the earliest documented use of red ochre by Neandertals.
11  a C to T transition in exon 53, creating an ochre codon (CAA to TAA).
12 r plasmid bearing a ColE1-type origin and an ochre codon in the beta-lactamase gene.
13 re, we have employed this system using a TAA ochre codon reversion assay to examine the fidelity of t
14 e internal amber codon, but at the following ochre codon.
15  single clone that was recovered harbored an ochre mutation in the cI gene after the first 128 amino
16 ght-member tRNA-Tyr gene family suppress the ochre mutation reporter, there are considerable phenotyp
17                                          The ochre mutation reverts to sense at a low frequency while
18  sensitive fluorescent reporter gene with an ochre mutation, fluorescence-activated cell sorting of a
19 clone which lacked the DNA downstream of the ochre mutation, pTRKH2::CI-per2, confirmed the phenotype
20 aromyces cerevisiae strain involving a cox15 ochre mutation, which acts as a reporter.
21 sgenic mice carrying a reporter gene with an ochre mutation.
22 ere tested for their ability to suppress the ochre nonsense alleles ade2-1, lys4-1, and met4-1.
23 een nsP3 and nsP4 was replaced with an opal, ochre, or amber stop codon.
24 assemblage including grinding stones, ground ochres, reflective additives and ground-edge hatchet hea
25 or tRNA concentration to the point where the ochre-suppressing tRNA(Ser) is in four- to fivefold exce
26                         The expression of an ochre suppressor mutant of the GluII(UUA) tRNA appears t
27 ng as colonies in 3-5 days) are slow-growing ochre suppressor mutants that probably existed in the cu
28 mature termination codon in vivo by using an ochre suppressor tRNA acting in an intact mouse.
29 luding the first report of a 21st synthetase-ochre suppressor tRNA pair.
30 cribe conditions for the import of amber and ochre suppressor tRNAs derived from Escherichia coli ini
31  further of importing a mixture of amber and ochre suppressor tRNAs for the insertion of two differen
32 s to sense at a low frequency while tRNA-Tyr ochre suppressors (SUP-o) arise at a very high frequency
33                          Glutamate-inserting ochre suppressors have been identified among late-arisin
34 allosuppressor alleles examined, an in-frame ochre (TAA) mutation was present in the SUP45 coding reg
35  the specific suppression of amber (UAG) and ochre (UAA) codons, respectively.
36 ected which enhanced suppression by the weak ochre (UAA) suppressor tRNA(Ser) SUQ5.
37 a (i.e., to the same time range as the early ochre use in the African record).
38 corated with a spiral groove filled with red ochre, which closely parallels similar marks that San ma

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