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1       The most commonly used pigment was red ochre.
2 escribe construction and characterization of Ochre, a GRO that fully compresses a translational funct
3 hesives from naturally sticky substances and ochre, a technical behavior proposed to mark the advent
4 ls, a behavior known from Neanderthals, high-ochre adhesives present a real benefit, improving their
5          UV-induced reversion of the arg4-17 ochre allele in Saccharomyces cerevisiae is largely depe
6        Escherichia coli WP2 bacteria with an ochre amino acid auxotrophy show no evidence of growth d
7 ete set of orthogonal 21st synthetase-amber, ochre and opal suppressor tRNA pairs including the first
8                                       Amber, ochre and opal suppressor tRNAs with a wide range of act
9                          We show that amber, ochre and opal suppressor tRNAs, derived from Escherichi
10  and for the regulated suppression of amber, ochre and opal termination codons in mammalian cells.
11 ting up to about 100,000 y ago, the engraved ochre and ostrich eggshell fragments from the South Afri
12 in two isolated areas confirmed two types of ochre and that the dark spots are charcoal remnants.
13 the beta-gal gene as a reporter, that amber, ochre, and opal suppressors derived from the serine and
14 ere assayed for the ability to complement an ochre B mutant and defects in the morphogenetic pathway
15 Paleolithic also used glues, but evidence of ochre-based compound adhesives is unknown.
16 ng regional variations within an overarching ochre-behavioral community of practice.
17 dere finds as hematite pushes the use of red ochre by (early) Neandertals back in time significantly,
18 onstitute the earliest documented use of red ochre by Neandertals.
19  a C to T transition in exon 53, creating an ochre codon (CAA to TAA).
20 r plasmid bearing a ColE1-type origin and an ochre codon in the beta-lactamase gene.
21 re, we have employed this system using a TAA ochre codon reversion assay to examine the fidelity of t
22 e internal amber codon, but at the following ochre codon.
23  processing rabbit pelts with and without an ochre compound, digging in sediment in and outside a cav
24 ains in association with rich assemblages of ochre, fauna and stone tools dated to ~100 ka.
25                                              Ochre fully compresses degenerate stop codons into a sin
26 sing intentional human burial and the use of ochre in burial contexts.
27                                              Ochre loads were so high that they lowered the adhesive'
28 y as the oldest known evidence for intensive ochre mining worldwide (~48,000 years ago).
29  single clone that was recovered harbored an ochre mutation in the cI gene after the first 128 amino
30 ght-member tRNA-Tyr gene family suppress the ochre mutation reporter, there are considerable phenotyp
31                                          The ochre mutation reverts to sense at a low frequency while
32  sensitive fluorescent reporter gene with an ochre mutation, fluorescence-activated cell sorting of a
33 clone which lacked the DNA downstream of the ochre mutation, pTRKH2::CI-per2, confirmed the phenotype
34 aromyces cerevisiae strain involving a cox15 ochre mutation, which acts as a reporter.
35 sgenic mice carrying a reporter gene with an ochre mutation.
36 ere tested for their ability to suppress the ochre nonsense alleles ade2-1, lys4-1, and met4-1.
37 een nsP3 and nsP4 was replaced with an opal, ochre, or amber stop codon.
38 s), and the earliest intensive use of ground ochre pigments in Sahul (the Pleistocene landmass of Aus
39 ern China, which includes the earliest known ochre-processing feature in east Asia, a distinctive min
40 ompositional analyses to determine localized ochre procurement strategies and long-distance transport
41                         Deep-time records of ochre provisioning span the final Middle Stone Age and L
42 assemblage including grinding stones, ground ochres, reflective additives and ground-edge hatchet hea
43                                          The ochre-stained skeleton of the Lapedo child, a juvenile a
44 or tRNA concentration to the point where the ochre-suppressing tRNA(Ser) is in four- to fivefold exce
45                         The expression of an ochre suppressor mutant of the GluII(UUA) tRNA appears t
46 ng as colonies in 3-5 days) are slow-growing ochre suppressor mutants that probably existed in the cu
47 mature termination codon in vivo by using an ochre suppressor tRNA acting in an intact mouse.
48 luding the first report of a 21st synthetase-ochre suppressor tRNA pair.
49 cribe conditions for the import of amber and ochre suppressor tRNAs derived from Escherichia coli ini
50  further of importing a mixture of amber and ochre suppressor tRNAs for the insertion of two differen
51 s to sense at a low frequency while tRNA-Tyr ochre suppressors (SUP-o) arise at a very high frequency
52                          Glutamate-inserting ochre suppressors have been identified among late-arisin
53 allosuppressor alleles examined, an in-frame ochre (TAA) mutation was present in the SUP45 coding reg
54                                              Ochre thus utilizes UAA as the sole stop codon, with UGG
55 itumen was mixed with high loads of goethite ochre to make compound adhesives at the type-site of the
56  the specific suppression of amber (UAG) and ochre (UAA) codons, respectively.
57 ected which enhanced suppression by the weak ochre (UAA) suppressor tRNA(Ser) SUQ5.
58 a (i.e., to the same time range as the early ochre use in the African record).
59 corated with a spiral groove filled with red ochre, which closely parallels similar marks that San ma