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1 onents during starvation-induced motility in Sulfolobus acidocaldarius.
2 ave used previously to characterize Dbh from Sulfolobus acidocaldarius.
3 ated from the thermoacidophilic crenarchaeon Sulfolobus acidocaldarius.
4 and inhibitor binding to CYP119, a P450 from Sulfolobus acidocaldarius.
5 degrees C) is near the growth temperature of Sulfolobus acidocaldarius.
6 ions are met by the extreme thermoacidophile Sulfolobus acidocaldarius.
7 nd the archaeal chromatin protein Sac7d from Sulfolobus acidocaldarius.
8 in-like modification pathway in the archaeon Sulfolobus acidocaldarius.
9  of a shuttle plasmid (pJlacS) propagated in Sulfolobus acidocaldarius.
10 egrees C) and pH (2 to 4) on the motility of Sulfolobus acidocaldarius, a thermoacidophilic archaeon.
11 onucleotide-mediated transformation (OMT) in Sulfolobus acidocaldarius and Escherichia coli as a func
12 al structures of the XPD catalytic core from Sulfolobus acidocaldarius and measured mutant enzyme act
13 l context, we used ECT to image the archaeon Sulfolobus acidocaldarius and observed a distinct protei
14 NA polymerases from the extreme thermophiles Sulfolobus acidocaldarius and Pyrodictium occultum (54%
15 proteins from the hyperthermophilic archaeon Sulfolobus acidocaldarius and S. solfactaricus, respecti
16 milar to the 7-kDa DNA binding proteins from Sulfolobus acidocaldarius and Sulfolobus solfataricus in
17     When cells of two auxotrophic mutants of Sulfolobus acidocaldarius are mixed and incubated on sol
18 extremely high temperature was developed for Sulfolobus acidocaldarius, based on the selection of pyr
19 kably, the ortholog of L30 from the archaeon Sulfolobus acidocaldarius binds specifically to the same
20                         In the crenearchaeon Sulfolobus acidocaldarius, biosynthesis of the archaellu
21                    Genetic transformation of Sulfolobus acidocaldarius by a multiply marked pyrE gene
22                                           In Sulfolobus acidocaldarius conjugation assays, recombinan
23 bled those of the thermoacidophilic archaeon Sulfolobus acidocaldarius, despite important molecular d
24               The hyperthermophilic archaeon Sulfolobus acidocaldarius exchanges and recombines chrom
25 mber of independent pyrimidine auxotrophs of Sulfolobus acidocaldarius for deletions and sequenced th
26 isolated from the thermoacidophilic archaeon Sulfolobus acidocaldarius grown at different temperature
27 hese and previously available sequences from Sulfolobus acidocaldarius, Haloferax volcanii and Methan
28 ) from the thermoacidophilic archaebacterium Sulfolobus acidocaldarius has been investigated.
29 ) from the thermoacidophilic archaebacterium Sulfolobus acidocaldarius have been studied by perylene
30 E) from the thermoacidophilic archaebacteria Sulfolobus acidocaldarius have been studied using two-ph
31 hnique to show that both S. solfataricus and Sulfolobus acidocaldarius have three functional origins.
32 o that of the adenylate kinase from archaeal Sulfolobus acidocaldarius in many respects such as the e
33  recombinant Sac7d from the hyperthermophile Sulfolobus acidocaldarius is mapped using multi-dimensio
34 nant Sac7d protein from the thermoacidophile Sulfolobus acidocaldarius is shown to be stable towards
35                                              Sulfolobus acidocaldarius is so far the only hyperthermo
36  shibatae, while no homologs were evident in Sulfolobus acidocaldarius, lending further support to th
37 317H variant of the thermostable CYP119 from Sulfolobus acidocaldarius maintains heme iron coordinati
38 archaeabacterium Sulfolobus solfataricus and Sulfolobus acidocaldarius, respectively.
39 i reverse gyrase (48% overall identity), the Sulfolobus acidocaldarius reverse gyrase (41% identity),
40 rize prototypical superfamily ATPase FlaI in Sulfolobus acidocaldarius, showing FlaI activities in ar
41 y dynamic and TBP from the archaeal organism Sulfolobus acidocaldarius strictly requires TFB for DNA
42 ochondrial aa3-type proton pump functions in Sulfolobus acidocaldarius terminal oxidase complexes.
43                       In S. solfataricus and Sulfolobus acidocaldarius, tfb3 is one of the most highl
44 on of strains of Sulfolobus solfataricus and Sulfolobus acidocaldarius that allow the incorporation o
45 tify saci_0568 and saci_0748, two genes from Sulfolobus acidocaldarius that are highly induced upon U
46  chromatin protein from the hyperthermophile Sulfolobus acidocaldarius that severely kinks duplex DNA
47 he relevance of this threat for the archaeon Sulfolobus acidocaldarius, the mode of GGCC methylation
48  of the extremely thermoacidophilic archaeon Sulfolobus acidocaldarius to assess genetic and physiolo
49 amics of the binding of the Sac7d protein of Sulfolobus acidocaldarius to double-stranded DNA has bee
50                                              Sulfolobus acidocaldarius utilizes glucose and xylose as
51             The 3 DNA replication origins of Sulfolobus acidocaldarius were mapped by 2D gel analysis
52     Sac7d is a small, chromatin protein from Sulfolobus acidocaldarius which induces a sharp kink in
53  chromatin protein from the hyperthermophile Sulfolobus acidocaldarius which kinks duplex DNA by appr
54    The genomic mutation rate of the archaeon Sulfolobus acidocaldarius, which inhabits a harsh and po

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