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1 T. thermophila has at least three other piggyBac-derived
2 T. thermophila Poc1 exhibits a protein incorporation pro
3 containing L. pneumophila cells, expelled by T. thermophila, and to characterize them on the basis of
5 with different coat defects to predation by T. thermophila paralleled the spores' sensitivities to l
8 kyl-dihydroxyacetone phosphate synthase from T. thermophila resulted the detection of various glycero
11 ese results we conclude that TGP2 is DLDH in T. thermophila and suggest that the G4-DNA binding capab
15 n in and around a predicted "fusion loop" in T. thermophila HAP2 were found to abrogate membrane pore
16 This finding of telomeric nucleosomes in T. thermophila suggests that the difference between vert
17 apparent modified Sox pathway we observed in T. thermophila is present in marine Thiobacillus and Thi
18 ports the hypothesis that the hv1 protein in T. thermophila and hv1-like proteins in other eukaryotes
20 At the administered MWCNT dose of 0.3 mg/L, T. thermophila accumulated up to (0.86 +/- 0.3) mug/mg a
22 ical mapping to aid the complete assembly of T. thermophila macronuclear chromosomes from shotgun seq
23 ically and physically mapping the genomes of T. thermophila: the micronuclear (germ-line) genome, whi
27 P2 is expressed in all seven mating types of T. thermophila and that fertility is only blocked when t
29 wild-type HTA3 gene was introduced into the T. thermophila cells, the endogenous chromosomal HTA3 co
31 of vertebrate telomeric mononucleosomes, the T. thermophila mononucleosomes were stable to micrococca
36 quences identical or nearly identical to the T. thermophila Cbs at sites of breakage flanking the ger
38 e localization of the novel protein DisAp to T. thermophila striated fibers (kinetodesmal fibers; KFs
39 tically reduced or eliminated in transformed T. thermophila lines containing these altered rRNAs.
40 endogenous RNAi pathways in the unicellular T. thermophila, a complexity previously demonstrated onl
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