ライフサイエンスコーパス: T. thermophila

1 T. thermophila has at least three other piggyBac-derived

2 T. thermophila Poc1 exhibits a protein incorporation pro

3 nd mu(S) and mu(G) to covary linearly across T. thermophila and 6 mammals, despite the independent or

4 containing L. pneumophila cells, expelled by T. thermophila, and to characterize them on the basis of

5 Spore killing by T. thermophila was by means of lytic enzymes within the

6 with different coat defects to predation by T. thermophila paralleled the spores' sensitivities to l

7 Genomic DNA from T. thermophila strain EPR85 contains genes homologous to

8 he expression of the standard eEF2 gene from T. thermophila.

9 chitecture adopted by telomeric repeats from T. thermophila and GQs in general.

10 kyl-dihydroxyacetone phosphate synthase from T. thermophila resulted the detection of various glycero

11 With the inclusion of these two genes, T. thermophila is the first organism whose entire comple

12 In T. thermophila, simple mass transformation and gene repl

13 ese results we conclude that TGP2 is DLDH in T. thermophila and suggest that the G4-DNA binding capab

14 Thus, an essential gene in T. thermophila can be defined by the fact that it can be

15 first demonstration of an essential gene in T. thermophila using these methods.

16 The youngest 90-bp exon LRR genes in T. thermophila are concentrated in pericentromeric and s

17 d for delivery of a key protease involved in T. thermophila mucocyst maturation.

18 n in and around a predicted "fusion loop" in T. thermophila HAP2 were found to abrogate membrane pore

19 The overall pattern of somatic mutations in T. thermophila also resembles that in mammals.

20 This finding of telomeric nucleosomes in T. thermophila suggests that the difference between vert

21 apparent modified Sox pathway we observed in T. thermophila is present in marine Thiobacillus and Thi

22 , the higher-order chromatin organization in T. thermophila is still largely unknown.

23 ports the hypothesis that the hv1 protein in T. thermophila and hv1-like proteins in other eukaryotes

24 These studies argue that, in T. thermophila, the histone ubiquitylation mechanism is

25 At the administered MWCNT dose of 0.3 mg/L, T. thermophila accumulated up to (0.86 +/- 0.3) mug/mg a

26 24 novel T. thermophila basal body proteins were identified, 19 o

27 ical mapping to aid the complete assembly of T. thermophila macronuclear chromosomes from shotgun seq

28 ically and physically mapping the genomes of T. thermophila: the micronuclear (germ-line) genome, whi

29 at the macronuclear btu1-1 (K350M) locus of T. thermophila strain CU522.

30 n organization in the two distinct nuclei of T. thermophila using the Hi-C and HiChIP methods.

31 Using a mutant strain of T. thermophila carrying a negatively selectable allele o

32 In addition, we reveal the structure of T. thermophila PARG in a complex with a novel rhodanine-

33 P2 is expressed in all seven mating types of T. thermophila and that fertility is only blocked when t

34 fe as well as the suitability for the use of T. thermophila as a valuable model to investigate the ev

35 ontrast to what we observe in human cells or T. thermophila, an organism with similar AT-content.

36 additional GRL-like genes were found in the T. thermophila genome.

37 wild-type HTA3 gene was introduced into the T. thermophila cells, the endogenous chromosomal HTA3 co

38 lication and rDNA gene amplification, is the T. thermophila origin recognition complex (TtORC).

39 of vertebrate telomeric mononucleosomes, the T. thermophila mononucleosomes were stable to micrococca

40 omatin organization in the two nuclei of the T. thermophila and suggest that the higher-order chromat

41 Phylogenetic analysis of the T. thermophila cathepsins, combined with prior work on t

42 The Km of the T. thermophila enzyme for pre-tRNAGln is 1.6 x 10(-7)M,

43 At one end of the T. thermophila micronuclear rDNA locus, a pair of short

44 Our structural and functional study of the T. thermophila respiratory chain reveals divergence in k

45 During the natural lengthening of the T. thermophila telomeric DNA tracts that occurs in veget

46 quences identical or nearly identical to the T. thermophila Cbs at sites of breakage flanking the ger

47 In contrast with the T. thermophila HHO and HTA3 genes, no introns were ident

48 e localization of the novel protein DisAp to T. thermophila striated fibers (kinetodesmal fibers; KFs

49 tically reduced or eliminated in transformed T. thermophila lines containing these altered rRNAs.

50 endogenous RNAi pathways in the unicellular T. thermophila, a complexity previously demonstrated onl

51 The unique T. thermophila gene, called PGM1, encodes a protein that