ライフサイエンスコーパス: thermotolerant

1 than C. difficile 630 Deltaerm and was less thermotolerant.

2 d-type HSF, and they are also constitutively thermotolerant.

3 ignificantly accelerated in cells first made thermotolerant.

4 Production of a protein-engineered thermotolerant (1, 3-1, 4)-beta-glucanase with the D hor

5 barley of 6.2% transgenic malt containing a thermotolerant (1,3-1,4)-beta-glucanase (4.28 microg.g(-

6 ora "type 1") increased its association with thermotolerant algal symbionts (Durusdinium glynnii) dur

7 ed to the reproductive adult, 63 retested as thermotolerant and 49 (80%) exhibited a >15% increase in

8 delay of complex formation was attenuated in thermotolerant and heat radiosensitization-resistant cel

9 neous interfacial method to develop superior thermotolerant and highly emissive solid-state metal hal

10 Instead, animals exposed to H(2)S are thermotolerant and long-lived.

11 Hsp70 transcription was similar between thermotolerant and naive cells during heat shock.

12 Hsp70 mRNA translation were similar between thermotolerant and naive cells during the post-stress pe

13 ing pollen tube growth by comparing a set of thermotolerant and thermosensitive tomato cultivars.

14 f invasive pulmonary infection caused by the thermotolerant ascomycetous fungus Gymnascella hyalinosp

15 characterization of the EctA enzyme from the thermotolerant bacterium Paenibacillus lautus (Pl).

16 on of the Rif1 homologue from methylotrophic thermotolerant budding yeast Hansenula polymorpha DL-1.

17 ults of E. coli, intestinal enterococci, and thermotolerant Campylobacter spp. in surface waters than

18 , or tumor necrosis factor was suppressed in thermotolerant cells and that Hsp72 accumulation was res

19 ddition, Hsp70 mRNA stability was reduced in thermotolerant cells as compared with naive cells follow

20 A number of polypeptides unique to thermotolerant cells have been uncovered by Boolean anal

21 These results suggest that thermotolerant cells limit Hsp70 expression by transcrip

22 sed by Western blotting, was negligible when thermotolerant cells were heat-shocked a second time.

23 Hsp70 after heat shock was compared between thermotolerant cells, which contain a large concentratio

24 the organelle, similar to that observed for thermotolerant cells.

25 spectrometry (MSP-MS) to globupain, a marine thermotolerant clostripain-like protease and show that i

26 taminated water, particularly as measured by thermotolerant coliform (TTC) bacteria, a WHO-approved i

27 9; p = 0.001) and 0.38 mean log(10)MPN fewer thermotolerant coliforms (95% CI: 0.14, 0.62; p = 0.002)

28 ater for the presence of Escherichia coli or thermotolerant coliforms (TTC) were included provided th

29 s, children's drinking water was assayed for thermotolerant coliforms (TTC), an indicator of faecal c

30 associated with the largest log reduction in thermotolerant coliforms (TTCs) ( - 0.66 log10 TTC most

31 Assessing the association between thermotolerant coliforms in drinking water and diarrhea:

32 barriers, a reduction of 27% E. coli and 24% thermotolerant coliforms mean counts.

33 EXX Colilert method to enumerate E. coli and thermotolerant coliforms most probable number (MPN).

34 icantly in thermosensitive cultivars than in thermotolerant cultivars.

35 We report the design of a thermotolerant, disulfide-free, and trimeric HA stem-fra

36 growing number of AGO pathways required for thermotolerant fertility in C. elegans and support a mod

37 IgE sensitisation to thermotolerant filamentous fungi, in particular A. fumig

38 thermosensitive bacterial species with more thermotolerant forms.

39 and such modulation was able to distinguish thermotolerant from thermosensitive Cladocopium goreaui

40 ldren with chronic asthma were sensitized to thermotolerant fungi compared with no children without a

41 Children sensitized to thermotolerant fungi have worse lung function, require m

42 Numerous thermotolerant fungi other than A. fumigatus can be cult

43 Sensitization to thermotolerant fungi, including filamentous fungi and Ca

44 acid and 6-benzylaminopurine to survive, but thermotolerant GCPs cultured at 38 degrees C +/- ABA do

45 us) extracellular signal-regulated kinase 1; thermotolerant GCPs retain this polypeptide.

46 potential as a genetic resource for breeding thermotolerant grapevine varieties.

47 ng of endothelial cells transfected with the thermotolerant green fluorescent protein-caveolin-1 cons

48 us and demonstrate that cgrA is required for thermotolerant growth and wild-type virulence of the org

49 is study, we elucidate a new EPS produced by thermotolerant (growth from 34-44 degrees C) strain Pseu

50 We reveal that thermotolerant kiwifruit species have increased expressi

51 olerance and set the foundation for breeding thermotolerant kiwifruits cultivars.

52 eloped from a lettuce cultivar (Salinas) and thermotolerant Lactuca serriola accession UC96US23 (UC),

53 Two independent thermotolerant lettuce seed mutant lines, TG01 and TG10,

54 (T22B3.2) and alg-4 (ZK757.3), in promoting thermotolerant male fertility.

55 cultative symbiosis in Oculina patagonica, a thermotolerant Mediterranean coral(5,6).

56 It is believed that such highly thermotolerant metal halide perovskites will unleash the

57 A newly isolated thermotolerant microalga produces reddish pigments under

58 ch mutant, bulked DNA samples of segregating thermotolerant (mutant) seeds were sequenced and analyze

59 The thermotolerant mutants of GFP greatly improve the sensit

60 in the dominance of Microcoleus vaginatus by thermotolerant, novel phylotypes of bundle-forming cyano

61 fer high temperatures and are among the most thermotolerant of marine organisms.

62 Despite observations that some of the most thermotolerant organisms grow under conditions of high p

63 ics and machine learning to mine 74 putative thermotolerant PET hydrolases.

64 pendent gene expression and acquisition of a thermotolerant phenotype.

65 s need, a fast and effect way of quantifying thermotolerant phenotypes is required.

66 to that contention, with psychrotolerant vs thermotolerant physiology being strain dependent, and co

67 ling in heat-stressed cells and seedlings of thermotolerant plants and suggest that even plants that

68 nitude of these calcium peaks was greater in thermotolerant plants, implying that these calcium signa

69 exposure of the mechanisms underpinning the thermotolerant properties of some alternative pathways;

70 sion, only minor alterations can transform a thermotolerant regulator into a thermosensor that allows

71 By isolating spontaneous thermotolerant revertants of the mdbA mutant at 37 degre

72 d form spores is temperature sensitive, with thermotolerant S. cerevisiae having a higher temperature

73 yces with different temperature preferences: thermotolerant Saccharomyces cerevisiae and cold-toleran

74 is study expands the number and diversity of thermotolerant scaffolds for enzymatic PET deconstructio

75 particularly during heat stress, to provide thermotolerant sperm-based fertility.

76 Here, we present a system which uses thermotolerant T4 DNA ligase and no UV.

77 rtantly, we found that pollen tubes from the thermotolerant Tamaulipas cultivar have enhanced growth

78 transcription was attenuated more rapidly in thermotolerant than naive cells immediately upon return

79 ginatus) being more psychrotolerant and less thermotolerant than the other (M. steenstrupii).

80 stress, its photosynthesis activity is more thermotolerant than the wild type.

81 der these conditions, is about 100-fold less thermotolerant than the wild type.

82 he Earth's temperature and are becoming more thermotolerant, which is enhancing fungal fitness and vi

83 By contrast, TaRca1-beta was more thermotolerant, with a thermal midpoint of 42 degrees C,