ライフサイエンスコーパス: rich media

1 d receptors, even in the presence of protein-rich media.

2 are also apparent when cystine is used or in rich media.

3 no acids at diverse sense codons in cells in rich media.

4 cytokines, even when stimulated in nutrient-rich media.

5 , although they prefer glucose when grown in rich media.

6 tions, Shewanella oneidensis, in minimal and rich media.

7 ression at levels similar to those seen with rich media.

8 ffect on growth of the bacterium in nutrient-rich media.

9 s, but had no detectable effect on growth in rich media.

10 -independent (HI) cells, cultured on peptone-rich media.

11 ent to disrupt spore germination in nutrient-rich media.

12 m 50 mL of Escherichia coli culture grown in rich media.

13 ir growth was significantly reduced in lipid-rich media.

14 ing growth in glucose-containing or nutrient-rich media.

15 Salmonella grown in the presence of salt in rich media.

16 A total of 85% of the genome is expressed in rich media.

17 that of the wild-type strain WU2 in vitro in rich media.

18 d of 99% in predicting nonessential genes in rich media.

19 genes that regulate gab operon expression in rich media.

20 nes are likely to be essential for growth on rich media.

21 robust aerobic growth of Escherichia coli in rich media.

22 urvival after treatment with alpha-factor in rich media.

23 d to prevent the accumulation of pyruvate in rich media.

24 rains displayed wild-type growth kinetics in rich media.

25 pendence on sigma(S) when cells are grown in rich media.

26 ces associated with culturing in minimal and rich media.

27 pores germinated very poorly in a variety of rich media.

28 ll mutants have no apparent growth defect on rich media.

29 f CFU was measured by plate count methods on rich media.

30 ressed at detectable levels during growth in rich media.

31 er stationary-phase cultures after growth in rich media.

32 ive to UV irradiation (UVS) and sensitive to rich media.

33 2 stimulates filamentation, even on nitrogen-rich media.

34 oxidized state in wild-type strains grown in rich media.

35 mutant shows a 40% decreased growth rate in rich media, a drastic reduction in loosely coupled ribos

36 expressed when cells are growing in nutrient-rich media, although different gene groups are affected

37 ty to growth inhibition by some component of rich media and by oxidized thiol compounds.

38 ly, mRNA half-lives were similar in nutrient-rich media and defined media in which the generation tim

39 es the Frz system for vegetative swarming on rich media and for cellular aggregation during fruiting

40 Fungal growth in rich media and minimal media containing select amino aci

41 l growth on nonfermentable carbon sources in rich media and normal frequencies of generation of petit

42 s autophagy in mammalian cells maintained in rich media and nutrient permease downregulation in yeast

43 e onset of nutrient limitation in amino acid rich media and responds to extracellular pyruvate.

44 Cells are large in rich media and small in poor media.

45 ol promoted the growth of the ccmG mutant on rich media and substantially restored spectroscopically

46 e transcriptional response of yeast grown in rich media and treated with rapamycin to investigate the

47 s growth defect at different temperatures in rich media, and analysis of yeast extracts suggests that

48 or normal growth on a variety of minimal and rich media, and any of the proteins is sufficient for no

49 ng is known to generate hydrogen peroxide in rich media, and because catalase and sodium pyruvate are

50 es spores only after prolonged incubation on rich media, and identifies a gene whose predicted protei

51 he wild type and overproduces antibiotics on rich media, and it identifies a gene whose predicted pro

52 (2) per cell than exponential-phase cells in rich media, and such excessive O(2) consumption causes r

53 bility to progress in development in glucose-rich media are manifestations of phenomena that occur in

54 t of these "dark oxygenations" require water-rich media associated with short (1)O(2) lifetimes, and

55 gene requirements for competitive growth in rich media between these two closely related serovars.

56 The two mutants grow normally in rich media but do not grow in defined media lacking arom

57 ants grow well and are slightly elongated in rich media but grow less well than wild-type cells in mi

58 echanism of catabolite repression control in rich media by Crc involves posttranscriptional regulatio

59 LAC include working equally well in nutrient-rich media, conceivably expanding applicability to any o

60 rently simple auxotroph did not grow well in rich media containing excess methionine, forming small c

61 to validate gene essentiality predictions in rich media, contextualize intra-screen discrepancies and

62 the addition of modest amounts of acetate to rich media (e.g., tryptone broth).

63 the nrf promoter is known to be repressed in rich media, especially in the presence of glucose, but t

64 ch, although capable of growing well in iron-rich media, failed to prosper under iron chelation.

65 n morphogenesis, overproduces antibiotics on rich media, fails to grow on minimal media, and identifi

66 he transcription factor Pho4, slow growth on rich media, failure to grow using galactose, lactate or

67 In rich media, FLO11 is regulated by mating type; it is exp

68 When cultured in rich media in shake flasks, pEVOL was capable of produci

69 n secreted by this strain of B. anthracis in rich media in vitro.

70 s undetectable during growth in a variety of rich media, including Luria-Bertani (LB) medium, or in m

71 in blood (output pool) compared to growth in rich media (input pool) were identified using DNA microa

72 yces cerevisiae cells transferred from spent rich media into water live for weeks, whereas the same c

73 from Bacillus thuringiensis spores grown in rich media is [N(1)C(4)H(12)](+).

74 st, Thr4, although dispensable for growth in rich media, is essential in phosphate-depleted or galact

75 In rich media, loss of PBPs 2c and 4 resulted in no obvious

76 n exponentially growing cultures in nutrient-rich media, meaning knowledge of such interactions under

77 Despite an impaired fitness in rich media, melanogenic mutants can inhibit their wild-t

78 Stress in nutrient-rich media necessitated SgrS regulation of only sugar tr

79 nal molecule luteolin in defined minimal and rich media or of strains altered in the expression of ke

80 Furthermore, when grown in rich media (repressing conditions), wild-type cells yiel

81 dium from stationary-phase cultures grown in rich media resulted in the premature activation of each

82 inization, and ammonia release on amino acid-rich media, similar to stp2Delta and ahr1Delta stp2Delta

83 When grown in rich media, single-celled organisms such as yeast and ba

84 ugh unable to germinate in standard nutrient-rich media, spores lacking SleB, CwlJ1, and CwlJ2 are ab

85 ype repression of FLO11 in diploids grown in rich media suffices to explain the inability of these ce

86 rain is able to form fruiting bodies on semi-rich media, suggest that Pkn5 and Pkn6 have reciprocal r

87 ompU2 displayed wild-type growth kinetics in rich media, suggesting that this is the true phenotype o

88 nder anaerobic conditions, cultures grown on rich media supplemented with d-glucose or glycerol produ

89 that it grows larger and faster in nutrient-rich media than in nutrient-poor media.

90 toylation as cells transition from growth in rich media to a growth-arrested state during nutrient de

91 nd expression data from yeast cells grown in rich media to learn the transcriptional network specific

92 h efficiency, low background and facility in rich media, tolC selection is a broadly applicable metho

93 Comparisons made between rich media under aerobic conditions vs low-oxygen condit

94 Repression of srrAB in rich media under aerobic growth conditions shows that Sr

95 y, even against bacteria growing in nutrient-rich media under favorable conditions.

96 In cells growing rapidly in nutrient-rich media, we find that RNAP is organized in 2-8 bands.

97 utants that can sustain hyphal elongation in rich media, we found hog1, ssk2, and pbs2 mutants of the

98 under multiple time-points during growth in rich media, we show that the binding regions of the two

99 for the Fis-deficiency, but during growth in rich media when the demand for ribosomes is high, this c

100 iratory mucosa and can be cultivated only on rich media, whereas E. coli is a saprophyte that can gro

101 , single cells (blastospores) predominate in rich media, whereas filaments composed of elongated cell

102 significant bacterial reduction in nutrient rich media, wherein experimental conditions more closely

103 e 13 ACPPs exert antimicrobial activities in rich media with broad spectrum of antibacterial activiti

104 t wild-type strain when cultured in nutrient-rich media with or without CO(2) in the atmosphere, alth

105 Gal- YAH1 cells were grown in standard rich media (YPD and YPGal) under O 2 or argon atmosphere