ライフサイエンスコーパス: baker's yeast

1 typically studying Saccharomyces cerevisiae (baker's yeast).

2 heres derived from Saccharomyces cerevisiae (Baker's yeast).

3 nd functional gating of the P2X2 receptor in baker's yeast.

4 extended to other species, such as humans or baker's yeast.

5 ther characterized mitochondrial proteins of baker's yeast.

6 ted in the commercial samples of vinegar and baker's yeast.

7 cation balance is achieved and modulated in baker's yeast.

8 teins in the nuclear pore complex (NPC) from baker's yeast.

9 h-containing breads from those leavened with baker's yeast.

10 grees C compared to 11.8 % for the reference baker's yeast.

11 Using baker's yeast, 125 genes were identified in a genetic sc

12 dition, we illustrate on the PPI networks of baker's yeast and human the ability of L-GRAAL to predic

13 s of nucleotides, enabling organisms such as baker's yeast and pathogenic fungi to survive in the pre

14 ra crassa, but is absent from the genomes of baker's yeast and plants.

15 ree model genomes (Homo sapiens, E. coli and baker's yeast), and the project will extend to other gen

16 organisms, including human fungal pathogens, baker's yeast, and common coliform bacteria, and uncover

17 The BIM motif is unique to the baker's yeast, and we show both BRD and BIM contribute t

18 Using baker's yeast as a convenient metabolic factory, we demo

19 Linkage of baker's-yeast beta-glucan to the glucan-deficient yeast

20 modifying the leavening agent (fresh or dry baker's yeast, biga, type II and type III sourdoughs), t

21 ssion of mouse Ctr1 functionally complements baker's yeast cells defective in high affinity Cu transp

22 interaction of horse ferricytochrome c with baker's yeast cytochrome c peroxidase and with six cytoc

23 ve largely been developed for and applied in baker's yeast, even as experimental systems have begun t

24 ell wall of living Saccharomyces cerevisiae (baker's yeast) exhibits local temperature-dependent nano

25 We sought to improve the performance of baker's yeast for beta-keto ester reductions by using re

26 develop strains of Saccharomyces cerevisiae (baker's yeast) for high-yielding biological production o

27 on heritable traits in a very large pool of baker's yeast from a multiparent 12th generation intercr

28 he proteins in the Saccharomyces cerevisiae (baker's yeast) genome.

29 Baker's yeast has equivalent proteins, branchpoint bindi

30 tail by in vitro and in vivo assays: the two baker's yeast helicases, ScPif1p and Rrm3p, the fission

31 ly, it reveals that 77.7% of proteins in the baker's yeast high-confidence PPI network participate in

32 ial application of alternative proteins from baker's yeast in food emulsions, examining how oil conte

33 technoeconomic analysis for integrated wine/baker's yeast industrial production, showed that the inv

34 Translation in baker's yeast involves the coordinated interaction of 20

35 ile the autoregulation of iron metabolism in Baker's yeast is well-understood, little is known about

36 We analysed 28 alleles of baker's yeast MLH1 that correspond to non-truncating hum

37 vage site into the Mlh1 linker arm domain of baker's yeast Mlh1-Pms1.

38 We have used baker's yeast open reading frames to study these questio

39 hate to glucose-6-phosphate (F6P --> G6P) by baker's yeast phosphoglucose isomerase (PGI) with regard

40 Genetic studies have established that the baker's yeast Pif1p DNA helicase is a negative regulator

41 Baker's yeast Pif1p is involved in the maintenance of mi

42 flow) using these different matrices on the Baker's yeast PPI network in cross-validation.

43 rge dataset of over 700 structural models of baker's yeast PPIs.

44 th free and immobilized yeast) combined with baker's yeast production (with minor nutrient supplement

45 C18 resin-binding fractions of Brewer's and Baker's yeast products and Epicor dose-dependently lower

46 imilar according to our measure in different baker's yeast protein interaction networks, outperformin

47 me sequences of over seventy isolates of the baker's yeast S. cerevisiae and its closest relative, Sa

48 is of two MIAs, serpentine and alstonine, in baker's yeast Saccharomyces cerevisiae and deploy it to

49 way of budding yeasts, including that of the baker's yeast Saccharomyces cerevisiae and the opportuni

50 y related yet contrasting yeast species, the baker's yeast Saccharomyces cerevisiae and the wild yeas

51 Here we engineer baker's yeast Saccharomyces cerevisiae as a chassis for

52 Diploid strains of baker's yeast Saccharomyces cerevisiae can grow in a cel

53 Remarkably, we show that the baker's yeast Saccharomyces cerevisiae does not reject m

54 The baker's yeast Saccharomyces cerevisiae encodes a single

55 The baker's yeast Saccharomyces cerevisiae expresses three h

56 eproducing experimental growth curves of the baker's yeast Saccharomyces cerevisiae growing in the pr

57 Baker's yeast Saccharomyces cerevisiae has gained import

58 ades the pheromone-induced mating pathway in baker's yeast Saccharomyces cerevisiae has served as a m

59 The baker's yeast Saccharomyces cerevisiae possesses a singl

60 The baker's yeast Saccharomyces cerevisiae possesses a singl

61 Here we engineer the baker's yeast Saccharomyces cerevisiae to produce and se

62 -cell high-throughput assay system using the baker's yeast Saccharomyces cerevisiae to screen for che

63 resistance to a toxic amino acid analogue in baker's yeast Saccharomyces cerevisiae with a mutation r

64 ion of previously inaccessible proteins from baker's yeast Saccharomyces cerevisiae, as well as two c

65 In the baker's yeast Saccharomyces cerevisiae, extracellular Cu

66 In baker's yeast Saccharomyces cerevisiae, the cellular pro

67 Using the well-characterized baker's yeast Saccharomyces cerevisiae, we employed a si

68 urbation using deletion mutant data from the baker's yeast Saccharomyces cerevisiae, which were obtai

69 the cell wall of yeasts, especially that of baker's yeast Saccharomyces cerevisiae.

70 es but are missing or highly diverged in the baker's yeast Saccharomyces cerevisiae.

71 fer functions in a eukaryote chassis, namely baker's yeast Saccharomyces cerevisiae.

72 virus (CaMV) genome for promoter activity in baker's yeast (Saccharomyces cerevisiae) and have identi

73 We apply RPL in both baker's yeast (Saccharomyces cerevisiae) and human cells

74 While whole cells of baker's yeast (Saccharomyces cerevisiae) are a convenien

75 Eighteen key reductases from baker's yeast (Saccharomyces cerevisiae) have been overp

76 Studies in baker's yeast (Saccharomyces cerevisiae) have shown that

77 tions remain the most popular application of baker's yeast (Saccharomyces cerevisiae) in organic synt

78 Features that distinguish C. albicans from baker's yeast (Saccharomyces cerevisiae) include the str

79 a substantially greater penetration into the baker's yeast (Saccharomyces cerevisiae) proteome compar

80 o its ability to complement the defects of a Baker's yeast (Saccharomyces cerevisiae) strain lacking

81 We engineered unicellular baker's yeast (Saccharomyces cerevisiae) to develop eith

82 In this study, baker's yeast (Saccharomyces cerevisiae) was considered

83 Eighteen known and putative reductases from baker's yeast (Saccharomyces cerevisiae) were tested for

84 protein of the large ribosomal subunit from baker's yeast (Saccharomyces cerevisiae), is stoichiomet

85 amydomonas reinhardtii, Escherichia coli and baker's yeast (Saccharomyces cerevisiae).

86 the whole-genome duplication (WGD) event in baker's yeast (Saccharomyces cerevisiae).

87 ses in mammals but are generally harmless to Baker's yeast (Saccharomyces cerevisiae).

88 i pisi cutinase (FsC) on the cell surface of Baker's yeast Sacchromycese cerevisiae and demonstrated

89 Baker's yeast strains bearing these constructs were grow

90 Here, we provide genetic evidence in baker's yeast that Exo1 promotes meiotic crossing over b

91 lular extract from Saccharomyces cerevisiae (Baker's yeast), the median inter-run relative standard d

92 o domestication events leading to the extant baker's yeasts, the population structure of S. cerevisia

93 tL homolog) proteins (primarily Mlh1-Pms1 in baker's yeast) then survey the genome for lesion-bound M

94 interference-responsive crossover pathway in baker's yeast, these breaks are resected to form 3' sing

95 Here we engineered baker's yeast to produce the medicinal alkaloids hyoscya

96 machinery for regulating lipid saturation in baker's yeast to study its molecular mechanism.

97 the model organism Saccharomyces cerevisiae (baker's yeast) to identify and characterize an iron home

98 y using a more tractable platform-the common baker's yeast-to create plant-like hyperaccumulators.

99 The oven rise obtained with standard baker's yeast was compared to 15 Saccharomyces cerevisia

100 his investigation, Saccharomyces cerevisiae (baker's yeast) was engineered to produce short hairpin R

101 y labeled 13C, 15N-labeled NAD prepared from baker's yeast) was measured.

102 In the interaction network of baker's yeast, we find that statistically proteins that

103 ities of products prepared from Brewer's and Baker's yeast were compared with the commercial yeast pr

104 sing a functional toxicogenomics approach in baker's yeast, which shares many cellular pathways and f

105 roducts were each prepared from Brewer's and Baker's yeasts, which suppressed production of interfero

106 lar inhibitors of the alpha-glucosidase from baker's yeast with Ki's near to 2 muM.