ライフサイエンスコーパス: baker's yeast

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

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

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

4 ther characterized mitochondrial proteins of baker's yeast.

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

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

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

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

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

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

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

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

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

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

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

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

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

18 Baker's yeast has equivalent proteins, branchpoint bindi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 The baker's yeast Saccharomyces cerevisiae encodes a single

37 The baker's yeast Saccharomyces cerevisiae expresses three h

38 The baker's yeast Saccharomyces cerevisiae possesses a singl

39 The baker's yeast Saccharomyces cerevisiae possesses a singl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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