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1 etylase, we studied Sir2 from another yeast, Kluyveromyces lactis.
2 nant proteins derived from the budding yeast Kluyveromyces lactis.
3 tional ancestral gene as is still present in Kluyveromyces lactis.
4 p formation in the unicellular budding yeast Kluyveromyces lactis.
5 om Saccharomyces kluyveri and of PET111 from Kluyveromyces lactis.
6 idues in the telomerase RNA of budding yeast Kluyveromyces lactis.
7 he cytoplasmic linear DNA killer plasmids of Kluyveromyces lactis.
8 ut accelerated the inactivation in that from Kluyveromyces lactis.
9  toxin secreted by some strains of the yeast Kluyveromyces lactis.
10 agues demonstrate that, in the budding yeast Kluyveromyces lactis, a DNA rearrangement associated wit
11 se Gal4 binding sites are not present in the Kluyveromyces lactis ACC1 gene.
12 isiae and the homologous KLLA0A09713 gene of Kluyveromyces lactis allow for cross-complementation of
13 bility of ICE to divergent yeasts, including Kluyveromyces lactis and alternative S. cerevisiae strai
14 ial beta-galactosidases (Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae) was analyse
15 beta-galactosidases from Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae.
16 sidase preparations from Aspergillus oryzae, Kluyveromyces lactis and Bacillus circulans.
17 at shock transcription factor from the yeast Kluyveromyces lactis and had shown it to be highly alpha
18 ase activity, as previously observed for the Kluyveromyces lactis and human telomerase RNA pseudoknot
19              Here we report that recombinant Kluyveromyces lactis and Saccharomyces cerevisiae Abd1 a
20 led to monitor carboxylic acid production by Kluyveromyces lactis and Saccharomyces cerevisiae during
21 p) and CDEIII (~25 bp) are conserved between Kluyveromyces lactis and Saccharomyces cerevisiae, but C
22 provided evidence that in the budding yeasts Kluyveromyces lactis and Saccharomyces cerevisiae, the t
23 egy to isolate LCB2 homologs from the yeasts Kluyveromyces lactis and Schizosaccharomyces pombe and a
24 e three-dimensional structure of Gal80p from Kluyveromyces lactis and show that it is structurally ho
25 st Saccharomyces cerevisiae, the dairy yeast Kluyveromyces lactis and the human pathogen Candida albi
26 ralog ORC4 (Origin Recognition Complex 4) in Kluyveromyces lactis and the Schizosaccharomyces pombe t
27  and gamma-subunits of ATP synthase in yeast Kluyveromyces lactis and trypanosome Trypanosoma brucei.
28 myces cerevisiae, Schizosaccharomyces pombe, Kluyveromyces lactis, and Candida albicans, as well as a
29 ree yeast species (Saccharomyces cerevisiae, Kluyveromyces lactis, and Debaryomyces hansenii) are rem
30  This work evaluated the saponins effects on Kluyveromyces lactis beta-galactosidase activity and cor
31 luate the negative effects of tannic acid on Kluyveromyces lactis beta-galactosidase catalytic activi
32                       We show here, by using Kluyveromyces lactis cells containing two types of telom
33               Telomeres in the budding yeast Kluyveromyces lactis consist of perfectly repeated 25-bp
34 5% of genes in the genome of the dairy yeast Kluyveromyces lactis (family Saccharomycetaceae).
35 dy, we uncovered a domesticated transposase, Kluyveromyces lactis hobo/Activator/Tam3 (hAT) transposa
36 the yeast heat-shock transcription factor of Kluyveromyces lactis (HSF_KL) suggests that these prolin
37    We present the 3.0-A crystal structure of Kluyveromyces lactis Hsv2, which shares significant sequ
38    Solubilisation of beta-galactosidase from Kluyveromyces lactis in Aerosol-OT water-in-isooctane mi
39 CrPV-IRES bound to the ribosome of the yeast Kluyveromyces lactis in both the canonical and rotated s
40 pression of the lactose-galactose regulon in Kluyveromyces lactis is induced by lactose or galactose
41 airy industry, and the enzyme from the yeast Kluyveromyces lactis is most widely used.
42 ing yeasts Saccharomyces cerevisiae (Sc) and Kluyveromyces lactis (Kl).
43 owever, deletion of the PNT1 orthologue from Kluyveromyces lactis, KlPNT1, caused a clear nonrespirat
44        Origin positions in four other yeasts-Kluyveromyces lactis, Lachancea kluyveri, Lachancea walt
45                         The mannan chains of Kluyveromyces lactis mannoproteins are similar to those
46                         The mannan chains of Kluyveromyces lactis mannoproteins are similar to those
47                             Mannan chains of Kluyveromyces lactis mannoproteins are similar to those
48        The corresponding domain of the yeast Kluyveromyces lactis Mig1 conferred glucose-regulated Ms
49           We report the crystal structure of Kluyveromyces lactis MIND and examine its partner intera
50  from MDCK cells of a recently characterized Kluyveromyces lactis mutant deficient in Golgi transport
51                                           In Kluyveromyces lactis mutants lacking telomerase, recombi
52 Saccharomyces cerevisiae, S. carlsbergensis, Kluyveromyces lactis, Neurospora crassa, Aspergillus nid
53                      Yarrowia lipolytica and Kluyveromyces lactis occur as part of Stilton cheese mic
54 in a telomerase-deletion mutant of the yeast Kluyveromyces lactis occurs through a roll-and-spread me
55            The solution NMR structure of the Kluyveromyces lactis pseudoknot, presented here, reveals
56  the telomerase RNA gene (TER1) in the yeast Kluyveromyces lactis results in gradual loss of telomeri
57      Here we report the crystal structure of Kluyveromyces lactis Rtr1, which reveals a new type of z
58 Golgi apparatus and of a mutant of the yeast Kluyveromyces lactis specifically defective in the trans
59        We characterized two mutations in the Kluyveromyces lactis telomerase RNA gene (TER1) template
60 knot elements in human and the budding yeast Kluyveromyces lactis telomerase RNAs contain unusual tri
61                                          The Kluyveromyces lactis ter1-16T strain contains mutant tel
62 omerase RNA gene (TER1) of the budding yeast Kluyveromyces lactis that were predicted to lead to synt
63                         In the budding yeast Kluyveromyces lactis, the incorporation of certain mutan
64                                           In Kluyveromyces lactis, the repeats synthesized by the wil
65                                 In the yeast Kluyveromyces lactis, the telomerase RNA (Ter1) template
66 ing ALT cells, such as the stn1-M1 mutant of Kluyveromyces lactis, the telomeres appear to be continu
67 zyme that converts the petite-negative yeast Kluyveromyces lactis to petite-positive.
68 the immobilization of B-d-galactosidase from Kluyveromyces lactis was developed, consisting of mesopo
69                                           In Kluyveromyces lactis, we have identified a novel allele
70 ed mating type and Sir proteins in the yeast Kluyveromyces lactis, which contains cryptic copies of t
71 plication and found that Orc1 from the yeast Kluyveromyces lactis, which diverged from S. cerevisiae
72 died telomere length regulation in the yeast Kluyveromyces lactis, which has long (25 base pairs) hom
73           Using the KlCYC1 gene of the yeast Kluyveromyces lactis, which includes a single promoter a
74  (OYE) reductase increases ROS resistance in Kluyveromyces lactis, while Saccharomyces cerevisiae mut
75 chore proteins Nkp1 and Nkp2, from the yeast Kluyveromyces lactis, with nanoflow electrospray ionizat