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1  to the results, the bread prepared by using Kluyveromyces aestuarii possessed the highest porosity p
2  conserved sequences in telomerase RNAs from Kluyveromyces budding yeasts.
3 at KAT1 was domesticated specifically in the Kluyveromyces clade of the budding yeasts.
4 ermini except for those of the Saccharomyces/Kluyveromyces clade that all contained a region homologo
5 5% of genes in the genome of the dairy yeast Kluyveromyces lactis (family Saccharomycetaceae).
6 the yeast heat-shock transcription factor of Kluyveromyces lactis (HSF_KL) suggests that these prolin
7 ing yeasts Saccharomyces cerevisiae (Sc) and Kluyveromyces lactis (Kl).
8 se Gal4 binding sites are not present in the Kluyveromyces lactis ACC1 gene.
9 isiae and the homologous KLLA0A09713 gene of Kluyveromyces lactis allow for cross-complementation of
10 bility of ICE to divergent yeasts, including Kluyveromyces lactis and alternative S. cerevisiae strai
11 ial beta-galactosidases (Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae) was analyse
12 beta-galactosidases from Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae.
13 sidase preparations from Aspergillus oryzae, Kluyveromyces lactis and Bacillus circulans.
14 at shock transcription factor from the yeast Kluyveromyces lactis and had shown it to be highly alpha
15 ase activity, as previously observed for the Kluyveromyces lactis and human telomerase RNA pseudoknot
16              Here we report that recombinant Kluyveromyces lactis and Saccharomyces cerevisiae Abd1 a
17 led to monitor carboxylic acid production by Kluyveromyces lactis and Saccharomyces cerevisiae during
18 p) and CDEIII (~25 bp) are conserved between Kluyveromyces lactis and Saccharomyces cerevisiae, but C
19 provided evidence that in the budding yeasts Kluyveromyces lactis and Saccharomyces cerevisiae, the t
20 egy to isolate LCB2 homologs from the yeasts Kluyveromyces lactis and Schizosaccharomyces pombe and a
21 e three-dimensional structure of Gal80p from Kluyveromyces lactis and show that it is structurally ho
22 st Saccharomyces cerevisiae, the dairy yeast Kluyveromyces lactis and the human pathogen Candida albi
23 ralog ORC4 (Origin Recognition Complex 4) in Kluyveromyces lactis and the Schizosaccharomyces pombe t
24  and gamma-subunits of ATP synthase in yeast Kluyveromyces lactis and trypanosome Trypanosoma brucei.
25  This work evaluated the saponins effects on Kluyveromyces lactis beta-galactosidase activity and cor
26 luate the negative effects of tannic acid on Kluyveromyces lactis beta-galactosidase catalytic activi
27                       We show here, by using Kluyveromyces lactis cells containing two types of telom
28               Telomeres in the budding yeast Kluyveromyces lactis consist of perfectly repeated 25-bp
29 dy, we uncovered a domesticated transposase, Kluyveromyces lactis hobo/Activator/Tam3 (hAT) transposa
30    We present the 3.0-A crystal structure of Kluyveromyces lactis Hsv2, which shares significant sequ
31    Solubilisation of beta-galactosidase from Kluyveromyces lactis in Aerosol-OT water-in-isooctane mi
32 CrPV-IRES bound to the ribosome of the yeast Kluyveromyces lactis in both the canonical and rotated s
33 pression of the lactose-galactose regulon in Kluyveromyces lactis is induced by lactose or galactose
34 airy industry, and the enzyme from the yeast Kluyveromyces lactis is most widely used.
35                         The mannan chains of Kluyveromyces lactis mannoproteins are similar to those
36                         The mannan chains of Kluyveromyces lactis mannoproteins are similar to those
37                             Mannan chains of Kluyveromyces lactis mannoproteins are similar to those
38        The corresponding domain of the yeast Kluyveromyces lactis Mig1 conferred glucose-regulated Ms
39           We report the crystal structure of Kluyveromyces lactis MIND and examine its partner intera
40  from MDCK cells of a recently characterized Kluyveromyces lactis mutant deficient in Golgi transport
41                                           In Kluyveromyces lactis mutants lacking telomerase, recombi
42                      Yarrowia lipolytica and Kluyveromyces lactis occur as part of Stilton cheese mic
43 in a telomerase-deletion mutant of the yeast Kluyveromyces lactis occurs through a roll-and-spread me
44            The solution NMR structure of the Kluyveromyces lactis pseudoknot, presented here, reveals
45  the telomerase RNA gene (TER1) in the yeast Kluyveromyces lactis results in gradual loss of telomeri
46      Here we report the crystal structure of Kluyveromyces lactis Rtr1, which reveals a new type of z
47 Golgi apparatus and of a mutant of the yeast Kluyveromyces lactis specifically defective in the trans
48        We characterized two mutations in the Kluyveromyces lactis telomerase RNA gene (TER1) template
49 knot elements in human and the budding yeast Kluyveromyces lactis telomerase RNAs contain unusual tri
50                                          The Kluyveromyces lactis ter1-16T strain contains mutant tel
51 omerase RNA gene (TER1) of the budding yeast Kluyveromyces lactis that were predicted to lead to synt
52 zyme that converts the petite-negative yeast Kluyveromyces lactis to petite-positive.
53 the immobilization of B-d-galactosidase from Kluyveromyces lactis was developed, consisting of mesopo
54 agues demonstrate that, in the budding yeast Kluyveromyces lactis, a DNA rearrangement associated wit
55 myces cerevisiae, Schizosaccharomyces pombe, Kluyveromyces lactis, and Candida albicans, as well as a
56 ree yeast species (Saccharomyces cerevisiae, Kluyveromyces lactis, and Debaryomyces hansenii) are rem
57 owever, deletion of the PNT1 orthologue from Kluyveromyces lactis, KlPNT1, caused a clear nonrespirat
58        Origin positions in four other yeasts-Kluyveromyces lactis, Lachancea kluyveri, Lachancea walt
59 Saccharomyces cerevisiae, S. carlsbergensis, Kluyveromyces lactis, Neurospora crassa, Aspergillus nid
60                         In the budding yeast Kluyveromyces lactis, the incorporation of certain mutan
61                                           In Kluyveromyces lactis, the repeats synthesized by the wil
62                                 In the yeast Kluyveromyces lactis, the telomerase RNA (Ter1) template
63 ing ALT cells, such as the stn1-M1 mutant of Kluyveromyces lactis, the telomeres appear to be continu
64                                           In Kluyveromyces lactis, we have identified a novel allele
65 ed mating type and Sir proteins in the yeast Kluyveromyces lactis, which contains cryptic copies of t
66 plication and found that Orc1 from the yeast Kluyveromyces lactis, which diverged from S. cerevisiae
67 died telomere length regulation in the yeast Kluyveromyces lactis, which has long (25 base pairs) hom
68           Using the KlCYC1 gene of the yeast Kluyveromyces lactis, which includes a single promoter a
69  (OYE) reductase increases ROS resistance in Kluyveromyces lactis, while Saccharomyces cerevisiae mut
70 chore proteins Nkp1 and Nkp2, from the yeast Kluyveromyces lactis, with nanoflow electrospray ionizat
71 etylase, we studied Sir2 from another yeast, Kluyveromyces lactis.
72 nant proteins derived from the budding yeast Kluyveromyces lactis.
73 tional ancestral gene as is still present in Kluyveromyces lactis.
74 om Saccharomyces kluyveri and of PET111 from Kluyveromyces lactis.
75 idues in the telomerase RNA of budding yeast Kluyveromyces lactis.
76 p formation in the unicellular budding yeast Kluyveromyces lactis.
77 he cytoplasmic linear DNA killer plasmids of Kluyveromyces lactis.
78 ut accelerated the inactivation in that from Kluyveromyces lactis.
79  toxin secreted by some strains of the yeast Kluyveromyces lactis.
80 on of a recombinant endopolygalacturonase of Kluyveromyces marxianus (KMPG) for the aroma enhancement
81 ive kinetochores from the thermophilic yeast Kluyveromyces marxianus and examined them by electron mi
82 dustrial interest (Saccharomyces cerevisiae, Kluyveromyces marxianus and kefir) by solid state fermen
83 ces pombe, and two Crabtree-negative yeasts, Kluyveromyces marxianus and Scheffersomyces stipitis, cu
84 t by Lactiplantibacillus plantarum BL011 and Kluyveromyces marxianus B0399, analysing cell viability,
85 d and pre-treated immobilized inulinase from Kluyveromyces marxianus NRRL Y 7571 and Aspergillus nige
86 ally validated sgRNAs designed by ALLEGRO in Kluyveromyces marxianus, Komagataella phaffii, Yarrowia
87 mine the structure and function of Usb1 from Kluyveromyces marxianus, which shares 25 and 19% sequenc
88 t phytate content (17.49 mg/5 g) belonged to Kluyveromyces marxianus.
89  emerged after WGD between the divergence of Kluyveromyces polysporus and Saccharomyces castellii fro
90 ere we report the 3.2 A crystal structure of Kluyveromyces polysporus Argonaute (KpAGO) fortuitously
91 tivity of a catalytically active fragment of Kluyveromyces polysporus Dcr1, which represents the nonc
92 ase RNAs of Saccharomyces cerevisiae and six Kluyveromyces species followed by mutagenesis of the S.
93 wine fermented with Torulaspora delbrueckii, Kluyveromyces thermotolerans and Saccharomyces cerevisia
94 ly examine 87 potential interactions between Kluyveromyces waltii proteins, whose one to one ortholog
95 ow evolution compared with the orthologue in Kluyveromyces waltii, a non-WGD species.
96 ome duplication, by sequencing and analysing Kluyveromyces waltii, a related yeast species that diver
97 e speciation event between S. cerevisiae and Kluyveromyces waltii, suggesting that the WGD occurred i
98 a core structure common to Saccharomyces and Kluyveromyces yeast species.