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1 horseradish peroxidase, and laccase from T. versicolor).
2 commercial laccase from the fungus Trametes versicolor.
3 e development of asthma after exposure to A. versicolor.
4 rboxypeptidases from the marine snail Nerita versicolor.
5 ription of canine aspergillosis caused by A. versicolor.
6 ide E was synthesized and fed to Aspergillus versicolor.
7 us sp. and a terrestrial-derived Aspergillus versicolor.
8 0 to 462 for A. terreus, and 45 to 84 for A. versicolor.
9 f Aspergillus terreus, and 15 of Aspergillus versicolor.
10 avus, A. niger, A. terreus, A. ustus, and A. versicolor.
11 terreus, Aspergillus ustus, and Aspergillus versicolor.
12 sympodialis are most closely linked to tinea versicolor.
13 three distinct alpha-expansin proteins in T. versicolor.
14 oth roots and shoots of in-vitro-cultured T. versicolor.
18 migatus, A. flavus, A. niger, A. terreus, A. versicolor, A. glaucus, A. nidulans, A. ustus, and A. sy
19 in roots of the parasitic plant Triphysaria versicolor after being exposed to the haustorium-inducin
20 trodes are prepared from laccase of Trametes versicolor and a series of osmium-based redox polymer me
22 etes, among which the co-culture of Trametes versicolor and Ganoderma applanatum demonstrated the str
23 assays to demonstrate that two WRF, Trametes versicolor and Gelatoporia subvermispora, funnel carbon
25 Orobanchaceae parasites, such as Triphysaria versicolor and Phtheirospermum japonicum, that can infec
26 nascus purpureus, Lentinula edodes, Trametes versicolor and Pleurotus ostreatus proved to be an effec
27 yrobaculum aerophilum, laccase from Trametes versicolor, and bilirubin oxidase from Myrothecium verru
28 rations, such as pityriasis alba, pityriasis versicolor, and progressive macular hypomelanosis, were
31 rne fungi (Alternaria alternata, Aspergillus versicolor, Bipolaris sorokiniana, Candida albicans, Cla
32 eans of fungal bioaugmentation with Trametes versicolor (BTV-systems) and compared with the effect of
34 f the parasitic Scrophulariaceae Triphysaria versicolor by treating them with exudates obtained from
35 ults suggest that a fungal treatment with T. versicolor could be a promising process for the remediat
36 eciprocal crosses between T. eriantha and T. versicolor demonstrated that DMBQ responsiveness was inf
37 terreus, Aspergillus ustus, and Aspergillus versicolor, differentiated 41 isolates (3 to 9 each of t
41 oots of the hemi-parasitic plant Triphysaria versicolor expressing the GUS reporter gene were allowed
42 gene discovery project involving Triphysaria versicolor (facultative hemiparasite), Striga hermonthic
44 s, 22 Aspergillus terreus, seven Aspergillus versicolor, five Aspergillus calidoustus, and two Asperg
46 iseases such as seborrheic dermatitis, tinea versicolor, folliculitis, atopic dermatitis, and scalp c
47 Polysaccharopeptide (PSP), from Coriolus versicolor, has been used as an adjuvant to chemotherapy
48 ment with fungus Pycnoporus sp. and Trametes versicolor increased qm up to 72.5 mg/g and 85.7 mg/g, r
50 and a predominately Th2 response, whereas A. versicolor induced a strong Th17 response and neutrophil
51 rates of hosts (larval gray treefrogs; Hyla versicolor) infected with Echinoparyphium 10 days prior
54 lavus, 59 A. niger, 35 A. terreus, and 24 A. versicolor isolates and 24 isolates of other Aspergillus
55 le, 0.5 (99.7%); voriconazole, 1 (99.1%); A. versicolor, itraconazole, 2 (100%); posaconazole, 1 (not
57 onsisting in AuNPs, fullerenols and Trametes versicolor Laccase (TvL) assembled layer by layer onto a
58 ntial of the T1 center in Fet3p and Trametes versicolor laccase (TvL) that have the same 2His1Cys lig
59 hrough the direct immobilization of Trametes versicolor laccase on graphene doped carbon paste electr
60 esting form in Rhus vernicifera and Trametes versicolor laccase, characterized by "normal" type 2 Cu
61 given for the blue copper oxidase, Trametes versicolor laccase, in which the rate of change of the S
63 upus erythematosus, capillaritis, pityriasis versicolor, nummular eczema, and cutaneous T-cell lympho
67 gnin with basidiomycetes, primarily Coriolus versicolor, pre-grown on kenaf/lignin agar followed by e
68 x lacteus, Dichomitus squalens, and Trametes versicolor proved most efficient and transformed more th
69 leurotus spp., Lentinula edodes and Trametes versicolor proved to be an effective method for the prod
70 laccases from Agaricus bisporus and Trametes versicolor, resulting in formation of the same coupling
71 formatics and transcriptional analysis of T. versicolor revealed a potential candidate gene (GI: 6366
72 or transcripts differentially abundant in T. versicolor root tips treated with the allelopathic quino
73 of two expansin transcripts increased in T. versicolor roots exposed to BAP, but not DMBQ or maize r
75 isolated cDNAs preferentially abundant in T. versicolor roots exposed to Trifolium repens (white clov
77 eady-state levels of AS mRNA increased in T. versicolor roots several-fold when seedlings were expose
81 PFOS, PFOA, and GenX on gray treefrog (Hyla versicolor) tadpoles, followed by a Bd challenge after m
83 selected included the laccase from Trametes versicolor, the laccase-like enzyme isolated from Bacill
84 t amphibian, the eastern gray treefrog (Hyla versicolor), to variation in photoperiod and measured it
86 hthonous fungal/bacterial communities and T. versicolor was studied using denaturing gradient gel ele
88 dy, we have shown that laccase from Trametes versicolor, where the T1 redox potential is increased by
89 sted with lipids from the spider Tetragnatha versicolor, which had been previously analyzed by deriva
90 roots of the hemiparasitic plant Triphysaria versicolor within a few hours of exposure to either maiz