ライフサイエンスコーパス: versicolor

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.

15 ), A. terreus (0.0%, 1.6%, and 3.2%), and A. versicolor (6.3%, 0.0%, and 0.0%).

16 Hyla versicolor, a tetraploid treefrog, is reported to have o

17 migatus, A. flavus, A. niger, A. terreus, A. versicolor, A. glaucus, A. nidulans, A. ustus, and A. sy

18 in roots of the parasitic plant Triphysaria versicolor after being exposed to the haustorium-inducin

19 trodes are prepared from laccase of Trametes versicolor and a series of osmium-based redox polymer me

20 Aspergillus versicolor and Cladosporium cladosporioides are common m

21 etes, among which the co-culture of Trametes versicolor and Ganoderma applanatum demonstrated the str

22 rations, such as pityriasis alba, pityriasis versicolor, and progressive macular hypomelanosis, were

23 T. versicolor AS cDNA clones were isolated and placed into

24 The T. versicolor AS message levels increased to a similar magn

25 rne fungi (Alternaria alternata, Aspergillus versicolor, Bipolaris sorokiniana, Candida albicans, Cla

26 eans of fungal bioaugmentation with Trametes versicolor (BTV-systems) and compared with the effect of

27 A. versicolor, but not C. cladosporioides, spores had incre

28 f the parasitic Scrophulariaceae Triphysaria versicolor by treating them with exudates obtained from

29 ults suggest that a fungal treatment with T. versicolor could be a promising process for the remediat

30 eciprocal crosses between T. eriantha and T. versicolor demonstrated that DMBQ responsiveness was inf

31 terreus, Aspergillus ustus, and Aspergillus versicolor, differentiated 41 isolates (3 to 9 each of t

32 For laccase of T. versicolor (E(e)(0) = 0.82), the optimum mediator potent

33 In Dectin-1-deficient mice, A. versicolor exposure resulted in markedly attenuated IL-1

34 R and eosinophilic inflammation following A. versicolor exposure.

35 oots of the hemi-parasitic plant Triphysaria versicolor expressing the GUS reporter gene were allowed

36 gene discovery project involving Triphysaria versicolor (facultative hemiparasite), Striga hermonthic

37 (Benth.) Chuang and Heckard, and Triphysaria versicolor Fischer and C.

38 s, 22 Aspergillus terreus, seven Aspergillus versicolor, five Aspergillus calidoustus, and two Asperg

39 several chronic diseases such as pityriasis versicolor, folliculitis, and seborrheic dermatitis.

40 iseases such as seborrheic dermatitis, tinea versicolor, folliculitis, atopic dermatitis, and scalp c

41 Polysaccharopeptide (PSP), from Coriolus versicolor, has been used as an adjuvant to chemotherapy

42 ment with fungus Pycnoporus sp. and Trametes versicolor increased qm up to 72.5 mg/g and 85.7 mg/g, r

43 Ninety percent of T. versicolor individuals responded, whereas only 40% of T.

44 and a predominately Th2 response, whereas A. versicolor induced a strong Th17 response and neutrophil

45 rates of hosts (larval gray treefrogs; Hyla versicolor) infected with Echinoparyphium 10 days prior

46 We report a case of disseminated A. versicolor infection presenting as diskospondylitis, ost

47 Tinea versicolor is common worldwide and is caused by Malassez

48 lavus, 59 A. niger, 35 A. terreus, and 24 A. versicolor isolates and 24 isolates of other Aspergillus

49 le, 0.5 (99.7%); voriconazole, 1 (99.1%); A. versicolor, itraconazole, 2 (100%); posaconazole, 1 (not

50 onsisting in AuNPs, fullerenols and Trametes versicolor Laccase (TvL) assembled layer by layer onto a

51 hrough the direct immobilization of Trametes versicolor laccase on graphene doped carbon paste electr

52 esting form in Rhus vernicifera and Trametes versicolor laccase, characterized by "normal" type 2 Cu

53 given for the blue copper oxidase, Trametes versicolor laccase, in which the rate of change of the S

54 upus erythematosus, capillaritis, pityriasis versicolor, nummular eczema, and cutaneous T-cell lympho

55 a, mice were repeatedly exposed to either A. versicolor or C. cladosporioides spores.

56 An inhibitory effect exerted by T. versicolor over bacterial populations was suggested.

57 ee types of infection will be covered: tinea versicolor, piedra, and tinea nigra.

58 gnin with basidiomycetes, primarily Coriolus versicolor, pre-grown on kenaf/lignin agar followed by e

59 x lacteus, Dichomitus squalens, and Trametes versicolor proved most efficient and transformed more th

60 leurotus spp., Lentinula edodes and Trametes versicolor proved to be an effective method for the prod

61 formatics and transcriptional analysis of T. versicolor revealed a potential candidate gene (GI: 6366

62 or transcripts differentially abundant in T. versicolor root tips treated with the allelopathic quino

63 of two expansin transcripts increased in T. versicolor roots exposed to BAP, but not DMBQ or maize r

64 e messages were similarly up-regulated in T. versicolor roots exposed to maize root exudates.

65 isolated cDNAs preferentially abundant in T. versicolor roots exposed to Trifolium repens (white clov

66 Reducing TvPirin transcripts in T. versicolor roots resulted in significantly less haustori

67 eady-state levels of AS mRNA increased in T. versicolor roots several-fold when seedlings were expose

68 Morphological responses of T. versicolor roots to these haustoria inducing factors (HI

69 We tested the function of TvPirin in T. versicolor roots using hairpin-mediated RNA interference

70 which may be ascribed to response against T.versicolor stress.

71 0(4-d)) killed 10-60% of gray treefrog (Hyla versicolor) tadpoles.

72 selected included the laccase from Trametes versicolor, the laccase-like enzyme isolated from Bacill

73 However, after 21 days, T. versicolor was no longer the main taxon in the fungal co

74 hthonous fungal/bacterial communities and T. versicolor was studied using denaturing gradient gel ele

75 lans, A. niger, A. terreus, A. ustus, and A. versicolor) was also designed.

76 roots of the hemiparasitic plant Triphysaria versicolor within a few hours of exposure to either maiz

77 cyclic tripeptide isolated from Aspergillus versicolor ZLN-60, is reported herein.