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1 esult of the infection process with Erysiphe necator.
2 tida, Sphingobium japonicum, and Cupriavidus necator.
3 alothiobacillus neapolitanus and Cupriavidus necator.
4 and 23.3-fold, respectively) and Cupriavidus necator (51.5- and 516.6-fold, respectively).
5 gulatory [NiFe]-hydrogenase from Cupriavidus necator, a model enzyme for the analysis of catalytic in
6 l-length GST protein from the human hookworm Necator americanus (and designated Na-GST-1, Na-GST-2, a
7                                              Necator americanus Ancylostoma-secreted protein 2 (Na-AS
8 llergen-like 1 protein (SmTAL1), SmTAL2, and Necator americanus Ancylostoma-secreted protein-2 (Na-AS
9                                              Necator americanus and gluten microchallenge promoted to
10                                              Necator americanus aspartyl protease 1 (Na-APR-1) is one
11                                 The hookworm Necator americanus establishes infections of impressive
12 k1 peptides from the Ancylostoma caninum and Necator americanus hookworms and assessed their structur
13      Cytokine and proliferative responses to Necator americanus infection were measured in a treatmen
14 our healthy volunteers were infected with 50 Necator americanus infective larvae (L3) in a controlled
15 excretory/secretory products of the hookworm Necator americanus inhibited eosinophil recruitment in v
16                                 The hookworm Necator americanus is the predominant soil-transmitted h
17 id arthritis, psoriasis, and autism, and the Necator americanus larvae for allergic rhinitis, asthma,
18             Subjects were inoculated with 20 Necator americanus larvae, and escalating gluten challen
19 53.7%) following challenge with heterologous Necator americanus larvae.
20 atic nature of infection, we argue here that Necator americanus might be approaching a mutualistic sy
21 e effect of excretory/secretory product from Necator americanus on superoxide radical anions generate
22 months after the cessation of all deworming, Necator americanus prevalence (the predominant species a
23 ished floors were also associated with lower Necator americanus prevalence in Bangladesh (0.52, 0.29-
24  nematodes - hookworms (Ancylostoma spp. and Necator americanus) and the ruminant parasite, Haemonchu
25        Trials using helminths like hookworm (Necator americanus) or porcine whipworm (Trichuris suis)
26 arum, hookworm (Ancylostoma duodenale and/or Necator americanus), Entamoeba histolytica/dispar, Mycob
27 icoides, hookworm (Ancylostoma duodenale and Necator americanus), Trichuris trichiura, and Strongyloi
28 ness among people infected with the hookworm Necator americanus, although the mechanisms underlying d
29            Primarily three hookworm species (Necator americanus, Ancylostoma duodenale, and Ancylosto
30 ed by infective larvae of the human hookworm Necator americanus, has been solved to resolution limits
31                          The human hookworm, Necator americanus, is a parasite that infects almost ha
32 o hookworm species, Ancylostomaduodenale and Necator americanus, the whipworm Trichuristrichiura, and
33                        Ascaris lumbricoides, Necator americanus, Trichuris trichiura, and Strongyloid
34 eption is infection with the human hookworm, Necator americanus, where virtually no protection ensues
35 her nematodes, including the human hookworm, Necator americanus, which also evaded NETs in vitro.
36  with the blood-feeding intestinal hookworm, Necator americanus.
37 ngyloides stercoralis, Ancylostoma spp., and Necator americanus.
38 is trichiura, Strongyloides stercoralis, and Necator americanus.
39 ichiura, hookworm [Ancylostoma duodenale and Necator americanus], and Strongyloides stercoralis).
40  of the grape powdery mildew fungus Erysiphe necator and a high-quality mitochondrial gene annotation
41                                           E. necator and A. carbonarius correlated negatively with st
42 ecies: Saccharomyces cerevisiae, Cupriavidus necator, and HEK293T cells.
43 bernet Sauvignon, which is susceptible to E. necator, and V. aestivalis cv. Norton, which is resistan
44                Botrytis cinerea and Erysiphe necator are among the most relevant fungi in viticulture
45  and the obligate biotrophic fungus Erysiphe necator are not understood in depth.
46 ort that Ralstonia eutropha H16 (Cupriavidus necator ATCC 17699) uses l-ascorbate as sole carbon sour
47 dated, showing that it was activated when C. necator cells were subjected to gentisic acid.
48 under aerobic conditions using a Cupriavidus necator chassis.
49  between transcriptome changes induced by E. necator colonization and those triggered by elevated SA
50 dsABG formate dehydrogenase from Cupriavidus necator (formerly known as Ralstonia eutropha) to cataly
51 01-589) of the class I PhaC from Cupriavidus necator (formerly Ralstonia eutropha) to 1.80 A resoluti
52 t a genome-scale metabolic model (GSM) of C. necator H16 (denoted iCN1361), which is directly constru
53 in the model chemolithoautotroph Cupriavidus necator H16 (Ralstonia eutropha H16) by characterizing t
54 g the system-level metabolic behaviour of C. necator H16 and can provide useful insights for designin
55 the hydrogen-oxidizing bacterium Cupriavidus necator H16 both with and without bound NADH.
56 of this network, inclusions from Cupriavidus necator H16 DeltaphaP were examined.
57                    The bacterium Cupriavidus necator H16 produces a family of linear lipopeptides whe
58                   In this regard Cupriavidus necator H16 represents a particularly promising microbia
59      In this work, we engineered Cupriavidus necator H16, a model autotrophic organism to express dif
60 tantly, better reflects PHB production in C. necator H16.
61  for gentisic acid metabolism in Cupriavidus necator H16.
62 alstonia eutropha (also known as Cupriavidus necator) H16, a facultatively chemolithoautotrophic soil
63  (AmpSeq), we show that the population of E. necator in Israel is composed of three genetic groups: G
64                             We found that C. necator invests a large fraction of its proteome in func
65 rmate dehydrogenase FdsDABG from Cupriavidus necator is capable of catalyzing both formate oxidation
66                                  Cupriavidus necator) is one of the best studied organisms for the sy
67      Further comparative analysis of five E. necator isolates revealed 203 polymorphic sites, but onl
68         The tcpRXABCYD operon of Cupriavidus necator JMP134 is involved in the degradation of 2,4,6-t
69 alcohol dehydrogenase (ADH) from Cupriavidus necator JMP134.
70                                       The E. necator mitochondrial genome consists of a circular DNA
71 rtial resistance to powdery mildew (Erysiphe necator, PM) in V. sylvestris from Central Asia.
72    Therefore, we suggest that the Israeli E. necator population was founded by at least two invasions
73 red the centre of origin and diversity of E. necator, previous reports on resistant native wild and d
74 y versatile 'knallgas' bacterium Cupriavidus necator reallocates protein resources when grown on diff
75  grape powdery mildew (PM) pathogen Erysiphe necator (Schw.) Burr triggers a major remodeling of the
76  to the powdery mildew fungus (PM), Erysiphe necator (Schw.) Burr., but little is known about the tra
77                                     Erysiphe necator, the causal agent of grape powdery mildew, is a
78 ere the substrate is upgraded by Cupriavidus necator to biopolymer with a maximum rate of 32 +/- 3.5
79 sDABG formate dehydrogenase from Cupriavidus necator to catalyze the exchange of solvent oxygen into
80  previously reported enzyme from Cupriavidus necator, we identify five thiolases with TAL production