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1 r oxygen are overlapping and complex in this obligate anaerobe.
2 ommensal Enterobacteriaceae and a decline of obligate anaerobes.
3 bactam caused the most severe declines among obligate anaerobes.
4         None of 10 control samples contained obligate anaerobes.
5 ellular building blocks and all appear to be obligate anaerobes.
6 ically many bacteria have been classified as obligate anaerobes.
7  composed of a collection of facultative and obligate anaerobes.
8 erobic bottles, with 15 (1.8%) containing 16 obligate anaerobes.
9  when co-resident with other facultative and obligate anaerobes.
10 c bottles, of which 384 (5.8%) contained 403 obligate anaerobes.
11 iotics was associated with lower richness of obligate anaerobes (adjusted risk ratio = 0.84[95% CI: 0
12 iotics was associated with lower richness of obligate anaerobes (adjusted risk ratio [aRR], 0.84; 95%
13  difficile is a Gram-positive, spore-forming obligate anaerobe and a major nosocomial pathogen of wor
14 ling of the OI variable from the proteins of obligate anaerobes and aerobes has established that the
15 e and duration of therapy on the richness of obligate anaerobes and known butyrate-producers in all i
16 ic dysentery and amebic liver abscess, is an obligate anaerobe, and derives energy from the fermentat
17   Thus aeration is a serious threat for this obligate anaerobe, and to cope it employs a set of defen
18  the class Armophorea, form a major clade of obligate anaerobes (APM ciliates) within the Spirotriche
19 acteroides thetaiotaomicron, a gram-negative obligate anaerobe, appears to utilize starch by first bi
20 concentration changes, indicating that these obligate anaerobes are more accurate than E. coli for fe
21                                              Obligate anaerobes are periodically exposed to oxygen, a
22 e in facultative anaerobes at the expense of obligate anaerobes, as well as molecular disruptions in
23 o-culture of human epithelial cells with the obligate anaerobe Bacteroides caccae and LGG results in
24 -inducible genes ahpCF, dps, and katB in the obligate anaerobe Bacteroides fragilis are controlled by
25  anaerobically prepared cell extracts of the obligate anaerobe Bacteroides fragilis.
26                                          The obligate anaerobe, Bacteroides fragilis, is a highly aer
27 rganism, Cytophaga hutchinsonii, and from an obligate anaerobe, Bacteroides thetaiotaomicron.
28 usly follow cellular chemistry within living obligate anaerobes by monitoring hydrogen bond structure
29 uld be used to study the pathogenesis of the obligate anaerobe C. difficile.
30 trointestinal tract with this Gram-positive, obligate anaerobe can lead to potentially life-threateni
31 ponent of the normal intestinal flora, is an obligate anaerobe capable of long-term survival in the p
32             Here we present a TU map for the obligate anaerobe Clostridium acetobutylicum ATCC 824.
33                            The Gram-positive obligate anaerobe Clostridium difficile causes potential
34 xybenzoate decarboxylase (4-HOB-DC) from the obligate anaerobe Clostridium hydroxybenzoicum JW/Z-1(T)
35 ical characterization of the enzyme from the obligate anaerobe Clostridium kluyveri, a ternary mechan
36                             In contrast, the obligate anaerobe Clostridium pasteurianum codes for a t
37 f the microbes within the human body are the obligate anaerobes, Clostridium spp., in the internal po
38               Porphyromonas gingivalis is an obligate anaerobe consistently associated with severe ma
39 obiota showed inter-individual variation and obligate anaerobe enrichment (e.g., Firmicutes).
40 the molecular mechanisms underlying how this obligate anaerobe forms infectious spores and how these
41 trong relationship between cyanobacteria and obligate anaerobes, from which cyanobacteria presumably
42 nd other species facilitated the survival of obligate anaerobes in aerated environments.
43 nvironment, and the continued use of Fe2+ by obligate anaerobes inhabiting high Fe2+ niches.
44                        The defining trait of obligate anaerobes is that oxygen blocks their growth, y
45 obic blood cultures only recovered 2 (0.69%) obligate anaerobes, it did allow for recovery of clinica
46  chronic or follow antibiotic treatment, and obligate anaerobes may be copathogens in ischemic or nec
47  short chain acyl-CoA dehydrogenase from the obligate anaerobe Megasphaera elsdenii was studied by ra
48 teroides fragilis (ETBF) is a Gram-negative, obligate anaerobe member of the gut microbial community
49 ost reducing to most oxidizing: methanogens, obligate anaerobes (nonmethanogenic), facultative aerobe
50                                              Obligate anaerobes other than Fusobacterium nucleatum co
51 zyme that mediates oxalate catabolism in the obligate anaerobe Oxalobacter formigenes, O. formigenes
52 e of facultative anaerobes and one confirmed obligate anaerobe, oxidase complexes (fox, sox, dox and
53 ies but also with otherwise-noncoaggregating obligate anaerobe-oxygen-tolerant species pairs.
54                                        These obligate anaerobes propagate under hyperthermophilic con
55 ells than bacterial cells, most of which are obligate anaerobes residing in the gut.
56 Porphyromonas gingivalis is a gram-negative, obligate anaerobe strongly associated with chronic adult
57  prevalent in many species (even facultative/obligate anaerobes), suggesting a key role for oxygen am
58  sulfate-reducing bacterium classified as an obligate anaerobe, swam to a preferred oxygen concentrat
59                 Oxalobacter formigenes is an obligate anaerobe that colonizes the human gastrointesti
60  Porphyromonas gingivalis is a Gram-negative obligate anaerobe that has been implicated in the etiolo
61 ified by qPCR as Akkermansia muciniphila, an obligate anaerobe that resides in the intestinal mucus b
62 amily, and are found in many facultative and obligate anaerobes that produce UFAs but lack fabA, sugg
63 omain of one such signaling protein from the obligate anaerobe Thermoanaerobacter tengcongensis at 1.
64 approach to elaborate cellular metabolism in obligate anaerobes using the pathogen Clostridioides dif
65 acteroides thetaiotaomicron, a gram-negative obligate anaerobe, utilizes polysaccharides by binding t
66                            In some patients, obligate anaerobes were isolated in pure culture.
67                                        These obligate anaerobes were not recovered using the conventi
68      If not for anaerobic bottles, all but 8 obligate anaerobes would have gone undetected.