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1 A after integration of this oxygen-respiring eubacterium.
2 phic merger between an archaebacterium and a eubacterium.
3 a, generated hydrogen sulfide to protect the eubacterium, a heterotrophic swimmer comparable to Spiro
8 tilizing bacteria producing butyrate, namely Eubacterium and Anaerostipes species, supported by incre
9 cluster resembling that from a gram-positive eubacterium and the other resembling a eubacterial V nit
11 roides, Oscillospira, Blautia, Ruminococcus, Eubacterium, and Christensenella species in the RS4 grou
12 ve abundance of Lactobacillus, Turicibacter, Eubacterium, and Clostridium, while decreased that of th
13 PC3 (positive loadings on Faecalibacterium, Eubacterium, and Roseburia) was associated with higher i
14 nsella, Coprobacillus, Desulfovibrio, Dorea, Eubacterium, and Ruminococcus, while greater adherence t
15 nella, Tannerella, Streptococcus, Atopobium, Eubacterium, and Treponema were elevated in disease.
16 dy, the PilT homologue from the thermophilic eubacterium Aquifex aeolicus was cloned, overexpressed,
19 UCG-005 ambiguous taxa and Anaerovoracaceae (Eubacterium) brachy group uncultured bacterium were incr
20 , CBM65A and CBM65B, derived from EcCel5A, a Eubacterium cellulosolvens endoglucanase, bind to a rang
23 M. smegmatis as the first known example of a eubacterium containing both Lon and a complete 20S prote
24 occus faecium, E. coli, Streptococcus avium, Eubacterium contortum, Peptostreptococcus productus, and
25 , and a Ro ortholog enhances survival of the eubacterium Deinococcus radiodurans after ultraviolet ir
26 s homolog encoded by the radiation-resistant eubacterium Deinococcus radiodurans and show that DNA bi
28 orthologue of Ro in the radiation-resistant eubacterium Deinococcus radiodurans contributes to survi
29 that a Ro protein in the radiation-resistant eubacterium Deinococcus radiodurans participates in ribo
32 all eukaryotic genomes whereas the number of eubacterium-derived genes is much more variable, suggest
33 centrations of Cd were associated with lower Eubacterium eligens (coef = -0.774, q-value = 0.045).
34 alue = 0.039) and negatively associated with Eubacterium eligens (coef = -0.794, q-value = 0.044).
35 erial species (Faecalibacterium prausnitzii, Eubacterium eligens, and Bacteroides thetaiotaomicron) a
36 of species from class Clostridia, including [Eubacterium] eligens, Butyrivibrio crossotus, and Lachno
37 rchaebacterium Methanococcus jannaschii, the eubacterium Escherichia coli, and the nematode, Caenorha
41 noma infections included those in the genera Eubacterium, Flavobacterium, Kocuria, Microbacterium, an
42 of Lactobacillus bulgaricus, a gram-positive eubacterium, for the conversion by an amidotransferase o
43 genera Capnocytophaga, Cytophaga, Dialister, Eubacterium, Fusobacterium, Gemella, Mogibacterium, Pept
44 rate producers-Akkermansia, Bifidobacterium, Eubacterium halii, unassigned Lachnospiraceae, Blautia,
45 nts in remission after FMT had enrichment of Eubacterium hallii and Roseburia inulivorans compared wi
46 d a reduction in the abundance of the genera Eubacterium hallii group and Dorea, and an increase in a
48 Using correlation analysis we found that Eubacterium hallii was negatively associated with fatigu
49 coccus cristatus, Capnocytophaga gingivalis, Eubacterium IR009, Campylobacter rectus, and Lachnospira
50 tcB is found in the human intestinal isolate Eubacterium limosum ATCC 8486, an acetogen that can grow
51 ember MtpB from the human intestinal isolate Eubacterium limosum ATCC 8486, an acetogen that excretes
52 Here, we show that the human gut acetogen Eubacterium limosum demethylates y-butyrobetaine and pro
54 ance of a bacterial group composed mostly of Eubacterium limosum in the validation set was associated
55 or carnitine metabolism in the gut bacterium Eubacterium limosum Instead of forming TMA, carnitine is
57 entified in the obligate anaerobic bacterium Eubacterium limosum, is composed of five previously unch
58 ns, and co-occurrence analysis revealed that Eubacterium minutum was correlated with Prevotella inter
59 We have shown that the genetically tractable eubacterium Mycobacterium smegmatis contains a 20S prote
61 a (86%/62%), Campylobacter rectus (90%/76%), Eubacterium nodatum (64%/30%), Prevotella intermedia (58
62 blue cluster (composed of antibodies against Eubacterium nodatum and Actinomyces naeslundii) was inve
63 associated with periodontitis, whereas high Eubacterium nodatum titers were associated with periodon
64 e (which included Actinomyces naeslundii and Eubacterium nodatum) was inversely associated (OR = 0.93
65 ae, Prevotella intermedia, Parvimonas micra, Eubacterium nodatum, and Campylobacter gracilis, a signi
66 obacterium polymorphum, Eikenella corrodens, Eubacterium nodatum, Campylobacter gracilis, Capnocytoph
68 species (ASF356 Clostridium species, ASF492 Eubacterium plexicaudatum, ASF500 Pseudoflavonifactor sp
69 tain Bacillota, while also reducing specific Eubacterium populations that may be more prevalent at ea
70 This genome fusion between a deep branching eubacterium, possibly an ancestor of the cyanobacterium
71 We describe properties of the recently found eubacterium proton pump from Exiguobacterium sibiricum (
72 lostridium, Lactobacillus, Ruminococcus, and Eubacterium, ranging from 4% to 19% relative abundance).
73 ridium coccoides (cluster XIVa), C coccoides-Eubacterium rectale (cluster XIVab), Bacteroidetes, and
75 relative abundance of Bacteroides, Roseburia-Eubacterium rectale and Bifidobacterium and an increase
76 inished genome sequences were generated from Eubacterium rectale and E. eligens, which belong to Clos
77 ry concentration), is produced in culture by Eubacterium rectale and is present in human faecal sampl
78 n some cases, discrete subspecies (e.g., for Eubacterium rectale and Prevotella copri) or continuous
80 t also known as the Clostridium coccoides or Eubacterium rectale group, contains species that have ev
85 om Bombyx mori and a group II intron RT from Eubacterium rectale Only the non-LTR RT supported robust
88 m populations: Bacteroides thetaiotaomicron, Eubacterium rectale, and Methanobrevibacter smithii.
92 teroides spp./Prevotella spp. (7.50-10.71%), Eubacterium rectale/Clostridium coccoides (1.37-3.70%),
94 thensis (37.9%), Capnocytophaga sp. (36.9%), Eubacterium saburreum (32.7%), Campylobacter rectus (17.
95 species (Cs), Porphyromonas gingivalis (Pg), Eubacterium saburreum (Es), and Fusobacterium nucleatum
96 esistant isolates of Gemella morbillorum and Eubacterium saburreum increased significantly at 6 month
99 lifactor alocis, Treponema lecithinolyticum, Eubacterium saphenum, Desulfobulbus sp./OT041, and Mogib
100 periodontitis-related unculturable bacteria (Eubacterium saphenum, Fretibacterium sp. human oral taxo
101 5 from the TM7 phylum, and the named species Eubacterium saphenum, Porphyromonas endodontalis, Prevot
102 pathogens and of Fretibacterium fastidiosum, Eubacterium saphenum, Porphyromonas endodontalis, Trepon
103 tructures of the THF-sensing domain from the Eubacterium siraeum riboswitch in the ligand-bound and u
105 to an alpha-hydroxysteroid dehydrogenase of Eubacterium sp. strain VPI 12708, a 25-kDa protein corre
108 ntermedia/nigrescens, Bacteroides forsythus, Eubacterium species, Campylobacter species, Fusobacteriu
109 were analyzed by differential isolation and eubacterium-specific PCR-denaturing gradient gel electro
112 ter spp., Selenomonas spp., Catonella morbi, Eubacterium spp., Filifactor alocis, Parvimonas micra, P
114 lum, a phylotype (clone BS095) of Dialister, Eubacterium sulci, a phylotype (clone DR034) of the uncu
116 etrans is a gram-positive, endospore-forming eubacterium that apparently is a member of the Bacillus-
117 otes as a fusion of an archaebacterium and a eubacterium that could not have been observed using phyl
120 properties of HU from the hyperthermophilic eubacterium Thermotoga maritima are shown here to differ
121 show here that HU from the hyperthermophilic eubacterium Thermotoga maritima HU bends DNA and constra
123 adenylosuccinate lyase from the thermophilic eubacterium Thermotoga maritima, the archaebacterial lya
124 tone-like protein from the hyperthermostable eubacterium Thermotoga maritima, TmHU as an efficient ge
126 de dismutase from the extremely thermophilic eubacterium Thermus thermophilus has been cloned and exp
131 exporter from the thermophilic Gram-negative eubacterium Thermus thermophilus; it is homologous to va
132 ed Ruminococcaceae, Christensenellaceae, and Eubacterium, Treponema, Senegalimassilia, Ruminiclostrid
133 , UCG003 and UCG005), LachnospiraceaeUCG001, Eubacterium ventriosum and Ruminococcusgauvreauiigroup,
136 equence of strain 195 indicated that it is a eubacterium without close affiliation to any known group
137 ured Lachnospiraceae (Firmicutes) related to Eubacterium xylanophilum and Butyrivibrio spp. were stro
138 group, Coprococcus 2, Escherichia-Shigella, [Eubacterium] xylanophilum group, Flavonifractor, Lachnoc