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1 resident symbiont Baumannia cicadellinicola (Gammaproteobacteria).
2 d may be the reason ZipA is essential in the gammaproteobacteria.
3 highly conserved, especially among beta- and gammaproteobacteria.
4 ividuals, who had a proportional increase of Gammaproteobacteria.
5 gain in the common ancestor of the Beta- and Gammaproteobacteria.
6 ilization pathway may be prevalent in marine Gammaproteobacteria.
7 sts and bacteria, mainly Dothideomycetes and Gammaproteobacteria.
8  conserved, but most studies have focused on Gammaproteobacteria.
9  by Alphaproteobacteria, Actinobacteria, and Gammaproteobacteria.
10 us and choline oxidation (betB) expressed by Gammaproteobacteria.
11 elative abundance of Alphaproteobacteria and Gammaproteobacteria.
12 f the gammanonins: actinonin homologues from Gammaproteobacteria.
13 ili and potentially other systems in certain gammaproteobacteria.
14 cytidine deaminase (CDDL), seen primarily in Gammaproteobacteria.
15 d to metal reduction in Shewanella and other Gammaproteobacteria.
16 cific Zetaproteobacteria and an unclassified Gammaproteobacteria.
17  86 (76%) were positive for bacteria, mainly Gammaproteobacteria.
18 n of active methylamine-utilizing Alpha- and Gammaproteobacteria.
19 tant growth substrate for representatives of Gammaproteobacteria.
20 iched for versatile heterotrophic Alpha- and Gammaproteobacteria.
21 rganisms and could represent a new family of Gammaproteobacteria.
22  Alphaproteobacteria, Betaproteobacteria and Gammaproteobacteria.
23 ested a strong allergy-protective effect for Gammaproteobacteria.
24 ira, Planctomycetes, and SUP05/ARCTIC96BD-19 Gammaproteobacteria.
25 and function are likely conserved throughout gammaproteobacteria.
26  are narrowly distributed to a few orders of Gammaproteobacteria.
27  taxonomic units were assigned to the phylum Gammaproteobacteria (25 +/- 15%, n = 5 electrodes).
28                     Deep-sea piezophile-like Gammaproteobacteria, along with Epsilonproteobacteria, c
29 rated potential for hydrocarbon degradation (Gammaproteobacteria, Alphaproteobacteria, Actinobacteria
30 y a specific, but undescribed, member of the gammaproteobacteria, also recovered previously from the
31 labile and stimulated growth of copiotrophic Gammaproteobacteria (Alteromonadaceae and Oceanospirilla
32   Phytoplankton blooms caused an increase of Gammaproteobacteria (Alteromonadaceae, SAR86 and Vibrion
33           Light-enhanced growth was found in Gammaproteobacteria (Alteromonadales) and Bacteroidetes
34 ained dsyB(8), but some alphaproteobacteria, gammaproteobacteria and actinobacteria used a methionine
35                                 Unclassified Gammaproteobacteria and Alphaproteobacteria (Magnetovibr
36 equencing, including largely uncharacterized gammaproteobacteria and alphaproteobacteria taxa.
37 emonstrate the efficacy of Mobile-CRISPRi in gammaproteobacteria and Bacillales Firmicutes at the ind
38                       Before administration, Gammaproteobacteria and Bacilli dominated the microbiota
39 ant temporal variation, with Actinobacteria, Gammaproteobacteria and Bacilli predominant indoors, whe
40 nd November, while members of Euryarchaeota, Gammaproteobacteria and Bacteroidetes dominated the PR e
41 ed by the treatment processes, shifting from Gammaproteobacteria and Betaproteobacteria in RW to Alph
42 ulose synthase operons in representatives of Gammaproteobacteria and Betaproteobacteria.
43 vel, DEHP exposure increased Bacteroidia and Gammaproteobacteria and decreased Verrucomicrobiae in bo
44 des compared to silicates, while taxa of the Gammaproteobacteria and Deltaproteobacteria were common
45 d relative abundance of the bacterial clades Gammaproteobacteria and Desulfovibrionaceae and decrease
46 nes for heterotrophic metabolisms implicates Gammaproteobacteria and diverse heterotrophs in hydrothe
47 ther primarily because of differences in the Gammaproteobacteria and Epsilonproteobacteria abundances
48             The dominance of piezophile-like Gammaproteobacteria and Epsilonproteobacteria, along wit
49     Variations between subjects in levels of Gammaproteobacteria and Erysipelotrichi were directly as
50 acterial phyla shifts from a predominance of Gammaproteobacteria and Firmicutes towards Bacteroidetes
51                                              Gammaproteobacteria and Firmicutes were consistently enr
52  been restricted to a related cluster within Gammaproteobacteria and have revealed distinctive featur
53 a rubisco is dominated by just two orders of gammaproteobacteria and SAR324, encoding either the form
54 t prominently members of the Flavobacteriia, Gammaproteobacteria and the alphaproteobacterial Roseoba
55 trophs belonging mainly to nifH clusters 1G (Gammaproteobacteria) and 3 (putative anaerobes) dominate
56 (Alphaproteobacteria, Betaproteobacteria and Gammaproteobacteria) and eukarya (Alveolata, Fungi, Stra
57 s a nutritional habitat (certain alveolates, Gammaproteobacteria) and organisms that resist digestive
58 estyle, feeding on photosynthetic anoxygenic Gammaproteobacteria, and absorption of host cytoplasm.
59 , SAR116, Roseobacter and Rhodospirillales), Gammaproteobacteria, and Actinobacteria.
60 the Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, and Deltaproteobacteria classes.
61 olute transporters were Alphaproteobacteria, Gammaproteobacteria, and Deltaproteobacteria, accounting
62 ia, enriched in either Betaproteobacteria or Gammaproteobacteria, and either unicellular Cyanobacteri
63  presence of Gram negative Enterobacterales, Gammaproteobacteria, and Fusobacteriaceae, which continu
64 ella prevented its reliable placement within Gammaproteobacteria, and high bias caused artifacts that
65 rophs, including Pelagibacter, SAR86-cluster Gammaproteobacteria, and marine Euryarchaea.
66 h hydrocarbons resulted in the enrichment of Gammaproteobacteria, and specifically the genera Pseudoa
67 including Actinobacteria, Alpha-, Beta-, and Gammaproteobacteria, and Sphingobacteria.
68 lvin-Benson-Bassham cycle, in Cyanobacteria, Gammaproteobacteria, and, surprisingly, Gemmatimonadetes
69 uding Shewanella, Pseudomonas, Psychromonas (Gammaproteobacteria), Arcobacter (Epsilonproteobacteria)
70                                              Gammaproteobacteria are important gut microbes but only
71      Organisms in the OM60/NOR5 clade of the Gammaproteobacteria are ubiquitous in the world's oceans
72 ) that harbor a community of closely related Gammaproteobacteria as intracellular endosymbionts in th
73 rved among Actinobacteria, Beta-, Delta- and Gammaproteobacteria-as the primary enzyme responsible fo
74  distinctive taxonomic profile, dominated by Gammaproteobacteria at class level and by Pseudomonas at
75 structed the genome of a Chromatiales (class Gammaproteobacteria) bacterium from a metagenomic sequen
76 assemblages were (1) dominated by Alpha- and Gammaproteobacteria, Bacteroidetes, and unclassified Bac
77 mic adaptation strategies in Bacteroidia and Gammaproteobacteria, both of which respond to organic ma
78                                              Gammaproteobacteria can biosynthesize both of these resp
79 cells of Deltaproteobacteria cluster SAR324, Gammaproteobacteria clusters ARCTIC96BD-19 and Agg47, an
80 dance of dinoflagellates, and DMSP-degrading gammaproteobacteria co-occurred with haptophytes.
81                                              Gammaproteobacteria-colonizing pancreatic tumors can deg
82 stimated (e.g. SAR11) or overestimated (e.g. Gammaproteobacteria) common marine taxa.
83  related to most other abundant unclassified Gammaproteobacteria commonly reported in EABs reducing O
84       They belong to type I methanotrophs of gammaproteobacteria, contain both mxaF and xoxF types of
85                  Four phylotypes, one within Gammaproteobacteria (corresponding to "Candidatus Gillia
86 novel, highly divergent marine member of the Gammaproteobacteria, currently without a cultured repres
87 itabine resistance was induced by intratumor Gammaproteobacteria, dependent on bacterial CDDL express
88  cultures, while methanotrophs affiliated to Gammaproteobacteria dominated the 10%-CH(4) cultures tha
89 microbial taxonomic diversity (P = 0.03) and Gammaproteobacteria (e.g., Enterobacteriaceae; P = 0.04)
90 oaBC-dut-algC gene clusters, in a variety of gammaproteobacteria, either as the sole PMM gene in the
91 ardless of sex and sexual practice including Gammaproteobacteria enrichment, Lachnospiraceae and Rumi
92  the sCD14 level; the relative abundances of Gammaproteobacteria, Enterobacteriales, and Enterobacter
93    The relative abundance of Proteobacteria, Gammaproteobacteria, Enterobacteriales, Enterobacteriace
94 liated with the classes Clostridia, Bacilli, Gammaproteobacteria, Epsilonproteobacteria, Bacteroidia,
95                                              Gammaproteobacteria exhibited high metabolic activity in
96 tion of airways disease are reflected by the gammaProteobacteria:Firmicutes (gammaP:F) ratio.
97 wellia, Cycloclasticus, and other members of Gammaproteobacteria, Flavobacteria, and Rhodobacteria.
98 th an unprecedented organization: an unnamed gammaproteobacteria, for which we propose the name Candi
99 oted an increase in the contribution of some Gammaproteobacteria groups (e.g. Alteromonadales) to the
100   The phylogeny of the large bacterial class Gammaproteobacteria has been difficult to resolve.
101          The Pseudomonas putida group in the Gammaproteobacteria has been intensively studied for bio
102          Isolated from coastal Oregon water, Gammaproteobacteria HTCC2148 and HTCC2080 are two member
103  we present the genome sequences of the OM60 Gammaproteobacteria HTCC2148 and HTCC2080.
104 e, Alphaproteobacteria (i.e., Thalassobius), Gammaproteobacteria (i.e., Pseudoalteromonas), Sphingoba
105                      A relative abundance of Gammaproteobacteria (ie, Gram-negative facultative bacil
106        Class-level analysis showed increased Gammaproteobacteria in CLD, the former associated with i
107 ded members of Campylobacterota, Alpha-, and Gammaproteobacteria in deposits, and Gammaproteobacteria
108 a-, and Gammaproteobacteria in deposits, and Gammaproteobacteria in plumes.
109                               The ecology of Gammaproteobacteria in the gut environment is poorly und
110 bundance in the gut, and enriched members of Gammaproteobacteria in the lung.
111 more, comparative analyses suggest that many Gammaproteobacteria, including all members of the Shewan
112                                         Most gammaproteobacteria, including Escherichia coli, encode
113 ed by phylogenetically related intracellular gammaproteobacteria, including the opportunistic pathoge
114                        Campylobacterota- and Gammaproteobacteria-infecting viruses reflected variatio
115 ed phylogenies this order does not belong to Gammaproteobacteria; instead, it (and, independently, "M
116 lete sulfide-driven denitrification by SUP05 Gammaproteobacteria is predicted to support inorganic ca
117     The functional role of the gram-negative gammaproteobacteria is supported by in vitro measurement
118      A hallmark of the SUP05 clade of marine Gammaproteobacteria is the ability to use energy obtaine
119  unique member of the OM60/NOR5 clade of the Gammaproteobacteria isolated from coastal seawater of Ka
120 erant, aerobic, methanotrophic member of the Gammaproteobacteria, isolated from coastal seawater.
121 n only the stationary phase in Gram-negative gammaproteobacteria, it is ubiquitous throughout all gro
122 ched for oligotrophic Actinobacteria OM1 and Gammaproteobacteria KI89A clades while nitrate enriched
123 cally the order Pseudomonadales in the class Gammaproteobacteria, known facultative hydrocarbonoclast
124 e abundance of Marinobacter and unclassified Gammaproteobacteria may have increased competitive press
125 e in situ macromolecular structures of three Gammaproteobacteria motors: Legionella pneumophila, Pseu
126                                      In many gammaproteobacteria, NO controls behavioral responses th
127 ommunities were markedly dominated by select Gammaproteobacteria, notably Escherichia species and Pse
128                                We found that gammaproteobacteria of type I methanotrophs are responsi
129 icrobiome that included Thioglobaceae (SUP05 Gammaproteobacteria), OM190 (Planctomycetota), ABY1 (Pat
130 and significantly lower generic diversity of gammaproteobacteria on their skin.
131 s a global CCM regulator in some lineages of Gammaproteobacteria operating as a functional replacemen
132 t reduction in the early pioneering bacteria Gammaproteobacteria (P = 0.03) and exhibited a trend for
133 s interaction was positively associated with Gammaproteobacteria (p=0.0010) and negatively associated
134 olitis), there were increased proportions of Gammaproteobacteria (p=0.0011) and lower proportions of
135 d Bifidobacteriaceae, and lower abundance of Gammaproteobacteria-particularly opportunistic Enterobac
136 ance by Deltaproteobacteria (Desulfobulbus), Gammaproteobacteria (Piscirickettsiaceae), Alphaproteoba
137 with n-hexadecane, and uncultured Alpha- and Gammaproteobacteria populations were enriched in the pol
138 ith relatively low levels of assimilation by Gammaproteobacteria populations, while copiotrophic Alph
139 has transferred horizontally across multiple Gammaproteobacteria, potentially driven by pressures to
140 affiliated with Competibacteraceae (GAO1), a Gammaproteobacteria PR6 and an Anaerolineae CH7.
141 R-associated transposon systems derived from Gammaproteobacteria, predicted all components essential
142 as putida, a versatile soil bacterium of the Gammaproteobacteria, processing a mixture of plant matte
143 ty of one or more highly conserved proteins; gammaproteobacteria produce two relevant proteins, ribos
144 erial strains on peptide decomposition, four Gammaproteobacteria (Pseudoalteromonas atlantica, Altero
145 bacteria KI89A clades while nitrate enriched Gammaproteobacteria SAR86, SAR92 and OM60 clades.
146          The heat shock sigma factors of all gammaproteobacteria sequenced have a histidine at this p
147 ), we identified a potential host-associated Gammaproteobacteria species (Serratia sp.) that was abse
148                                        Three Gammaproteobacteria species are maternally transmitted.
149 ar patterns are observed in select Beta- and Gammaproteobacteria species.
150 eobacteria yet before the betaproteobacteria/gammaproteobacteria split.
151 gae-dominated reefs had higher abundances of Gammaproteobacteria (such as Alteromonadales, Pseudomona
152 ibiotic bacterial taxa were chemoautotrophic Gammaproteobacteria, such as Thiotrichaceae and Methyloc
153 th pilin proteins from other species of soil gammaproteobacteria suggest that these structural differ
154 tarved copepods were Vibrio spp. and related Gammaproteobacteria, suggesting they represent the most
155            Actinobacteria, Bacilli, and many Gammaproteobacteria taxa discriminated birds from mammal
156                Throughfall samples contained Gammaproteobacteria that have been previously found to b
157  phylogenetically unique member of the class Gammaproteobacteria that is only distantly related to it
158 n our EABs was an unclassified member of the Gammaproteobacteria that was phylogenetically closely re
159 acteria, specifically Betaproteobacteria and Gammaproteobacteria, the likely major players.
160 ransmitted microbes consistently include two Gammaproteobacteria, the obligate mutualists Wiggleswort
161 cession of bacterial classes from Bacilli to Gammaproteobacteria to Clostridia, interrupted by abrupt
162 ies are dominated by Alphaproteobacteria and Gammaproteobacteria using the Calvin-Benson-Bassham path
163 P103(T) (ATCC BAA-332(T)) is a member of the Gammaproteobacteria utilizing n-alkanes as the sole sour
164 tatively involved in peroxide reduction from gammaproteobacteria were abundant in the VCs, suggesting
165 st, the genomes of organic-matter-responsive Gammaproteobacteria were characterized by high densities
166                                   Pathogenic Gammaproteobacteria were more resistant to non-antibioti
167 rom low abundance organisms of the NOR5/OM60 gammaproteobacteria were observed later in the experimen
168 bon substrates and belonging, e.g., to class Gammaproteobacteria were significantly enriched on PHB/H
169 reas Actinobacteria, Alphaproteobacteria and Gammaproteobacteria were the most abundant taxa outdoors
170 e SUP05 group of uncultured sulfur-oxidizing Gammaproteobacteria, which are abundant in widespread an
171 l five leech species revealed a dominance of gammaproteobacteria, which were distinct from each other
172 s and increases in the relative abundance of Gammaproteobacteria with distance from treatment plants
173 Alphaproteobacteria, Betaproteobacteria, and Gammaproteobacteria, with effect directions depending on
174 S) protein is a DNA binding factor, found in gammaproteobacteria, with functional equivalents in dive

 
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