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1 obal regulatory protein conserved within the Vibrionaceae.
2 l system for studying TMAO reductases in the Vibrionaceae.
3 es are predominantly vertically inherited in Vibrionaceae.
4 ant marine bacterium belonging to the family Vibrionaceae.
5 that toxR is an ancestral gene of the family Vibrionaceae.
6 ndent acetone formation is widespread in the Vibrionaceae.
7 s conserved in diverse members of the family Vibrionaceae.
8 res the secretion of these proteins from the Vibrionaceae.
9 d influences virulence in certain members of Vibrionaceae.
10 a clinically important bacterial family, the Vibrionaceae.
11 orporated core proteome data from the family Vibrionaceae; 35% of the virulence-associated proteins h
12               Vibrio fischeri belongs to the Vibrionaceae, a large family of marine gamma-proteobacte
13 conserved among diverse genera of the family Vibrionaceae and encodes an origin binding protein.
14                Our results demonstrated that Vibrionaceae and Flavobacteriaceae abundances were stron
15 To gain insight into the frequency of HGT in Vibrionaceae and its possible impact on speciation, we a
16 aproteobacteria (Alteromonadaceae, SAR86 and Vibrionaceae) and shift in dominance from SAR11 to Rhodo
17 n above Vibrio fischeri (gamma-Protebacteria-Vibrionaceae) bacterial biofilms of either symbiotic or
18 icial symbionts, make up the majority of the Vibrionaceae, but none of these species has been similar
19 dings support the hypothesis that the second Vibrionaceae chromosome arose from an ancestral plasmid,
20                           All members of the Vibrionaceae harbour LuxO, a response regulator that int
21 sformation is prevalent among members of the Vibrionaceae, including the pathogen Vibrio cholerae.
22 ly 35,000 possible mutual interactions among Vibrionaceae isolates from the ocean, we show that genot
23                             Studies of other Vibrionaceae members highlight the general importance of
24 d the number of qrr genes in fully sequenced Vibrionaceae members.
25 hesive genotypic clusters of closely related Vibrionaceae, only an intermediate percentage of genotyp
26 cted sequence exhibits DNA homology to other Vibrionaceae phospholipases.
27 to several ecophysiologically differentiated Vibrionaceae populations adapted to different physical f
28 mong FadR homologues of the GntR family, the Vibrionaceae protein is unusual in that it contains a C-
29 gests the most recent common ancestor of all Vibrionaceae shared a single, ancestral qrr gene, which
30             Sequence comparisons reveal that Vibrionaceae species possessing only qrr1 do not have th
31 ial and temporal resource partitioning among Vibrionaceae strains coexisting in coastal bacterioplank
32        The discovery of 'super-integrons' in Vibrionaceae suggests a greater impact of this gene acqu
33 d Vibrio vulnificus, the only members of the Vibrionaceae that have had their genome sequences report
34      Despite being widely distributed in the Vibrionaceae, this is the first demonstration of a bona
35 ond to an additional ligand allows FadR from Vibrionaceae to function as a more efficient regulator.

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