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1 nd temporary suppression of both Clostridium coccoides and Clostridium leptum group organisms.
2 tant show a striking morphology of irregular coccoids and aberrant DNA replication.
3  how cellular clusters of unexpectedly large coccoids and tubular sheath-like envelopes were trapped
4 ganized biofilm-like community consisting of coccoid bacteria that ultimately filled most of the cyto
5                                  In most non-coccoid bacteria, this shape is also determined by an in
6                                Strain 195, a coccoid bacterium that dechlorinates tetrachloroethene t
7 to as Bacteroidetes), Clostridium leptum, C. coccoides, bifidobacteria, Escherichia coli and Archaea
8        Clone libraries targeting Clostridium coccoides (C. coccoides) in sewage samples demonstrated
9 , the submucosal microbiota was dominated by coccoid cells.
10 rized by increased proportion of Clostridium coccoides (cluster XIVa), C coccoides-Eubacterium rectal
11 th SS and HC (P = 0.006) and higher fecal C. coccoides compared to those with SS (P = 0.04).
12 ion resulted in a revised growth model where coccoid cyanobacteria predominate in mat communities for
13 ommunities develop, which include endolithic coccoid cyanobacteria.
14                         Thus, in common with coccoids, Drosophila is capable of generating an imprint
15 n of Clostridium coccoides (cluster XIVa), C coccoides-Eubacterium rectale (cluster XIVab), Bacteroid
16 es uniformis, Eggerthella lenta, and Blautia coccoides-Eubacterium rectale groups (P < 0.05).
17  against Bacteroides, Prevotella and Blautia coccoides-Eubacterium rectale.
18                        Here we show that the coccoid form of H. pylori, in contrast to the spiral for
19 environment transforms into a nonculturable, coccoid form, which frequently results in the failure to
20 ake and a morphological shift from spiral to coccoid form.
21 iral form to the nonreplicating, but viable, coccoid form.
22  The organism has the propensity to become a coccoid form.
23 nd a nonculturable, but viable, metabolizing coccoid form.
24 .05) and in an increase in the proportion of coccoid forms (P <0.0001) relative to baseline.
25        Because only spiral organisms-and not coccoid forms-are capable of inducing interleukin-8 secr
26 so adopt straight rod, elongated helical and coccoid forms.
27  the planktic cyanobacterium, Microcystis, a coccoid genus that at the present-day commonly forms blo
28 otags encompassed the previously reported C. coccoides group.
29                                              Coccoid H. pylori, which are thought to be terminally di
30 ibraries targeting Clostridium coccoides (C. coccoides) in sewage samples demonstrated that Lachnospi
31              Strain SL100 is a gram-positive coccoid isolate prototype with an adhesin specific for g
32                                        These coccoids modify the sediment, forming thicker lithified
33 demonstrate here that iron depletion induces coccoid morphology in strains lacking cagA.
34 at the role of this endopeptidase in forming coccoid morphology may be critical for pathogenesis.
35 nd undergoes a premature transformation to a coccoid morphology.
36 d the normal transition to a densely packed, coccoid morphology.
37 res from which the poles disappear, yielding coccoid or lemon-shaped forms.
38 dult human gut also known as the Clostridium coccoides or Eubacterium rectale group, contains species
39 s zoonotic disease caused by a Gram-negative coccoid rod bacterium, Francisella tularensis.
40 ere, in some species, most notably among the coccoids (scale insects and allies), the differential ma
41  strains treated with CBR-4830 transition to coccoid shape, consistent with MreB inhibition or deplet
42 , we hypothesise that most major lineages of coccoids shifted from gymnosperms onto angiosperms when
43 aled endocarditis with small silver positive coccoid structures in endothelial cells.
44                         The difference in C. coccoides was no longer significant after adjusting for

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