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1 showed reduced binding (64 to 87% of that of piliated AAr176) to 16HBE14o(-) and ME180 cells, hifA an
2 transposon insertions in these ORFs were non-piliated and failed to express pilus-associated phenotyp
3  events predominated, which differed between piliated and non-piliated progeny.
4 l in situ structure of a T4bP machine in its piliated and non-piliated states.
5 ng of biofilm development differ between the piliated and non-piliated strains.
6                 T1P are phase variable (both piliated and nonpiliated bacteria exist in a clonal popu
7 D66c) were detected 4 h after infection with piliated and nonpiliated gonococci.
8 6 was induced equally by the interactions of piliated and nonpiliated meningococci, whereas lipopolys
9 pilus machine, or T4PM) in situ, in both the piliated and nonpiliated states, at a resolution of 3 to
10  optimized to each other, and that they give piliated bacteria significant advantages in rapidly chan
11 vors of RecA expression are enriched for non-piliated bacteria that carry large deletions of the pilE
12  pilus expression and independently of fully piliated bacteria.
13 des a protein found in the outer membrane of piliated bacteria; and cooB.
14  shown that pilT and pilU mutants, which are piliated but defective in twitching motility, display re
15                                              Piliated but not nonpiliated gonococci adhered to cells
16                                              Piliated, but not nonpiliated, N. gonorrhoeae strain F62
17  protein shown previously to localize to the piliated cell pole before and during pilus assembly, con
18 nly one pole that most likely identifies the piliated cell pole.
19                                 We show that piliated cells mostly contain a single pilus that is not
20 In addition, the phage were unable to infect piliated cells overexpressing MS2 coat protein, a resist
21  phase variation, reducing the proportion of piliated cells, reduced mannose binding 8-fold, and decr
22               The interaction between type 1 piliated E. coli and bladder epithelial cells leads to t
23                        Infection with type 1-piliated E. coli can trigger a number of host responses,
24 cultures compared to infection with a type 1 piliated E. coli K-12 strain.
25 sults demonstrate that the binding of type 1-piliated E. coli to vaginal epithelial cells correlates
26  uroepithelial cells are activated by type 1 piliated E. coli.
27 hat CooC is an outer membrane protein of CS1-piliated E. coli.
28    Acute UTIs are typically caused by type 1-piliated Escherichia coli and result in urothelial apopt
29 lls, and human tracheal explants with type 1-piliated Escherichia coli mediated a marked (25-50-fold)
30                          Adherence of type 1-piliated Escherichia coli to carbohydrate structures of
31 lex cell cycle involving sessile-stalked and piliated, flagellated swarmer cells.
32 zation approach can reduce interactions of a piliated form of this opportunistic pathogen with respir
33 sponse was limited to cultures infected with piliated gonococci and was more vigorous in the endocerv
34 ilus gene cluster had decreased adherence of piliated H. influenzae to mucins, and Fab fragments of a
35 ng NF-kappaB activity increased the level of piliated HB101-induced apoptosis to the level of apoptos
36                                              Piliated hemolytic Moraxella bovis is recognized as the
37 HifD and HifE proteins, respectively, of all piliated Hib and NTHI strains tested.
38 fD or HifE of strain Eagan also bound to all piliated Hib strains but did not bind to the piliated NT
39 d most of the mature protein reacted more to piliated Hib than to nonpiliated Hib or to a mutant cont
40                                          The piliated isolates formed either spreading/corroding or n
41                            Furthermore, such piliated L. lactis cells evoked a higher TNF-alpha respo
42                                              Piliated MS11Deltaopa cells formed dispersed microcoloni
43 quired for biofilm formation as evident by a piliated mutant of S. elongatus that develops biofilms.
44                     Intriguingly, one of the piliated mutants that does not exhibit spreading retains
45                                Attachment of piliated Neisseria gonorrhoeae or Neisseria meningitidis
46            Expression of the ChoP epitope on piliated neisseriae displayed phase variation, both link
47 pproximately 5000 sialylated or unsialylated piliated, non-opaque (P+Opa-, transparent) colony type g
48 piliated Hib strains but did not bind to the piliated NTHI strains.
49 was induced within 3 h of exposure to type 1 piliated NU14 and was dependent upon interactions mediat
50 s which were visually distinct from those of piliated Opa-expressing MS11 cells.
51 earrangements reported here are triggered by piliated, Opa- and Opc- strains and also by nonpiliated
52 ype of the inoculation strain to the P+Opa+ (piliated, opaque) phenotype 12-60 h before onset of dise
53 ildren whose nasopharynges were colonized by piliated organisms, the corresponding middle ear isolate
54                         This assay employs a piliated parental Gc variant with a recA allele whose pr
55                                              Piliated PilT mutants and a panel of pilus assembly muta
56 as observed to localize predominantly to the piliated pole.
57 analysis of piliated variants arising from a piliated progenitor.
58 quencing the pilE locus in randomly selected piliated progeny of both MS11 and FA1090 in recB and rec
59 ted, which differed between piliated and non-piliated progeny.
60  small percentage of pneumococci appeared as piliated, RrgA-expressing, DivIVA-negative single cocci,
61                            In peritrichously piliated species, it is unclear how multiple pili are co
62 armer cell with several polar pili and a non-piliated stalked cell.
63 re of a T4bP machine in its piliated and non-piliated states.
64  slow in vitro, it is rapid in vivo as a non-piliated strain lacking the other fim recombinases rapid
65   Using microarray analysis, we found that a piliated strain showed increased expression of the gene
66 s higher growth rate compared to that of the piliated strain.
67 sed protection against challenge by the four piliated strains that we have examined (PAK, PAO, KB7 an
68  CooD minor pilin (when overexpressed in CS1-piliated strains) was detected in periplasmic intermolec
69 elopment differ between the piliated and non-piliated strains.
70 in found exclusively in the periplasm of CS1-piliated strains.
71 n involving the irreversible transition from piliated to nonpiliated variants.
72 n involving the irreversible transition from piliated to nonpiliated variants.
73                     Here we show that type 1-piliated uropathogens can invade the superficial epithel
74 roviding the first comprehensive analysis of piliated variants arising from a piliated progenitor.
75                             On solid medium, piliated variants form small (S-phase), corroding coloni
76                             On solid medium, piliated variants form small (S-phase), corroding coloni
77 tory and nonendocarditis blood isolates were piliated, while the majority of joint fluid, bone, and e

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