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1  MR/P fimbriae but does not appear to be the fimbrial adhesin.
2  decreased stress and elevated expression of fimbrial adhesins.
3 tively encode P and type 1 receptor-specific fimbrial adhesins.
4                                              Fimbrial adhesins allow bacteria to interact with and at
5 date structure and function of this class of fimbrial adhesins and assess the feasibility of an adhes
6 niformly contained allele 41 of fimH (type 1 fimbrial adhesin) and a narrow range of alleles of gyrA
7                                          K88 fimbrial adhesins are filamentous surface appendages who
8 icularly rich in genes that encode potential fimbrial adhesins, autotransporters, iron-sequestration
9 ia the colonization factor antigen I (CFA/I) fimbrial adhesin CfaE.
10 o HEp-2 cells by virtue of a plasmid-encoded fimbrial adhesin designated aggregative adherence fimbri
11          Three antigenic variants of the K88 fimbrial adhesin exist in nature, K88ab, K88ac, and K88a
12  with a corresponding segment of the type 1C fimbrial adhesin FocH leads to a loss of the multivalent
13 ent discovery that allele III of papG (the P fimbrial adhesin gene) predominates among human cystitis
14 ructure was resolved based on fimH sequence (fimbrial adhesin gene: H subclone assignments), multiloc
15  host-associated nsSNPs for FimH, the type 1 fimbrial adhesin, highlights the role of key allelic res
16 itis-associated P fimbrial adhesin), sfaS (S fimbrial adhesin), hlyA (hemolysin), cnf1 (cytotoxic nec
17 brial structural subunit), papG allele II (P fimbrial adhesin), iha (putative adhesin siderophore), a
18                                   A range of fimbrial adhesins in ETEC strains determines host and ti
19 acterization of the fimH genes, encoding the fimbrial adhesins, indicated two allelic variants.
20 nic Escherichia coli expressing the K88 (F4) fimbrial adhesin (K88 ETEC) is a significant source of m
21 have centered on a subset of plasmid-encoded fimbrial adhesins known as colonization factors and heat
22                                              Fimbrial adhesins mediate the attachment of pathogenic E
23 lele III (which encodes variant III of the P-fimbrial adhesin molecule PapG).
24                    The Klebsiella pneumoniae fimbrial adhesin, MrkD, mediates adherence to the basola
25  fumC) but similar to that seen with another fimbrial adhesin of E. coli, papG-II, also implicated in
26 tudy, we identified a receptor for the K88ad fimbrial adhesin of Escherichia coli in neutral glycosph
27           FimH, the mannose-specific, type 1 fimbrial adhesin of Escherichia coli, acquires amino aci
28     Here, by using a common mannose-specific fimbrial adhesin of Escherichia coli, FimH, we demonstra
29                     The std operon encodes a fimbrial adhesin of Salmonella enterica serotype Typhimu
30 t not primary) structure to FimH, the type 1 fimbrial adhesin of uropathogenic E. coli, which shows s
31 MTGP-2) as receptors for the K88ab and K88ac fimbrial adhesins of Escherichia coli.
32     Recent studies show that the coupling of fimbrial adhesins of uropathogenic Escherichia coli and
33  it belongs) to genes that encode a putative fimbrial adhesin required for biofilm formation.
34  fimH, which encodes mannose-specific type 1 fimbrial adhesin, resulting in functionally distinct cop
35  prerequisite for invasion and that distinct fimbrial adhesins select different target cells for inva
36 luded papG allele III (cystitis-associated P fimbrial adhesin), sfaS (S fimbrial adhesin), hlyA (hemo
37                                      The non-fimbrial adhesin ShdA is a fibronectin binding protein r
38  of urinary tract infections (UTI), utilizes fimbrial adhesins to colonize the uroepithelium.
39 is of cystitis and to develop a FimH (type 1 fimbrial adhesin) vaccine, was assessed for extended vir
40  that AAF adhesins represent a new family of fimbrial adhesins which mediate aggregative adherence in

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