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1 larridgeiae and more distantly related to B. bacilliformis.
2 ot result from the recent introduction of B. bacilliformis.
3 on with the alpha-proteobacterium Bartonella bacilliformis.
4 ) of the cell and is actively secreted by B. bacilliformis.
5  a role for ialB as a virulence factor in B. bacilliformis.
6  date that characterizes a lipoprotein of B. bacilliformis.
7 onella henselae, Bartonella quintana, and B. bacilliformis.
8 onstrated previous infection with Bartonella bacilliformis.
9  suis, Mycoplasma genitalium, and Bartonella bacilliformis.
10 e, a bacterium that is closely related to B. bacilliformis.
11 ction with Leishmania species and Bartonella bacilliformis.
12              The groESL operon of Bartonella bacilliformis, a facultative intracellular, Gram-negativ
13                                   Bartonella bacilliformis, a useful model organism for the genus, ha
14    Infection of cultured endothelium with B. bacilliformis also resulted in induction of angiopoetin-
15 but phylogenetically distant from Bartonella bacilliformis and considerably divergent from other know
16                       Distinction between N. bacilliformis and N. elongata can be made confidently by
17 ) test for the detection of antibodies to B. bacilliformis and then tested its performance as an aid
18 tient, who was inapparently infected with B. bacilliformis and who presumably acquired infection in a
19  syndrome caused by the bacterium Bartonella bacilliformis, and is characterized by the development o
20  principal vectors of Leishmania, Bartonella bacilliformis, and some arboviruses.
21 ect humans, henselae, quintana, elizabethae, bacilliformis, and vinsonii.
22     The IFA is 82% sensitive in detecting B. bacilliformis antibodies in acute-phase blood samples of
23 ly uncharacterized resolvase from Bartonella bacilliformis ("Bart").
24  Our findings suggest that infection with B. bacilliformis causes a broad spectrum of disease that is
25                                   Bartonella bacilliformis causes bartonellosis, a potentially life-t
26 and heterologous expression of the Neisseria bacilliformis class III RNR and show that it can catalyz
27 s to offer a well-supported assessment of B. bacilliformis diversity, and the genotypic differences i
28  that an ftsZ gene similar in size to the B. bacilliformis gene is present in Bartonella henselae, a
29          Deduced amino acid sequences for B. bacilliformis GroEL and GroES revealed a high degree of
30                                   Bartonella bacilliformis has caused debilitating illness since pre-
31 ), showed significant homology to Bartonella bacilliformis IalA (invasion associated locus).
32 e for IalB in erythrocyte parasitism, the B. bacilliformis ialB gene was disrupted by insertional mut
33 loped and used to confirm the presence of B. bacilliformis in the biopsied skin lesions.
34 family member were the best predictors of B. bacilliformis infection.
35                       Recent epidemics of B. bacilliformis infections associated with atypical sympto
36                 To further localize IalB, B. bacilliformis inner and outer membranes were fractionate
37 ovided to show that the 43-kDa antigen of B. bacilliformis is a lipoprotein and that it is likely to
38     Recombinant IalA protein from Bartonella bacilliformis is a monomeric adenosine 5'-tetraphospho-5
39  the test is 89% in an area of Peru where B. bacilliformis is endemic and where the point prevalence
40                                           B. bacilliformis is endemic in Peru and Ecuador, where it c
41 e region of Caraz, Ancash, in Peru, where B. bacilliformis is endemic.
42              The causative agent, Bartonella bacilliformis, is endemic in specific regions of Peru an
43 relationships and genomic diversity of 18 B. bacilliformis isolates (10 isolates from a region where
44  pattern were most similar to a subset of B. bacilliformis isolates from the region of Caraz, Ancash,
45 strongly to two out of the three Peruvian B. bacilliformis isolates tested, and EC-01 antigen reacted
46                 The immunogenicity of the B. bacilliformis LppB homologue was demonstrated by Western
47     This study suggests that the range of B. bacilliformis may be expanding from areas of endemicity
48 ic diversity among 26 isolates of Bartonella bacilliformis obtained from different areas of Peru, and
49 degree of amino acid identity between the B. bacilliformis protein (FtsZ[Bb]) and the other FtsZ prot
50  jejuni, Helicobacter pylori, and Bartonella bacilliformis, require flagellar motility to efficiently
51 enus Neisseria, for which the name Neisseria bacilliformis sp. nov. is proposed.
52                                         A B. bacilliformis strain containing the intact groES-groEL o
53 e results of this study show that Bartonella bacilliformis, the agent of Oroya fever and verruga peru
54 a from an organism that resembled Bartonella bacilliformis, the causative agent of Oroya fever, which
55 asion of human red blood cells by Bartonella bacilliformis, the causative agent of several diseases,
56              A genomic library of Bartonella bacilliformis was constructed and screened with human an
57                                   Bartonella bacilliformis was continuously internalized into human e
58 iserum specific for the LppB homologue of B. bacilliformis was generated.
59 sing an immunoreactive antigen of Bartonella bacilliformis was isolated by screening a genomic DNA li
60 ed infection in a region of Ecuador where B. bacilliformis was not thought to be endemic.
61 ed locus A and B genes (ialAB) of Bartonella bacilliformis were previously shown to confer an erythro
62 dothelial cells undergoing infection with B. bacilliformis, with maximal activation and translocation