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1 and an internal fragment of an NRAMP gene in Burkholderia cepacia.
2 and in the use of a prolonged incubation for Burkholderia cepacia.
3 is and other species, including (cultivable) Burkholderia cepacia.
4 bors, such as Burkholderia thailandensis and Burkholderia cepacia.
5 olysis of anchovy oil with lipase PS-DI from Burkholderia cepacia.
6 oteobacteria including a clinical isolate of Burkholderia cepacia.
7 ise bacteria previously identified merely as Burkholderia cepacia.
13 ying a suspension of immobilized lipase from Burkholderia cepacia (Amano PS-IM) in a mixture of vinyl
14 ont Rhizobium NGR234 and the root-colonizing Burkholderia cepacia AMMD, conferred to Escherichia coli
15 cretion genes in the gram-negative bacterium Burkholderia cepacia, an important pulmonary pathogen in
16 MN(+) mice survived after being administered Burkholderia cepacia, an opportunistic pathogen in CGD p
17 ese reactive species in host defense against Burkholderia cepacia and Chromobacterium violaceum, orga
20 gative pathogens, including Yersinia pestis, Burkholderia cepacia, and Acinetobacter haemolyticus, sy
22 s of IS285 from Yersinia pestis, IS1356 from Burkholderia cepacia, and ISRm3 from Rhizobium meliloti.
23 late isolates of Pseudomonas aeruginosa and Burkholderia cepacia are associated with differences in
27 ueous Pb(II) sorbed at the interface between Burkholderia cepacia biofilms and hematite (alpha-Fe(2)O
28 during apoptosis induced by phagocytosis of Burkholderia cepacia, Borrelia hermsii, Listeria monocyt
29 spp., Ralstonia spp., Burkholderia gladioli, Burkholderia cepacia, Burkholderia thailandensis, and Ps
31 rbaspirillum species can be misidentified as Burkholderia cepacia by commercially available microbial
32 n the pathogenesis of respiratory disease in Burkholderia cepacia-colonized cystic fibrosis (CF) pati
33 ost described the use of selective media for Burkholderia cepacia complex (99%), Staphylococcus aureu
49 Antimicrobial susceptibility testing for the Burkholderia cepacia complex (BCC) is often used to dete
50 oacae, Stenotrophomonas maltophilia, and the Burkholderia cepacia complex (BCC) may be able to produc
52 cystic fibrosis (CF), airway infection with Burkholderia cepacia complex (Bcc) species or Burkholder
53 undred thirty-eight clinical isolates of the Burkholderia cepacia complex (Bcc) were identified using
55 terization of the opportunistic pathogens of Burkholderia cepacia complex (BCC), a group composed of
63 initive identification of the species in the Burkholderia cepacia complex by routine clinical microbi
66 fe threatening infection with species of the Burkholderia cepacia complex frequently occurs as a resu
67 or the rapid detection and identification of Burkholderia cepacia complex genomovars directly from sp
68 n >500 ug/L), and for a lung transplant 6.3 (Burkholderia cepacia complex infection for 1 y or less).
70 t pathogens that account for the majority of Burkholderia cepacia complex infections in cystic fibros
75 r relative levels of accuracy in identifying Burkholderia cepacia complex isolates recovered from cys
77 PCR primers targeting loci in the current Burkholderia cepacia complex multilocus sequence typing
78 Pseudomonas aeruginosa and members of the Burkholderia cepacia complex often coexist in both the s
80 thods is difficult, and differentiation from Burkholderia cepacia complex organisms may be especially
83 rosis (CF) patients including members of the Burkholderia cepacia complex that cause a high rate of m
84 ted from biofilms produced by species of the Burkholderia cepacia complex were shown to possess clust
87 ia cenocepacia is an important member of the Burkholderia cepacia complex, a group of closely related
88 s species and closely related species in the Burkholderia cepacia complex, accurate identification is
89 elective media designed for the isolation of Burkholderia cepacia complex, along with two media desig
91 epacia strain K56-2, a representative of the Burkholderia cepacia complex, is part of the epidemic an
92 ortunistic pathogens, such as members of the Burkholderia cepacia complex, likewise display elevated
93 LIs with a focus on clinical utility against Burkholderia cepacia complex, Stenotrophomonas maltophil
94 Gram-negative bacterium and a member of the Burkholderia cepacia complex, which is frequently associ
103 We investigated the utility of PCR to detect Burkholderia cepacia directly in sputum samples at two c
104 more active than other tetracyclines against Burkholderia cepacia, Escherichia coli, Serratia marcesc
105 on of the related toluene o-monooxygenase of Burkholderia cepacia G4 and a previously reported T4MO G
106 vity of toluene ortho-monooxygenase (TOM) of Burkholderia cepacia G4 for both chlorinated ethenes and
107 ion and toluene ortho-monooxygenase (TOM) of Burkholderia cepacia G4 hydroxylates at the ortho positi
109 alyzed a collection of 97 well-characterized Burkholderia cepacia genomovar III isolates to evaluate
114 model leading to complete protection against Burkholderia cepacia infection, and restored healthy don
124 egorize patients into panresistant (n = 27) (Burkholderia cepacia, n = 6, and Pseudomonas aeruginosa,
127 ied within a 27-kb region of DNA cloned from Burkholderia cepacia R34, a strain that grows using 2,4-
128 oblematic, and analysis of isolates from the Burkholderia cepacia Research Laboratory and Repository
129 ng a panel of 102 isolates obtained from the Burkholderia cepacia Research Laboratory and Repository.
130 ferredoxins (the Thermus Rieske protein, the Burkholderia cepacia Rieske-type biphenyl dioxygenase fe
131 veral clinical and environmental isolates of Burkholderia cepacia secreted ATP-utilizing enzymes to t
132 m of this study was to compare RGM medium to Burkholderia cepacia selective agar (BCSA) and a standar
133 ients with CF by extending incubation of the Burkholderia cepacia selective agar (BCSA) from 5 to 14
137 dation of tryptophan through anthranilate by Burkholderia cepacia, several plasposon mutations were c
138 ung disease including Staphylococcal aureus, Burkholderia cepacia, Stenotrophomonas maltophilia, Achr
139 led tobramycin did not increase isolation of Burkholderia cepacia, Stenotrophomonas maltophilia, or A
140 y reviewing isolates initially identified as Burkholderia cepacia susceptible to all antibiotics test
143 rgillus fumigatus, Staphylococcus aureus, or Burkholderia cepacia were compared in wild-type, X-CGD m
145 incubated with P. aeruginosa strain PAK and Burkholderia cepacia, while little activation was observ