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1 e expressed in propagating populations of M. fermentans.
2 ritis, only one of whom was infected with M. fermentans.
3 gdorferi, Treponema pallidum, and Mycoplasma fermentans.
4 against part of the two 16S rRNA genes of M. fermentans.
5 activating lipopeptide, on the surface of M. fermentans.
6 rees C, the optimal growth temperature of A. fermentans.
7  the anaerobic gut bacterium Acidaminococcus fermentans.
8                                    Pelosinus fermentans 16S rRNA gene sequences have been reported fr
9 kb Ureaplasma urealyticum, 1.2-Mb Mycoplasma fermentans, 2.3-Mb Streptococcus pneumoniae, and 4.6-Mb
10 riation is shown here to occur in Mycoplasma fermentans, a chronic human infectious agent and possibl
11 gdorferi, Treponema pallidum, and Mycoplasma fermentans activated cells heterologously expressing TLR
12 1 control subjects were also positive for M. fermentans and M. genitalium by PCR.
13 nated by species closely related to Geothrix fermentans, Azospira restricta and Cellulomonas oligotro
14 from the anaerobic bacterium Acidaminococcus fermentans bifurcates the electrons of NADH, sending one
15 from the anaerobic bacterium Acidaminococcus fermentans bifurcates the electrons of NADH, sending one
16 tans, binds human HeLa cells and inhibits M. fermentans binding to these cells, in both a quantitativ
17 undant P29 surface lipoprotein of Mycoplasma fermentans, binds human HeLa cells and inhibits M. ferme
18 re with the incognitus and PG18 strains of M fermentans, but surprisingly not with some other strains
19 ta-FAD in each subunit) from Acidaminococcus fermentans catalyze electron bifurcation which reduces l
20 CoA dehydrogenase (Bcd) from Acidaminococcus fermentans catalyze the endergonic reduction of ferredox
21 kunkelii, Mycoplasma pulmonis and Mycoplasma fermentans cluster together and are more similar to TraE
22 e MALP-404 surface lipoprotein of Mycoplasma fermentans comprises a membrane-anchored N-terminal lipi
23                  Membrane preparations of A. fermentans contain a highly active ferredoxin/flavodoxin
24                              Acidaminococcus fermentans degrades glutamate via the hydroxyglutarate p
25  in our laboratory to study the effect of M. fermentans DnaK expression in vivo.
26 regard, we previously showed that Mycoplasma fermentans DnaK, an HSP70 chaperone protein, hampers the
27         We previously showed that Mycoplasma fermentans DnaK, an HSP70 family chaperone protein, hamp
28 ome sequence reported here suggested that D. fermentans employs membrane-bound hydrogenases and novel
29                      In eight isolates of M. fermentans examined, malp occurred upstream of an operon
30 onspicua produced white colonies; the Pichia fermentans group and C. krusei did not.
31                                   Mycoplasma fermentans had previously been isolated from patients wi
32                        Since 1970 Mycoplasma fermentans has been suspected of being associated with r
33 ermentans incognitus and other strains of M. fermentans have been associated with rheumatoid arthriti
34                                           M. fermentans incognitus alone induced an incomplete arrest
35                                           M. fermentans incognitus and other strains of M. fermentans
36                    While cell extracts of M. fermentans incognitus can induce changes in murine and h
37                                   Mycoplasma fermentans incognitus has been isolated from human tissu
38  inflammation, we examined the effects of M. fermentans incognitus on surface markers and functions o
39                                           M. fermentans incognitus only minimally affected changes in
40 posed to phorbol myristate acetate (PMA), M. fermentans incognitus, or both.
41            We examined effects of Mycoplasma fermentans infection on the continuing survival and immo
42 e the movement of a previously identified M. fermentans insertion sequence (IS)-like element.
43  A new insertion sequence (IS) of Mycoplasma fermentans is described.
44 t of succinic, oxalic and acetic acids by P. fermentans is reported for the first time in this work,
45                  The malp gene of Mycoplasma fermentans is shown to occur in single copy but to encod
46                              Desulfurococcus fermentans is the first known cellulolytic archaeon.
47 ed sites of chromosomal integration among M. fermentans isolates suggest a role for ICEF in promoting
48                                    Pelosinus fermentans JBW45 is an anaerobic, lactate-fermenting bac
49 y dramatically in ratio among isolates of M. fermentans occur on the mycoplasma surface: (i) MALP-404
50               In comparison, live Mycoplasma fermentans or M. penetrans infection for 4 to 5 weeks in
51  <5 copies of Mycoplasma hominis, Mycoplasma fermentans, or a molecular mimic control in synovial flu
52  is present in four copies in the Mycoplasma fermentans PG18 chromosome, accounting for approximately
53 approximately 16 kb genome of the Mycoplasma fermentans phiMFV1 prophage is described, and its mobili
54  we show that recombinant flavodoxin from A. fermentans produced in Escherichia coli can replace ferr
55 nted in a series of clonal derivatives of M. fermentans propagated in culture.
56 ed ICEF (integrative conjugal elements of M. fermentans), resemble conjugative, self-transmissible in
57 lipid-modified surface protein of Mycoplasma fermentans, reveal phase variation of surface epitopes o
58                                In various M. fermentans strains, phiMFV1 was either absent or integra
59 re present in the genomes of at least two M. fermentans strains.
60 ween the expression of a specific Mycoplasma fermentans surface antigen (Pra, proteinase-resistant an
61     We present the genome sequence of the P. fermentans type strain R7 (DSM 17108) and genome sequenc
62                                           M. fermentans was detected in 23 of 26 (88%) rheumatoid art
63              In the current study Mycoplasma fermentans was found to adhere to the glass surface form
64                       The distribution of M. fermentans was studied in the synovial fluid of patients
65                                           M. fermentans was therefore found to be a variable and very
66 t and the cellulolytic bacterium Actinotalea fermentans, we are able to achieve methyl halide product
67 rtance (Mycoplasma pneumoniae and Mycoplasma fermentans) were examined using a novel approach involvi
68 CoA dehydrogenase (BcdAf) of Acidaminococcus fermentans, which couple the exergonic reduction of crot
69 e 5.8S internal transcribed spacer as Pichia fermentans, Wickerhamomyces anomalus and Candida oleophi
70 ts suggest that the direct interaction of M. fermentans with a ligand on the HeLa cell surface involv