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1 ens (2 with Ehrlichia chaffeensis and 1 with Mycoplasma pneumoniae).
2 of these differences by analysing RuvA from Mycoplasma pneumoniae.
3 rat and human SP-D with the human pathogen, Mycoplasma pneumoniae.
4 m 8% for Methanococcus jannaschii to 37% for Mycoplasma pneumoniae.
5 tococcus pneumoniae, Legionella species, and Mycoplasma pneumoniae.
6 ld-type copies, including the ruvA gene from Mycoplasma pneumoniae.
7 is (MLVA) method for the molecular typing of Mycoplasma pneumoniae.
8 oplasma genitalium and its closest relative, Mycoplasma pneumoniae.
9 ted B/C proteins (P90/P40), respectively, in Mycoplasma pneumoniae.
10 al organelle of the cell wall-less bacterium Mycoplasma pneumoniae.
13 micdadei, 9 and 80 CFU/ml, respectively; for Mycoplasma pneumoniae, 5 CFU/ml; and for Chlamydia (Chla
15 e increased inflammatory response induced by Mycoplasma pneumoniae, a pathogen known to exacerbate as
16 ccus pneumoniae, Haemophilus influenzae, and Mycoplasma pneumoniae accounting for most identified bac
20 ypical bacteria Chlamydophila pneumoniae and Mycoplasma pneumoniae and asthma pathogenesis; however,
21 urine pneumococcal and legionella antigens, Mycoplasma pneumoniae and Chlamydia pneumoniae antibodie
23 these processes in the pathogenic bacterium Mycoplasma pneumoniae and its close relatives have also
24 genes encoding the P30 adhesin (one UGA) of Mycoplasma pneumoniae and methionine sulfoxide reductase
28 mnose was detected in the d configuration in Mycoplasma pneumoniae and Mycoplasma pulmonis, and in bo
30 sciscella tularensis, Ehrlichia chaffeensis, Mycoplasma pneumoniae, and Escherichia coli, although ot
32 sthma inception, while Chlamydia pneumoniae, Mycoplasma pneumoniae, and latent adenovirus infections
33 the cytadherence-associated protein P65 from Mycoplasma pneumoniae, and MGA_0928, the M. gallisepticu
34 species representing the Mycoplasma hominis, Mycoplasma pneumoniae, and Spiroplasma phylogenetic clus
37 n technology, was used to initially identify Mycoplasma pneumoniae as the causative agent in this out
39 he smallest and simplest of all known cells, Mycoplasma pneumoniae builds a surprisingly large and co
44 espiratory syncytial virus A (RSV A), RSV B, Mycoplasma pneumoniae, Chlamydophila pneumoniae, Legione
45 as Bordetella pertussis pertussis toxin and Mycoplasma pneumoniae community-acquired respiratory dis
50 surface protein P65 is a constituent of the Mycoplasma pneumoniae cytoskeleton and is present at red
52 e (82%) predictive values when compared with Mycoplasma pneumoniae enzyme-linked immunosorbent assay.
59 mucosal pathogens, Mycoplasma genitalium and Mycoplasma pneumoniae, has helped define the essential f
61 tes known, and yet several species including Mycoplasma pneumoniae have a remarkably complex cellular
62 preceding respiratory tract infections with Mycoplasma pneumoniae have been reported in some cases,
63 rom patients involved in a large outbreak of Mycoplasma pneumoniae in a closed religious community in
65 ectrum of neurologic disease attributable to Mycoplasma pneumoniae in children is incompletely unders
68 incidence of atypical bacteria LRIs (notably Mycoplasma pneumoniae) in children is now recognized.
69 ed the effects of different timing of airway Mycoplasma pneumoniae infection on bronchial hyperrespon
70 onic eosinophilic pneumonia complicated with Mycoplasma pneumoniae infection was diagnosed on the bas
71 To investigate the pathogenesis of acute Mycoplasma pneumoniae infection, BALB/c mice were anesth
74 ting human herpes virus (HHV1-HHV7), HEV, or Mycoplasma pneumoniae infections using throat swab virus
75 lung inflammatory responses to bacteria (eg, Mycoplasma pneumoniae) involved in lung disease exacerba
76 iratory distress syndrome (CARDS) toxin from Mycoplasma pneumoniae is a 591-amino-acid virulence fact
78 e of the cell wall-less pathogenic bacterium Mycoplasma pneumoniae is a complex structure involved in
101 nducting airways of humans by the prokaryote Mycoplasma pneumoniae is mediated by a differentiated te
106 licobacter pylori, Methanococcus jannaschii, Mycoplasma pneumoniae, M. genitalium, and Synechocystis
107 t S. pneumoniae, or Chlamydia pneumoniae and Mycoplasma pneumoniae may facilitate the clinical manage
113 d recognition and degradation of an extended Mycoplasma pneumoniae (MP) tmRNA tag by the MP-Lon prote
115 atory infections, such as atypical bacterium Mycoplasma pneumoniae (Mp), have been proposed to worsen
118 athogens Staphylococcus aureus (SaEf-Tu) and Mycoplasma pneumoniae (MpnEf-Tu), and the porcine pathog
119 neous, hemadsorption-negative (HA-) class II Mycoplasma pneumoniae mutants that displayed P30 adhesin
120 mophilus influenzae, Neisseria meningitidis, Mycoplasma pneumoniae, Mycobacterium tuberculosis, and B
121 l of antimicrobial susceptibility testing of Mycoplasma pneumoniae, Mycoplasma hominis, and Ureaplasm
123 ned the structure of full length HPrK/P from Mycoplasma pneumoniae (PD8 ID, 1KNX) to 2.5A resolution.
125 no recommended epidemic-control measures for Mycoplasma pneumoniae pneumonia outbreaks in closed comm
131 the bacterial species Mycoplasma genitalium, Mycoplasma pneumoniae, Shewanella putrefaciens, Synechoc
133 emophilus influenzae, Mycoplasma genitalium, Mycoplasma pneumoniae, Synechocystis sp. strain PCC6803,
134 ediatric patient secondary to infection with Mycoplasma pneumoniae that progressed to cardiac tampona
136 teins required for adherence of the pathogen Mycoplasma pneumoniae to host respiratory epithelial cel
137 six bacteria that have varied genome sizes (Mycoplasma pneumoniae, Treponema pallidum, Helicobacter
138 The presence of Chlamydophila pneumoniae or Mycoplasma pneumoniae was ascertained by serologic analy
140 trongly conserved mycoplasmal 16S RNA genes, Mycoplasma pneumoniae was found in the synovial fluid of
144 herichia coli, Streptococcus pneumoniae, and Mycoplasma pneumoniae, which exemplify gram-negative, gr
145 ficant sequence homology to the ORF6 gene of Mycoplasma pneumoniae, which has been shown to play an a
146 identified two surface proteins of virulent Mycoplasma pneumoniae with molecular masses of 45 and 30
147 ly become available for Escherichia coli and Mycoplasma pneumoniae, yielding 443 and 116 heteromultim
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