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1 omitans and the porcine respiratory pathogen Actinobacillus pleuropneumoniae.
2 pendent growth of Haemophilus influenzae and Actinobacillus pleuropneumoniae.
3 day infection with Salmonella typhimurium or Actinobacillus pleuropneumoniae.
4 ting acyl-transferase (TAAT) from pathogenic Actinobacillus pleuropneumoniae.
6 previous studies demonstrated that Adh from Actinobacillus pleuropneumoniae (A. pleuropneumoniae) is
7 -ray crystal structure of the Cu,Zn SOD from Actinobacillus pleuropneumoniae, a major porcine pathoge
8 of its ability to confer NAD independence on Actinobacillus pleuropneumoniae and H. influenzae, has b
9 ting of two fastidious veterinary pathogens, Actinobacillus pleuropneumoniae and Haemophilus somnus,
10 nimals intranasally co-infected (n = 7) with Actinobacillus pleuropneumoniae and Pasteurella multocid
11 steurellaceae indicates that M. haemolytica, Actinobacillus pleuropneumoniae, and Haemophilus ducreyi
12 genic Neisseriaceae, Haemophilus influenzae, Actinobacillus pleuropneumoniae, and M. catarrhalis.
16 Haemophilus parasuis, Pasteurella multocida, Actinobacillus pleuropneumoniae, Bordetella bronchisepti
23 system, we introduced the P5PAB operon from Actinobacillus pleuropneumoniae into an Escherichia coli
31 s, which differentiates serovars 3, 6, and 8 Actinobacillus pleuropneumoniae isolates, is described.
33 sequence optimized for glycosylation by the Actinobacillus pleuropneumoniae N-glycosyltransferase (N
34 directly quantify glycopeptide formation by Actinobacillus pleuropneumoniae NGT and determine its su
36 t a vaccine prepared from outer membranes of Actinobacillus pleuropneumoniae serotype 5 can elicit pr
38 ee extracts isolated from colony biofilms of Actinobacillus pleuropneumoniae serotype 5 were found to
40 tiplex PCR assays were developed to identify Actinobacillus pleuropneumoniae serotypes 1, 2, and 8.