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1 omitans and the porcine respiratory pathogen Actinobacillus pleuropneumoniae.
2 ting acyl-transferase (TAAT) from pathogenic Actinobacillus pleuropneumoniae.
3 pendent growth of Haemophilus influenzae and Actinobacillus pleuropneumoniae.
4 day infection with Salmonella typhimurium or 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 steurellaceae indicates that M. haemolytica, Actinobacillus pleuropneumoniae, and Haemophilus ducreyi
11 genic Neisseriaceae, Haemophilus influenzae, Actinobacillus pleuropneumoniae, and M. catarrhalis.
14 Haemophilus parasuis, Pasteurella multocida, Actinobacillus pleuropneumoniae, Bordetella bronchisepti
28 s, which differentiates serovars 3, 6, and 8 Actinobacillus pleuropneumoniae isolates, is described.
30 directly quantify glycopeptide formation by Actinobacillus pleuropneumoniae NGT and determine its su
32 t a vaccine prepared from outer membranes of Actinobacillus pleuropneumoniae serotype 5 can elicit pr
34 ee extracts isolated from colony biofilms of Actinobacillus pleuropneumoniae serotype 5 were found to
36 tiplex PCR assays were developed to identify Actinobacillus pleuropneumoniae serotypes 1, 2, and 8.
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