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1 acteria including Haemophilus influenzae and Pasteurella multocida.
2 Haemophilus spp., Neisseria gonorrhoeae, and Pasteurella multocida.
3 5 from Haemophilus influenzae and Oma87 from Pasteurella multocida.
4 ia meningitidis, Haemophilus influenzae, and Pasteurella multocida.
5 nia pestis and the human and animal pathogen Pasteurella multocida.
6 tion of the pig's upper respiratory tract by Pasteurella multocida.
7 ely related species, Actinobacillus suis and Pasteurella multocida.
8 ilus influenzae, Neisseria meningitidis, and Pasteurella multocida.
10 l pathogens, including Haemophilus parasuis, Pasteurella multocida, Actinobacillus pleuropneumoniae,
11 c nonfastidious species were as follows: for Pasteurella multocida and staphylococci tested on Muelle
12 ents were conducted with a zoonotic pathogen Pasteurella multocida and the fluoroquinolone enrofloxac
13 Synechocystis sp., Deinococcus radiodurans, Pasteurella multocida, and Actinobacillus actinomycetemc
15 zae, Proteus mirabilis, Vibrio fischeri, and Pasteurella multocida are all cleaved by RNase III as pr
17 ly potent against the Gram-negative pathogen Pasteurella multocida both in vitro and in a mouse infec
18 eir potencies against the bacterial pathogen Pasteurella multocida both in vitro and in mouse infecti
22 oop sequences from Enterococcus faecalis and Pasteurella multocida gamma-GCS-GS, isoforms that are in
25 gmented genomic DNA from the animal pathogen Pasteurella multocida has identified a gene encoding a p
26 P]UDP products made by the purified class II Pasteurella multocida HAS were not released by adding un
31 the literature, of ocular infections due to Pasteurella multocida include: endophtalmitis, keratitis
39 e rapid, accurate method to detect toxigenic Pasteurella multocida is needed for improved clinical di
43 bacteria, including Haemophilus influenzae, Pasteurella multocida, Neisseria gonorrhoeae, Neisseria
44 se of rapidly evolving conjunctivitis due to Pasteurella multocida, occurring after direct inoculatio
45 enes encoding Haemophilus influenzae D15 and Pasteurella multocida Oma87 protective outer membrane an
47 an synthases from the Gram-negative bacteria Pasteurella multocida, PmHS1 and PmHS2, were efficiently
48 The intracellularly acting protein toxin of Pasteurella multocida (PMT) causes numerous effects in c
49 hase, PmCS, from the Gram-negative bacterium Pasteurella multocida polymerize the glycosaminoglycan (
51 isolates and 4 attenuated vaccine strains of Pasteurella multocida recovered from multiple avian spec
53 Neuraminidases produced by 16 strains of Pasteurella multocida (serotypes 1 to 16) were character
55 -ray crystal structures of a multifunctional Pasteurella multocida sialyltransferase (Delta24PmST1) w
56 he structures of a truncated multifunctional Pasteurella multocida sialyltransferase (Delta24PmST1),
58 ntical for P. multocida subsp. multocida and Pasteurella multocida subsp. gallicida but differs from
59 e more than 17 species of Pasteurella known, Pasteurella multocida subsp. multocida and Pasteurella m
61 , Pasteurella multocida subsp. multocida and Pasteurella multocida subsp. septica are among the most
62 mediates adhesion of serogroup A strains of Pasteurella multocida to elicited turkey air sac macroph
63 as assessed by exposing broth suspensions of Pasteurella multocida to perflubron for various times.
64 agonists and phospholipase C is activated by Pasteurella multocida toxin (a G(q) alpha-subunit agonis
70 atalytic and receptor-binding domains of the Pasteurella multocida toxin (PMT) were investigated.
71 not obvious and is explored with recombinant Pasteurella multocida toxin (rPMT, a Galpha(q) agonist).
72 ion on its own, it potentiated the effect of Pasteurella multocida toxin by 2-fold and ionomycin by 3
73 quires protein kinase C and MEK activity) by Pasteurella multocida toxin, a Galpha(q) agonist that pr
74 er these conditions, treatment of cells with Pasteurella multocida toxin, a selective inhibitor of Ga
75 channel current inhibition was diminished by Pasteurella multocida toxin, mimicked by constitutively
79 des tryptophanase; as well as a homologue of Pasteurella multocida tsaA, which encodes an alkyl perox
80 in a single polypeptide as was found for the Pasteurella multocida Type A PmHAS, the hyaluronan synth
85 The extracellular polysaccharide capsules of Pasteurella multocida types A, D, and F are composed of
86 ue of the NeuA C-terminal domain (Pm1710) in Pasteurella multocida was also shown to be an esterase,
88 ytica and three matched pairs of isolates of Pasteurella multocida were isolated by using a nasal swa
89 The major outer membrane protein (OmpH) of Pasteurella multocida X-73 was purified by selective ext
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