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5 is subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in blood samples from infected
15 c assay is a highly discriminatory assay for B. canis genotyping, and can serve as a useful molecular
17 hesion process, the structure of Bc28.1 from B. canis appears unrelated to the previously published s
18 ferentiate Babesia gibsoni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. ca
19 nd discriminate B. gibsoni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. ca
20 rRNA genes from B. gibsoni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. rossi, and B. ca
22 e, marine mammal isolates (no species name), B. canis, and B. suis, confirmed that all but the latter
24 es-Brucella abortus, B. melitensis, B. suis, B. canis, and B. ovis-using whole-genome comparisons.
25 non-endemic countries in Europe suggest that B. canis infection should be considered in European pati
28 ni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in
29 ni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in
30 ni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. rossi, and B. canis subsp. canis but not