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1 titution experiments with proteins from both M. capricolum and E. coli showed that EI(DeltaHD) can do
5 Gram-negative glycerol kinase activity, the M. capricolum EIIA has no effect on the homologous glyce
10 e information and its transplantation into a M. capricolum recipient cell to create new M. mycoides c
14 o specific peptide determinants of predicted M. capricolum subsp. capricolum gene products, and (iii)
16 the mycoides cluster, including a strain of M. capricolum subsp. capricolum identical to that found
17 A to vmcF) expressing distinct Vmc (variable M. capricolum subsp. capricolum) lipoproteins is demonst
18 lysis of the membrane-associated proteome of M. capricolum subsp. capricolum, a novel set of six gene
19 n a latex agglutination test (LAT), detected M. capricolum subsp. capripneumoniae antigen in the seru
20 tinated strongly in the presence of purified M. capricolum subsp. capripneumoniae capsular polysaccha
21 icity of the LAT exactly mirrored that of an M. capricolum subsp. capripneumoniae CPS-specific monocl
23 using genomic DNA and bacterial culture from M. capricolum subsp. capripneumoniae strain ILRI181, whi
24 he assay using a specific target sequence in M. capricolum subsp. capripneumoniae, as found in the ge
25 ed agglutinating activity in the presence of M. capricolum subsp. capripneumoniae, strongly suggestin
27 h approximately 50% alpha-helix content from M. capricolum were used to further elucidate the nature
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