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1                    Reverse transcriptions of alpha antigen (85B protein) mRNA and 16S rRNA were perfo
2  system for the detection of M. tuberculosis alpha-antigen (85B protein) mRNA and to demonstrate the
3 els of 16S rRNA, fbpB mRNA (encoding the 85B alpha antigen), and aroB mRNA (encoding dehydroquinate s
4 ese epitopes are uniquely present within the alpha antigen as expressed from the bca gene.
5  cells were negative for CD34, CD14, and CD8 alpha antigens but expressed low levels of the myeloid m
6 lected on or before day 14 were positive for alpha-antigen DNA.
7             In contrast to previous studies, alpha antigen expression does not appear to play a role
8 sly cloned, sequenced, and characterized the alpha antigen gene, bca, and showed that the alpha C pro
9           To evaluate expression of the CD79 alpha antigen in acute myeloid leukemia (AML), we studie
10 r allowed a simple and fast detection of TNF alpha antigen in human serum and satisfied recoveries (9
11 monstrated cytoplasmic staining for the CD79 alpha antigen, including one M1, nine M3, and one M5 AML
12  first 24 h, suggesting that the role of the alpha antigen is important in the initial stages of the
13          Native 30-kD antigen, also known as alpha antigen, is a fibronectin-binding protein that is
14     Levels of mRNA encoding the 85B protein (alpha-antigen), IS6110 DNA, and 16S rRNA were compared i
15 , we measured levels of M. tuberculosis 85B (alpha antigen) messenger RNA (mRNA), 16S ribosomal RNA (
16 or to the start of therapy were positive for alpha-antigen mRNA, compared with 1 of 8 (13%), 2 of 8 (
17          Stimulation with PPD and the 30-kDa alpha antigen of MTB (30-kDa antigen) induced greater se
18  oxidation of catechol, determination of TNF-alpha antigen was based on its obstruction to the electr
19        A fivefold increase in levels of IL-1 alpha antigen was measured in cell lysate samples by enz
20 tion between anti-TNF alpha antibody and TNF alpha antigen were monitored by cyclic voltammetry (CV)

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