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1 stases using barcodes specific to each shRNA transductant.
2 ating genetic element and form an "abortive" transductant.
3 perinfection killing during the selection of transductants.
4 ility mediated by IL-2 secretion of the IL-2 transductants.
5 mutant with reduced ability to form abortive transductants.
6 erted within the chromosomes of PS12 and the transductants.
7 expression or stability; and Ii(+) and Ii(-) transductants activate human CD4+ T cells to DRB1*0701-r
9 e in transepithelial resistance in claudin-5 transductants and a reduction in conductance of monovale
10 FHIT, in comparison with that of the control transductants and untreated cells, was eliminated in viv
11 e genes affected by PRC silencing in the two transductants, and the functional identities of these ov
13 ional culture, in that the proportion of the transductants becoming K19+ in response to RA was marked
14 ells of strain A216 (deltanox 438-760::kan), transductants (Cmr Kmr) were obtained at a frequency of
17 eric leukocyte function-associated antigen 1 transductants demonstrate that the site required for Lkt
18 which compensates for loss of NHEJ in these transductants does not introduce any gross abnormalities
19 ression is silenced >95% in CIITA/CD80/siRNA transductants; down-regulation of Ii does not affect HLA
23 ete knockdown of PRC protein, whereas shRNA4 transductants expressed PRC protein at approximately 15%
26 3-kb BamHI fragment were isolated from SAB11 transductants in which growth but not enterobactin synth
27 TrkA and increased phosphorylation of signal transductants in, albeit not specific for, the TrkA-MEK-
28 th RS1varphi, followed by inoculation of the transductants into the adult rabbit intestine, caused el
29 s confirms that formation and/or survival of transductants is dependent on components of the NHEJ pat
30 ons at this temperature therefore eliminated transductant killing and lysogeny, as did inclusion of c
31 PRC expression levels in the two independent transductant lines argues that the defects result from P
33 h-expression green fluorescent protein (GFP) transductant of human lung cancer cell line H460 (H460-G
34 tPMP resistant [tPMP(r)]); or 757-5 (tPMP(r) transductant of the ISP479R genotype in the ISP479 paren
36 he recipient chromosome to form a "complete" transductant, or it can establish itself as an expressib
38 from approximately 2 x 10(-7) to 1 x 10(-8) transductants/PFU depending upon the marker being transd
40 s mode of DNA synthesis proposed to generate transductants, sequences located between the vectors' tw
41 ely diminished respiratory growth rate, both transductants showed markedly reduced growth on glucose
44 ere added to the packaging reaction mixture, transductants that are resistant to both the antibiotics
45 sduction frequency and reduced the number of transductants that were lysogenized during the transduct
46 mutant, ISP479R, and two bacteriophage back-transductants, TxA and TxB, exhibit reduced in vitro sus
50 rulent Salmonella strains, and the resultant transductants were screened for virulence in mice and ac
52 he infected population, and in the number of transductants, were also observed in the presence of a d
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