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1 mercial kits to determine the extent of this cross-reaction.
2 ucrose-containing medium showed little or no cross-reaction.
3 genic virus via viral interference or immune cross-reaction.
4 -dimensional features that may promote their cross-reaction.
5 ce of homogeneous DRAG and glutaraldehyde in cross-reaction.
6 This raises the potential problem of cross-reaction.
7 due to a multiple infection rather than to a cross-reaction.
8 only one sample may allow for confusion with cross reactions.
9 graph theory to disentangle the few existing cross-reactions.
10 000 TCR-peptide MHC class I interactions for cross-reactions.
11 tically significant B. burgdorferi serologic cross-reactions.
12 ligand mimetics have low affinities and show cross-reaction among the three selectins, precluding eff
14 he mechanism corresponds more to trapping by cross-reaction and coaggregation rather than classical s
15 nd rye might also trigger EoE as a result of cross-reaction and/or cross-contamination with wheat.
16 studies were performed using seroconversion, cross-reaction, and interference panels, archived clinic
19 most efficient method of diagnosis, although cross-reactions are possible in patients recently vaccin
26 apoptosis, although there are no detectable cross-reactions between externally added and endogenous
29 es ( approximately 1/30,000), explaining why cross-reactions between unrelated pathogens are infreque
31 ce acids and bases in both self-exchange and cross reactions, by stepwise mechanisms utilizing the fa
33 CDR3beta loop that, when altered, modify the cross-reaction capability of the TCR to position 4 and p
35 3+/2+-His18 couple, and E0' = 176 mV for the cross-reaction couple, His82-Fe3+-His18 + e- --> Met80-F
37 s homology filtering, minimizes non-specific cross-reaction, filters target sites based on RNA duplex
38 and HPV-45) exhibited detectable serological cross-reaction for the class of antibodies that inhibit
42 calculations highlight the need to consider cross reactions in the cell and suggest that localizatio
43 he sole carbon source showed a high anti-MTD cross-reaction in the cytoplasm, whereas cells that were
44 al for the probability of celecoxib inducing cross-reactions in AERD patients was calculated to be be
46 ver, the directionality and quality of these cross-reactions is critical in determining their biologi
47 constant for the Cr(aq)OO(2+)/CH(3)C(O)OO(*) cross reaction, k(Cr) = 1.5 x 10(8) M(-1) s(-1), was det
50 oduce [(tpy)(bpy)Ru(III)OH](2+); and (3) the cross reaction of [(tpy)(bpy)Ru(III)OH](2+) and [(bpy)(2
51 -alpha and PCaPK-beta, and the immunological cross-reaction of expressed cloned fragments of these ge
53 normal host self-proteins, thus leading to a cross-reaction of immune response against virus with hos
54 Paraneoplastic retinopathy is caused by the cross-reaction of neoplasm-directed autoantibodies again
56 n within the ventricle can be explained by a cross-reaction of the anti-KChIP2 antibody with a differ
57 an anti-keratin 19 antibody, which is due to cross-reaction of the antibody with Nmi, and suggests an
58 plex V in leaves was not meaningful due to a cross-reaction of the antibody with the chloroplast form
59 pe II/1b (primers 389 and 492) abolished the cross-reaction of the antisense primer for genotype II/1
61 tudied plant enzymes was demonstrated by the cross-reaction of the yeast enzyme to a antiserum direct
63 ns to evaluate whether co-reactions are true cross-reactions or co-sensitizations by allergens with t
65 t (k(11)) has then been calculated from each cross reaction rate constant using the Marcus cross rela
67 oton and electron transfer self-exchange and cross-reaction rates have been determined for reactions
69 motifs revealed a hierarchy in the degree of cross-reaction: The more frequent an allergen was positi
74 Plasma immune to DENV showed substantial cross-reaction to ZIKV and was able to drive antibody-de
79 timization of the microarray composition and cross-reaction was performed using an original approach
80 PE membrane were observed as expected, while cross reactions were spotted for P(4,5)BP/PtdIns(4)P and
88 Arabidopsis mitochondrial RecA protein shows cross-reaction with a soybean protein of about 44 kDa, i
90 atory pathogens showed only one low-level H3 cross-reaction with an H10N7 avian strain and only at 5.
93 A, cMyc and AcV5 tags show relatively little cross-reaction with endogenous proteins in a variety of
94 hought to be pathogenic in the kidney due to cross-reaction with glomerular antigens, leading subsequ
95 west detection limit of 60ng/ml and shows no cross-reaction with other analogous organophosphates or
103 ose of the nonimprinted films and negligible cross-reaction with the tested nonspecific analyte.
107 nical strains of S. porcinus were tested for cross-reactions with group B streptococcal reagents from
110 f 0.2 ng/ml for C. difficile toxin B with no cross-reactions with other enterotoxins, nontoxigenic C.
112 parvum DNA in human stool, and there are no cross-reactions with other parasites commonly found ther
113 nt IgM and syphilitic sera in the absence of cross-reactions with rabbit antisera to avirulent trepon
114 by serologic methods test their reagents for cross-reactions with selected S. porcinus cultures or an
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