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1 t (i.e., in the absence of space- and object-based selection).
2 even error-prone DNA polymerases function in base selection.
3 ith the replicating base pair, thus relaxing base selection.
4 cile extrusion from the helix in its damaged base selection.
5 cyclic re-entry to ensure efficient affinity-based selection.
6 ndicating that DETC development involves TCR-based selection.
7 This was not due to a TCR-based selection.
8 red from cells that have undergone lethality-based selection.
9 ide library that was formatted for autocrine-based selection.
10 cycles of targeted mutagenesis and affinity-based selection.
11 such selection mechanisms: space- and object-based selection.
12 small molecule were identified by microarray-based selection.
13 ct is not a spatially global form of feature-based selection.
14 zes directed domain shuffling and rapid cell-based selections.
15 eered PKS design by learning from laboratory-based selection; adoption of DNA design software and aut
16 anning and enzyme-linked immunosorbent assay-based selection afforded a panel of nine scFv-phage clon
17 RNA recombination with a powerful host range-based selection allowed by the interspecies chimeric vir
19 567) is a key determinant of the fidelity of base selection and that the Pol and Exo functions are st
20 provide a conceptual framework for rationale-based selection and combination of anticancer drugs for
21 gut microbiotas include chance events, host-based selection and interactions among microorganisms wi
22 sh N(-) B cells in adult life via repertoire-based selection and suggest the possibility of a TdT-def
23 h were used to examine the effect of feature-based selection and the competitive influence of a secon
24 forming a conceptual framework for rationale-based selection (and combination) of immunosuppressive a
25 at was part of the same object (i.e., object-based selection), and at an uncued location that was par
30 scovery typically uses hybridoma- or display-based selection approaches, which lack the advantages of
31 rstanding the direct impacts of ecologically based selection, as well as the indirect effects due to
33 cillatory responses, suggesting that feature-based selection at ignored locations during visual searc
34 et detection at a cued location (i.e., space-based selection), at an uncued location that was part of
35 as length distribution, paired distance, and base selection bias of vsiRNA sequences reflect differen
36 f the same object (i.e., resulting in object-based selection), but little is known about the relation
37 d type and suggest that enhanced fidelity of base selection by a polymerase active site can result in
38 ase is achieved in a multiplicative process: base selection by its polymerase activity and removal of
41 ic flounders is the trait under ecologically based selection causing reproductive isolation, directly
42 g MS-, physical-chemical, and chromatography-based selection criteria including HRMS/MS fragmentation
46 incorporating this information, the entropy-based selection (EBS) scheme is useful for selecting an
48 face of Galphas and argues that mRNA display-based selection/evolution is a powerful route for target
49 demonstrate this notion, we preformed growth-based selection experiments at nonpermissive temperature
51 50 to 80 years to estimate outcomes of risk-based selection for CT lung screening, assuming screenin
52 ation of new lineages under host- or element-based selection for function, in either case followed by
54 of infection and suggest that genetic marker-based selection for resistance to bTB has the potential
56 binding site previously identified by a PCR-based selection from random oligonucleotides by using re
59 zF72 was generated and subjected to a growth based selection in a chorismate mutase deficient strain.
60 mechanisms appear to operate during feature-based selection in much the same manner as has been show
62 regulators of p53, we have used a phenotype-based selection in which a total cDNA library in a retro
66 imary electrophysiological marker of feature-based selection is the N2pc, a lateralized posterior neg
68 Dendritic cell maturation and TCR affinity-based selection mechanisms control the recruitment and e
71 such enzymes, we have developed an activity-based selection method which isolates polymerase mutants
72 site, identified by a combinatorial activity-based selection method, within genomic and subgenomic RN
74 elements of both modular design and activity-based selection methods typically used for generation of
75 t and validate a scoring system for evidence-based selection of bariatric and metabolic surgery proce
78 is paper are the starting point for pedigree based selection of cultivars with high levels of resista
81 pportunity for genomics- and transcriptomics-based selection of patients for rationally designed ther
82 ful procedure that permits an unbiased trait-based selection of plant samples based on such phenotypi
83 In this study, structure- and computation-based selection of the predicated VDAC1 dimerization sit
84 The reports further suggest that the marker-based selection of the tumor cell population will facili
89 this problem, we have developed a population-based selection procedure to increase aggression in Dros
92 We find that the time-course of the object-based selection process is well explained by a 'growth-c
93 minate the use of helper phage from phagemid-based selection protocols; reducing the amount of techni
94 population-level signature of global feature-based selection reflects a sequence of hierarchically or
97 lter intein specificity, we developed a cell-based selection scheme to evolve split inteins that spli
101 oral data to determine how space- and object-based selection simultaneously evolve under conditions t
102 ng resulting from a spatial cue (i.e., space-based selection) spreads to uncued locations if those lo
103 Targeted therapy arms that used a biomarker-based selection strategy (n = 57 trials) were associated
105 ifunctional gp17, we developed an expression-based selection strategy to select for mutants that are
110 Given the large library sizes our bacterial-based selection system can handle, this method should pr
111 t the development and application of a yeast-based selection system designed to functionally interrog
112 By combining a previously developed FACS-based selection system for functional expression with ul
113 he efficacy of the non-invasive fluorescence-based selection system is promising for its application
115 ss, making it more general than biologically based selection systems because it is not limited to rea
116 cally not amenable to traditional antibiotic-based selection systems, and may be used in combination
117 ific tools, including promoters for reporter-based selection systems, that we employed to improve lov
119 lygenic resistance and field- vs. laboratory-based selection, the application of molecular cloning to
120 pansion, somatic hypermutation, and affinity-based selection, the combination of which results in the
121 ate progressive but discontinuous repertoire-based selection throughout B cell development supporting
122 he G185V substitution was used in a function-based selection to identify mutations that would further
123 impede anaerobic growth, followed by growth-based selection to isolate suppressor mutants that resto
124 Here, we adapted a phage display library-based selection to screen and identify binding peptides
125 rgo somatic hypermutation (SHM) and affinity-based selection toward antigen in activated germinal cen
126 ralleled advantage over traditional pedigree-based selection (TS) methods by reducing the time commit
127 ing bacteria and methanogens indicate energy-based selection typical of anoxic marine sediments, 5-15
128 dinated network of water molecules acting in base selection upstream of the GGAA core and the structu
130 or the isolation of bona fide hiPSCs in FACS-based selection using an optimized combination of cell s
132 MS analysis of the suspension after density-based selection yielded a sensitivity of 72.1% and a spe
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