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1 fers several tools including a sophisticated multifactor analysis of relevant physicochemical propert
8 95% confidence intervals obtained by using a multifactor bootstrap-resampling approach contain the tr
10 expression changes were driven by a stepwise multifactor cascading control mechanism, where the speci
12 Thus, NAP-1 appears to be one component of a multifactor chromatin assembly machinery that mediates t
14 mains that have been implicated in the yeast multifactor complex (eIF1-eIF3-eIF5-eIF2-GTP-Met-tRNA(i)
15 erated from purified human proteins a stable multifactor complex (MFC) comprising eIF1, eIF2, eIF3 an
16 tions that disrupt eIF2-eIF3 contacts in the multifactor complex (MFC) diminished 40S-bound TC, indic
17 e eIF2.tRNA(i)(Met.)GTP complex (TC) and the multifactor complex (MFC) required for translation initi
19 It is recruited to the 43 S complex in the multifactor complex (MFC) with eIF2, eIF3, and eIF5 via
20 (eIF3) of Saccharo myces cerevisiae forms a multifactor complex (MFC) with eIFs 1, 2, 5 and Met-tRNA
21 nd eIF3c, thereby mediating formation of the multifactor complex (MFC), an important intermediate for
22 duced 40S binding of all constituents of the multifactor complex (MFC), comprised of these three fact
23 binds the eIF3/eIF1/eIF5 complex to form the multifactor complex (MFC), whereas eIF2.GDP binds the pe
24 acts with eIF3-eIF1-eIF5 complex to form the multifactor complex (MFC), while eIF2GDP associates with
26 to, and stabilizes, the eIF3-eIF5- eIF1-eIF2 multifactor complex and is required for the normal level
27 to interact with eIF1, eIF2, and eIF3 in the multifactor complex and with eIF4G in the 48S complex.
28 C loading on 40S subunits or destabilize the multifactor complex containing eIF1, eIF3, eIF5, and TC,
29 F3, was shown to bind to, and stabilize, the multifactor complex containing eIFs 1, 2, 3, and 5 and M
32 mutation in eIF5-CTD, which destabilizes the multifactor complex in vivo, reduced the binding of Met-
34 to the silencer leads to the formation of a multifactor complex that induces silencer function and r
35 which mRNAs undergo polyadenylation; CPSF, a multifactor complex that interacts with the near-ubiquit
37 ith CARM1, CBP, c-Jun, and Sp1 and that this multifactor complex was formed in a p53-dependent manner
38 It is recruited to the 40 S subunit in a multifactor complex with Met-tRNA(i)(Met), eIF2, eIF3, a
39 est the occurrence of an eIF3/eIF1/eIF5/eIF2 multifactor complex, which was observed in cell extracts
40 These results suggest that the stability of multifactor complexes at promoters and regulatory elemen
43 cation, few have examined these effects in a multifactor context or recorded how these effects vary s
44 ntly, the context provided by multimodal, or multifactor delivery represents a key element of most bi
46 mbinatorial approach, namely the generalized multifactor dimensionality reduction (GMDR) method, whic
47 ormed Neural Networks (NNs), and Model-based Multifactor Dimensionality Reduction (MB-MDR) models.
48 fied analysis, combined effect analysis, and multifactor dimensionality reduction (MDR) analysis.
52 this problem, we have previously developed a multifactor dimensionality reduction (MDR) method for co
53 To address this problem, we have developed a multifactor dimensionality reduction (MDR) method for co
54 everal combinatorial approaches, such as the multifactor dimensionality reduction (MDR) method, have
55 Recent combinatorial approaches, such as the multifactor dimensionality reduction (MDR) method, the c
56 MDR-Phenomics, a novel approach based on the multifactor dimensionality reduction (MDR) method, to de
57 and BAT3) were investigated by entropy-based multifactor dimensionality reduction (MDR), classificati
58 f the AMBIENCE algorithm was compared to the multifactor dimensionality reduction (MDR), generalized
59 3.95, P = 7.8 x 10(-5) [FDR </=0.05], P for multifactor dimensionality reduction = 5.9 x 10(-45)).
63 teractions were assessed through model-based multifactor dimensionality reduction in the PIAMA study,
69 ts show that SIPI has higher power than MDR (Multifactor Dimensionality Reduction), AA_Full, Geno_Ful
70 o-head comparisons with the relevance-chain, multifactor dimensionality reduction, and PDT methods, t
71 o-head comparisons with the relevance-chain, multifactor dimensionality reduction, and the pedigree d
74 ve refined independent marker sets, extended multifactor-dimensionality reduction (EMDR) analysis was
77 e, long-term ecosystem-scale studies testing multifactor effects on plants and soils are urgently req
78 These findings indicate the importance of a multifactor experimental approach to understanding ecosy
79 ariable climate and atmosphere simulator for multifactor experimentation on natural or artificial eco
82 ctive importance of these processes requires multifactor experiments under realistic field conditions
86 n the longest-running, best-replicated, most-multifactor global-change experiment at the ecosystem sc
89 es and profiles, which might be explained by multifactors including charge, size, helicity, hydrophob
92 story of reflux is an important risk for EA, multifactor interactions also play important roles in EA
93 f analytical tools for identifying nonlinear multifactor interactions and unraveling the genetic arch
97 upervisors and 179 supervisees completed the Multifactor Leadership Questionnaire and a demographic s
100 tions of soil carbon dynamics and results of multifactor manipulations to calibrate a model that can
103 trophic magnification factors (TMFs), and a multifactor model that included delta(15)N-derived troph
104 range overlap of environmental variables in multifactor models controlling for phylogeny to simultan
108 on the magnitude of each interacting factor, multifactor, multilevel experiments are required, but ar
111 distinguish metazoan cells are specified by multifactor regulatory complexes containing distinct com
112 ngle factors (i.e., Ea or DeltaS alone); (2) multifactor scenarios of photosynthetic temperature accl
113 , these data reveal the power of integrating multifactor sequencing of chromatin immunoprecipitates w
114 er, our data demonstrate the requirement for multifactor signal integration by Arp2/3 complex and hig
116 perature ranges to determine whether and how multifactor thermal acclimation of photosynthesis occurs