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1 ted proteomics offers higher throughput over global analyses.
2 ripts that were largely hidden from previous global analyses.
3 tional design of media for both targeted and global analyses.
4 l modifications at genomic scale enable such global analyses and are challenging some assumptions abo
5                           We validated these global analyses by demonstrating that both IHF and LuxR
6                               In addition to global analyses, five regions were evaluated where potat
7                                       Recent global analyses have determined that many Drosophila and
8 debate, especially because most regional and global analyses have not considered the influence of agr
9  the most parsimonious conclusion from these global analyses is that APOBEC3B-catalyzed genomic uraci
10                                              Global analyses of cancer transcriptomes demonstrate tha
11                                              Global analyses of DNase I-hypersensitive sites and 3D g
12                                        These global analyses of DV effects on cellular gene expressio
13                  Transcriptome profiling and global analyses of ETV1-binding sites suggest that ETV1
14  calculated for conventional independent and global analyses of experiments with noninteracting solut
15                                              Global analyses of gene expression correlation combined
16                                    RNA-based global analyses of gene expression have led to the ident
17                                              Global analyses of gene expression in regulatory T (Treg
18                                              Global analyses of gene expression were conducted on mai
19 ese gene products are combined with dynamic, global analyses of gene expression.
20  designing arrays and interpreting data from global analyses of gene regulation because regulatory in
21                These analyses were the first global analyses of genes conditionally required for low-
22                              Here we present global analyses of histone acetylation and histone H3 Ly
23 d its activity, as defined by individual and global analyses of its transcriptional targets.
24 his general kinetic scheme was then used for global analyses of liver alcohol dehydrogenase anisotrop
25                                              Global analyses of metabolites and transcripts were carr
26 Advances in systems biology have allowed for global analyses of mRNA and protein expression, but larg
27 ed approach described here can be applied to global analyses of mRNA turnover and translation and can
28 ng both local-scale data from Costa Rica and global analyses of over 11 000 Bd infection assays.
29                                       Recent global analyses of Pol II and elongation factors, mechan
30                                              Global analyses of protein complex assembly, composition
31                                              Global analyses of RNA expression levels are useful for
32 oordinates and is therefore inconvenient for global analyses of the chemotactic bacterial migration.
33                                              Global analyses of the gene expression data revealed alt
34                                         Most global analyses of the innate immune response have focus
35                               Here we employ global analyses of the mouse liver transcriptome to demo
36 ximately 500 kilobases upstream, and enabled global analyses of the relationship between gene dosage
37                                              Global analyses of the ST-EPR data using a newly develop
38                                              Global analyses of the transcriptomic data set indicate
39                                     Although global analyses of transcription factor binding provide
40                              Here, we report global analyses of two prototypical SR proteins, SRSF1 (
41                                        These global analyses reveal that most core cell cycle regulat
42                                              Global analyses suggest that splicing noise (due to stoc
43                                              Global analyses that assume a sustained CO(2) fertilizat
44 e observations, we performed the appropriate global analyses to ascertain that SD70 inhibits the andr
45       To evaluate the current feasibility of global analyses to contribute to this aim, we evaluated
46               To validate the ability of our global analyses to identify functionally important RNA s
47                                 Next, we use global analyses to show where and how much no-take marin
48                                          Our global analyses yield thermodynamic parameters for the u

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