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