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 he generality of this pattern is unknown, as
global analyses are lacking.
6 We validated these
global analyses by demonstrating that both IHF and LuxR
7 d deterioration with higher sensitivity than
global analyses by using predefined non-overlapping subs
8 Previous
global analyses described increased yield volatility fro
9 In addition to
global analyses,
five regions were evaluated where potat
10 Recent
global analyses have determined that many Drosophila and
11 debate, especially because most regional and
global analyses have not considered the influence of agr
12 the most parsimonious conclusion from these
global analyses is that APOBEC3B-catalyzed genomic uraci
13 Global analyses of cancer transcriptomes demonstrate tha
14 Global analyses of DNase I-hypersensitive sites and 3D g
15 These
global analyses of DV effects on cellular gene expressio
16 Transcriptome profiling and
global analyses of ETV1-binding sites suggest that ETV1
17 calculated for conventional independent and
global analyses of experiments with noninteracting solut
18 Global analyses of gene expression correlation combined
19 RNA-based
global analyses of gene expression have led to the ident
20 Global analyses of gene expression in regulatory T (Treg
21 Global analyses of gene expression were conducted on mai
22 ese gene products are combined with dynamic,
global analyses of gene expression.
23 designing arrays and interpreting data from
global analyses of gene regulation because regulatory in
24 These analyses were the first
global analyses of genes conditionally required for low-
25 Global analyses of genome dynamics across 46 species wer
26 Here we present
global analyses of histone acetylation and histone H3 Ly
27 d its activity, as defined by individual and
global analyses of its transcriptional targets.
28 his general kinetic scheme was then used for
global analyses of liver alcohol dehydrogenase anisotrop
29 Global analyses of metabolites and transcripts were carr
30 Advances in systems biology have allowed for
global analyses of mRNA and protein expression, but larg
31 ed approach described here can be applied to
global analyses of mRNA turnover and translation and can
32 Although there have been regional and
global analyses of NAPs from a One Health and policy per
33 increasingly well documented for some taxa,
global analyses of non-native species in local assemblag
34 ng both local-scale data from Costa Rica and
global analyses of over 11 000 Bd infection assays.
35 Recent
global analyses of Pol II and elongation factors, mechan
36 Global analyses of projected heatwaves can inform decisi
37 Global analyses of protein complex assembly, composition
38 Global analyses of RNA expression levels are useful for
39 oordinates and is therefore inconvenient for
global analyses of the chemotactic bacterial migration.
40 Global analyses of the gene expression data revealed alt
41 Most
global analyses of the innate immune response have focus
42 Here we employ
global analyses of the mouse liver transcriptome to demo
43 ximately 500 kilobases upstream, and enabled
global analyses of the relationship between gene dosage
44 Global analyses of the ST-EPR data using a newly develop
45 Global analyses of the transcriptomic data set indicate
46 Although
global analyses of transcription factor binding provide
47 Here, we report
global analyses of two prototypical SR proteins, SRSF1 (
48 about IFDARs and IPDARs, and lack synthetic
global analyses of variation in form of these three cate
49 Here, we present
global analyses of viral transcript levels to further un
50 Global analyses reveal hotspots of species richness, tog
51 These
global analyses reveal that most core cell cycle regulat
52 In
global analyses,
rEZR was associated with the mean avera
53 Global analyses suggest that splicing noise (due to stoc
54 Global analyses that assume a sustained CO(2) fertilizat
55 e observations, we performed the appropriate
global analyses to ascertain that SD70 inhibits the andr
56 To evaluate the current feasibility of
global analyses to contribute to this aim, we evaluated
57 To validate the ability of our
global analyses to identify functionally important RNA s
58 Next, we use
global analyses to show where and how much no-take marin
59 Our
global analyses yield thermodynamic parameters for the u