1 countries, with no consistent and comparable
global analysis.
2 max approximately 790 nm) were determined by
global analysis.
3 EEK LKALEEK G-NH(2) (Baby L9C) is derived by
global analysis.
4 econd transient absorption spectroscopy with
global analysis.
5 tions, underscoring the need for a synthetic
global analysis.
6 rder to unite these data for the purposes of
global analysis,
a new web-based resource of heme protei
7 Global analysis afforded a second-order rate constant k(
8 we present here a computationally efficient
global analysis algorithm for the analysis of time-corre
9 ow-noise thermogram integration approach and
global analysis allow for more precise parameter estimat
10 are recent additions to the tool set for the
global analysis and decomposition of microarray co-expre
11 BIOEQS is a
global analysis and simulation program for complex biomo
12 Historically, the dual approach of
global analysis and target modelling has been used to el
13 New kinetic (
global analysis)
and computational (DFT) data explain th
14 We have demonstrated that the
global analysis approach allows the concentration and di
15 -angle X-ray scattering (SAXS) and present a
global analysis approach for the deconvolution of hetero
16 ependent BSI traces are directly fit using a
global analysis approach to characterize the interaction
17 While
global analysis approximates the data to the sum of a sm
18 erent components or their molar ratio in the
global analysis are introduced.
19 ities of LDA with those of the more familiar
global analysis,
as well as providing a number of statis
20 Here, we present the first
global analysis,
based on data from 163 drip sites, from
21 the 3-nt periodicity is observed mostly in a
global analysis,
but not in individual transcripts.
22 Our
global analysis calculates the total potential damage ca
23 Global analysis combining sedimentation velocity and flu
24 We present an in-depth
global analysis examining the impact of aging on classic
25 Additionally, our
global analysis has revealed a number of interesting bio
26 This
global analysis identified > 1300 proteins, of which 215
27 Multicomponent
global analysis implicates the generation of additional
28 Global analysis in yeast, using an H2AQ105me-specific an
29 FA and MD histograms of whole brain and GM (
global analysis)
in healthy control subjects and MS pati
30 repellency was very low in our sites and the
global analysis indicated high repellency only in sites
31 Our
global analysis indicates that the division of labor by
32 on based on singular value decomposition and
global analysis is applied to estimate the binding affin
33 In this work, we present a
global analysis linking chemical features to adverse dru
34 sumption of linear combinations of decays in
global analysis means the technique is unable to describ
35 The EPR spectra were modeled by using a
global analysis method.
36 METHODS AND Quantitative
global analysis,
methylated and hydroxymethylated DNA se
37 gus Batrachochytrium dendrobatidis (Bd) in a
global analysis of 32 291 amphibian hosts.
38 Here we present a
global analysis of 403 tropical and temperate tree speci
39 We conducted a
global analysis of 5'-truncated mRNA ends that mapped to
40 A
global analysis of 65,421 prokaryotic genomes revealed 3
41 The
global analysis of a series of spectra, from fibers tilt
42 Here, we report a
global analysis of abundance trends of 304 widely distri
43 Global analysis of activated regions of the genome, as d
44 Global analysis of active RNAPII reveals that hypoxia-in
45 Altogether, this study provides the first
global analysis of AI-2 signaling in Y. pestis and ident
46 Expansion of the BURST analysis to a
global analysis of all known pneumococcal STs (as of 27
47 res, we have conducted a bioinformatic-based
global analysis of all orphan diseases with known diseas
48 radigms by conducting, for the first time, a
global analysis of all the naturally occurring mutations
49 Global analysis of all three proteins indicated that the
50 between-experiment variation that enabled a
global analysis of all transgenic lines from the four in
51 overy cohort, we used microarrays to perform
global analysis of alternative splicing in DM1 and DM2.
52 d high-density exon-sensitive microarray for
global analysis of alternative splicing.
53 Our study provides a
global analysis of an entire DNA repair pathway and reve
54 transcript sequence data sets are enabling a
global analysis of AS in many plant species.
55 r role of TbZFP3 in parasite transmission, a
global analysis of associating transcripts was carried o
56 Here we provide a
global analysis of associations between migratory behavi
57 The
global analysis of auxin response gene expression and th
58 Through a
global analysis of binding kinetics data obtained from s
59 Global analysis of BUD13 knockdown and BUD13 cross-linki
60 protein microarray and used it to study the
global analysis of CaM/CML interactions.
61 n of cell type specific genes as well as for
global analysis of cell type specific gene expression in
62 Global analysis of cellular mRNA abundance and translati
63 A
global analysis of cellular phospholipids demonstrates t
64 by a variety of stressors, no comprehensive
global analysis of change in kelp abundances currently e
65 A
global analysis of circular dichroism kinetic traces for
66 ional networks, we performed a comprehensive
global analysis of cis-regulatory element activity and i
67 We present a
global analysis of CO2 emission reductions from the ligh
68 in 5-hydroxytryptamine 2C (5-HT2C) receptor,
global analysis of construct quantal brightness was cons
69 This
global analysis of context-dependent protein interaction
70 rtical patterning, we carried out an in vivo
global analysis of cortical gene expression in Fgfr1 mut
71 Our recent
global analysis of CpG island hypermethylation and gene
72 A
global analysis of cross-talk suggests that many externa
73 Here, we present a
global analysis of cumulative human impacts on threatene
74 Global analysis of data sets collected at multiple PR-A
75 ercially available programs do not allow for
global analysis of different physical observables.
76 calculated from a linear combination of the
global analysis of each substrate reveals a detailed lan
77 f concept for a method allowing simultaneous
global analysis of endogenous protein complexes that beg
78 le of PIMT in brain function, we undertook a
global analysis of endogenous substrates for PIMT in mou
79 implemented in the software SEDPHAT, for the
global analysis of equilibrium data at multiple rotor sp
80 Finally, the
global analysis of equilibrium profiles at multiple roto
81 Global analysis of equilibrium substrate binding and ste
82 Here a
global analysis of exon usage in AML samples revealed di
83 We highlight the power of a
global analysis of experimental time courses acquired un
84 We report here
global analysis of expressed genes in a naturally occurr
85 with extinction according to the 2010 first
global analysis of extinction risk.
86 ss-spectrometry-based shotgun lipidomics for
global analysis of fatty acids including isomers and mod
87 Global analysis of FCS data provides association (k(+))
88 Global analysis of fluorescence and associated anisotrop
89 Global analysis of gene expression by using DNA microarr
90 Global analysis of gene expression demonstrated distinct
91 Collectively, these data provide the first
global analysis of gene expression during sub-zero accli
92 Our
global analysis of gene expression identified 162 genes
93 We performed a
global analysis of gene expression in normal squamous es
94 biomarkers of affected muscles, we compared
global analysis of gene expression in two distinct muscl
95 Our
global analysis of gene expression of common translocati
96 Finally, a
global analysis of gene expression revealed extensive al
97 Global analysis of gene expression via RNA sequencing wa
98 atform of knowledge-based algorithms for the
global analysis of gene expression, together with conven
99 NA microarrays provide a powerful method for
global analysis of gene expression.
100 lidity and the utility of this comprehensive
global analysis of gene function by analyzing two breast
101 A arrayed libraries enable the comprehensive
global analysis of gene function.
102 rigination and extinction but immigration, a
global analysis of genera and subgenera of marine bivalv
103 In addition,
global analysis of genes associated with groups of drugs
104 Global analysis of Genevestigator data indicated that At
105 However, no
global analysis of germ-line transcription throughout th
106 Global analysis of glycoproteins shows great promise for
107 Global analysis of glycosylated proteins identifies 109
108 Moreover,
global analysis of H3K4me3/2 revealed that enhancers of
109 Furthermore, our
global analysis of high-elevation soils from the Andes,
110 er descriptors on leaflet outlines provide a
global analysis of highly heritable, intricate aspects o
111 Wamstad et al have provided a robust
global analysis of histone markers and gene expression a
112 ed proteomics of enriched ECM extracts for a
global analysis of human glomerular ECM in vivo and iden
113 ditional potential Dcp2 substrate mRNAs by a
global analysis of human mRNAs containing a similar pred
114 Using a
global analysis of iceberg samples, we reveal that icebe
115 Here, we report the first
global analysis of immune dysfunction in patients with a
116 Recent scientific advances now allow a
global analysis of immune parameters that capture novel
117 el organism,Bacillus subtilis, facilitated a
global analysis of internal 5' ends that are generated o
118 ovide an online platform that enables robust
global analysis of kinetic data without the need for ext
119 We apply this method to the
global analysis of kinetic progress curves for bovine al
120 Global analysis of kinetics data has previously shown th
121 A
global analysis of known IYSV nucleocapsid gene (N gene)
122 Our results offer a general approach to the
global analysis of lateral organization and receptor clu
123 Elliptical Fourier descriptors provide a
global analysis of leaf outlines and lobe positioning, w
124 We have carried out an unbiased
global analysis of m5C in total and nuclear poly(A) RNA
125 Finally, a
global analysis of mammalian herbivore transport is pres
126 bon of aldose sugars and will facilitate the
global analysis of metabolic flux in carbohydrate pathwa
127 lomics tool box and provides a framework for
global analysis of metabolic fluxes.
128 Additionally, we report for the first time a
global analysis of miRNA epi-transcriptomic modification
129 ted by epigenetic mechanisms, we undertook a
global analysis of miRNA expression and epigenetic state
130 Global analysis of miRNA-target gene interactions identi
131 This
global analysis of miRNAs and their potential targets in
132 We report the first
global analysis of mitochondrial transport during axonal
133 We present a comprehensive,
global analysis of modern extinction in plants.
134 bed here provides a general platform for the
global analysis of mRNA turnover and transcription and c
135 By performing a
global analysis of MSI2-RNA interactions, we show that M
136 njection was comparable to that obtained for
global analysis of multiple standard injections.
137 We performed a
global analysis of nitrogen in fruits consumed by primat
138 Our
global analysis of NLP reveals that microbial interplay
139 we combine singular value decomposition and
global analysis of NMR chemical shift perturbations caus
140 Here we present a
global analysis of no-till-induced changes of soil C and
141 ALL samples, and combined locus-specific and
global analysis of NOTCH1-driven epigenetic changes.
142 Overall, our studies provide a
global analysis of O-GlcNAc dynamics during T cell activ
143 A
global analysis of one of the largest marine clades at t
144 This study provided a
global analysis of P. gingivalis transcriptional respons
145 Global analysis of p27 and cJun chromatin binding and ge
146 methylation landscape of the human genome by
global analysis of patterns of CpG depletion and by dire
147 We present a
global analysis of pest and pathogen distributions, to d
148 Overall, our collection opens the door to
global analysis of photosynthesis and early seedling dev
149 We conducted the first
global analysis of plasticity in Deltapitlp and related
150 First, ParticleStats:Directionality for the
global analysis of polarity, for example microtubule plu
151 ed in response to DNA damage, we conducted a
global analysis of poly(A) site usage in Saccharomyces c
152 Mass spectrometry enables
global analysis of posttranslationally modified proteofo
153 Global analysis of pre-steady state and equilibrium bind
154 alanine racemase clearly refutes claims that
global analysis of progress curves can be used to extrac
155 In a
global analysis of protected areas, we show that kilomet
156 enrichment method that can be applied to the
global analysis of protein adducts with various naturall
157 Methods for the
global analysis of protein expression offer an approach
158 Quantitative proteome analysis, the
global analysis of protein expression, is increasingly b
159 ample restrictions can be widely applied for
global analysis of protein O-GlcNAcylation in different
160 s of signaling pathways are now commonplace,
global analysis of protein phosphorylation and kinase ac
161 Here we present a
global analysis of protein profiles of 82 apparently nor
162 every extracellular event, but compared with
global analysis of proteins, comprehensive and site-spec
163 Global analysis of protiated and deuterated progress cur
164 To facilitate the
global analysis of PTPs, we designed and synthesized two
165 have been determined at pH 6.9 and 8.9 from
global analysis of racemization progress curves.
166 the selection of the BAC clones analyzed, a
global analysis of random sequence reads indicates that
167 Global analysis of RARalpha binding and enhancer mapping
168 Comparative
global analysis of RNA synthesis vs steady state levels
169 By performing an integrative, systematic,
global analysis of RNA turnover utilizing 4-thiouridine
170 d for synchronizing cell growth that enabled
global analysis of S. meliloti cell cycle-regulated gene
171 In a recent
global analysis of satellite-derived atmospheric NH(3) d
172 Through a
global analysis of sequence and structural similarity, i
173 We performed
global analysis of short capped RNAs and Pol II Chromati
174 cture-function relationships, we performed a
global analysis of similarities across the entire superf
175 no-, bi-, and tri-exponential TRFAs from the
global analysis of simulated I(VV)(t) and I(VH)(t) fluor
176 A
global analysis of single- and double-jump kinetic data,
177 kinetic mechanism for PheH was determined by
global analysis of single-turnover data in the reaction
178 Through
global analysis of SOX10-binding sites and epigenetic ch
179 The
global analysis of spectra at two frequencies yielded va
180 The
global analysis of spectra obtained at two microwave fre
181 Global analysis of SR4-associated differential gene expr
182 Here, we report that a
global analysis of SRC-1 target genes suggested that SRC
183 Global analysis of steady-state and transient kinetic da
184 We used a
global analysis of STRF shape based on a large database
185 ty transcript profiling to perform the first
global analysis of SUMO chain function.
186 We have undertaken a
global analysis of sumoylated proteins in Saccharomyces
187 Global analysis of surface glycoproteins will result in
188 Global analysis of synthetic lethality promises to ident
189 Global analysis of TFIIIC distribution revealed disperse
190 Global analysis of TFs has only been performed for three
191 We performed
global analysis of the canola genes that were expressed
192 is method can be extensively applied for the
global analysis of the cell-surface N-glycoproteome.
193 Global analysis of the Cy3 and Cy5 FRET time-courses, us
194 These demonstrations revealed the power of a
global analysis of the data contained within gene expres
195 Global analysis of the data supports the hypothesis that
196 esent a comprehensive kinetic model based on
global analysis of the data.
197 Global analysis of the deletion collection was carried o
198 refolding and unfolding, not included in the
global analysis of the dimeric protein, reflects the pre
199 e seven homoeologous chromosome groups and a
global analysis of the entire mapped wheat EST data set.
200 Here, we provide a comprehensive
global analysis of the evolutionarily distant unicellula
201 Global analysis of the experimental results preferential
202 Our
global analysis of the FG domain requirements in mRNA ex
203 This study is the first
global analysis of the GAS transcriptome during invasive
204 Here, we describe a
global analysis of the genomes of Lonesome George-the ic
205 ject Consortium enables for the first time a
global analysis of the genomic distribution of transcrip
206 en together, these results provide the first
global analysis of the human preimplantation embryo tran
207 an early stage of visual processing prior to
global analysis of the image.
208 Detailed
global analysis of the kinetic data clearly demonstrates
209 ion via an intermediate are examined using a
global analysis of the kinetic data, and the most likely
210 Global analysis of the kinetic data, based on a sequenti
211 The
global analysis of the kinetic folding mechanism reveals
212 Further,
global analysis of the kinetics and the transient absorp
213 The
global analysis of the large number of low-abundance sph
214 However, additional regional studies and a
global analysis of the Late Ordovician mass extinction t
215 of Sac7d has been well-characterized with a
global analysis of the linkage of folding, protonation,
216 li to determine the best methods to approach
global analysis of the metabolome.
217 Global analysis of the pH dependence of the trimer-dodec
218 A
global analysis of the proteins in budding yeast classif
219 We hypothesized that a
global analysis of the proteomes of human ASD vs. contro
220 used to perform a quantitative and unbiased
global analysis of the rates at which newly synthesized,
221 We present a
global analysis of the relationship of FPE to stand-age
222 A
global analysis of the resulting data allowed determinat
223 To enable a
global analysis of the results, we introduce the concept
224 o provide for the first time an unbiased and
global analysis of the role of Ubqln2 in controlling the
225 Global analysis of the SAXS/WAXS patterns recovered time
226 Global analysis of the sedimentation equilibrium data de
227 This emerging technology provides data for a
global analysis of the selection process and for simulta
228 Global analysis of the severe SMNDelta7 SMA mouse model
229 For [Ru(tpy)(bpy)(dmso)](2+),
global analysis of the spectra reveals changes that are
230 Global analysis of the structural ensemble shows that th
231 Global analysis of the temperature and static field depe
232 Using a sequential model,
global analysis of the time-dependent scattering differe
233 A
global analysis of the time-resolved pyrene monomer and
234 Here, a
global analysis of the total lipid repertoire of Plasmod
235 Here we report a
global analysis of the transcriptional programme control
236 h-throughput microarray data has enabled the
global analysis of the transcriptome, driving the develo
237 For trans-[Ru(tpy)(pic)(dmso)](+),
global analysis of the transient spectra reveals time co
238 A
global analysis of the translation efficiency of HCMV mR
239 Global analysis of the unimolecular unfolding transition
240 Global analysis of the upstream promoter regions of diff
241 chronic HIV infection on aging, we report a
global analysis of the whole-blood DNA methylomes of 137
242 RNAi Screening Center (DRSC), we performed a
global analysis of their activity in 30 genome-wide scre
243 Multiwavelength
global analysis of these data provide two charge-recombi
244 Here, we provide a
global analysis of these data.
245 However,
global analysis of these events is currently limited.
246 Global analysis of these signatures confirms known assoc
247 Global analysis of this effect using microarrays indicat
248 a proteomic approach as the first step in a
global analysis of this important body fluid.
249 The
global analysis of time courses under different conditio
250 Global analysis of time- and frequency-resolved transien
251 By
global analysis of TPP1 side chain requirements for holo
252 Here, we present a spatially explicit
global analysis of tradeoffs between carbon stocks and c
253 a genomic scale, offering the potential for
global analysis of transcription factor occupancy in a s
254 A
global analysis of transcription revealed that loss of M
255 By performing a
global analysis of transcripts and protein production co
256 Comparative
global analysis of transcripts under induced and nonindu
257 fic ribosome profiling strategy that enables
global analysis of translation in defined subcellular lo
258 Global analysis of translation regulation has recently b
259 osome profiling is an emerging technique for
global analysis of translation that offers direct and ex
260 and ribosomal density that we observed in a
global analysis of translation.
261 No consistent and comparable
global analysis of trends has been done.
262 Global analysis of tRNA methylation in S. pombe showed a
263 ray platforms to perform a comprehensive and
global analysis of tumors arising in a model of metastat
264 In addition,
global analysis of viral transcripts by RNA sequencing i
265 An unbiased,
global analysis of where CREB binds has not been perform
266 Global analysis of WUE reveals existence of strong regio
267 The highly coupled nature of
global analysis often results in a significantly slower
268 ex and have been held to index the effect of
global analysis on local feature encoding.
269 When we performed a
global analysis on the brains of mice exposed to MeHg by
270 ity was evaluated, leading to a quantitative
global analysis on the relative effects of LOF and GOF o
271 A
global analysis over such a range of conditions permitte
272 Global analysis performs better than unconstrained data
273 nalysis of gene expression (SAGE) provides a
global analysis platform for profiling mRNA populations
274 This
global analysis removes some of the experimental inconve
275 The
global analysis revealed a transcriptome that bears sign
276 A
global analysis revealed changes in the abundances of 25
277 Global analysis revealed increased expression of the tra
278 Global analysis revealed significant genomic hypomethyla
279 Specifically, our
global analysis revealed that most genes with paused Pol
280 Global analysis reveals double Benioff zones in 30 segme
281 In total, this
global analysis reveals post-transcriptional regulators
282 Global analysis reveals that the TFIIIB-TFIIIC transcrip
283 Global analysis shows that all Ace2-only genes are bound
284 Global analysis shows that the thermal reactions for bot
285 nt calorimetric titration experiments into a
global analysis,
statistical analysis of binding paramet
286 Global analysis suggests that the nuclear surveillance m
287 Further evidence for this comes from the
global analysis that identified a crucial overlap betwee
288 In a follow-up
global analysis,
there were 161 genes that covaried with
289 , we conduct an innovative and comprehensive
global analysis to determine the potential contribution
290 ultural productivity and carbon storage in a
global analysis to find where agricultural extensificati
291 e of lncRNAs in brain cancer, we performed a
global analysis to identify and characterize all annotat
292 ed by present data, and outline a route from
global analysis to more detailed and focused studies of
293 y, however, be more robustly extracted using
global analysis to simultaneously fit the fluorescence d
294 A
global analysis underlined the predominance of induction
295 We interrogate this coincidence by
global analysis using a simplified model generally appli
296 experiments typically take 1-2.5 h each, and
global analysis usually takes 10-20 min.
297 To test this concept a second
global analysis was undertaken of earliest Cenozoic (Pal
298 Using a
global analysis,
we show that the >100 vascular plant fa
299 In this
global analysis,
we use the International Model for Poli
300 ingly labeled alphabetaTm were combined in a
global analysis with doubly labeled alphabetaTm.