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 tions, underscoring the need for a synthetic
global analysis.
5 econd transient absorption spectroscopy with
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 the 3-nt periodicity is observed mostly in a
global analysis,
but not in individual transcripts.
21 Our
global analysis calculates the total potential damage ca
22 Global analysis combining sedimentation velocity and flu
23 This
global analysis detected 123 known proteins and 29 "new"
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 Global analysis indicated the presence of five kinetic c
32 Our
global analysis indicates that the division of labor by
33 on based on singular value decomposition and
global analysis is applied to estimate the binding affin
34 chiometry and with affinities, determined by
global analysis,
K(d) = 4.8 +/- 0.2 nM for p65 and K(d)
35 In this work, we present a
global analysis linking chemical features to adverse dru
36 sumption of linear combinations of decays in
global analysis means the technique is unable to describ
37 The EPR spectra were modeled by using a
global analysis method.
38 METHODS AND Quantitative
global analysis,
methylated and hydroxymethylated DNA se
39 Here we present a
global analysis of 403 tropical and temperate tree speci
40 We conducted a
global analysis of 5'-truncated mRNA ends that mapped to
41 A
global analysis of 65,421 prokaryotic genomes revealed 3
42 The
global analysis of a series of spectra, from fibers tilt
43 ndmark genomic scanning (RLGS) is useful for
global analysis of aberrant methylation of CpG islands,
44 Global analysis of activated regions of the genome, as d
45 Global analysis of active RNAPII reveals that hypoxia-in
46 Altogether, this study provides the first
global analysis of AI-2 signaling in Y. pestis and ident
47 Expansion of the BURST analysis to a
global analysis of all known pneumococcal STs (as of 27
48 res, we have conducted a bioinformatic-based
global analysis of all orphan diseases with known diseas
49 radigms by conducting, for the first time, a
global analysis of all the naturally occurring mutations
50 Global analysis of all three proteins indicated that the
51 between-experiment variation that enabled a
global analysis of all transgenic lines from the four in
52 overy cohort, we used microarrays to perform
global analysis of alternative splicing in DM1 and DM2.
53 d high-density exon-sensitive microarray for
global analysis of alternative splicing.
54 Our study provides a
global analysis of an entire DNA repair pathway and reve
55 transcript sequence data sets are enabling a
global analysis of AS in many plant species.
56 r role of TbZFP3 in parasite transmission, a
global analysis of associating transcripts was carried o
57 The
global analysis of auxin response gene expression and th
58 These data demonstrate a new approach to the
global analysis of B. burgdorferi genes that are prefere
59 ences with array hybridization has allowed a
global analysis of bacterial gene expression occurring i
60 Through a
global analysis of binding kinetics data obtained from s
61 protein microarray and used it to study the
global analysis of CaM/CML interactions.
62 By combining these data with previous
global analysis of cell cycle transcription patterns and
63 n of cell type specific genes as well as for
global analysis of cell type specific gene expression in
64 Global analysis of cellular mRNA abundance and translati
65 A
global analysis of cellular phospholipids demonstrates t
66 Global analysis of cellular transcription indicated that
67 by a variety of stressors, no comprehensive
global analysis of change in kelp abundances currently e
68 A
global analysis of circular dichroism kinetic traces for
69 We present a
global analysis of CO2 emission reductions from the ligh
70 in 5-hydroxytryptamine 2C (5-HT2C) receptor,
global analysis of construct quantal brightness was cons
71 This
global analysis of context-dependent protein interaction
72 rtical patterning, we carried out an in vivo
global analysis of cortical gene expression in Fgfr1 mut
73 Our recent
global analysis of CpG island hypermethylation and gene
74 A
global analysis of cross-talk suggests that many externa
75 Global analysis of data sets collected at multiple PR-A
76 r dot TATA interactions have been modeled by
global analysis of detailed kinetic and thermodynamic da
77 ercially available programs do not allow for
global analysis of different physical observables.
78 calculated from a linear combination of the
global analysis of each substrate reveals a detailed lan
79 f concept for a method allowing simultaneous
global analysis of endogenous protein complexes that beg
80 le of PIMT in brain function, we undertook a
global analysis of endogenous substrates for PIMT in mou
81 implemented in the software SEDPHAT, for the
global analysis of equilibrium data at multiple rotor sp
82 Finally, the
global analysis of equilibrium profiles at multiple roto
83 Global analysis of equilibrium substrate binding and ste
84 We highlight the power of a
global analysis of experimental time courses acquired un
85 We report here
global analysis of expressed genes in a naturally occurr
86 with extinction according to the 2010 first
global analysis of extinction risk.
87 ss-spectrometry-based shotgun lipidomics for
global analysis of fatty acids including isomers and mod
88 Global analysis of FCS data provides association (k(+))
89 Global analysis of fluorescence and associated anisotrop
90 Global analysis of gene expression by using DNA microarr
91 Global analysis of gene expression demonstrated distinct
92 Collectively, these data provide the first
global analysis of gene expression during sub-zero accli
93 A
global analysis of gene expression events during shoot d
94 Our
global analysis of gene expression identified 162 genes
95 We performed a
global analysis of gene expression in normal squamous es
96 To provide a
global analysis of gene expression in the aging heart, w
97 biomarkers of affected muscles, we compared
global analysis of gene expression in two distinct muscl
98 Our
global analysis of gene expression of common translocati
99 Finally, a
global analysis of gene expression revealed extensive al
100 Global analysis of gene expression via RNA sequencing wa
101 atform of knowledge-based algorithms for the
global analysis of gene expression, together with conven
102 NA microarrays provide a powerful method for
global analysis of gene expression.
103 lidity and the utility of this comprehensive
global analysis of gene function by analyzing two breast
104 A arrayed libraries enable the comprehensive
global analysis of gene function.
105 rigination and extinction but immigration, a
global analysis of genera and subgenera of marine bivalv
106 In addition,
global analysis of genes associated with groups of drugs
107 Global analysis of Genevestigator data indicated that At
108 However, no
global analysis of germ-line transcription throughout th
109 Global analysis of glycoproteins shows great promise for
110 Global analysis of glycosylated proteins identifies 109
111 Moreover,
global analysis of H3K4me3/2 revealed that enhancers of
112 Furthermore, our
global analysis of high-elevation soils from the Andes,
113 er descriptors on leaflet outlines provide a
global analysis of highly heritable, intricate aspects o
114 Wamstad et al have provided a robust
global analysis of histone markers and gene expression a
115 ed proteomics of enriched ECM extracts for a
global analysis of human glomerular ECM in vivo and iden
116 ditional potential Dcp2 substrate mRNAs by a
global analysis of human mRNAs containing a similar pred
117 Here, we report the first
global analysis of immune dysfunction in patients with a
118 Recent scientific advances now allow a
global analysis of immune parameters that capture novel
119 el organism,Bacillus subtilis, facilitated a
global analysis of internal 5' ends that are generated o
120 e (TATAAAAG) promoters have been modeled via
global analysis of kinetic and thermodynamic data obtain
121 ovide an online platform that enables robust
global analysis of kinetic data without the need for ext
122 We apply this method to the
global analysis of kinetic progress curves for bovine al
123 A
global analysis of known IYSV nucleocapsid gene (N gene)
124 Our results offer a general approach to the
global analysis of lateral organization and receptor clu
125 Elliptical Fourier descriptors provide a
global analysis of leaf outlines and lobe positioning, w
126 We have carried out an unbiased
global analysis of m5C in total and nuclear poly(A) RNA
127 Finally, a
global analysis of mammalian herbivore transport is pres
128 bon of aldose sugars and will facilitate the
global analysis of metabolic flux in carbohydrate pathwa
129 lomics tool box and provides a framework for
global analysis of metabolic fluxes.
130 Additionally, we report for the first time a
global analysis of miRNA epi-transcriptomic modification
131 ted by epigenetic mechanisms, we undertook a
global analysis of miRNA expression and epigenetic state
132 This
global analysis of miRNAs and their potential targets in
133 We report the first
global analysis of mitochondrial transport during axonal
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 we combine singular value decomposition and
global analysis of NMR chemical shift perturbations caus
139 ALL samples, and combined locus-specific and
global analysis of NOTCH1-driven epigenetic changes.
140 Overall, our studies provide a
global analysis of O-GlcNAc dynamics during T cell activ
141 A
global analysis of one of the largest marine clades at t
142 This study provided a
global analysis of P. gingivalis transcriptional respons
143 methylation landscape of the human genome by
global analysis of patterns of CpG depletion and by dire
144 We present a
global analysis of pest and pathogen distributions, to d
145 In this study, a
global analysis of physiological changes of the plant sa
146 We conducted the first
global analysis of plasticity in Deltapitlp and related
147 First, ParticleStats:Directionality for the
global analysis of polarity, for example microtubule plu
148 ed in response to DNA damage, we conducted a
global analysis of poly(A) site usage in Saccharomyces c
149 Global analysis of pre-steady state and equilibrium bind
150 alanine racemase clearly refutes claims that
global analysis of progress curves can be used to extrac
151 In a
global analysis of protected areas, we show that kilomet
152 enrichment method that can be applied to the
global analysis of protein adducts with various naturall
153 Methods for the
global analysis of protein expression offer an approach
154 Quantitative proteome analysis, the
global analysis of protein expression, is increasingly b
155 s of signaling pathways are now commonplace,
global analysis of protein phosphorylation and kinase ac
156 Global analysis of protiated and deuterated progress cur
157 To facilitate the
global analysis of PTPs, we designed and synthesized two
158 Through a
global analysis of pulmonary gene expression in the lung
159 have been determined at pH 6.9 and 8.9 from
global analysis of racemization progress curves.
160 the selection of the BAC clones analyzed, a
global analysis of random sequence reads indicates that
161 Global analysis of RARalpha binding and enhancer mapping
162 Comparative
global analysis of RNA synthesis vs steady state levels
163 By performing an integrative, systematic,
global analysis of RNA turnover utilizing 4-thiouridine
164 d for synchronizing cell growth that enabled
global analysis of S. meliloti cell cycle-regulated gene
165 Through a
global analysis of sequence and structural similarity, i
166 To facilitate the
global analysis of serine hydrolase activities in comple
167 software SEDPHAT is introduced, allowing the
global analysis of several sedimentation velocity and eq
168 We performed
global analysis of short capped RNAs and Pol II Chromati
169 cture-function relationships, we performed a
global analysis of similarities across the entire superf
170 A
global analysis of single- and double-jump kinetic data,
171 kinetic mechanism for PheH was determined by
global analysis of single-turnover data in the reaction
172 Through
global analysis of SOX10-binding sites and epigenetic ch
173 The
global analysis of spectra at two frequencies yielded va
174 The
global analysis of spectra obtained at two microwave fre
175 Global analysis of SR4-associated differential gene expr
176 Here, we report that a
global analysis of SRC-1 target genes suggested that SRC
177 Global analysis of steady-state and transient kinetic da
178 Furthermore, a
global analysis of stopped-flow CD kinetic data is consi
179 We used a
global analysis of STRF shape based on a large database
180 Here, we review recent literature on the
global analysis of subcellular organelles and briefly di
181 ty transcript profiling to perform the first
global analysis of SUMO chain function.
182 We have undertaken a
global analysis of sumoylated proteins in Saccharomyces
183 Global analysis of synthetic lethality promises to ident
184 Global analysis of TFIIIC distribution revealed disperse
185 Global analysis of TFs has only been performed for three
186 A
global analysis of the activity, subcellular distributio
187 The
global analysis of the binding data by a combinatorial a
188 We performed
global analysis of the canola genes that were expressed
189 is method can be extensively applied for the
global analysis of the cell-surface N-glycoproteome.
190 Global analysis of the chlorophyll a fluorescence lifeti
191 The advantages of a
global analysis of the complete screening data set are d
192 Global analysis of the Cy3 and Cy5 FRET time-courses, us
193 These demonstrations revealed the power of a
global analysis of the data contained within gene expres
194 Global analysis of the data supports the hypothesis that
195 esent a comprehensive kinetic model based on
global analysis of the data.
196 Global analysis of the deletion collection was carried o
197 refolding and unfolding, not included in the
global analysis of the dimeric protein, reflects the pre
198 e seven homoeologous chromosome groups and a
global analysis of the entire mapped wheat EST data set.
199 Here, we provide a comprehensive
global analysis of the evolutionarily distant unicellula
200 Global analysis of the experimental results preferential
201 Our
global analysis of the FG domain requirements in mRNA ex
202 This study is the first
global analysis of the GAS transcriptome during invasive
203 ject Consortium enables for the first time a
global analysis of the genomic distribution of transcrip
204 en together, these results provide the first
global analysis of the human preimplantation embryo tran
205 an early stage of visual processing prior to
global analysis of the image.
206 Detailed
global analysis of the kinetic data clearly demonstrates
207 Global analysis of the kinetic data shows that the favor
208 ion via an intermediate are examined using a
global analysis of the kinetic data, and the most likely
209 Global analysis of the kinetic data, based on a sequenti
210 The
global analysis of the kinetic folding mechanism reveals
211 Further,
global analysis of the kinetics and the transient absorp
212 The
global analysis of the large number of low-abundance sph
213 However, additional regional studies and a
global analysis of the Late Ordovician mass extinction t
214 of Sac7d has been well-characterized with a
global analysis of the linkage of folding, protonation,
215 li to determine the best methods to approach
global analysis of the metabolome.
216 Global analysis of the pH dependence of the trimer-dodec
217 A
global analysis of the proteins in budding yeast classif
218 used to perform a quantitative and unbiased
global analysis of the rates at which newly synthesized,
219 A
global analysis of the resulting data allowed determinat
220 To enable a
global analysis of the results, we introduce the concept
221 Global analysis of the SAXS/WAXS patterns recovered time
222 Global analysis of the sedimentation equilibrium data de
223 This emerging technology provides data for a
global analysis of the selection process and for simulta
224 Global analysis of the severe SMNDelta7 SMA mouse model
225 For [Ru(tpy)(bpy)(dmso)](2+),
global analysis of the spectra reveals changes that are
226 of this dual robustness and sensitivity in a
global analysis of the structure of a conductance-based
227 Global analysis of the temperature and static field depe
228 Using a sequential model,
global analysis of the time-dependent scattering differe
229 A
global analysis of the time-resolved pyrene monomer and
230 Here, a
global analysis of the total lipid repertoire of Plasmod
231 h-throughput microarray data has enabled the
global analysis of the transcriptome, driving the develo
232 For trans-[Ru(tpy)(pic)(dmso)](+),
global analysis of the transient spectra reveals time co
233 A
global analysis of the translation efficiency of HCMV mR
234 Global analysis of the unimolecular unfolding transition
235 Global analysis of the upstream promoter regions of diff
236 A
global analysis of the urea- and temperature-induced equ
237 Global analysis of the UV/vis spectral kinetic data show
238 chronic HIV infection on aging, we report a
global analysis of the whole-blood DNA methylomes of 137
239 RNAi Screening Center (DRSC), we performed a
global analysis of their activity in 30 genome-wide scre
240 Multiwavelength
global analysis of these data provide two charge-recombi
241 Here, we provide a
global analysis of these data.
242 However,
global analysis of these events is currently limited.
243 Global analysis of these signatures confirms known assoc
244 Global analysis of this effect using microarrays indicat
245 a proteomic approach as the first step in a
global analysis of this important body fluid.
246 The
global analysis of time courses under different conditio
247 Global analysis of time- and frequency-resolved transien
248 By
global analysis of TPP1 side chain requirements for holo
249 Here, we present a spatially explicit
global analysis of tradeoffs between carbon stocks and c
250 a genomic scale, offering the potential for
global analysis of transcription factor occupancy in a s
251 A
global analysis of transcription revealed that loss of M
252 By performing a
global analysis of transcripts and protein production co
253 Comparative
global analysis of transcripts under induced and nonindu
254 fic ribosome profiling strategy that enables
global analysis of translation in defined subcellular lo
255 Global analysis of translation regulation has recently b
256 osome profiling is an emerging technique for
global analysis of translation that offers direct and ex
257 and ribosomal density that we observed in a
global analysis of translation.
258 No consistent and comparable
global analysis of trends has been done.
259 Global analysis of tRNA methylation in S. pombe showed a
260 ray platforms to perform a comprehensive and
global analysis of tumors arising in a model of metastat
261 In addition,
global analysis of viral transcripts by RNA sequencing i
262 An unbiased,
global analysis of where CREB binds has not been perform
263 Global analysis of WUE reveals existence of strong regio
264 The highly coupled nature of
global analysis often results in a significantly slower
265 We have conducted a
global analysis on a group of regulatory determinants th
266 ex and have been held to index the effect of
global analysis on local feature encoding.
267 ity was evaluated, leading to a quantitative
global analysis on the relative effects of LOF and GOF o
268 A
global analysis over such a range of conditions permitte
269 Global analysis performs better than unconstrained data
270 nalysis of gene expression (SAGE) provides a
global analysis platform for profiling mRNA populations
271 Such
global analysis provides a link between septation and th
272 This
global analysis removes some of the experimental inconve
273 The
global analysis revealed a transcriptome that bears sign
274 Global analysis revealed an unexpected correlation: Ribo
275 A
global analysis revealed changes in the abundances of 25
276 Global analysis revealed increased expression of the tra
277 Specifically, our
global analysis revealed that most genes with paused Pol
278 Global analysis reveals double Benioff zones in 30 segme
279 In total, this
global analysis reveals post-transcriptional regulators
280 Global analysis reveals that the TFIIIB-TFIIIC transcrip
281 Global analysis shows that all Ace2-only genes are bound
282 Global analysis shows that the thermal reactions for bot
283 nt calorimetric titration experiments into a
global analysis,
statistical analysis of binding paramet
284 ensities, were simultaneously analyzed using
global analysis techniques and fit to a two independent
285 a two independent receptor-class model using
global analysis techniques.
286 Further evidence for this comes from the
global analysis that identified a crucial overlap betwee
287 In a follow-up
global analysis,
there were 161 genes that covaried with
288 ultural productivity and carbon storage in a
global analysis to find where agricultural extensificati
289 e of lncRNAs in brain cancer, we performed a
global analysis to identify and characterize all annotat
290 ed by present data, and outline a route from
global analysis to more detailed and focused studies of
291 y, however, be more robustly extracted using
global analysis to simultaneously fit the fluorescence d
292 A
global analysis tool for competitive NF-kappa B/Ig kappa
293 A
global analysis underlined the predominance of induction
294 We interrogate this coincidence by
global analysis using a simplified model generally appli
295 Whole-cell
global analysis using this method allowed FRET measureme
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 Global analysis with a statistical mechanical model iden
300 ingly labeled alphabetaTm were combined in a
global analysis with doubly labeled alphabetaTm.