1 We extended our analysis to 17 MYC-negative high-grade B
2 When
we extended the study to 3 months of quiescence, we conf
3 Here,
we extended the analysis to 33 directly measured and 13
4 We extended our previous analysis to 6.5 years after the
5 nue to be discovered as technologies evolve,
we extended the investigation to 6809 putative miRNAs en
6 s in viral RNA recombination, in this paper,
we extended the screening to 800 essential yeast genes p
7 To show the versatility of the model,
we extend it to a multiple minima system comprising seve
8 We extend our analysis to a mouse model of OPMD and demo
9 Here,
we extend our observations to a single BIR domain contai
10 In this work,
we extend our PSAM approach to a highly hydrophobic pept
11 Here,
we extend SHAPE chemistry to a benzoyl cyanide scaffold
12 Here
we extend such an analysis to a songbird, the zebra finc
13 In this paper,
we extend the BEAGLE API to a multiple Field Programmabl
14 To model these constraints,
we extend the LCT to a new structure, the partially labe
15 Here
we extend the technique to a more complex, biologically
16 In detail,
we extend the tomographic volume to a tensorial set of v
17 We extend these early findings to a very large high-prec
18 In this study,
we extend this principle to a strong synergism between t
19 Furthermore,
we extended our framework to a cross-species setting, id
20 We extended the study to a larger cohort of newborn and
21 We extended these analyses to a recent multiethnic T2D c
22 We extended this study to a larger cohort and found that
23 Here
we extend a model, developed to account for both the tim
24 We extend our approach to account for low-coverage seque
25 In particular,
we extend our model to account for the bias in the recom
26 We extend the methodology to account for correlations in
27 Here,
we extend dielectrophoretic nanowire assembly to achieve
28 Here
we extend this approach to achieve rapid, reversible, an
29 We extended this approach to additional targets and demo
30 Furthermore,
we extend our framework to address the pervasive problem
31 In this paper,
we extend this work to address the three following quest
32 phase proteins in the brain and circulation,
we extended our investigation to address whether changes
33 Based on scaling arguments,
we extend our modeling to all of Greenland and estimate
34 Also,
we extend its functionality to allow users to trade off
35 Finally,
we extend our analysis to allow for adaptive specificati
36 tly colonized with multiple strains of MRSA,
we extend the model to allow patients to be co-colonized
37 Here
we extend this theory to allow multiple steps during ada
38 Here
we extend two colocalization methods to allow for the sh
39 In the present article,
we extend this strategy to alpha-L-LNA: i.e., one of the
40 We extended these findings to an in vivo model.
41 Here,
we extend our methods to analyze whether this is attribu
42 We extend this framework to analyze single-cell RNA-seq
43 Using subtractive pharmacology,
we extend these findings to anandamide, a promiscuous en
44 We extended this approach to another toxic intermediate
45 Subsequently,
we extended this study to another gene, PHO5 (carrying t
46 Here,
we extend previous approaches to antigenic cartography,
47 We extend this technique to apply to the case where rare
48 Here,
we extend that analysis to approximately eighty organic
49 Herein,
we extend the reaction to aryl and vinyl bromides.
50 es have been created using the SST approach,
we extend it to assemble complex two-dimensional shapes
51 lammatory increases in vascular permeability.
We extended this approach to attenuate physiological inc
52 In this study
we extended the analysis to Broad and E74 and found that
53 Here
we extend this method to building custom three-dimension
54 We extend these observations to cell culture and tissue
55 ired by Feynman's path integral formulation,
we extend the theory to classical interacting systems.
56 We extend Smaldino's approach to collaboration and socia
57 Here
we extended these studies to compare the standard i.n./i
58 Here
we extend our method to compute these transmembrane curr
59 We extended these observations to confirm that S1PR1 (sp
60 individual standing in direct sunlight; here
we extend this approach to consider a walking hominin, h
61 Finally,
we extend this perspective to consider three contemporar
62 Here,
we extend this work to consider how the fate of a novel
63 Finally,
we extended HMM-DB to correct the baseline drift in sing
64 Here, using our new speleothem data,
we extend the Chinese record to cover the full uranium/t
65 Here
we extend our studies to demonstrate that MNV-1 replicat
66 We extend these findings to demonstrate that T cells fro
67 We extend these results to demonstrate a correlation bet
68 Importantly,
we extend these studies to demonstrate that even the ear
69 Here,
we extend this observation to demonstrate the selective
70 We extend those findings here to demonstrate antibody-me
71 We extend this method to derive epsilon values for both
72 In this study,
we extend previous results to describe a genetic circuit
73 Here
we extend the consensus strategy to design a globular pr
74 In doing so,
we extend GERMLINE, a method to detect IBD from exome se
75 We extended Drop-seq to detect dynamic expression change
76 Here
we extend these correlational studies to determine if in
77 In the present study,
we extended our previous investigations to determine whe
78 We extended particle tracking microrheology to determine
79 We extended the study to determine the peptide sensitivi
80 Here
we extend our efforts to dissect the mechanism of inhibi
81 We extended these observations to dissociated DRG neuron
82 Subsequently,
we extended this method to DNA extracts from human clini
83 To further boost the prediction accuracy,
we extend dRW to dRW-kNN.
84 Here,
we extend RBT to enable simultaneous monitoring of addit
85 We extend SpIDA to enable analysis of high-order oligome
86 Here
we extend this test to enable the characterization of a
87 Here
we extend this observation to establish that A20 is requ
88 Here
we extend a statistical framework to estimate rates of v
89 We extend statistical methods to estimate the frequency,
90 We extend this analysis to evaluate control strategies t
91 Here
we extend this work to examine the effectiveness of diff
92 Here
we extend this model to explain the reversal of SERCA2a
93 Herein
we extend our studies to explore the origin of these eff
94 We extend our theoretical framework to explore how trade
95 In the current study,
we extend this work to explore the longitudinal associat
96 We extend SpRL to extract discourse level spatial relati
97 Here,
we extend such work to flexible, multidomain proteins an
98 Here,
we extend the muChopper concept to fluorescence detectio
99 We extend classic theory to founder populations, giving
100 Finally
we extend our analysis to functions with more exotic top
101 Here,
we extend these studies to further characterize a varian
102 Here
we extend this approach to generate the first SC-beta ce
103 ms-level sensitivity analysis technique, and
we extended this analysis to generate other parameter-in
104 Furthermore,
we extended this technique to generate a 3D rendering of
105 Here,
we extend LplA-based labeling to green- and red-emitting
106 We extend GRAPPA to handle transpositions.
107 Here,
we extend MS2LDA to handle multiple metabolomics experim
108 s in the case of single-metabolite analysis,
we extend the methods to handle metabolite sets as well.
109 Here
we extend this modelling framework to heterogeneous musc
110 We extend this concept to higher electric multipole mome
111 Here
we extend this characterization to how repeated stress a
112 ve been based solely on transcript analysis,
we extended our analysis to HOXA5 protein localization i
113 Here
we extend these findings to HSV-1 strain 17syn+-derived
114 We extend these experiments to human RBCs and demonstrat
115 Here,
we extend these findings to human cells.
116 Here
we extend these findings to human mast cells and offer a
117 In this study
we extend these previous data to human cells and show th
118 We extended our findings to human thyroid cancer using T
119 We extended our studies to human orthologs and found tha
120 We extended these findings to human clinical samples and
121 Here,
we extend these findings to humans.
122 We extended these observations to humans, a species repo
123 Here
we extend our previous findings to identify the mechanis
124 In this paper,
we extend the software to identify putative cis-regulato
125 Here,
we extend these findings to identify GLI1, a transcripti
126 ccumulate intron-containing pre-mRNA in vivo
We extend this analysis to identify genetic interactions
127 Subsequently,
we extended our efforts to identify PI3Kalpha-specific i
128 Here
we extend that work to imputed genome-wide genotypes and
129 Here,
we extend this system to in vivo applications and use tT
130 selection and induced fit models considered,
we extend ANM to include concurrent but differentiated i
131 prehensive carbohydrate sequencing strategy,
we extend earlier reports to include the characterizatio
132 In this article,
we extend McVean's model to include gene conversion.
133 Finally,
we extend our model to include an immediate quit rate, a
134 We extend the analysis to include a comparison of surviv
135 ove the accuracy of our predicted relations,
we extend the integration methodology to include additio
136 Here,
we extend the model to include detailed models of protei
137 Here,
we extend the MSCE model to include clonal expansion of
138 Here
we extend the standard framework to include costly punis
139 Here,
we extend the study to include the effects of cell size
140 We extend the study to include two hexacene derivatives
141 Here,
we extend the technique to include a small amount of def
142 We extend the variance decomposition to include dominanc
143 In this report
we extend these findings to include a detailed character
144 In this study,
we extend these findings to include a large panel of fib
145 We extend these models to include groups of people isola
146 We extend these studies to include GATC sites involved i
147 Here
we extend this approach to include superhelical crucifor
148 Moreover,
we extend this approach to include the correspondence be
149 Herein,
we extend this methodology to include a bioinspired, cat
150 We extend this modeling approach to include searcher res
151 We extended our assays to include a limited number of ca
152 Here,
we extended previous theory to include exploitable resou
153 ger than the persistence length of dsDNA, so
we extended the model to include multiple parallel colli
154 of these compounds as drug-abuse treatments,
we extended the previous assessments to include a wider
155 no peer-reviewed studies of AXO effects, so
we extended the search to include grey literature.
156 Herein,
we extended this approach to include metabolic pathways,
157 We extended this investigation to include 20 grey matter
158 We extended this treatment approach to include children
159 In addition,
we extend the model to incorporate isotope information t
160 rrive at satisfactory results in such cases,
we extended NMF to incorporate preexisting qualitative k
161 Second,
we extended our method to incorporate external reference
162 Here
we extend the adhesion model to investigate the adhesive
163 In this work,
we extend these studies to investigate formation of the
164 Here,
we extended our research to investigate the role of Puma
165 Here
we extend this technique to ion-selective photoacoustic
166 Here
we extend these analyses to jawless vertebrates.
167 Here
we extend TimeSTAMP to label new protein copies by fluor
168 We extend brightness analysis to large macromolecular pr
169 We extend these findings to laser-capture microdissected
170 Then, with this concept,
we extend the supracrystalline growth to lattice-mismatc
171 ance of direct and indirect climate effects,
we extend metabolic scaling theory to link hypothesized
172 We extend our concept to liquid loads, generalizing the
173 Here,
we extend this work to look at physiological and cogniti
174 We extended our analysis to look for genes and proteins
175 Here,
we extend our observations to mammary carcinomas from mi
176 We extend our approach to map the stylistic topography o
177 Furthermore,
we extend the thermodynamic analysis to model the entire
178 Furthermore,
we extended our study to molecular assemblies in which e
179 In this work
we extend the stochastic model to more realistic BKCa-Ca
180 We extend these findings to more naturalistic conditions
181 In the work presented here,
we extend these studies to motif D, a region that forms
182 Here,
we extended our studies to mouse.
183 We extend the algorithm to multiple sequences by a consi
184 late the expressivity of the epialleles, and
we extended our paradigm to naturally occurring phenotyp
185 Here
we extend our observations to neurons in the pallidal [v
186 ting of imaging and therapeutic agents; here
we extend its use to oligonucleotide delivery.
187 Herein,
we extend this tactic to organic photochemistry.
188 We extend this approach to other ethnic groups and ident
189 Here
we extend this work to other X-H...pi interactions.
190 We extended our analysis to other cancer-related genes t
191 We extended our studies to other members of the importin
192 We extended the reaction to other carboxylic acids, demo
193 Here,
we extend this paradigm to pediatric bipolar disorder (B
194 Here,
we extend previous approaches to perform a Temporal Expr
195 Furthermore,
we extend this approach to perform single base-pair modi
196 We extended the proteomic analysis to phosphoproteomic p
197 ically achievable concentrations of CPX, and
we extended this effect to piroctone, 8-hydroxyquinoline
198 We extend the method to predict downstream effects on bi
199 Here,
we extend this methodology to prepare thin films and nan
200 To examine the later cyclization stages,
we extended this strategy to prepare stabilized cyclic i
201 Here
we extend those observations to primary leukemia cells a
202 ions are detected frequently in benign nevi,
we extended our studies to primary human melanocytes.
203 Finally,
we extended these findings to primary clinical specimens
204 Here
we extend it to probe spin moment change in the entire t
205 Here,
we extend the technique to probing the interfacial dynam
206 ng meiosis) functions drive oncogenesis, and
we extend this to propose that meiotic factors could be
207 underpinning psiko to bear in such studies,
we extended it to psiko2, which we introduce here.
208 To surmount this challenge,
we extend traction force microscopy to quantify the spat
209 Here
we extend the method to quantifying CnClm by introducing
210 We extend DDFT to quantum systems for application to den
211 We extended the study to reactive transport scenarios co
212 Here,
we extend ribosome profiling methodology to reveal a hig
213 Here,
we extend these observations to reveal a novel role for
214 Here,
we extend this concept to Salmonella typhimurium.
215 Further,
we extend AUC data analysis to sedimentation processes i
216 Here
we extend our studies to shewasin D, the pepsin homolog
217 In this article,
we extend our findings to show that similarly to humans,
218 Here,
we extend our studies to show a direct association betwe
219 In this work,
we extend our studies to show that poliovirus polymerase
220 We extend our work to show that in the presence of both
221 We extend previous theory to show that conditional expre
222 When drift dominates,
we extend Robertson's argument to show that, for any for
223 Here,
we extend these findings to show that elevated glucose m
224 In the current study
we extend these findings to show that the ability of ast
225 Here,
we extend these results to show that virus-specific T ce
226 In the present report,
we extend these studies to show that MN9D cytoplasmic pr
227 We extend this work to show that in addition to matrix m
228 that FliG was required for flagellation, and
we extend those findings to show that all four switch pr
229 that was dependent on the cag PAI T4SS; here
we extend those findings to show that the elevated respo
230 In this study,
we extended our findings to show that further sequential
231 We extended our findings to show that in mammalian cells
232 Moreover,
we extended our studies to show EHD1 regulates BIN1 indu
233 We extended this analysis to show that ICP22 can also be
234 Here
we extend the group model to signed directed networks su
235 We extended numeric examinations to simulate INCX in the
236 We extended our model to simulate the combination of APO
237 We extend this analysis to situations in which informati
238 Here
we extend this technology to stand-alone linear ion-trap
239 Here,
we extended our initial finding to structurally diverse
240 We extend our model to study crosstalk between multiple
241 In a second step,
we extend our models to study whether the subunits withi
242 Here,
we extend this work to study the collective behavior of
243 We extended the model to synthetic circuits that incorpo
244 We extend this evolutionary procedure to take into accou
245 Here,
we extend microscale thermophoresis to target immunologi
246 Here
we extend those results to targeting of a therapeutic ra
247 We extended the TDT to test for RV associations using fo
248 Here
we extend brightness analysis to the nuclear envelope (N
249 We extend here this formalism to the case of the Abeta40
250 Furthermore,
we extend it to the truncated group-lasso (TGL), and pro
251 We extend our analysis to the community level, exploring
252 We extend our analysis to the motor level by showing tha
253 Here
we extend our initial observation to the entire mouse ge
254 We extend our observation to the murine male germline, w
255 We extend our previous method to the more general case o
256 Finally,
we extend our work to the case of a population connected
257 Here,
we extend that work to the study of the biogenesis of NK
258 Here,
we extend these statistics to the simultaneous compariso
259 Here
we extend this approach to the green lineage by assembli
260 We extend this concept to the case of weighted brain net
261 Here,
we extend this construct to the assessment of cerebral i
262 Here
we extend this culture system to the propagation of prim
263 Here,
we extend this functionality to the domain of magnetic r
264 Here
we extend this idea to the world's electricity sectors b
265 Ultimately,
we extend this macrophage ratio to the tissue scale and
266 Here,
we extend this strategy to the generation of periodic pr
267 Herein,
we extend this study to the double-stranded helix.
268 Herein,
we extend this study to the synthesis of various glycosi
269 We extend this theory to the realm of unicellular organi
270 Here
we extend this understanding to the synthesis of hexagon
271 (PR-A) assembly at multiple promoters; here
we extend this work to the role of PR-A in mediating pro
272 Here
we extend those observations to the hippocampus and neoc
273 Furthermore,
we extended our analysis to the formation of stress-indu
274 We extended our investigation to the population level by
275 phagocytophilum isolates share this ability,
we extended our studies to the geographically diverse st
276 Here,
we extended the study to the biologically relevant micel
277 Recently,
we extended the study to the case of recurrent epidemics
278 Moreover,
we extended the technique to the assembly of lipid-stabi
279 We extended these findings to the development of a modul
280 In the current study,
we extended this analysis to the entire GR transcriptome
281 Focusing on the post-translocational state,
we extended this assessment to the single-residue level,
282 We extend these observations to their functions at enhan
283 Here
we extend May's results to these relationships and find
284 Here,
we extended our analysis to three syn point mutants: A85
285 Here,
we extend this stimulation protocol to time-dependent br
286 Here
we extend this approach to tissues that strongly scatter
287 using a computationally efficient approach,
we extend this idea to tune more general properties of n
288 Here,
we extend the fRMA algorithm to two new microarray platf
289 We extended our analysis to two studies containing trans
290 Here
we extend that study to understand better how Pcdh15 ope
291 We extend this approach to understand the effects of sid
292 We extended our study to unsymmetrical substrates and co
293 Here
we extend existing methodology to use dosage data on SNP
294 by applying it within the same species, then
we extend it to use data available in closely related sp
295 We extended these observations to virological synapses i
296 We extended photoswitching to visible wavelengths >400 n
297 Using photoactivatable GFP (paGFP),
we extended our protocol to visualize single functionall
298 Similar conclusions emerged when
we extended the survey to viviparous amphibians and rept
299 We extend these findings to X-DC human patient cells in
300 We extend our technology to yeast RNA-binding proteins (