1 Guided by the 2(N + 1)2 electron-counting rule for spher
2 Guided by experimental Phi-values, a putative transition
3 Guided by findings in linkage mapping, a genome-wide ass
4 Guided by structural simulation, a fused pol Sdbh with n
5 Guided by these results, a cultured retinal microglia mo
6 Guided by structural models, active site engineering of
7 on the LASAGNA (Length-Aware Site Alignment
Guided by Nucleotide Association) algorithm.
8 Guided by the histopathologic map, all spectroscopy voxe
9 Guided by the structures, an optimized molecule was gene
10 Guided by these parameters, an arterial spin labeling MR
11 Guided by computer modeling studies, and taking advantag
12 Guided by features of molecular, cellular, and circuit d
13 Guided by the Prp28*AMPPNP structure, and that of the Dr
14 Guided by a computational modeling approach, appropriate
15 Guided by nuclear magnetic resonance (NMR) binding assay
16 Guided by nuclear magnetic resonance (NMR) binding assay
17 Guided by the data, calculations show that electron-hole
18 Guided by extensive theoretical analysis, cellular struc
19 Guided by structure based design, changes to P2' and P3
20 Guided by single guide (sg)RNAs, dCas9-AID-P182X (AIDx)
21 Guided by optical simulation, each of the active layer t
22 Guided by numerical simulations, experiments are designe
23 Guided by bioinformatics, four diastereomers were synthe
24 Guided by X-ray cocrystal structures, fragment 1 was ela
25 Guided by comparative genomics, here we reverse-engineer
26 Guided by metabolomic analyses, here we employ a combina
27 Guided by MM results, high-resolution differential scann
28 Guided by initial microarray analysis, in vitro studies
29 Guided by solution NMR experiments, it could be shown th
30 Guided by the geometrical analysis, linkers with differe
31 Guided by this structure, mutations were introduced into
32 Guided by microscale X-ray CT, nanoscale X-ray CT is use
33 Guided by the 'directionality' of cell development along
34 Guided by this data, optimal design parameters were esta
35 Guided by the computational models, reaction between 2,3
36 Guided by biochemical data, rigid body modeling of subun
37 Guided by the neutron reflectivity measurements, suitabl
38 Guided by a kinetic model, the oligomer dissociation rat
39 Guided by structural-biology information, the binding-po
40 Guided by the optimized calculated spectra, the tunabili
41 Guided by molecular modeling, this series was evolved to
42 Guided by topology, two flexible isomeric MOFs, compound
43 Guided by these predictions, we demonstrated, via gain-
44 Guided by a "proximate determinants" approach, we focus
45 Guided by a computational model, we fabricated a patch c
46 Guided by available evidence, we present an algorithm fo
47 Guided by bioinformatic analysis, we demonstrated that s
48 Guided by ChR2-EYFP fluorescence, we recorded systematic
49 Guided by cognitive deficits, we demonstrated that mutan
50 Guided by comparative sequence considerations, we have e
51 Guided by computational analysis, we designed variants o
52 Guided by computational design, we optimized the interfa
53 Guided by endonuclease restriction maps, we chose PCR pr
54 Guided by functional magnetic resonance studies, we expl
55 Guided by functional maps, we recorded neurons in the la
56 Guided by ion motion simulations, we designed elevator a
57 Guided by mechanistic studies, we disclose the selective
58 Guided by molecular modeling, we investigated the molecu
59 Guided by molecular modeling, we synthesized and studied
60 Guided by multiple sequence alignments, we used site-dir
61 Guided by power calculations, we used statistical infere
62 Guided by predictions of this model, we found that the d
63 Guided by predictive modelling, we enhanced the circuit'
64 Guided by previous experimental observations, we have st
65 Guided by protein dimerization properties, we examined D
66 Guided by Rasch analysis, we constructed and validated a
67 Guided by recent experimental reports, we propose that t
68 Guided by results from transcriptional profiling, we ide
69 Guided by RNA sequencing expression profiling, we have d
70 Guided by sequence alignment, we created IDL deletions i
71 Guided by six central questions, we propose an integrati
72 Guided by structural information, we identified a unique
73 Guided by structure-based mutagenesis, we identify amino
74 Guided by structure-based optimization, we were able to
75 Guided by the computational results, we used chemical pr
76 Guided by the crystal structures, we engineered a series
77 Guided by the disease phenotype, we investigated the rol
78 Guided by the Drosophila studies, we reasoned that a dow
79 Guided by the model, we developed two signatures consist
80 Guided by the model, we tested the hypothesis that AIPL1
81 Guided by the motif rotamer searches, we made improvemen
82 Guided by the mouse genetic analysis, we demonstrate tha
83 Guided by the receptor docking model, we have mapped the
84 Guided by the strongest signal, we evaluate thousands of
85 Guided by the structural information, we generated a num
86 Guided by the structures, we engineered disulfide cross-
87 Guided by thermodynamics, we have synthesized two mixed-
88 Guided by these "knobs" and "holes", we designed variant
89 Guided by these data, we designed fluorogenic peptide su
90 Guided by these findings, we were able to generate artif
91 Guided by these imaging findings, we undertook a focused
92 Guided by these observations, we present an alternative
93 Guided by these phylogenetic analyses, we developed a ne
94 Guided by these results, we assessed the FOXP3 and EZH2
95 Guided by these results, we demonstrate that a subset of
96 Guided by these results, we discover that bacterial sign
97 Guided by these rules, we designed sequences predicted t
98 Guided by these structural models, we expressed and puri
99 Guided by these studies, we analyzed mouse placentas and
100 Guided by these studies, we identified a regulon of appr
101 Guided by these studies, we next sought to examine the t
102 Guided by this evolutionary genomic analysis, we generat
103 Guided by this finding, we determine the activation barr
104 Guided by this finding, we have further interrogated the
105 Guided by this information, we identified KEAP1 (also kn
106 Guided by this information, we mutated Dbs to alter sign
107 Guided by this model, we showed that 7-9 N-terminal amin
108 Guided by this scaling law, we then perform Monte Carlo
109 Guided by this screening excise, we showed that netropsi
110 Guided by this sequence, we computationally identified 1
111 Guided by this structural information, we design peptide
112 Guided by this structure, we remodeled the surface of th
113 Guided by this structure, we use protein-engineering app
114 Guided by this structure, we used tryptophan-scanning mu
115 Guided by this, we devise an experimental protocol using
116 Guided by Y-chromosome sequence, we localized breakpoint