1 We tried to address this by optically detecting the conf
2 s on molecular and imaging technologies, and
we try to address questions about where we may go in the
3 erization, and electrochemical measurements,
we try to address the key issues of the ongoing debate t
4 In this study,
we try to address this challenge and present a novel par
5 Here,
we try to address this problem by using a framework to m
6 In this paper,
we try to address this question.
7 The question
we are trying to answer in this work is: are there any s
8 In our studies of subtilisin,
we are trying to answer two basic questions: why does su
9 pened up a host of intriguing questions that
we have tried to answer over the last 35 years.
10 ways and processes that may be implicated as
we try to answer these important questions in the months
11 We try to answer this by summarizing the main challenges
12 In this Perspective,
we try to answer this question.
13 In our response,
we try to argue that an explicitly atheoretical, purely
14 In the additional experiments reported here,
we tried to ascertain the preferred conformation in the
15 Here,
we try to ascertain whether two of these Wolbachia-types
16 Given this,
we tried to build an interpretable model that mimics the
17 In this study
we try to characterise the effect of proline on the geom
18 To address these general questions,
we are trying to characterize all the rate constants gov
19 We tried to characterize the downstream process by PBM,
20 In this study
we try to circumnavigate the inherent problems associate
21 On the basis of these findings,
we tried to circumvent the problem by simply diluting pr
22 We tried to clarify the nature of this step by searching
23 Additionally,
we try to clarify controversial issues concerning possib
24 ridization, RNA-sequencing, and marker data,
we try to compare how and when stem cell niches are esta
25 We tried to compile information on antidiabetic, antihyp
26 Herein,
we have tried to confirm 2 previous reports of HPV16 E6
27 We tried to confirm this by using the PLC inhibitor U731
28 r ring diameter determines septal thickness,
we tried to construct different SepF chimeras with the p
29 Here,
we have tried to correlate the function of MG and detect
30 ia length or percent ciliation was expected,
we tried to correlate ex-vivo tracheal cilia ciliary bea
31 Here
we try to cut through some of this hyperbole and review
32 When
we are trying to decrease caloric intake by reducing fat
33 We tried to define the best primary intention-to-treat s
34 synthetic and theoretical approaches (DFT),
we tried to demonstrate the usefulness of this method an
35 We try to deploy the retinal fovea to optimally scrutini
36 e of rodent and human cell lines and organs,
we tried to detail ATAD3 gene expression profiles and to
37 Here,
we have tried to determine the structural model for the
38 factors responsible for the inhibition, and
we have tried to determine where in the complement pathw
39 In the present study,
we tried to determine more precisely which of these site
40 We tried to determine whether morphine mimics preconditi
41 Thus, in this study,
we tried to develop NG-loaded macrophage membrane-coated
42 Instead,
we have tried to discuss particular findings that provid
43 We have tried to distinguish between these two models by
44 Here
we try to draw an arc from initiation of acute inflammat
45 In this study,
we tried to eliminate ImCs in an attempt to improve anti
46 We tried to elucidate the underlying mechanism for this
47 In three experiments,
we tried to elucidate whether listeners rely on formant
48 We are trying to emulate the cell-specific consequences
49 In this study,
we try to enhance this combination by "arming" ONYX-015
50 Finally,
we tried to establish the optimal time interval between
51 In an fMRI study
we tried to establish whether this depends on areas that
52 In this study,
we try to establish a more accurate model to address thi
53 We tried to estimate the direct and the indirect costs o
54 It is what
we are trying to explain.
55 In this study,
we tried to explain the remaining difference.
56 Here
we try to explain how that review moved the field forwar
57 This question is becoming crucial as
we try to explain the emergent scale-free topology of th
58 Here,
we try to explain these individual differences under nor
59 In this review article,
we have tried to explore as well as compile the role of
60 We tried to explore synthetic MR-based relaxometry to di
61 We try to explore here the consequences of gain versus l
62 Here,
we try to extensively investigate whether these loci con
63 We tried to extract flagellar filaments from such cells
64 metadata are correlated with the communities
we are trying to find.
65 Overall,
we try to fit these fecundity-limitation phenomena into
66 Our eyes move constantly, even when
we try to fixate our gaze.
67 From a definition of science
we try to foresee how simulation and theory will interac
68 From a definition of science
we try to foresee how simulation and theory will interac
69 aphic supports with quasi unlimited freedom,
we tried to formulate an answer to the question of how t
70 We have tried to gather a comprehensive view of the bios
71 cy, and this problem becomes even worse when
we try to generalize to other data types such as scATAC-
72 Rab5 isoforms in endocytosis in Leishmania,
we tried to generate null-mutants of LdRab5a and LdRab5b
73 We tried to get a rough insight on it from a theoretical
74 We try to give a proof that this sensing platform is ver
75 We have tried to highlight all the recent developments i
76 When possible
we have tried to highlight systems that use supramolecul
77 In doing so,
we have tried to identify gaps where they exist in the h
78 Here,
we have tried to identify the KCNQ subunits that are inv
79 In this study,
we tried to identify a universal association factor betw
80 In this study,
we tried to identify atypical N-glycosylation sites usin
81 We tried to identify components of the NorR regulon by p
82 In this study
we tried to identify factors in RNAseq data missingness.
83 improve the management of uncontrolled DCD,
we tried to identify factors predictive of outcome.
84 Here,
we tried to identify pathways and targets affected by th
85 Finally,
we tried to identify putative LdRab5a and LdRab5b effect
86 We tried to identify statistics whose power was robust o
87 We tried to identify statistics whose power was robust o
88 adually vanishes from academic institutions,
we tried to identify the sequences of inhibitory protein
89 We try to impart a sense of the scope and complexity of
90 By using a nomogram
we are trying to improve on the current practice of usin
91 pharmacophoric motif (d-Phe-Arg-Trp) fixed,
we tried to improve selectivity and physicochemical para
92 We tried to improve these outcomes by treating patients
93 In this review,
we have tried to incorporate the reported pathways used
94 When
we tried to induce immune responses to five mouse melano
95 In this study, therefore,
we tried to induce Th17 cells in cultures of severely bu
96 Here,
we tried to induce totipotent stem cells by mimicking DN
97 Here,
we try to induce a pan-H1N1 antibody response in pigs by
98 Here
we try to infer genome-wide recombination within a speci
99 ting what happens in our mind and brain when
we try to influence others, these results begin to expla
100 icance of apoptosis and autophagy in cancer,
we tried to investigate how HO-1 controls these events t
101 In this study,
we tried to investigate the roles of CXCR4 and CXCR2 sig
102 We tried to investigate whether advanced fibrosis screen
103 f the apparently metastatic behavior of LAM,
we tried to isolate LAM cells from body fluids.
104 Microsaccades, the small saccades made when
we try to keep the eyes still, were once believed to be
105 We tried to limit confounding bias through exact matchin
106 In particular,
we try to link information theoretic (variational) and t
107 m channels in the Drosophila nervous system,
we have tried to locate upstream cis-acting regulatory e
108 one that epidemiologists often encounter as
we try to locate the mediating processes between exposur
109 constantly making small movements even when
we try to maintain a fixed gaze.
110 plore the limit of electronic metastability,
we tried to make the related quadruply charged pyrene-1,
111 We tried to more fully characterize StcE activity to bet
112 In this study,
we tried to observe both of PI3Kgamma inhibitor Eganelis
113 Here,
we tried to observe if mammographic density also affects
114 velopment of the peptidyl transfer reaction,
we tried to obtain peptide bond formation without the ri
115 In this review
we tried to outline new pathophysiological and therapeut
116 In the translation,
we tried to preserve the content of the narrative while
117 With HSM
we try to propose a hybrid system based formalism that i
118 Here,
we have tried to provide a comprehensive review that syn
119 At this point,
we try to pull the reader up, giving the opposing view o
120 At this point,
we try to pull the reader up, giving the opposing view o
121 At this point,
we try to pull the reader up, giving voice to the opposi
122 Herein,
we tried to recapitulate mild, moderate, and severe BPD,
123 In this review,
we try to reconcile the different views of the transcrip
124 In this essay,
we try to reconcile these ideas and consider classes of
125 We try to reconcile these two meanings, positing that sy
126 n inference and design is that in the former
we try to reconstruct the system that has given rise to
127 We have tried to remedy these short-comings in the Roche
128 We found no evidence of interaction when
we tried to replicate previously reported interactions.
129 es and sample sizes used in the studies that
we tried to replicate, we suggest that many-if not all-o
130 odeling work on surround suppression is that
we have tried to reproduce realistic lengthscales that a
131 c fibrosis caused by the DeltaF508 mutation,
we tried to reproduce and extend the pre-clinical data o
132 Here,
we have tried to review the current understanding of the
133 In this article,
we tried to review different aspects of keratoconus stem
134 We try to shed light on the complex relationship of GBS
135 In this perspective,
we try to shed light on the state-of-the-art technology
136 In this manner,
we tried to simulate the conditions at the time of the i
137 Until now,
we have tried to study subtle and complex biological pro
138 In this review,
we have tried to summarize research--with an emphasis on
139 Thus, in this review
we try to summarize almost 40 years' worth of studies on
140 In this article
we try to summarize current knowledge on the function of
141 In this paper,
we try to summarize how DS accelerated the transition to
142 Here,
we try to summarize the contribution of biotechnology to
143 Here,
we try to tackle this challenge by introducing the conce
144 Over the last 10 years
we have tried to understand the roles of PIP(2) in regul
145 are distinct from other MCs, and for years,
we have tried to understand their origin and peculiariti
146 In this study,
we tried to understand why the abundant NMIIA does not l
147 lay an essential role in the coming years as
we try to understand the many ways actin filaments can t
148 examining the effects of neuroinflammation,
we try to understand the role that MMPs might have in ne
149 Here,
we try to understand the solid-solid phase transition oc
150 In this work,
we try to understand the structural preferences of AuI(3
151 We tried to use NPPV for 30 minutes in our clinic, and t
152 We tried to validate the putative TFF3 receptors CXCR4 a