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 Here,
we try to address this problem by using a framework to m
4 The question
we are trying to answer in this work is: are there any s
5 In our studies of subtilisin,
we are trying to answer two basic questions: why does su
6 pened up a host of intriguing questions that
we have tried to answer over the last 35 years.
7 In our response,
we try to argue that an explicitly atheoretical, purely
8 In the additional experiments reported here,
we tried to ascertain the preferred conformation in the
9 Here,
we try to ascertain whether two of these Wolbachia-types
10 In this study
we try to characterise the effect of proline on the geom
11 To address these general questions,
we are trying to characterize all the rate constants gov
12 On the basis of these findings,
we tried to circumvent the problem by simply diluting pr
13 We tried to clarify the nature of this step by searching
14 Additionally,
we try to clarify controversial issues concerning possib
15 Herein,
we have tried to confirm 2 previous reports of HPV16 E6
16 We tried to confirm this by using the PLC inhibitor U731
17 Here
we try to cut through some of this hyperbole and review
18 We tried to define the best primary intention-to-treat s
19 e of rodent and human cell lines and organs,
we tried to detail ATAD3 gene expression profiles and to
20 factors responsible for the inhibition, and
we have tried to determine where in the complement pathw
21 In the present study,
we tried to determine more precisely which of these site
22 We tried to determine whether morphine mimics preconditi
23 Instead,
we have tried to discuss particular findings that provid
24 We have tried to distinguish between these two models by
25 In this study,
we tried to eliminate ImCs in an attempt to improve anti
26 We tried to elucidate the underlying mechanism for this
27 In three experiments,
we tried to elucidate whether listeners rely on formant
28 We are trying to emulate the cell-specific consequences
29 In this study,
we try to enhance this combination by "arming" ONYX-015
30 Finally,
we tried to establish the optimal time interval between
31 In an fMRI study
we tried to establish whether this depends on areas that
32 In this study,
we try to establish a more accurate model to address thi
33 In this study,
we tried to explain the remaining difference.
34 This question is becoming crucial as
we try to explain the emergent scale-free topology of th
35 In this review article,
we have tried to explore as well as compile the role of
36 We try to explore here the consequences of gain versus l
37 Here,
we try to extensively investigate whether these loci con
38 We tried to extract flagellar filaments from such cells
39 metadata are correlated with the communities
we are trying to find.
40 Overall,
we try to fit these fecundity-limitation phenomena into
41 Our eyes move constantly, even when
we try to fixate our gaze.
42 Rab5 isoforms in endocytosis in Leishmania,
we tried to generate null-mutants of LdRab5a and LdRab5b
43 We tried to get a rough insight on it from a theoretical
44 We try to give a proof that this sensing platform is ver
45 We have tried to highlight all the recent developments i
46 When possible
we have tried to highlight systems that use supramolecul
47 In doing so,
we have tried to identify gaps where they exist in the h
48 Here,
we have tried to identify the KCNQ subunits that are inv
49 In this study,
we tried to identify atypical N-glycosylation sites usin
50 We tried to identify components of the NorR regulon by p
51 Here,
we tried to identify pathways and targets affected by th
52 Finally,
we tried to identify putative LdRab5a and LdRab5b effect
53 We tried to identify statistics whose power was robust o
54 We tried to identify statistics whose power was robust o
55 We try to impart a sense of the scope and complexity of
56 By using a nomogram
we are trying to improve on the current practice of usin
57 pharmacophoric motif (d-Phe-Arg-Trp) fixed,
we tried to improve selectivity and physicochemical para
58 We tried to improve these outcomes by treating patients
59 In this review,
we have tried to incorporate the reported pathways used
60 When
we tried to induce immune responses to five mouse melano
61 In this study, therefore,
we tried to induce Th17 cells in cultures of severely bu
62 ting what happens in our mind and brain when
we try to influence others, these results begin to expla
63 icance of apoptosis and autophagy in cancer,
we tried to investigate how HO-1 controls these events t
64 In this study,
we tried to investigate the roles of CXCR4 and CXCR2 sig
65 f the apparently metastatic behavior of LAM,
we tried to isolate LAM cells from body fluids.
66 Microsaccades, the small saccades made when
we try to keep the eyes still, were once believed to be
67 We tried to limit confounding bias through exact matchin
68 In particular,
we try to link information theoretic (variational) and t
69 m channels in the Drosophila nervous system,
we have tried to locate upstream cis-acting regulatory e
70 one that epidemiologists often encounter as
we try to locate the mediating processes between exposur
71 constantly making small movements even when
we try to maintain a fixed gaze.
72 plore the limit of electronic metastability,
we tried to make the related quadruply charged pyrene-1,
73 We tried to more fully characterize StcE activity to bet
74 velopment of the peptidyl transfer reaction,
we tried to obtain peptide bond formation without the ri
75 In the translation,
we tried to preserve the content of the narrative while
76 With HSM
we try to propose a hybrid system based formalism that i
77 Here,
we have tried to provide a comprehensive review that syn
78 In this essay,
we try to reconcile these ideas and consider classes of
79 n inference and design is that in the former
we try to reconstruct the system that has given rise to
80 We have tried to remedy these short-comings in the Roche
81 We found no evidence of interaction when
we tried to replicate previously reported interactions.
82 c fibrosis caused by the DeltaF508 mutation,
we tried to reproduce and extend the pre-clinical data o
83 Here,
we have tried to review the current understanding of the
84 We try to shed light on the complex relationship of GBS
85 In this manner,
we tried to simulate the conditions at the time of the i
86 Until now,
we have tried to study subtle and complex biological pro
87 In this review,
we have tried to summarize research--with an emphasis on
88 Thus, in this review
we try to summarize almost 40 years' worth of studies on
89 In this article
we try to summarize current knowledge on the function of
90 Here,
we try to summarize the contribution of biotechnology to
91 Here,
we try to tackle this challenge by introducing the conce
92 Over the last 10 years
we have tried to understand the roles of PIP(2) in regul
93 In this study,
we tried to understand why the abundant NMIIA does not l
94 lay an essential role in the coming years as
we try to understand the many ways actin filaments can t
95 examining the effects of neuroinflammation,
we try to understand the role that MMPs might have in ne
96 In this work,
we try to understand the structural preferences of AuI(3
97 We tried to use NPPV for 30 minutes in our clinic, and t