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1 f the Saccharomyces cerevisiae Rad52 protein to learn how a cell controls its quantity and longevity.
2 great challenges for molecular biologists is to learn how a protein sequence defines its three-dimens
3                                              To learn how AAV interacts with host cells, we investiga
4                                              To learn how activation of keratinocyte nicotinic recept
5 he protein rigid, as in docking, with a view to learning how approximations made in docking affect ac
6 cal Record and Genomics (eMERGE) Network are to learn how best to return research results to patient/
7                                              To learn how building blocks of the pore can create spec
8                                              To learn how C. elegans Dicer, DCR-1, functions in multi
9 cteristics of pneumococci and, consequently, to learn how CBPs may affect nonspecific interactions wi
10                  This mouse model allows one to learn how cells of contrasting genotype functionally
11                                              To learn how certain ESCRT-IIIs shape positively curved
12 tigate the role of ICL4 in CFTR function and to learn how CF mutations in this region disrupt functio
13 proaches may be useful in other cancer types to learn how critical regulators of tumor lineage are li
14          Single molecule studies can be used to learn how different modes of preinitiation complex as
15                                              To learn how dystrophic musculature responds to altered
16 equirement for a single E2F site in vivo and to learn how E2F-mediated repression is regulated during
17 strength of these relationships is essential to learn how ecology scales up to affect microbiome asse
18 iencies, and further research should be done to learn how efficiency can be increased.
19 emarkable ability not only to learn but also to learn how fast it should learn.
20  multicancer screening saves lives, but also to learn how frequently it causes harm.
21            This will give us the opportunity to learn how genetics can contribute to better diagnosis
22                                              To learn how genomic sequence influences multiscale thre
23 and genome-wide levels-and how they are used to learn how GRNs operate as a function of time.
24                         The model is applied to learn how human brain networks vary across individual
25  which has enabled drug discovery scientists to learn how it may be possible to overcome such resista
26           We have cloned gon-4 in an attempt to learn how it regulates gonadogenesis.
27 tructure of the human CaMKIIalpha holoenzyme to learn how its ring architecture abets function.
28                                 In an effort to learn how mating systems evolve, we have cloned tra-2
29  requires skills and efforts of all involved to learn how members of the respective other tradition t
30  in extracellular vesicles was characterized to learn how miR-1 directed extracellular vesicle functi
31                                              To learn how monosomy-X may impact embryonic development
32 etter understand the function of Arg-347 and to learn how mutations at this site disrupt channel acti
33                      In particular, I wanted to learn how myxococcus builds its multicellular fruitin
34                                              To learn how NAPRTase uses this hydrolytic energy, we ha
35                                              To learn how nebulin functions in the assembly and maint
36 how neuronal diversity is generated, we need to learn how neuroblast-specific gene expression is esta
37 -diffusion equations provide a valuable tool to learn how new dynamics could emerge from quantitative
38                                              To learn how PHYB and GAs interact in the control of flo
39 lecular genetic approaches, we are beginning to learn how plants perceive ethylene and how this signa
40                                              To learn how plasma fibronectin stabilizes platelet-rich
41                                              To learn how proline side-chains could be structurally a
42                                              To learn how RAG-catalyzed transposition is inhibited in
43                                              To learn how retinal precursors segregate, we followed i
44                                              To learn how revertant mutations influence G551D-CFTR fu
45                                    We sought to learn how rheumatologists use evaluative laboratory t
46 ng inhibition in vitro was followed in order to learn how RNA polymerase II begins transcription at t
47                      An entire field emerged to learn how RNAs that lack the chemical versatility of
48 ework, for example that provided by the sun, to learn how stimuli are distributed in space and to rep
49  hairpin ribozyme cleavage activity in yeast to learn how structure-function relationships defined fo
50                                              To learn how such clocks influence behavioral and physio
51                                              To learn how TH elicits seemingly opposite responses in
52           Functionally, it will be important to learn how the ACSL isoforms can direct their acyl-CoA
53                                              To learn how the behavior of individual cells contribute
54                           We have only begun to learn how the brain represents social rank(5-9) and g
55                    This survey was conducted to learn how the career decisions of women and men in ca
56 r samples, including meteorites, can help us to learn how the Earth was made and acquired the ingredi
57                                              To learn how the firing of different clusters combines t
58                                              To learn how the interaction of granzyme B (GrB) with se
59                                     We hoped to learn how the introduction of cooperative cells into
60 nome variation and patterns of gene exchange to learn how the lake community evolved.
61                                              To learn how the MD-PFC thalamocortical network is engag
62                                    Expecting to learn how the mutations lead to loss of function, we
63       Here, we apply a quantitative approach to learn how the notochord forms during the development
64                                              To learn how the presence of Usp14 on 26S proteasomes in
65                                     In order to learn how the retention of PCNA on DNA might interfer
66 d have been uncovered, we are only beginning to learn how the specificity for the activation of each
67  molecular modelling of the hairpin ribozyme to learn how the two domains (A and B) might fold and ap
68           The overall goal of this study was to learn how the VAT Treg transcriptome adapts to differ
69                       In the future, we have to learn how these features change with disease or inter
70                       We made double mutants to learn how these genes might interact.
71 re enriched in different types of phagosomes to learn how these molecules work together to tailor inf
72                                              To learn how these networks reach a consensus, we model
73  health research fosters better science, and to learn how these partnerships have been able to flouri
74 ecisions are made at U.S. academic MICUs and to learn how these practices compare with the recommenda
75 ic iron inputs must be traced and quantified to learn how they affect primary productivity and climat
76 signing trials and should be further studied to learn how they can be favorably modified.
77 ble nephron numbers, it would be interesting to learn how they fare compared to living donor kidneys
78                                              To learn how this family of metalloenzymes functions, a
79                                              To learn how this interaction leads to bacterial death,
80                                              To learn how this occurs, a series of single point mutat
81                                              To learn how this pathway is established during developm
82 ion in humans emphasize that it is important to learn how this receptor influences lipoprotein metabo
83                    However, it is imperative to learn how to apply information derived from functiona
84                                      We need to learn how to approach the analysis of the complex dat
85 yanus loach is taken as the bionic prototype to learn how to avoid or slow down the mucus loss throug
86 racterized by high volatility and a tendency to learn how to avoid punishment rather than how to gain
87                   Further research is needed to learn how to best structure these conversations in th
88  be a necessary component of clinical trials to learn how to best tailor therapy to the patient.
89                                              To learn how to control the aqueous and membrane behavio
90 olecules behave randomly, so suddenly we had to learn how to deal with stochastic processes." Here I
91 but is not absolutely required for the cells to learn how to desensitize.
92 d here as supramolecular energy materials is to learn how to design soft materials containing light-h
93     A key challenge in stem cell research is to learn how to direct the differentiation of stem cells
94 lications of these materials it is important to learn how to drive transitions from one phase to anot
95 examined these complex interactions in order to learn how to introduce changes into the retroviral pr
96 or physicians who are asked to lead and want to learn how to lead well.
97                    There is, however, a need to learn how to make best use of this new resource.
98 flammatory bowel disease have lifelong needs to learn how to manage their symptoms and life situation
99 ization and provides a rational path forward to learn how to modulate these to improve therapy.
100                                We often need to learn how to move based on a single performance measu
101 omparison with sequential PET/MR imaging and to learn how to optimize an imaging examination.
102 in use similar brute-force fitting processes to learn how to perceive and act upon the world?
103  tools and resources for clinicians who want to learn how to perform QI specifically in the field of
104 , there has been tremendous effort worldwide to learn how to predict reaction rates and equilibrium c
105                         Bumblebees are known to learn how to recognize rewarding flower colors by wat
106                                     Research to learn how to respond to violence must be strengthened
107 h; some children may need guidance and rules to learn how to self-select appropriate portion sizes.
108  tooth development in this model may help us to learn how to stimulate growth of adult teeth in mamma
109 pK(a) calculations in proteins, we will need to learn how to treat this coupling between ionization o
110 ing that developing the ability of the brain to learn how to use an implant may be as important as fu
111                               As we continue to learn how to use targeted therapies in the context of
112 memory reactivation during sleep contributes to learning how to execute a novel action.
113                            Our next goal was to learn how Ung and Fpg affect susceptibility to homolo
114 nce of adopting qualitative research methods to learn how users work with data and digital tools, and
115                                              To learn how virus maintains and reactivates from latenc
116                                              To learn how well ungapped sequence comparisons of multi

 
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