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1  the single-cell level as well as via bulk biochemistry and will be advantageous for the study of neurotropic viruses in
2 ys to anticipate and manage the ongoing microbial challenge will be critical for achieving the United Nations Sustainable
3 ut the membrane-inserted state of SecA is still lacking and will be critical for elucidating the bacterial protein transp
4                                             Such a compound will be critical for elucidating the biological roles of this
5          Predictive biomarkers and mechanistic explorations will be critical for identifying appropriate patients for fut
6                         Continued research on CRF mutations will be critical for our future understanding of cancer biolo
7 cute and chronic activation of these inflammatory pathways, will be critical for the development of novel therapeutic str
8 on induced by immune-mediated lysis of infected hepatocytes will be critical for the future design of curative antiviral
9                     Understanding physiological acclimation will be critical for the large carbon stores in these ecosyst
10 entia (bvFTD) poses a daunting challenge for clinicians but will be critical for the success of disease-modifying therapi
11 pansion in vivo of PGCs and controlling follicle activation will be essential for continuing maintenance of the functiona
12 individuals and demonstrate that individual baseline values will be essential for predicting disease presence and progres
13  the view that accounting for disequilibrium range dynamics will be essential for realistic forecasts of patterns of biod
14 g of the molecular composition and characteristics of DPANs will be essential for the development of mechanism-based ther
15              Structural information for the Rho*-GT complex will be essential for understanding the molecular mechanism o
16 ibody is most sensitive to and provided novel insights that will be helpful for appropriate calibration of ELISAs.
17  further expands the mutation spectrum of RP2 and RPGR, and will be helpful for further study molecular pathogenesis of X
18 een pKa and chloride anion affinity of these receptors that will be important for designing future anion receptors and or
19                                           This new approach will be important for improving estimates of species distribu
20  formed when polycations interact with lipid membranes that will be important for predicting polycation-membrane interact
21              Such stratification, based on genomic drivers, will be important for selecting patients for clinical trials.
22                These SOD1-specific ALS natural history data will be important for the design and implementation of clinic
23                                                This finding will be important for women and caregivers considering preven
24                                                  This clock will be instrumental for understanding the biology of ageing
25 g information while maintaining deterministic detection and will be invaluable for long distance classical and quantum co
26 nsistent methods and routine reporting in the public domain will be necessary for tracking progress towards the 90-90-90
27                                     Significant preparation will be needed for a thorough, synchronized, and full withdra
28 geted agents, novel immunotherapies and combinations likely will be needed for most subtypes.
29 can be either positive or negative, but long term responses will be negative for all populations, with the timing of the
30  the basis for future investigation of enzyme variants that will be useful for applications in detoxifying chemicals haza
31 ment of a meta-analysis and to provide recommendations that will be useful for carrying out meta-analyses and for readers
32 itionally, the outlined expression strategy and strain sets will be useful for decoupling other downstream morphogenetic
33 he importance of more flexible sheep grazing management and will be useful for developing guidelines to optimize livestoc
34                                                   This work will be useful for developing novel strategies to deliver saf
35            Further, these results indicate that this system will be useful for functional and gene expression studies of
36                 We concluded that this improved mmLD method will be useful for future genome-wide association studies and
37 od-stage vaccine candidate, and we propose that this system will be useful for future vaccine candidate discovery.
38 and lincRNA-AK170409 as NF-kappaB regulators, and this tool will be useful for identifying additional genes involved in r
39 on model has both face and construct validity and therefore will be useful for investigating the neurobiological basis of
40 of porous materials for nucleation of protein crystals, and will be useful for optimal design of such materials.
41  nearly ideal two-dimensional Heisenberg ferromagnet and so will be useful for studying fundamental spin behaviours, open
42                            We anticipate that this approach will be useful for studying neural development and disease, a
43                                Significantly, SECM-based CV will be useful for the in situ characterization of various el
44           We believe the FKBP-based PB transposon induction will be useful for transposon-mediated genome engineering, in
45                                               These results will be useful for vector selection for various applications.
46                                 The updated homology models will be useful for virtual screening and drug design.
47 on of different diazonium reagents were also observable and will be valuable for applications of 1-20 nm organic films in
48                                   The models developed here will be valuable for evaluating the effects of filament shape
49                                 This newly developed system will be valuable for studying ZIKV disease because it more cl
50 opy number variations on neuropeptides and receptors, which will be valuable for the design of peptide-based cancer progn

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