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1 cancer therapy, efficient reovirus reverse genetics rescue will accelerate production of recombinant reoviruses as candi
2 We argue that mesic microenvironments will act as species-specific refugia only if the nature and s
4 Such independent genetic control suggests that breeders will be able to select semi-independently for mean phenotype
5 is of chronic thromboembolic pulmonary hypertension (CTEPH) will be accelerated by an animal model that replicates the ph
7 nated by zoophilic vectors, existing vector control tactics will be insufficient to achieve elimination, even if maximize
8 ildren (57.3%; 95% uncertainly interval [UI], 55.2 to 60.0) will be obese at the age of 35 years, and roughly half of the
11 ly no validated biomarkers that predict which mRCC patients will benefit from antiangiogenic therapy.
14 ced AA and AR, their effect on subsequent guideline updates will depend on the methodology and evidence model used by eac
16 ut also for possibly identifying peripheral biomarkers that will eliminate the need for scalp biopsies.
18 tion and management of common postoperative conditions they will encounter as new surgical interns.
20 Building on this success, CRACKLE II will expand the network to hospitals across the United States
22 ion of compliance, and analyses of treatment mediators that will facilitate further therapeutic development.
24 eable in retrospective measurements of peripouch fat, which will foster future investigation of the role of mesentery fat
25 We therefore hypothesized that IL-15(-/-) mice will have reduced inflammatory responses during the developme
26 lower baseline Abeta1-42 level is an important finding that will have to be replicated in other cohorts.
27 port long-term survival and differentiation of repair cells will help identify, and eventually correct, the failures that
28 Interventions that target these events will interrupt tuberculosis transmission and accelerate the d
29 results suggest that combined, elevated CO2 and temperature will lead to long-term declines in the amount of carbon store
30 Validating these associations in vivo will lead to new diagnostic tools for Alzheimer disease and b
32 ing flowering and grain filling using donors such as NL-44, will minimize the negative impact of heat stress and increase
33 However, extant plant trait distributions will not allow extrapolations to novel community assemblages
34 on with a substantially increased resolution of gene models will not only further our understanding of the biological pro
35 see text] Although finite temperature equilibrium dynamics will not yield hyperuniform states, driven, nonequilibrium dy
38 testing results), the integrated cheminformatics algorithm will optimize the extracted biological data using in vitro-in
40 ange, we estimate that the population of sub-Saharan Africa will probably lose 2.3 million disability-adjusted life-years
41 es for the study of ancient plant populations and, in time, will provide higher taxonomic resolution and more precise est
42 nts, especially those with HER2 and ER negative tumors, who will receive one of the widely-accepted chemotherapy regimens
43 ns to novel community assemblages in future climates, which will require a mechanistic understanding of the trade-offs th
44 ng treated with alternative programs, comparison of results will require general agreement on definitions of response, re
45 ing one-stop diagnosis and treatment for all people with TB will require simpler, more sensitive diagnostics and broader
46 rgan shortage, preservation of average post-transplant eGFR will require sustained improvement in immunosuppression and o
47 r to realize high-density, low-power neuromorphic computing will require very large numbers of nanoscale nonlinear oscill
49 vious survey suggesting that one-third of patients might be willing to donate at imminent death, we estimate that between
50 e in the state of Wisconsin would be medically eligible and willing to donate each year at the time of imminent death.
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