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1 Understanding of their development is of high interest for pl
3 g complexes with sufficiently long values of T2 requires an understanding of precisely how the position of nuclear spins
4 Moreover, this single-cell approach provides a better understanding of how prostate cancer cells respond heterogene
5 fluke infection, it is imperative that we develop a better understanding of the basic biology of this parasite and how i
6 adins, LMW subunits and antigenic epitopes to gain a better understanding of the technology at a molecular level.
7 Active community-based surveillance allows for a better understanding of the true burden and seasonality of disease t
10 ates of the carbon budget in China's forests and for better understanding of effects of climate and stand characteristics
11 tness screening described by Glorius et al., builds a broad understanding of the impact of individual functional groups o
12 trations in humans.This study sought to advance the current understanding of placental vitamin D metabolism and its role
13 efinition of E dimers as the key antigenic target, and deep understanding of neutralizing mechanisms, multiple vaccine st
14 ly regulated by individual isoforms, necessitating a deeper understanding of how the distinct transcriptional programs co
15 in an iterative manner, with the aim of obtaining a deeper understanding of stem cell fate computation, in order to infl
17 e, we aim to discover new catalysts by obtaining a detailed understanding of the initial steps of CO2 electroreduction on
22 ty, and we highlight how such improvements enable a greater understanding of the pathogenesis of disease and the realizat
25 d degradation taking place throughout the tropics, improved understanding of the magnitude and spatial variation in deadw
28 blages in future climates, which will require a mechanistic understanding of the trade-offs that determine trait diversit
30 ium and their neighboring mesenchymal partners provides new understanding of how different cell types are maintained in t
33 identification of centriole components have accelerated our understanding of its assembly, function, evolution, and its r
34 This study significantly enhances our understanding of the EAV carrier state in stallions by unequi
36 nisms controlling cardiac specification is critical for our understanding of how heart formation is initiated during embr
37 creased resolution of gene models will not only further our understanding of the biological processes of this plant model
38 iological systems and tissue types will further improve our understanding of ancient DNA breakdown dynamics.
39 morphological profiling with great potential to improve our understanding of cellular heterogeneity through discovering n
40 iable in research is absolutely essential for improving our understanding of disease mechanisms contributing to risk and
41 g point for handedness, implying a fundamental shift in our understanding of the ontogenesis of hemispheric asymmetries i
43 t reflexes in the lower urinary tract and contribute to our understanding of the pathophysiology of urinary retention and
44 therapies for either FTD or NCL, in part because of a poor understanding of how mutations in genes such as GRN contribut
45 However, there is a fundamental gap in our quantitative understanding of the role of local ECM size and arrangement i
46 ovascular complications may be accomplished through a sound understanding of the hemodynamic and physiological consequenc
48 espite these limitations, there has been an increase in the understanding of pathophysiology and important risk factors b
49 In recent years, significant progress has been made in the understanding of proteasome assembly, structure, and function
50 1971;93(1):1-9) was an important contribution to the understanding of the epidemiology of cardiovascular diseases,
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