ライフサイエンスコーパス: to further explore

1 To further explore how bilayer lipids affect or are affected

2 To further explore how EEL-1 functions, here we performed aff

3 To further explore how the B. subtilis cell wall structure ca

4 To further explore its physiologic functions in hematopoietic

5 To further explore its structure-activity relationship, a new

6 To further explore reward deficits we used intracranial self-

7 To further explore the cooperative relationship of spin, ener

8 To further explore the differences in reactivity, thiiranium

9 To further explore the effects of Ddr1 ablation, Ddr1(-/-) mi

10 To further explore the impact of lifestyles and electrificati

11 To further explore the mechanism of channel formation, we per

12 To further explore the population-level resistance profiles o

13 To further explore the relationship between transcriptional r

14 To further explore these effects, we implemented a computatio

15 To further explore this interaction, the transcription profil

16 To further explore this phenomenon, we conducted a population

17 To further explore this relationship, 22 human blood samples

18 Therefore, we aimed to further explore their lipoprotein metabolism and to charac

19 rize genes that are co-expressed with ACE2 and TMPRSS2, and to further explore their biological functions and potential a

20 We use two independent approaches to further explore this controversy.

21 d our previous RNA-seq data and performed phenotypic assays to further explore the impact of PF on A. baumannii's microbi

22 We applied MAP-C to further explore the biochemical mechanism of these contact

23 GRA in Toxoplasma and provide a resource for the community to further explore the function of Toxoplasma genes that dete

24 s and site-level likelihood comparisons were then conducted to further explore the introgressed signal within our dataset

25 The authors examine national data to further explore allograft (kidney and pancreas) and patien

26 Collectively, the results of study provide a foundation to further explore the biology of mitoviruses.IMPORTANCE Caps

27 mula: see text] This paper paves the experimental framework to further explore chip-scale axon and neuron specific neural

28 th miRNAs and mRNAs from DA neurons of each treatment group to further explore the altered genes and related biological p

29 ns, Hg concentration, and Hg/TOC ratios, and Re-Os isotopes to further explore their causal relationship.

30 We then used this model to further explore geometric and kinetic factors that may inf

31 de a solid basis for the application of pre-clinical models to further explore the potential of gene editing against FA,

32 Prospective studies are necessary to further explore risk factors for SCR and to identify which

33 Further studies are necessary to further explore what constitutes best practice for informe

34 There is a need to further explore differences in underlying pathophysiologic

35 gy and thus more basic and translational studies are needed to further explore this topic.

36 Here we use STD-NMR to further explore the different driving forces that are resp

37 scriptome, opening new diagnostic avenues and opportunities to further explore the interplay of regulatory mechanisms wit

38 However, our promising results open up new possibilities to further explore the action of cardosins on whey proteins f

39 These include the potential to further explore alternate electrode materials, use of ion

40 Relevant links are provided to further explore knowledge about the target gene, the small

41 o promote healthy work environments, and promoting research to further explore practical strategies to address, mitigate,

42 For this study, we sought to further explore the functional consequences of PDK4 defici

43 /MM1/H3N2 challenge virus can be utilized in future studies to further explore pathogenesis and immunity and to evaluate

44 ular target for S1P in cell survival regulation, and a tool to further explore the biochemical and biological functions o

45 lated pelagiphages and their genome sequences will allow us to further explore their infectivities and ecological strateg

46 Initial murine studies led us to further explore a potential intracellular antiviral activi

47 s and allows for efficient data collection that can be used to further explore and understand differences in conference p

48 Kaplan-Meier analysis was used to further explore the association between biochemical marker

49 Nevertheless, large population-based studies are warranted to further explore the role of MALAT-1 SNPs in HCC incidence

50 Our work paves the way to further exploring topological phases in driven optical sys