ライフサイエンスコーパス: our understanding of

1 Our understanding of the frequency of large earthquakes at ti

2 Our understanding of the pathophysiological basis of chronic

3 and identification of centriole components have accelerated our understanding of its assembly, function, evolution, and i

4 fluence of early and midlife exposures will further advance our understanding of the disease.

5 sular alterations for FND and PTSD symptoms and may advance our understanding of FND.

6 Two recent papers advance our understanding of how the cancer genome evolves as the pri

7 f FANCD2 in governing cellular ATP production, and advances our understanding of how defective FA signaling contributes t

8 leukocyte extravasation and transmigration, which advances our understanding of the complex contribution of CtsB to angi

9 ons can inform better measurements of network structure and our understanding of collective phenomena.

10 c Bcl-2 proteins in human pancreatic beta-cells, broadening our understanding of cytokine-induced beta-cell apoptosis in

11 rain length and width, is an important yield component, but our understanding of the underlying genes and mechanisms is l

12 d with biotic changes in photosynthetic infrastructure, but our understanding of the relative effects of these factors ac

13 Critically, our understanding of ROS-mediated PTP oxidation is not yet su

14 abnormalities are remarkably common in early human embryos, our understanding of early embryonic somatic mutations is ver

15 experienced from social and ecological factors, and enhance our understanding of the dynamics of natural populations.

16 Next-generation sequencing has substantially enhanced our understanding of the genetics of primary brain tumors by

17 This study significantly enhances our understanding of the EAV carrier state in stallions by un

18 necessary for dynactin-mitochondria interaction, enhancing our understanding of how mitochondria properly localize in ax

19 Our finding can enrich our understanding of nanoscale energy transfer in molecular e

20 Work with this model system has enriched our understanding of the cyclopropanation-Cope rearrangement

21 A critical examination of these interactions could expand our understanding of viruses and be exploited for epidemiolog

22 The results extend our understanding of human CSF flux and open important clinic

23 This study facilitates our understanding of the fate and transformation of IAPP in v

24 echanisms controlling cardiac specification is critical for our understanding of how heart formation is initiated during

25 y increased resolution of gene models will not only further our understanding of the biological processes of this plant m

26 However, our understanding of N deposition effects on microbial commun

27 RNA signature associated with HLA class I-DSA could improve our understanding of ABMR and be useful for diagnostic or the

28 se biological systems and tissue types will further improve our understanding of ancient DNA breakdown dynamics.

29 These findings may improve our understanding of the mechanisms involved in rotor-guided

30 ant morphological profiling with great potential to improve our understanding of cellular heterogeneity through discoveri

31 Our work has the potential to improve our understanding of the role of global methylation in human

32 hypothesis which can be experimentally validated to improve our understanding of what triggers and maintains the growth o

33 tions into FRED to fill gaps in trait coverage will improve our understanding of changes in fine-root traits across space

34 accounting for Allee effects in social species will improve our understanding of the ecological and evolutionary implicat

35 udy, together with physiological measurements, has improved our understanding of the biological responses during droughts

36 Intensive research over the previous decades has improved our understanding of this complex arrhythmia while unraveling

37 an explore the identity of these genetic factors, improving our understanding of how they shape retinal function.

38 variable in research is absolutely essential for improving our understanding of disease mechanisms contributing to risk

39 nover to local, species-level effects, ultimately improving our understanding of spatial community dynamics.

40 This article reviews recent advances in our understanding of the proteasome's multistep ATP-dependent

41 However, until recently, deficiencies in our understanding of the nature of these cell populations, co

42 A major gap in our understanding of biodiversity-ecosystem function relation

43 rting point for handedness, implying a fundamental shift in our understanding of the ontogenesis of hemispheric asymmetri

44 also discuss how single-molecule approaches have increased our understanding of the dynamic behavior of complex multipro

45 identified key in vivo functions of ADAR enzymes, informing our understanding of the biological importance of A-to-I edit

46 ntal impairment in model mice in vivoSIGNIFICANCE STATEMENT Our understanding of the basis for intellectual impairment in

47 wever, are still unclear and represent a major challenge to our understanding of glacial climates.

48 ndent reflexes in the lower urinary tract and contribute to our understanding of the pathophysiology of urinary retention

49 Thus, this study contributes to our understanding of protein function within different Norovi

50 iew, I examine recent paradigm shifts that have transformed our understanding of pediatric ocular motor disease at the pr