ライフサイエンスコーパス: we demonstrate that

1 We demonstrate that clemizole binds to serotonin receptors an

2 We demonstrate that deregulated necroptosis results in system

3 We demonstrate that double heterojunctions designed into coll

4 We demonstrate that elevated Ctnnd1 expression contributes to

5 We demonstrate that Env-specific HLA-B*14-restricted activity

6 We demonstrate that even though the direction of force might

7 We demonstrate that Hoxb8 mutants contain corticostriatal cir

8 We demonstrate that long-range electrostatic fields emanating

9 We demonstrate that loss of Wnt5a results in cerebellar hypop

10 We demonstrate that optical spatial solitons with non-rectili

11 We demonstrate that ovarian cancer exhibits a targetable alte

12 We demonstrate that partial loss of p85alpha increases the am

13 We demonstrate that particle morphology and evaporation is de

14 We demonstrate that Si(OH)4 cycling through the Holocene alte

15 We demonstrate that targeted next-generation DNA sequencing r

16 We demonstrate that the Co(III)2(IV)2 cubane may be electroch

17 We demonstrate that the polo-like kinase PLK-1 mediates the r

18 We demonstrate that this unusual cyclic behaviour is governed

19 We demonstrate that YonO is a bona fide RNAP of the SPbeta ba

20 t rats while recording single unit and population activity, we demonstrate that PNN removal alters the balance between in

21 In addition, we demonstrate that Nbeal2 is primarily localized in the cyto

22 In this article, we demonstrate that a human ornithine transcarbamylase gene c

23 ansport measurements and electronic structure calculations, we demonstrate that the intercalation is driven by the exchan

24 Following gene inactivation and replacement in human cells, we demonstrate that CENP-A mutants that cannot be phosphoryla

25 s, hRETNTg(+)Tlr4(-/-) mice, and human immune cell culture, we demonstrate that hRetn binds the LPS receptor Toll-like re

26 Finally, we demonstrate that MAPPIN outperforms CADD and Eigen in pred

27 Furthermore, we demonstrate that the transcriptional regulation by the psy

28 Here we demonstrate that key RQC activities-Ltn1p-dependent ubiqui

29 Here we demonstrate that mate choice in the fruit fly Drosophila m

30 Here we demonstrate that sub-nanosecond spin-orbit torque pulses c

31 Here we demonstrate that the expression of an endogenous Braf(D631

32 Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) Shewan

33 Here, we demonstrate that comprehensive two-dimensional gas chromat

34 Here, we demonstrate that CRISPR/Cas9 genome editing of promoters g

35 Here, we demonstrate that interplay of p300-HDAC2-Sin3A in the chro

36 Here, we demonstrate that Ssp1 activates a second ARK, Ssp2/AMPKalp

37 Here, we demonstrate that the antidepressant-like efficacy of three

38 Here, we demonstrate that the FX/SR-AI-complex comprises a third pr

39 Herein, we demonstrate that cucurbit[7]uril (CB[7]) can catalyse Diel

40 Here, using human in vivo deuterium labeling, we demonstrate that classical monocytes emerge first from mar

41 Lastly, we demonstrate that SHF ventricular and OFT progenitors exhib

42 tion between carbon networks and polymerized ionic liquids, we demonstrate that carbon-based porous nanoarchitectures can

43 Using a malaria transmission model we demonstrate that in such regions dominated by zoophilic ve

44 sing the regenerating mouse digit tip as a mammalian model, we demonstrate that macrophages are essential for the regener

45 Using a glioma mouse model, we demonstrate that doxorubicin-loaded (D)CDX-RBCNPs have sup

46 Through simulation we demonstrate that the gene tree probabilities computed by S

47 rphic effects of morphine in the rat.SIGNIFICANCE STATEMENT We demonstrate that periaqueductal gray (PAG) microglia contr

48 In this study, we demonstrate that binding domains from autolysins and lysin

49 In this study, we demonstrate that culturing cells in different physical env

50 In this work we demonstrate that such a photosensitiser, chlorin e6, can b