ライフサイエンスコーパス: show that

1 esults in the context of topological superconductivity, and show that the observed critical supercurrent enhancement is c

2 Here the authors show that MRAP2 also regulates ghrelin receptor signalling in

3 Our resource estimates show that, even when taking into account the substantial over

4 Multiple lines of evidence show that cold stadials in the North Atlantic were accompanie

5 Finally, gain-of-function experiments show that Pth4 can alter calcium/phosphorus levels and affect

6 Genetic experiments show that ectopic dATM is sufficient to promote DNA synthesis

7 Our findings show that, in the striatum, a brain region implicated with mo

8 Hierarchical regression analyses further show that variations in spatial precision account for much of

9 ed the same patterns in human transcriptomes and we further show that AS rates correlate with the fitness cost of splicin

10 e results of chemically detailed simulations presented here show that this is not the case; pronounced deviations of the

11 Current results show that FLIm parameters linked to the amount of structural

12 Model results show that agonist-induced intracellular calcium dynamics can

13 Our results show that PTEN controls multicellular assembly through a memb

14 Our results show that the major insect opsin class (SW) that typically co

15 The results show that saccadic preparation and visual sensitivity oscilla

16 Here we use biochemical and structural methods to show that two molecules of Cas2/3 assemble with four molecule

17 Finally, we utilized the expanded cerebral organoids to show that infection with Zika virus impairs cortical growth a

18 helman et al. applied single-molecule force spectroscopy to show that an adhesin protein can regenerate its thioester in

19 Here we use resting-state fMRI data from 176 subjects to show that signals from the human white-matter contain meaning

20 We show that HSP22E and HSP22F are major chloroplast-targeted sH

21 We show that signalling through the TrpA1 thermo-sensor is requi

22 We show that such a framework is consistent with the stationary-

23 We show that the expression of many miRNAs is dramatically regul

24 We show that the line-shape of the measured resonant elastic X-r

25 We show that the photochemical reaction mechanisms for alpha-ket

26 We show that the same as for genes SPAD follows a beta distribut

27 We show that TSRI estimators with modified standard errors have

28 In this article, we show that CXCL8 expression, prior to proliferation, is common

29 these enhanced sgRNAs (e-sgRNA) and mRNA encoding Cas9, we show that a single intravenous injection into mice induces >8

30 4 wild-type parasites at multiple stages of development, we show that sexually committed, AP2-G(+) mature schizonts speci

31 nt learning simulations, and behavioral experimentation, we show that the resolution to this tension-and the adaptation o

32 Finally, we show that knockdown of EmMBD2/3 expression disrupts normal ce

33 Further, we show that an rpsA polymorphism previously identified in a PZA

34 Here we show that a microfluidic system supports murine ovarian folli

35 Here we show that assumption ii is not valid, due to strong intraannu

36 Here we show that drugs that inhibit important kinases in the BCR sig

37 Here we show that in mice DND1 binds a UU(A/U) trinucleotide motif pr

38 Here we show that mice with an adipose-tissue-specific knockout of th

39 Here, we show that both 2009 pandemic H1N1 influenza A (H1N1) virus an

40 Here, we show that knockdown of Hop in the germ line nurse cells (GLKD

41 Here, we show that lamin A/C expressing cells can form an actin cap to

42 Here, we show that modeling of neural sound representations in terms o

43 Here, we show that mutation of the mouse orthologue of GPSM2 affects a

44 Here, we show that NKT-specific deletion of Hdac3 results in a severe

45 Here, we show that Tomt/Comt2, the murine ortholog of LRTOMT, has an u

46 cess to nanotubes presorted by surfactant-based methods, we show that the resulting DNA-wrapped carbon nanotubes can be f

47 mice with the cecal contents of neonatal and adult mice, we show that the neonatal microbiota is unable to prevent coloni

48 Using three mouse infection models, we show that the SIP signaling pathway is active during infectio

49 By utilizing these novel structures we show that (i) the detection limit for dopamine can be improve

50 Using the Xenopus system, we show that RARbeta2 plays a specific role in somite number and