ライフサイエンスコーパス: we show that

1 We show that FC-A stabilizes a complex between 14-3-3 and the

2 We show that HSP22E and HSP22F are major chloroplast-targeted

3 We show that human participants report seeing a third flash w

4 We show that OnGuard2 faithfully reproduces the kinetics of s

5 We show that signalling through the TrpA1 thermo-sensor is re

6 We show that SiO2 first undergoes a change in Si-O coordinati

7 We show that such a framework is consistent with the stationa

8 We show that the expression of many miRNAs is dramatically re

9 We show that the line-shape of the measured resonant elastic

10 We show that the photoacids can be used as fluorescent marker

11 We show that the photochemical reaction mechanisms for alpha-

12 We show that the same as for genes SPAD follows a beta distri

13 We show that TSRI estimators with modified standard errors ha

14 Here, we directly monitor RNA proof-reading by RIG-I and we show that it is controlled by a set of conserved amino aci

15 In this article, we show that CXCL8 expression, prior to proliferation, is com

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

17 NF54 wild-type parasites at multiple stages of development, we show that sexually committed, AP2-G(+) mature schizonts sp

18 ement learning simulations, and behavioral experimentation, we show that the resolution to this tension-and the adaptatio

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

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

21 Here we show that a microfluidic system supports murine ovarian fo

22 Here we show that a significant variation in the rate of microeart

23 Here we show that assumption ii is not valid, due to strong intraa

24 Here we show that drugs that inhibit important kinases in the BCR

25 Here we show that ER-localized THBS1 is cytoprotective to rat, mou

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

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

28 Here we show that ripple bursts in CA1 and medial entorhinal corte

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

30 Here, we show that by using specific intracellular immunolabelling

31 Here, we show that knockdown of Hop in the germ line nurse cells (G

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

33 Here, we show that modeling of neural sound representations in term

34 Here, we show that mutation of the mouse orthologue of GPSM2 affect

35 Here, we show that NKT-specific deletion of Hdac3 results in a seve

36 Here, we show that stimulants like cocaine and methamphetamine grea

37 Here, we show that the Arabidopsis (Arabidopsis thaliana) ADF3 is r

38 Here, we show that the C-type lectin receptor CD69 controls tTreg c

39 Here, we show that the cytokine activin-A instructs the generation

40 Here, we show that Tomt/Comt2, the murine ortholog of LRTOMT, has a

41 process to nanotubes presorted by surfactant-based methods, we show that the resulting DNA-wrapped carbon nanotubes can b

42 ee mice with the cecal contents of neonatal and adult mice, we show that the neonatal microbiota is unable to prevent col

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

44 selectively depleted in myeloid cells, such as neutrophils, we show that FlnA negatively regulates beta2 integrin adhesio

45 Using Aspergillus nidulans, we show that AP-2 has a clathrin-independent essential role i

46 Despite this high baseline rate, we show that NAGC slows down as duplicate sequences diverge-u

47 Second, we show that, whereas the thermopower is diffusion driven for

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

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

50 Therefore, we show that both habit-like attention and goal-directed proc