ライフサイエンスコーパス: we show that

1 We show that 21-plex DiLeu tags generate strong reporter ions

2 We show that chemometric analysis of peanut leaflet spectra p

3 We show that CSB forms a stable complex with Pol II and acts

4 We show that epimutations arise spontaneously at a rate appro

5 We show that exposure of leukemia cells to daunorubicin activ

6 We show that glycolysis is required to maintain the plasma me

7 We show that inhibitory phosphorylation of eIF2alpha (P-eIF2a

8 We show that mantis shrimp rely on navigational strategies cl

9 We show that neutral evolution and nucleotide substitution ra

10 We show that NVP was readily taken up by dendritic cells (DCs

11 We show that Rho can prematurely terminate transcription of b

12 We show that tatM2NX inhibits over 90% of TRPM2 channel curre

13 We show that the increased cytokinin signaling in ARR1 gain-o

14 We show that the non-canonical tubulin Tuba8, transiently exp

15 We show that the phosphorylation of the RNA-DNA binding prote

16 We show that these dendrites develop by retrograde extension,

17 We show that this is due to acid inhibition of monocarboxylat

18 In addition, we show that phosphorylation of Ser(3) may be an additional m

19 Using genetic and pharmacological approaches, we show that depletion of the hyaluronic acid precursor UDP-g

20 well-known oncoprotein overexpressed in most human cancers, we show that FBXL16 stabilizes C-MYC by antagonizing FBW7-med

21 Using ChIP, we show that the occurrence of G4 structures peaks at the lat

22 In conclusion, we show that MEKi leads to CD8(+) T cell reprogramming into T

23 variation in media markets for 771 matched rural counties, we show that rural residents are more likely to practice soci

24 y integrating multiple sources of genetic and genomic data, we show that putative G-quadruplex forming sequences (pG4) in

25 stems-encompassing plants, protists, and algae with grazers-we show that this method predicts the results of unobserved e

26 Here we show that beta-cells express abundant Kindlin-2 and deleti

27 Here we show that beta4*nAChRs also are involved in non-nicotine-m

28 Here we show that dynamically growing somatosensory neurons in the

29 Here we show that keratin intermediate filaments directly regulate

30 Here we show that primary mouse and human T cells engage in macrop

31 Here we show that using prior knowledge to facilitate learning is

32 polymorphisms can affect RNA secondary structure, and here we show that single nucleotide polymorphisms can affect RNA-p

33 Here, we show that adrenergic stimulation of BAT activates a PKA-de

34 Here, we show that adult animals respond to ascarosides produced un

35 Here, we show that an AT-hook motif-containing nuclear localized (A

36 Here, we show that constrained 31-residue-peptides ('msR4Ms') desig

37 Here, we show that cytotoxic chemotherapies induce dynamic changes

38 Here, we show that expression of a fusion protein combining wheat G

39 Here, we show that histone H4 lysine 16 acetylation (H4K16ac) is ma

40 Here, we show that LDs induced by the yeast triacylglycerol (TAG)-s

41 Here, we show that SOX11 confers distinct features to ER-negative D

42 Here, we show that Syrian hamsters, in contrast to mice, are highly

43 Here, we show that the three major classes of LCCBs activate STIM/O

44 Here, we show that this toughness design approach can be applied to

45 Here, we show that tree mortality concomitant with drought has led

46 ication of intravacuolar pathogens such as Salmonella Here, we show that this mechanism requires aconitate decarboxylase

47 e and an ensemble approach to CNN parameter interpretation, we show that our trained network ("AI-TAC") does so by redisc

48 ing the melanoma lineage survival oncogene MITF as a model, we show that low-affinity binding sites act as a competitive

49 Here, using focal trans-synaptic anterograde tracing, we show that the motor-action-related topographical organizat

50 In this work, we show that there exists a correlation which is not attainab