ライフサイエンスコーパス: we present evidence for

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1 We present evidence for a novel role of astrocytes in PA flow

2 We present evidence for an A-type K(+) current in spinal CPG

3 We present evidence for cytoplasmic translocation of RNase II

4 We present evidence for functional A2A receptors, which have

5 We present evidence for intercellular communication in the br

6 We present evidence for lake redox stratification, establishe

7 We present evidence for photoreception via the light-sensitiv

8 We present evidence for the co-variation of the Type III comp

9 We present evidence for the existence of two different reacti

10 We present evidence for the imbalance between inflammatory an

11 We present evidence for the presence of two distinct mechanis

12 We present evidence for the role of alpha2 in facilitating PT

13 We present evidence for two inactivation pathways that are op

14 We present evidence for vessel-to-neuron communication in the

15 zing a variety of computational and biochemical approaches, we present evidence for a class of nuclear introns that relie

16 tion, molecular dynamics simulations, and electrochemistry, we present evidence for two populations of PmB molecules: pep

17 Finally, we present evidence for an electrostatic interaction between

18 Here we present evidence for a different mechanism in which two se

19 Here we present evidence for a neural mechanism for feature bindin

20 Here we present evidence for a neuronal computation that maximizes

21 Here we present evidence for a palaeo-subglacial lake on the Antar

22 Here we present evidence for a preponderance of exocellular As in

23 Here we present evidence for a separate generator in local circuit

24 Here we present evidence for an alternate view of core formation b

25 Here we present evidence for hyperphosphorylation as a mechanism a

26 Here we present evidence for microtubule (MT)-based targeting of a

27 Here we present evidence for persistent active drainage networks-i

28 Here we present evidence for phosphorylation-driven regulation of

29 Here we present evidence for previously unappreciated B-cell immun

30 Here we present evidence for strong diastereomeric interaction eff

31 Here we present evidence for successful use of morpholino oligomer

32 Here we present evidence for the formation of aerosol particles fr

33 Here, we present evidence for a direct recruitment of UHRF1 by the

34 Here, we present evidence for a third strategy: directionally selec

35 Here, we present evidence for a unique, tonically active, excitator

36 Here, we present evidence for DNA damage as an unexpected means to

37 Here, we present evidence for glucagon-like peptide 1 (GLP-1)-media

38 Here, we present evidence for multiplexed encoding of tactile skin

39 Here, we present evidence for oncogene-directed cancer metabolic re

40 Here, we present evidence for the influence of phospholipid bilayer

41 Using this novel method, we present evidence for direct proportionality of volumetric

42 Using Arabidopsis thaliana as a model, we present evidence for the involvement of a plastidial cis-p

43 first report of N-N coupling between NO molecules in a MOF, we present evidence for a species that is consistent with a f

44 In this paper we present evidence for this mechanism in nanograined Yttria

45 In the present paper, we present evidence for the idea that speech motor learning i

46 In this report, we present evidence for an alternative mechanism of deglutath

47 rges after the first retinal synapse.SIGNIFICANCE STATEMENT We present evidence for spatially antagonistic interactions b

48 In this study, we present evidence for the intracellular delivery and ultras

49 In this study, we present evidence for two spontaneous mutations as the mole

50 Thus, we present evidence for a new mechanism of Zap1-mediated gene

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