ライフサイエンスコーパス: anticorrelation

1 ed state is less structured, do not show the anticorrelation.

2 ern, with increased DMN integration and more anticorrelation.

3 siological fidelity of BOLD correlations and anticorrelations.

4 ach with its own pattern of correlations and anticorrelations.

5 shows full lateral correlation and vertical anticorrelation across the interlayers.

6 The anticorrelations are supported by DFT calculations of st

7 We interpret this anticorrelation as a sign that a number of phase-one int

8 data of lung adenocarcinoma, we confirmed an anticorrelation between AMPK and HIF-1 activities and th

9 .36 degrees S, 161.71 degrees W) features an anticorrelation between conductivity and Hdye(+), likely

10 or networks, and a restoration of the normal anticorrelation between dorsal attention/motor regions a

11 in tail, providing a molecular basis for the anticorrelation between glutamylation and glycylation ob

12 l resources by upstream mRNAs can lead to an anticorrelation between protein counts.

13 -wide significant signal, but it revealed an anticorrelation between R2 and DNA methylation in many o

14 ring erythropoiesis shows an almost complete anticorrelation between regions of elevated lysine 9 met

15 places of the D'' discontinuity and (ii) the anticorrelation between shear and bulk velocity anomalie

16 d higher within-DMN connectivity and greater anticorrelation between SN and DMN and between SN and EC

17 These results explain the anticorrelation between the bulk velocity and shear velo

18 te cross-network interactions, and show that anticorrelation between the default mode network and par

19 e peptide bond N-H orientations shows a weak anticorrelation between the deviation of the peptide bon

20 We found a striking anticorrelation between the gray matter volume of primar

21 The model ensemble shows strong anticorrelation between the short-lived and long-lived R

22 eralogy between Pv and PPv may result in the anticorrelation between the V(Phi) and V(S) anomalies at

23 g H3K4me3 modifications reveals the expected anticorrelation between them at active promoters but an

24 ntral attention networks, as well as reduced anticorrelation between these networks.

25 n response to thermal anomalies suggest that anticorrelations between bulk sound and shear wave veloc

26 th rest and task, patients exhibited reduced anticorrelations between MPFC and DLPFC, a region that w

27 Anticorrelations between N and LMA followed general LES

28 taneous correlations within each network and anticorrelations between networks.

29 association cortex, interactions (including anticorrelations) between brain networks and insights in

30 are given opposite contrast in the two eyes (anticorrelation), both components of the vergence respon

31 an indirect measure of neuronal activity and anticorrelations can be introduced by preprocessing step

32 in the standard and switch sessions, and the anticorrelation covaried with switch performance.

33 This anticorrelation demonstrates how a combinatorial tubulin

34 ns dominate ribosomal fluctuations, a strong anticorrelation extremum reliably occurs near the transi

35 by reward magnitude and probability, showed anticorrelation for better and worse options, and covari

36 al interspacing for the components and their anticorrelation in intensities.

37 rent levels of the NMR to MS correlation and anticorrelation matrixes.

38 An anticorrelation motion between Tyr229-OH and Asn168-OD1

39 well as directly acyl migrated products and anticorrelation observed between signals from compounds

40 activation at the cell tips and reduces the anticorrelation of active Cdc42 oscillations.

41 the human brain's global architecture is the anticorrelation of default-mode vs. task-positive system

42 erent left DLPFC TMS sites is related to the anticorrelation of each site with the subgenual cingulat

43 We have now obtained an excellent anticorrelation of nuFeN and nuNO, via resonance Raman s

44 Furthermore, we find an anticorrelation of phase-one intron positions with modul

45 Anticorrelation of SN-DMN predicted outcomes with higher

46 f the polypeptide backbone manifested by the anticorrelation of the backbone torsion angles phi(i) an

47 Based on the anticorrelation of the characteristic dimensions, we con

48 An anticorrelation of the recurrence times of SU UMa dwarf

49 ulus by approximately 6%, resulting in local anticorrelation of Vb and Vs anomalies; this behavior ex

50 ramework developed for CO adducts, involving anticorrelations of nuFeC and nuCO, has seemed not to ap

51 rs showed higher correlation in autism (less anticorrelation), possibly representing weaker inhibitor

52 Anticorrelation suggests competition for active Cdc42 or

53 ression to BOLD signals results in some BOLD anticorrelations that are not apparent in the ECoG data,

54 y to supplementary motor area and functional anticorrelation to primary motor cortex (p < 0.001).

55 ducts show large deviations from the modeled anticorrelation when there are distal H-bonds or positiv

56 reduced integration within the DMN and less anticorrelation with the cognitive control network (CCN)

57 ntrol network, which also lacked the typical anticorrelation with the default mode network; 2) hypoco

58 h the ventral attention network, and greater anticorrelation with the dorsal attention network.

59 parts of primary visual cortex showed focal anticorrelation with the dorsolateral and ventromedial p