ライフサイエンスコーパス: to measure

1 To measure EPFRs in PM samples, high volume samplers are requ

2 To measure NF-kappaB activity we used a line of transgenic mi

3 To measure resident surgeon technical and nontechnical skills

4 To measure spatial variation of mechanical properties, one mu

5 traction, introduces undesirable biases, it is advantageous to measure miRNA in a crude cell lysate.

6 tional Congestive Heart Failure (INTER-CHF) study, we aimed to measure mortality at 1 year in patients with heart failure

7 This study aims to measure and analyze unregulated compound emissions for two

8 : the development of a low cost, portable red cell analyzer to measure these parameters.

9 g the Gamma = (0, 0) and X = (pi/aFe, 0) points of FeSe and to measure the corresponding superconducting energy gaps.

10 departments to seek emergency care in larger hospitals, and to measure the association between rural hospital bypass and

11 School of Dentistry, University of California, Los Angeles) to measure the diffusion flux and determine the diffusivity o

12 V reservoirs exist, but there is currently no optimal assay to measure HIV reservoirs in HIV eradication interventions.

13 BATs to measure upregulation of basophil CD203c and induction of a

14 We then performed a pilot clinical study using BiliSpec to measure total bilirubin in neonates at risk for jaundice a

15 ple a quantum dot to a high-quality-factor microwave cavity to measure with exceptional sensitivity the dot's electronic

16 vitamin D3 (25(OH)D3), however, is particularly challenging to measure in such a format due to complexities involved in s

17 rt (primary outcome), and blood was collected from children to measure cytokine production relevant to asthma (secondary

18 We used chronoamperometry to measure protease-digested GA samples.

19 A methodology has been developed to measure nanoparticle mass and density, by combining centri

20 e tested this hypothesis using electroencephalography (EEG) to measure stimulus-evoked visual responses from human subjec

21 guish ACh and Cho, we used single-channel electrophysiology to measure resting affinities (binding free energies) of thes

22 We describe the use of thioester exchange equilibria to measure the propensities of amino acid residues to partici

23 We do not derive global estimates to measure the depth of impoverishment but focus on the media

24 e conclude that these variables are not useful risk factors to measure to predict progression to death after coronary hea

25 eter have all been measured, including 2395 trees harvested to measure aboveground biomass.

26 evious growth) and encourage the on-going discussion of how to measure and compare growth rates.

27 esis using ultra-fast functional magnetic resonance imaging to measure BOLD activity at precisely defined receptive field

28 Using the Global Peace Index to measure conflict, a curvilinear (quadratic) relationship b

29 avoiding large vessels, on imager-generated parametric maps to measure hepatic PDFF.

30 Here, we report a fluorometric method to measure carboxypeptidase activities that cleave the prolin

31 PET was developed in the 1970s as an in vivo method to measure regional pathophysiologic processes.

32 lso challenge the prospect of using neuroscientific methods to measure utility in a context-free manner and have importan

33 RATIONALE: There are several methods to measure cardiomyocyte and muscle contraction, but these re

34 We applied novel fetal resting-state functional MRI to measure brain function in 32 human fetuses in utero and fo

35 ounsaturated model membranes using magic angle spinning NMR to measure these interactions through both (1)H nuclear Overh

36 These findings open new possibilities to measure maximal absolute coronary blood flow and minimal m

37 In practice, however, it is hardly possible to measure fitness for all genotypes in a natural population.

38 tors of death, disease, and injury incidence and prevalence to measure the burden of diseases and injuries in Japan and i

39 We have used these reporters to measure differences in BER capacity across a panel of cell

40 tion imaging analysis, which employs statistical resampling to measure the Eph receptor aggregation distribution within e

41 cation of HEs becomes crucial and hence clinicians now seek to measure the area of HEs in the digital colour fundus (CF)

42 ingle glomerular stimulation in mouse olfactory bulb slices to measure the synaptic dynamics of afferent-evoked input at

43 We tested the ability of the tag to measure vibration in excised whiskers in a flume in respon

44 ng, subjects were exposed to a series of error-clamp trials to measure the temporal characteristics of the feedforward mo

45 encoded mutant green fluorescent proteins, which allowed us to measure the rates of selectively neutral mutations represe

46 can be linked to the approval of new diagnostic assays used to measure efficacy or to predict response.

47 With new pulse sequences, we show how hdNMR can be used to measure with high precision the (1)H(alpha)-(13)C(alpha) d

48 Flow cytometry was used to measure IFN-gamma, IL-13, IL-9, IL-17, and IL-22 cytokines

49 udy, a new analytical procedure was developed and validated to measure tobacco-related alkaloids, carcinogens, and their

50 Our goal was to measure the association of CXCL5 and molecular phenotypes