ライフサイエンスコーパス: were measured

1 Nasal and serum IFN-inducible protein 10 (IP-10) were measured after doses 1 and 8, then 1 (follow-up visit [F

2 Faradaic efficiencies of approximately 95% were measured in the gas phase for oxygen evolution in alkali

3 from Aldhahira and Sharqia regions of Sultanate of Oman and were measured using NIR spectroscopy in absorption mode in th

4 ntal contaminants (Dioxins, PCBs, HBCD, Zn, Cu, Cd, Pb, As) were measured at significantly higher levels in organic sampl

5 Benefits were measured in quality-adjusted life-years gained.

6 hosphate (ATP) synthesis rates of osteosarcoma cybrid cells were measured before and after CPC and BAK treatment.

7 Risk factor differences between the cohorts were measured using the independent t test, Wald chi(2), and

8 The TXRF spectra of the compounds were measured using variable X-ray energies in the vicinity o

9 , a marker of kidney function) and serum PFOA concentration were measured in blood samples collected during 2005-2006.

10 ctivation, matricellular protein release, and tissue damage were measured at admission.

11 inactive versions (cortisone and 11-dehydrocorticosterone) were measured by LC-MS/MS in maternal and cord plasma from 25

12 nce, as well as the duration of recommendation development, were measured.

13 E), thio-dimethylarsinoylacetate (thio-DMAA), and thio-DMA) were measured in spot urine samples prior to seaweed consumpt

14 ed, extracted with ethanol and metabolite (13)C enrichments were measured.

15 ucible factor 1-alpha (HIF-1alpha) and erythropoietin (EPO) were measured as potential mechanisms for exercise-induced EP

16 and vascular endothelial growth factor (VEGF)-C expression were measured.

17 agen fractional synthesis rate (FSR) and plasma lumican FSR were measured based on (2) H labeling using tandem mass spect

18 ic culture for 12 hours, after which viability and function were measured.

19 on-fasting blood sugar, body mass index and abdominal girth were measured.

20 sion, education, and health-related quality of life (HRQOL) were measured.

21 Plasma metabolites and insulin were measured at baseline, 15, 30, 60, 90 and 120 min after f

22 Viability and cell cycle kinetics were measured by using flow cytometry.

23 n a total of 370 seedlings, whose shoot and taproot lengths were measured repeatedly during the early stage of growth.

24 factor I, triglycerides, cholesterol, cortisol, and leptin, were measured after an overnight fast.

25 Serum cytokine and chemokine levels were measured at baseline and after BV.

26 Histamine and leptin levels were measured by enzyme immunoassay.

27 Claudin-18.1 mRNA levels were measured in airway epithelial brushings from healthy con

28 ic substudy from 4 phase 2 trials, circulating PCSK9 levels were measured at baseline and then weekly at weeks 8 through

29 g protein, troponin T, and brain natriuretic peptide levels were measured.

30 enes characterizing type 1, type 2, and type 17 lymphocytes were measured in sputum samples from 48 participants with ast

31 (GMD), urinary nitric oxide (NO), and inflammatory markers were measured before and after FBX treatment.

32 ndrial function, autophagy, ER stress, and lipid metabolism were measured in pancreatic tissue, acinar cells, and isolate

33 Fecal methanogens were measured by quantitative polymerase chain reaction.

34 m levels of 25-hydroxy VD, TGF-beta1, TIMP-1, MMP2 and MMP9 were measured at baseline and at the end of the 6-week study

35 Diastolic pulmonary artery pressure and mean PAWP were measured to calculate the DPD as per usual practice (dia

36 Serum concentrations of PBDEs were measured using gas chromatography-tandem mass spectromet

37 ntrations of free choline, betaine, and phosphatidylcholine were measured with the use of liquid-chromatography-stable-is

38 cosity, density, and coagulation rate of human blood plasma were measured along with the standard coagulation time.

39 +/- 5% for Br(-) oxidation and 94 +/- 2% for H2 production were measured.

40 to sequential epitopes derived from five major CM proteins were measured with a peptide microarray-based immunoassay.

41 ike peptide 1 (GLP-1), and peptide tyrosine tyrosine (PYY)] were measured, and ad libitum energy intake was quantified fr

42 Degradation percentages and rates were measured in pure water exposed to simulated natural sunl

43 Allergic airways responses were measured 48 h after the last challenge.

44 Viral replication and cellular responses were measured using quantitative real time PCR and multiplex

45 enic concentration in household tap water and urine samples were measured using inductively coupled mass spectrometry (IC

46 n increase ratio (SAIR), and subjective image quality score were measured and compared between the SAFIRE and Filter back

47 tal and allergen-specific IgE, IgG and basophil sensitivity were measured before and 8 weeks after challenge.

48 s of PFASs and of antibodies against diphtheria and tetanus were measured and were compared with data from the previous e

49 f three milk types, five fish species, and two coffee types were measured using electrospray ionization, desorption elect

50 and arachidonic acid [AA]) in blood samples at age 8 years were measured for 940 children from the prospective Swedish b