ライフサイエンスコーパス: were analyzed by

1 One hundred seventy OCT pullbacks were analyzed by 2 independent observers with intravascular i

2 the edible part of Chamelea gallina and Tapes philippinarum were analyzed by a proteomic approach based on a two-dimensio

3 Payments from 2013 to 2014 were analyzed by anti-VEGF agent, payment category, and dolla

4 , and its mechanical properties and dynamics at equilibrium were analyzed by atomic force microscopy.

5 bers and cellulose fibers extracted from rice and oat husks were analyzed by chemical composition, morphology, functional

6 Abeta10-40 conformations were analyzed by computing secondary structure, backbone fluc

7 Results were analyzed by descriptive statistics followed by generaliz

8 Changes from baseline in pulmonary function at Week 48 were analyzed by emphysema extent.

9 Compounds 1-3 were analyzed by EPR and NMR spectroscopy, DFT calculations,

10 n aqueous solutions at110 degrees C for 3h and the residues were analyzed by ESI/qTOF/MS using MS/MS and isotope labeling

11 re de Montilla-Moriles" and "Vinagre de Condado de Huelva", were analyzed by excitation-emission fluorescence spectroscop

12 -2 seropositive or seronegative and HIV-uninfected controls were analyzed by flow cytometry.

13 and sulfur-containing) analytes found in low-concentrations were analyzed by Fourier transform ion cyclotron resonance ma

14 Skeletal muscle, liver, and plasma samples were analyzed by gas chromatography time-of-flight mass spect

15 Age-matched nBmp2NLS(tm) and wild type mice were analyzed by immunohistochemistry, behavioral tests, and

16 Leaves were analyzed by LC-HRMS and a comprehensive statistical work

17 Data were analyzed by linear mixed models or generalized linear mi

18 baumannii, P seudomonas aeruginosa, and E nterobacter spp. were analyzed by MALDI-TOF-MS in negative ion mode to obtain

19 After elution and proteolysis, the peptides were analyzed by mass spectrometry to identify proteins assoc

20 Stool samples were analyzed by mass spectrometry.

21 sue mast cells, respectively, and their releasate proteomes were analyzed by mass spectrometry.

22 f CD63(hi) basophils, irrespective of whether the specimens were analyzed by means of conventional flow cytometry or cyto

23 Samples were analyzed by means of liquid chromatography-quadrupole ti

24 Potential moderators of efficacy were analyzed by meta-regression.

25 nitrogen source and to different concentrations of ammonium were analyzed by microarray and reverse transcription quantit

26 ecutive function and memory scores over 8 years (2002-2010) were analyzed by mixture models among 10,241 adults aged >/=5

27 our obtained from nine cultivars of different qualities and were analyzed by nanoUPLC and Ultra Definition Mass Spectrome

28 DATA EXTRACTION: Extracted data were analyzed by pairwise and network meta-analysis.

29 samples obtained from subjects undergoing bariatric surgery were analyzed by qRT-PCR for expression of WNT/PCP genes.

30 and patients without colon inflammation (controls, n = 23) were analyzed by quantitative polymerase chain rection to mea

31 rtant genes related to cardiac differentiation and function were analyzed by real-time quantitative polymerase chain reac

32 The intratumoral TSL and dox distribution were analyzed by single-photon emission computed tomography (

33 consecutive fresh blood cultures received in the laboratory were analyzed by the Accelerate Pheno system within 0 to 8 h

34 ples, a fresh leaf leachate and two humic-rich lake waters, were analyzed by the direct method presented here and in comp

35 SD for refractory VT or VT storm at 5 international centers were analyzed by the International Cardiac Sympathetic Denerv

36 MS/MS spectra available for 828 of these annotations were analyzed by translating experimentally known fragmentati

37 rted to the ASRS ReST Committee following laser vitreolysis were analyzed by type to gain an understanding of the spectru

38 somal RNA gene amplicon sequencing, and metabolite profiles were analyzed by ultrahigh-performance liquid chromatography-

39 Presentation" standard-dose mammograms and synthetic images were analyzed by using a fully automated algorithm.

40 Data were analyzed by using analysis of variance, t test, or chi(2

41 and their analytical performances in cancer cell detection were analyzed by using electrochemical impedance spectroscopy

42 Cell markers were analyzed by using immunohistochemistry, the Luminex Mult

43 n inhalational challenge was performed, and cough responses were analyzed by using nonlinear mixed-effects modeling to es

44 Nuclear magnetic resonance (NMR) profiles were analyzed by using partial least-squares discriminant ana

45 xty-four matched samples-127 primary and 37 relapse samples-were analyzed by using RNA sequencing.

46 In total, 50 samples were analyzed by using SMRT sequencing.

47 ism, reaction intermediates, and final degradation products were analyzed by UV/vis, NMR, GC-MS, and EPR.

48 nd other ST382 isolates not associated with these outbreaks were analyzed by whole-genome sequencing (WGS) analysis.

49 Data were analyzed by Wilcoxon, Mann-Whitney U, and permutation te

50 wever, variations in degree of overlap were noted when data were analyzed by year.