ライフサイエンスコーパス: we assayed

1 We assayed 25 species of asymptomatic native grasses for the

2 ecific autoantibodies characteristic of APS-I patients, and we assayed 26 thymoma samples for transcripts for AIRE and 16

3 We assayed 5-LO levels in brain samples from patients with ta

4 We assayed 712 genes for requirements during preimplantation.

5 We assayed a TEM-1 beta-lactamase variant and levoglucosan ki

6 of the paraaortic lymph nodes, which represented non-SLNs, we assayed all lymph nodes for radioactivity and fluorescence

7 We assayed blood samples from SB polar bears to assess prior

8 r Orn is the primary enzyme responsible for degrading pGpG, we assayed cell lysates of WT and orn strains of P. aeruginos

9 ammonium compounds (QACs) are exuded by germinating seeds, we assayed chemotaxis of S. meliloti towards betonicine, chol

10 In this study, to address the cause of these abnormalities, we assayed CSR in Lig4(R/R) B cells generated via preassemble

11 oidism leads to growth defects and premature death in mice, we assayed for changes in thyroid and pituitary hormones.

12 Here we assayed Gal80-Gal80 interactions and tested for effects of

13 fy epigenetic changes associated with lipid concentrations, we assayed genome-wide DNA methylation at cytosine-guanine di

14 myces cerevisiae model expressing the P. vivax DHFR enzyme, we assayed growth rate and resistance of all 16 combinations

15 We assayed individual behaviour and electronically tagged hun

16 Therefore, we assayed locomotor activity and immobility-defined sleep in

17 We assayed markers for neurons and glia, along with genes tha

18 the Pregnancy Exposures and Preeclampsia Prevention Study, we assayed NEFA levels in nonfasting serum collected at a mea

19 We assayed over 10(8) antibody-peptide interactions in 569 hu

20 ut of the spinal cord and myelinate peripheral motor axons, we assayed perineurial glial development, maturation, and res

21 We assayed peripheral blood leucocyte global gene expression

22 Following behavioral characterization, we assayed PFC gene expression using a targeted PCR array and

23 We assayed plasma soluble suppression of tumorigenicity-2 (n

24 We assayed propidium(2+) (Pro(2+)) influx kinetics during NLR

25 For comparison we assayed recessive ca1ca4 carbonic anhydrase double mutant

26 We assayed recombination across a 40Kb region of Drosophila p

27 We assayed serum soluble alpha-klotho in 2496 participants wi

28 We assayed SOC decomposition from these incubations by combin

29 We assayed the ability of the Lenski Escherichia coli populat

30 We assayed the activation phenotype and the responsiveness in

31 ensity) and the potent vasoconstrictor endothelin 1 (EDN1); we assayed the activity of angiotensin I converting enzyme (A

32 We assayed the assembly reaction for a range of ushers and pr

33 Here, we assayed the binding of five essential TFs over multiple st

34 tions affected domain organization in biological membranes, we assayed the effects of BAs on biomimetic synthetic liposom

35 Using in vitro competition experiments, we assayed the fitness of eleven isogenic S. Typhi strains wi

36 We assayed the GBM methylome with MeDIP-seq and MRE-seq, adju

37 ween genome architecture and gene regulation in Plasmodium, we assayed the genome architecture of P. falciparum at three

38 To assess the role of CdaS in sporulation, we assayed the germination of wild type and cdaS mutant spore

39 lore their broader potential for therapeutic interventions, we assayed the global lipid landscape during P. falciparum se

40 l factors on the evolution of the great ape gut microbiota, we assayed the gut communities of sympatric and allopatric po

41 Here, we assayed the key Th2 cytokine, IL-4, and its soluble and me

42 We assayed the presence of DCs by immunohistochemistry and fl

43 Here, we assayed the toxicity and adhesiveness of 90 MRSA (methicil

44 oter activity that depends in part on the hexameric domain, we assayed the transcriptional regulatory effects of varying

45 ain-specific reporter, paired with FACS and RNA sequencing, we assayed the transcriptome of the gynoecial medial domain w

46 We assayed thermodynamic stability of each domain by equilibr

47 We assayed these sites 3 h postinoculation with transcript ar

48 Here, we assayed virological factors and AKT expression in liver ti

49 Since synapsin is a target of protein kinase A (PKA), we assayed whether activity-dependent synaptic growth is regu

50 We assayed Zap70 and Syk content in NK cells from healthy hum