ライフサイエンスコーパス: we monitored

1 Here, we monitored 39 children shortly before and after allogeneic

2 ures using EMGs, which are performed on quiescent patients, we monitored activity during treadmill running aiming to dete

3 To identify neuronal correlates of behavior, we monitored brainwide activity with subcellular resolution a

4 TRPV1-lineage reporter mice and primary afferent cultures, we monitored capsaicin-induced effects on afferent terminals

5 of intracellular reorganization with morphological changes, we monitored centrosome positioning during EMT in vivo, in de

6 We monitored concentrations of per- and polyfluoroalkyl subst

7 For each cell line, we monitored constitutive PARP activation, spontaneous DNA da

8 Here, we monitored cortex-wide activity of the mouse brain using wi

9 We monitored CTCF-chromatin interactions by live cell single

10 We monitored detailed physiological responses, including shoo

11 stage viable tumor growth in a mouse model of human cancer, we monitored early tumor growth of engineered human ovarian c

12 We monitored Hh:GFP after pulsed expression, and analyzed the

13 Using longitudinal multi-modal MRI, we monitored hippocampal injury and tissue reorganization dur

14 sing intravital microscopy in Lgr5(EGFP-Ires-CreERT2) mice, we monitored individual crypt dynamics over multiple days wit

15 Here, using intracellular recording, we monitored inputs and plasticity-inducing complex spikes (C

16 We monitored long-term safety and efficacy for 3 years after

17 We monitored mast cell degranulation in real time by exploiti

18 We monitored MDSC frequency and function in SIV-infected rhes

19 To investigate the role of miRNAs, we monitored miRNA expression in the mosquito Anopheles gambi

20 By FRAP and imaging we monitored mobility of calsequestrin as [Ca(2+)] in the SR-

21 We monitored nighttime activity of adult great tits, Parus ma

22 ide the irradiated field at 1 and 4 days after irradiation, we monitored oxidatively induced clustered DNA lesions (OCDL)

23 -treated patients and 103 patients who received daily St-Cp We monitored patients with standardized protocols and adjuste

24 We monitored plasmid DNA degradation using gel electrophoresi

25 Throughout the flowering season, we monitored pollinator visitation and collected seeds to mea

26 of TRUB1 using massively parallel reporter assays in which we monitored Psi levels at thousands of synthetically designe

27 We monitored pupil size from ADHD and control subjects, durin

28 We monitored ROS, mitochondrial area and respiratory paramete

29 , carbon fiber amperometry, and magnetic resonance imaging, we monitored stimulus-coupled glandular secretion into the fl

30 clamp electrophysiology and rat cerebral arterial myocytes, we monitored STOCs in the presence and absence of agents that

31 To determine the winter export of N and P, we monitored stormwater outflow in a residential watershed in

32 tain deeper insights into the control of floral initiation, we monitored the activity of LFY in the absence of AP1/CAL fu

33 ly visualize cellular metabolic responses mediated by GAD1, we monitored the cytosolic NADH:NAD(+) equilibrium in tumor c

34 We monitored the density of 46 populations representing 28 sp

35 Here we monitored the dynamics of copy number alterations (CNAs) i

36 an RAD52 with replication protein A (RPA)-coated ssDNA, and we monitored the fate of RAD52 during assembly of the presyna

37 Next, we monitored the lifetime fitness of the terrestrial adults i

38 In this study, we monitored the movement of Agrobacterium-delivered VirE2 in

39 We monitored the progression of viral growth in tissues, bloo

40 We monitored the regulation of chloroplast transcription in p

41 We monitored the stability of these astaxanthin beads under f

42 ole of SPA proteins in COP1 nucleocytoplasmic partitioning, we monitored the subcellular localization of COP1 in a spa123

43 We monitored the survivorship of bees following antibiotic tr

44 Using high-speed microscopy, we monitored the swimming behavior of the monopolarly flagell

45 In this study, we monitored the thermal formation of early ribose-glycine Ma

46 In this study, we monitored the transcriptomic divergence of the maize (Zea

47 We monitored the viral load of MJNV RNA in various tissues of

48 Moreover, we monitored their frequencies in untreated and fingolimod- o

49 Here we monitored translation of the mammalian genome as cells bec

50 loped a high resolution multilevel well (HR-MLW) with which we monitored water across the interface of the unsaturated an