1 At baseline and 4 months post-treatment,
we measured (
1) LV global longitudinal strain, twisting, and
2 Here,
we measured 2-HG, mIDH2 allele burden, and co-occurring somat
3 We measured 6920 synapses in mouse motor and sensory cortices
4 Toward the end of each phase,
we measured arterial blood gases, inspiratory effort, and wor
5 We measured arterial oxygen partial pressure continuously wit
6 We measured binding affinity for four synbodies against VLPs
7 We measured binocular interactions in visual cortex of anesth
8 We measured biomarkers from plasma samples collected in 211 p
9 We measured BPA concentration in urine samples collected at a
10 We measured brain activity with functional magnetic resonance
11 Here,
we measured carbon, nitrogen, phosphorus, and biomass allocat
12 Simultaneously,
we measured changes in cerebral blood volume (CBV) as a proxy
13 We measured concentrations of angiopoietin-1, angiopoietin-2,
14 w a different protein scaffold can modulate these energies,
we measured DeltaDeltaGsc(o) for all 20 amino acids using the
15 l sclerosis (ALS), a progressive neurodegenerative disease,
we measured electromyogram (EMG) activity in hind limb muscle
16 Here,
we measured ex vivo sensitivity of 246 blood cancers to 63 dr
17 Here,
we measured fecal-associated bacterial, archaeal, and fungal
18 We measured fitness of approximately 14,000 E. coli strains,
19 To test this hypothesis,
we measured fMRI BOLD responses to task-irrelevant stimuli ac
20 In healthy subjects,
we measured forearm blood flow (Doppler ultrasound) and calcu
21 To quantify these effects,
we measured gas- and particle-phase emissions from 82 light-d
22 We measured HCV replication, entry, spread, production, and r
23 Using a single-copy assay,
we measured HIV-1 RNA levels in CSF and plasma specimens from
24 To test for elevational movements,
we measured hydrogen isotope (delta(2) H) values of metabolic
25 design using basic features of revealed preference theory,
we measured in rhesus monkeys the frequency of repeated choic
26 On day 4 post-challenge,
we measured increased antibody levels, ASCs and HAI titers wi
27 In vivo,
we measured interactions on length scales of 80-120 mum, whic
28 METHODS AND
We measured LTL by quantitative polymerase chain reaction in
29 We measured mechanical properties of a particular chordotonal
30 n = 109) falciparum malaria, and healthy controls (n = 50),
we measured parasite biomass, systemic inflammation (interleu
31 We measured particle size distribution of wheat flour, photog
32 loying any a priori assumptions concerning the floral cues,
we measured,
predicted, and finally artificially recreated mu
33 Significantly,
we measured proteins involved in 83% of all predicted enzymat
34 observational study of cardiovascular risk in black adults,
we measured serum endothelin-1 level at baseline (2000-2004;
35 We measured significant increases in mRNAs associated with a
36 We measured strain diversity within and between genomically c
37 Here
we measured systematically the thermodynamic stabilities of h
38 Here,
we measured the absolute abundance of RPs in translating ribo
39 We measured the abundance of T cells in circulation and intes
40 We measured the assembly quality in terms of reference genome
41 In this study,
we measured the concentrations of 65 flame retardants in wate
42 We measured the density of the adsorbed motor protein (heavy
43 We measured the derivatives of the well-known anti-inflammato
44 entation will not be an effective anemia reduction strategy.
We measured the effect of daily oral iron with or without mul
45 We measured the expression of 45 confirmed and putative restr
46 We measured the first wave of de novo transcription in living
47 To test this,
we measured the levels of Idh1-GFP, Idh2-GFP, Trx2-GFP, Pdr5-
48 METHODS AND
We measured the Life's Simple 7 ideal cardiovascular health m
49 Using the Crooks fluctuation theorem,
we measured the mechanical work produced during the breaking
50 Here
we measured the responses of a marine diatom, Thalassiosira p