1 To tackle this problem,
we utilized a 3D co-culture model incorporating ER+ breast ca
2 We utilized a formulation of VTM described by the CDC that wa
3 To test this possibility,
we utilized a full allogeneic mismatch murine transplant mode
4 We utilized a high-throughput full-factorial experimental sys
5 We utilized a human neuronal cell line model of HSV latency a
6 We utilized a molecular replacement strategy in which exogeno
7 We utilized a mouse model carrying a knockout of the mitochon
8 Here
we utilized a mouse model of maternal immune activation (MIA)
9 he role of ataxin-3's non-polyglutamine domains in disease,
we utilized a new, allelic series of Drosophila melanogaster.
10 We utilized a novel personalized approach to treating APOE4 s
11 Here,
we utilized a reconstituted system with a defined set of sign
12 We utilized a reverse genetics system to generate a GFP repor
13 To this end,
we utilized a sequential panning of a phage library on cultur
14 tabolism and its ability to adapt to metabolic engineering,
we utilized a series of in vitro and in vivo experiments to c
15 In this article,
we utilized a smartphone-based image acquisition method for c
16 In this study,
we utilized a three species biofilm model to understand the i
17 In this study,
we utilized an antisense oligonucleotide (ASO) to reduce IDOL
18 Herein,
we utilized an electronic nose and computer vision to check t
19 To functionally validate these findings,
we utilized an ex vivo model of angiogenesis.
20 We utilized an optimized orthotopic murine osteosarcoma model
21 a double-blind, placebo-controlled, parallel group design,
we utilized an ultra-high field multimodal brain imaging appr
22 For the treatment component,
we utilized data from the Georgia National HCV treatment prog
23 We utilized GBM neurospheres that display GSC characteristics
24 In a complementary approach,
we utilized HaXS8 cross-linking reactions between Halo and SN
25 We utilized in vitro E2F2 ChIP-chip and over expression data
26 Here,
we utilized induced pluripotent stem cell-derived retinal pig
27 We utilized interindividual variation in developmental rate a
28 We utilized knockin and transgenic mouse models to evaluate t
29 We utilized mass spectrometry enhanced by affinity hydrogel p
30 We utilized mass spectrometry imaging to spatially map N-glyc
31 To address this issue,
we utilized microdilution checkerboard assays to evaluate nin
32 We utilized molecular genetics, biochemistry, and cryo-electr
33 In this study,
we utilized novel electrospun fibrin microfiber sheets of dif
34 To address this fundamental question in immunology,
we utilized our knowledge of HIV-1 dynamics to compare the ki
35 In this study,
we utilized PPR skin biopsy explants to integrate both differ
36 To address these gaps,
we utilized quantitative multiplexed single-molecule fluoresc
37 We utilized sequence kernel association testing and polygenic
38 , our former gamma-secretase modulator (GSM) lead compound,
we utilized sequential structural replacements to improve the
39 Here,
we utilized single prolonged stress, a validated rodent model
40 In this study,
we utilized strand specific high-throughput RNAseq to identif
41 Here,
we utilized subcellular fractionation coupled with tandem mas
42 nding effects of cardiomyopathy on mitochondrial phenotype,
we utilized Taz-shRNA knockdown (Taz(KD) ) mice, which exhibi
43 We utilized the 2016 National Inpatient Sample-a nationally r
44 Here
we utilized the cell-to-cell variation in morphological featu
45 Here
we utilized the chicken (Gallus gallus) model to investigate
46 Here,
we utilized the rich diversity of the Collaborative Cross mic
47 We utilized the small molecule inhibitor, pifithrin-alpha, to
48 We utilized these high-quality annotations to assess gene fam
49 We utilized this setup to investigate the salt-induced aggreg
50 For a subset of validated candidates,
we utilized total internal reflection fluorescence microscopy