1 In this work,
we utilized a 7-dimethylamino flavylium heterocycle to constr
2 minants of immunodominance among several dominant epitopes,
we utilized a cell free antigen processing system and allowed
3 Finally,
we utilized a combined QSRR-DoE approach to propose an optima
4 al sclerosis-linked SOD1 mutants, SOD1(G93A) and SOD1(G85R)
We utilized a computational algorithm for mapping protein sur
5 We utilized a database of daily cardiovascular- and respirato
6 llite cells during muscle recovery following a burn injury,
we utilized a genetically modified mouse model (Pax7(CreER) -
7 Here,
we utilized a humanized mouse model to recapitulate the low i
8 Here,
we utilized a loss-of-function HR-reporter substrate to simul
9 In this study,
we utilized a mouse model of cGVHD to examine whether HC-HA/P
10 IMCL) and extramyocellular lipid (EMCL) content in obesity,
we utilized a new four-dimensional multi echo echo-planar cor
11 Here
we utilized a recently developed nanoplasmonic fiber tip prob
12 Here,
we utilized a series of experiments to examine the effects of
13 Here,
we utilized a shuttle vector method to examine the efficiency
14 To examine its function in AKI,
we utilized a specific function-blocking antibody to inhibit
15 inocyte stem cells in beta-HPV-induced skin carcinogenesis,
we utilized a transgenic mouse model in which the keratin 14
16 Here,
we utilized alive tumor tissues in ex-vivo platform termed CA
17 To further characterize the melanin pathway,
we utilized an advanced Aspergillus nidulans heterologous sys
18 Here,
we utilized an integrated approach to find potential key tran
19 We utilized computational approaches to identify putative tra
20 We utilized CRISPR/Cas9 genome editing in human induced pluri
21 We utilized ex vivo spinal cord slice cultures (SCSC) to demo
22 We utilized genetic code expansion and site-specific bioortho
23 To study the role of Copb2 in neural development,
we utilized genome-editing technology to generate an allelic
24 In this study,
we utilized high-throughput screening (HTS) in vitro data of
25 Herein,
we utilized immunohistochemistry (IHC) staining and public mi
26 In this study,
we utilized in vivo two-photon imaging to directly monitor th
27 In addition,
we utilized individual SNP lookups and polygenic score analys
28 To overcome this hurdle,
we utilized non-canonical amino acids and bio-orthogonal chem
29 In addition,
we utilized our mutual exclusivity analysis in support of a p
30 We utilized pharmacological augmentation and depletion combin
31 Here,
we utilized primary and immortalized PSC obtained from mice a
32 We utilized questionnaire data from a large general populatio
33 We utilized sequence similarity and gene expression to catego
34 We utilized the apoE(-/-) mouse model to compare atherosclero
35 Here,
we utilized the broad anatomical coverage of iEEG recordings
36 In the current study,
we utilized the close interaction between astrocytes and reti
37 Finally,
we utilized the expanded cerebral organoids to show that infe
38 We utilized the fact that many plant small RNAs direct cleava
39 We utilized the fast-growing pathogenic basiodiomycete formin
40 In this study,
we utilized the hybrid nanocrystal concept and studied the ki
41 We utilized the large variance in response to antidepressant
42 To determine the effect of alcohols on fusion rates,
we utilized the nystatin/ergosterol fusion assay to measure f
43 affecting cag PAI T4SS activity at the host cell interface,
we utilized the Phyre structural threading program and found
44 Here,
we utilized the Shank3B mutant mouse model of autism to inves
45 We utilized the Ugi multicomponent reaction to create a small
46 To circumvent this limitation,
we utilized the unique structural features of N-glycan molecu
47 In this study
we utilized the Xenopus oocyte expression system to shed ligh
48 We utilized this method to construct a functional lycopene bi
49 utations and other rare sequence variants on TRIO function,
we utilized two FRET-based biosensors: a Rac1 biosensor to st
50 We utilized untargeted metabolomics to identify novel metabol