1 e gastric cancer cell line MKN45 to 5-FU for >100 passages,
we established a 5-fluorouracil (5-FU)-tolerant line, MKN45/5
2 Here,
we established a cell culture model to characterize the cell-
3 We established a feline HFpEF model induced by slow-progressi
4 We established a gas chromatography-mass spectrometry method,
5 We established a hypothesis whereby the variability in the co
6 roscopy (TIRFM) and kinetic and thermodynamic measurements,
we established a kinetic model of Ena/VASP-mediated actin fil
7 We established a large-scale, prospective clinical sequencing
8 Overall,
we established a molecular diagnosis in 63/197 (32%) individu
9 We established a mouse model of developmental nonalcoholic st
10 We established a mouse xenograft model of human acute myeloid
11 We established a multi-step protocol involving protein immobi
12 To understand its role in placental development,
we established a novel Egfl7 knockout mouse.
13 To address their relative dependence on MHC-II,
we established a novel ENU-induced mutant mouse on the C57BL/
14 We established a novel mice model of HTG-AP by poloxamer 407
15 In this work,
we established a phage-display platform to select for specifi
16 We established a prospective registry to determine the risks
17 Through medicinal chemistry exploration,
we established a robust structure-activity relationship of th
18 In this study,
we established a role for lncRNAs in chondrocyte differentiat
19 With data from five trials,
we established a series of diary events based on peak expirat
20 We established a standardized mouse model of high fat diet (H
21 We established a systematic, standardised surveillance of blo
22 We established a transient expression system in Nicotiana ben
23 In terms of human specificity,
we established an in vitro invasion-differentiation trophobla
24 To address this deficit, in the present study,
we established an in vitro mouse brain slice preparation that
25 We established an in vitro system to evaluate lymphatic TEM f
26 We established and analyzed transcriptome datasets from leaf
27 In this study,
we established another Arabidopsis mutant line harbouring a d
28 We established Bacillus amyloliquefaciens LoaP as a paradigm
29 We established experimental maize plots in western Kenya to a
30 We established experimentally warmed and nonwarmed common gar
31 Using 2D NMR spectroscopy,
we established for the first time that MK-2 has a folded conf
32 We established how cause of death varied between these groups
33 We established in-vitro and ex-vivo susceptibility profiles f
34 In this study,
we established organotypic cell cultures of AT explants to st
35 We established our assay for the simultaneous analysis of thr
36 We established primary cultures from follicular epithelium in
37 facilitate the study of cellular mechanisms in human cells,
we established several human stem cell lines: human embryonic
38 t as "windows of opportunity" for changes in cell identity,
we established synchronized cultures of mouse embryonic stem
39 Using chemical inhibitors,
we established that inhibition of p38, but not ERK or JNK, re
40 We established that oligosaccharide stannanes could be prepar
41 of MS, isotope labeling, and (1)H and (13)C NMR techniques,
we established that the major product, MftA*, is a tyramine-v
42 (k = 17.3 +/- 1.3 m(-1) s(-1) at pH 7.4 and 25 degrees C),
we established that the measured decay of the intrinsic PDI f
43 Finally,
we established that UbFluor can quantify activation or inhibi
44 We established the decellularization of porcine urethras to p
45 We established the impact of intervention on food intake, bod
46 In conclusion, in this study
we established the involvement of the complement system in th
47 Based on the temporal patterns of gene-specific regulation,
we established the network architectures underlying distinct
48 In this study,
we established the optical trapping technique for determining
49 We established two levels (high/low quality) of within-patch
50 In response,
we established under the auspices of the UNEP/SETAC Life Cycl