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9461
The size of particle free areas (holes) characterize the simulated patterning process.
Published 2019“…B: Expansion rate of individual holes, as a function of their size. We identified areas that did not merge with adjacent holes during a 30 minute time interval, and determined the change in their size. …”
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9462
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9463
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9464
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9465
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9466
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9467
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9468
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9469
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9470
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9471
Mcl-1 degradation is slowed by a T163E mutation (but not T163A) in transfected CHO cells.
Published 2012“…In Panel B, the decline in Mcl-1 expression at 3 hours in 2 independent experiments ranged from 53–66% with WT-Mcl-1, 25–54% with Mcl-1-S162A, and 25–50% with Mcl-1-T163A. While the decline in expression with WT-Mcl-1 appeared be slightly greater than that seen with Mcl-1-T163A, this was not a consistent finding. …”
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9472
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9473
DRP2B is partially required for flg22-induced endocytosis of FLS2.
Published 2014“…Representative maximum-intensity projection images and zoomed insets of FLS2-GFP fluorescence are shown, with bright pixels corresponding to increased abundance of FLS2-GFP at a given location. Scale bars = 10 µm. (D) Quantification of FLS2-GFP in puncta at 0, 35–45 or 50–60 min after elicitation with 1 µM flg22 indicates that loss of <i>DRP2B</i> resulted in ∼20% decrease in flg22-stimulated endocytosis of FLS2-GFP (35–45 min, P = 0.0204; 50–60 min, P = 0.0396). …”
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9474
Table_5_Multi-omics analysis reveals the association between elevated KIF18B expression and unfavorable prognosis, immune evasion, and regulatory T cell activation in nasopharyngea...
Published 2023“…Validated by immunofluorescence assay, the high KIF18B expression group displayed a notable rise in Tregs infiltration, accompanied by a substantial decrease in the infiltration of CD8<sup>+</sup> T cells and macrophages. …”
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9475
Table_4_Multi-omics analysis reveals the association between elevated KIF18B expression and unfavorable prognosis, immune evasion, and regulatory T cell activation in nasopharyngea...
Published 2023“…Validated by immunofluorescence assay, the high KIF18B expression group displayed a notable rise in Tregs infiltration, accompanied by a substantial decrease in the infiltration of CD8<sup>+</sup> T cells and macrophages. …”
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9476
DataSheet_1_Multi-omics analysis reveals the association between elevated KIF18B expression and unfavorable prognosis, immune evasion, and regulatory T cell activation in nasophary...
Published 2023“…Validated by immunofluorescence assay, the high KIF18B expression group displayed a notable rise in Tregs infiltration, accompanied by a substantial decrease in the infiltration of CD8<sup>+</sup> T cells and macrophages. …”
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9477
Table_3_Multi-omics analysis reveals the association between elevated KIF18B expression and unfavorable prognosis, immune evasion, and regulatory T cell activation in nasopharyngea...
Published 2023“…Validated by immunofluorescence assay, the high KIF18B expression group displayed a notable rise in Tregs infiltration, accompanied by a substantial decrease in the infiltration of CD8<sup>+</sup> T cells and macrophages. …”
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9478
Table_1_Multi-omics analysis reveals the association between elevated KIF18B expression and unfavorable prognosis, immune evasion, and regulatory T cell activation in nasopharyngea...
Published 2023“…Validated by immunofluorescence assay, the high KIF18B expression group displayed a notable rise in Tregs infiltration, accompanied by a substantial decrease in the infiltration of CD8<sup>+</sup> T cells and macrophages. …”
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9479
Table_2_Multi-omics analysis reveals the association between elevated KIF18B expression and unfavorable prognosis, immune evasion, and regulatory T cell activation in nasopharyngea...
Published 2023“…Validated by immunofluorescence assay, the high KIF18B expression group displayed a notable rise in Tregs infiltration, accompanied by a substantial decrease in the infiltration of CD8<sup>+</sup> T cells and macrophages. …”
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9480
Tracking cell divisions post-irradiation for the cellular automaton computational modeling.
Published 2017“…Using the ModFit LT3.2 software, raw data (black lines) were fit and modeled for proliferation that results in decreased PKH-26 fluorescent intensity. The number of divisions (1 = orange, 2 = green, 3 = pink, etc.) from the (A) initial untreated day 0 cells with PKH-26 stain (blue) or without (grey) were measured at day 14 following (B.) 0Gy, (C.) 8Gy or (D.) 16Gy irradiation. …”