The ectodomains determine ligand function in vivo and selectivity of DLL1 and DLL4 toward NOTCH1 and NOTCH2 in vitro
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Title
The ectodomains determine ligand function in vivo and selectivity of DLL1 and DLL4 toward NOTCH1 and NOTCH2 in vitro
Authors
Keywords
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Journal
eLife
Volume 7, Issue -, Pages -
Publisher
eLife Sciences Publications, Ltd
Online
2018-10-05
DOI
10.7554/elife.40045
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Note: Only part of the references are listed.- Dynamic Ligand Discrimination in the Notch Signaling Pathway
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- The intracellular domains of Notch1 and Notch2 are functionally equivalent during development and carcinogenesis
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- Structural basis for Notch1 engagement of Delta-like 4
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- Context-Dependent Functional Divergence of the Notch Ligands DLL1 and DLL4 In Vivo
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- Spatiotemporal oscillations of Notch1, Dll1 and NICD are coordinated across the mouse PSM
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- (2014) E.-B. Braune et al. MOLECULAR AND CELLULAR BIOLOGY
- O-fucosylation of the Notch Ligand mDLL1 by POFUT1 Is Dispensable for Ligand Function
- (2014) Julia Müller et al. PLoS One
- The Extracellular Domain of Notch2 Increases Its Cell-Surface Abundance and Ligand Responsiveness during Kidney Development
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- Cross-talk between endothelial cells and tumor via delta-like ligand4/Notch/PTEN signaling inhibits lung cancer growth
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- Direct Comparison of Dll1- and Dll4-Mediated Notch Activation Levels Shows Differential Lymphomyeloid Lineage Commitment Outcomes
- (2010) M. Mohtashami et al. JOURNAL OF IMMUNOLOGY
- DLL1-mediated Notch activation regulates endothelial identity in mouse fetal arteries
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- Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development
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