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Publication : Polynomial algebra reveals diverging roles of the unfolded protein response in endothelial cells during ischemia-reperfusion injury.

First Author  Le Pape S Year  2014
Journal  FEBS Lett Volume  588
Issue  17 Pages  3062-7
PubMed ID  24945730 Mgi Jnum  J:213560
Mgi Id  MGI:5585331 Doi  10.1016/j.febslet.2014.05.065
Citation  Le Pape S, et al. (2014) Polynomial algebra reveals diverging roles of the unfolded protein response in endothelial cells during ischemia-reperfusion injury. FEBS Lett 588(17):3062-7
abstractText  The unfolded protein response (UPR)--the endoplasmic reticulum stress response--is found in various pathologies including ischemia-reperfusion injury (IRI). However, its role during IRI is still unclear. Here, by combining two different bioinformatical methods--a method based on ordinary differential equations (Time Series Network Inference) and an algebraic method (probabilistic polynomial dynamical systems)--we identified the IRE1alpha-XBP1 and the ATF6 pathways as the main UPR effectors involved in cell's adaptation to IRI. We validated these findings experimentally by assessing the impact of their knock-out and knock-down on cell survival during IRI.
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