Amathematical model of the unfolded protein stress response reveals the decision mechanism for recovery, adaptation and apoptosis Kamil Erguler*, Myrtani Pieri and Constantinos Deltas* Background: The unfolded protein response (UPR) is a major signalling cascade acting in the quality control of protein folding in the endoplasmic reticulum (ER). The cascade is known to play an accessory role in a range of genetic and environmental disorders including neurodegenerative and cardiovascular diseases, diabetes and kidney diseases. The three major receptors of the ER stress involved with the UPR, i.e. IRE1α, PERK and ATF6, signal through a complex web of pathways to convey an appropriate response. The emerging behaviour ranges from adaptive to mal...
When protein folding in the endoplasmic reticulum (ER) is disrupted by alterations in homeostasis in...
The endoplasmic reticulum (ER) is the main site in the cell for the folding and processing of secret...
Copyright © 2015 Marianna Holczer et al. This is an open access article distributed under the Creati...
Protein-folding stress at the endoplasmic reticulum (ER) is a salient feature of specialized secreto...
The endoplasmic reticulum (ER) is a key subcellular compartment involved in the folding and maturati...
Abstract: The endoplasmic reticulum (ER) is responsible for processing of proteins that are destined...
Disruption of protein folding homeostasis in the endoplasmic reticulum activates a signaling pathway...
The unfolded protein response is the mechanism by which cells control endoplasmic reticulum (ER) pro...
Since its discovery more than 25 years ago, great progress has been made in our understanding of the...
Eukaryotic cells fold and assemble membrane and secreted proteins in the endoplasmic reticulum (ER),...
One of the early cellular responses to endoplasmic reticulum (ER) stress is the activation of the un...
International audienceThe unfolded protein response (UPR) is an integrated, adaptive biochemical pro...
International audienceEndoplasmic Reticulum (ER) stress signaling is an adaptive mechanism triggered...
Study of the unfolded protein responses (UPR) is mainly addressed by challenging eukaryotic cells wi...
ER homeostasis is vital for cellular function and survival. Alterations in the folding capacity of t...
When protein folding in the endoplasmic reticulum (ER) is disrupted by alterations in homeostasis in...
The endoplasmic reticulum (ER) is the main site in the cell for the folding and processing of secret...
Copyright © 2015 Marianna Holczer et al. This is an open access article distributed under the Creati...
Protein-folding stress at the endoplasmic reticulum (ER) is a salient feature of specialized secreto...
The endoplasmic reticulum (ER) is a key subcellular compartment involved in the folding and maturati...
Abstract: The endoplasmic reticulum (ER) is responsible for processing of proteins that are destined...
Disruption of protein folding homeostasis in the endoplasmic reticulum activates a signaling pathway...
The unfolded protein response is the mechanism by which cells control endoplasmic reticulum (ER) pro...
Since its discovery more than 25 years ago, great progress has been made in our understanding of the...
Eukaryotic cells fold and assemble membrane and secreted proteins in the endoplasmic reticulum (ER),...
One of the early cellular responses to endoplasmic reticulum (ER) stress is the activation of the un...
International audienceThe unfolded protein response (UPR) is an integrated, adaptive biochemical pro...
International audienceEndoplasmic Reticulum (ER) stress signaling is an adaptive mechanism triggered...
Study of the unfolded protein responses (UPR) is mainly addressed by challenging eukaryotic cells wi...
ER homeostasis is vital for cellular function and survival. Alterations in the folding capacity of t...
When protein folding in the endoplasmic reticulum (ER) is disrupted by alterations in homeostasis in...
The endoplasmic reticulum (ER) is the main site in the cell for the folding and processing of secret...
Copyright © 2015 Marianna Holczer et al. This is an open access article distributed under the Creati...