Neurodegenerative conditions commonly involve loss of neuronal connectivity, synaptic dysfunction with excessive pruning, and ionic imbalances. These often serve as a prelude to cell death either through the activation of apoptotic or necrotic death routines or excess autophagy. In many instances, a local or generalized Ca2+ deregulation is involved in signaling or executing cell death. We have recently shown that in brain ischemia, and during excitotoxicity triggered by excess glutamate, the irreversible Ca2+ deregulation leading to necrosis is due to calpain-mediated modulation of the plasma membrane Na+/Ca2+ exchanger (NCX). Here we show that the NCX can also be cleaved by caspases in neurons undergoing apoptosis, which suggests that cle...
The ubiquitous, Ca2+-dependent, neutral proteases mu-calpain and m-calpain are heterodimeric regulat...
Physiological Ca2+ signals are essential for cell function and survival. On the other hand, perturba...
The molecular mechanisms responsible for A1-42-peptide induced intracellular Ca2+ homeostasis dysre...
AbstractIn brain ischemia, gating of postsynaptic glutamate receptors and other membrane channels tr...
Abstract In brain ischemia, gating of postsynaptic glutamate receptors and other membrane channels t...
Abstract—Although Ca2 signals are necessary for cell communication and survival, abnormal cellular ...
Neuronal death, which follows ischemic injury or is triggered by excitotoxins, can occur by both apo...
It is widely accepted that a critical factor in determining neuronal death during cerebral ischemia ...
Proteolytic cleavage of the Na+/Ca2+ exchanger (NCX) by calpains impairs calcium homeostasis, leadin...
AbstractProgrammed neuronal cell death is required during development to achieve the accurate wiring...
Excitotoxicity resulting from excessive Ca²+ influx through glutamate receptors contributes to neuro...
Role of calcium ion (Ca2+) in the functioning of neurons from their naive state to mature state is o...
The pathogenesis of various acute and chronic neurodegenerative disorders has been linked to excitot...
t is widely accepted that a critical factor in determining neuronal death during cerebral ischemia i...
Excitotoxicity resulting from excessive Ca(2+) influx through glutamate receptors contributes to neu...
The ubiquitous, Ca2+-dependent, neutral proteases mu-calpain and m-calpain are heterodimeric regulat...
Physiological Ca2+ signals are essential for cell function and survival. On the other hand, perturba...
The molecular mechanisms responsible for A1-42-peptide induced intracellular Ca2+ homeostasis dysre...
AbstractIn brain ischemia, gating of postsynaptic glutamate receptors and other membrane channels tr...
Abstract In brain ischemia, gating of postsynaptic glutamate receptors and other membrane channels t...
Abstract—Although Ca2 signals are necessary for cell communication and survival, abnormal cellular ...
Neuronal death, which follows ischemic injury or is triggered by excitotoxins, can occur by both apo...
It is widely accepted that a critical factor in determining neuronal death during cerebral ischemia ...
Proteolytic cleavage of the Na+/Ca2+ exchanger (NCX) by calpains impairs calcium homeostasis, leadin...
AbstractProgrammed neuronal cell death is required during development to achieve the accurate wiring...
Excitotoxicity resulting from excessive Ca²+ influx through glutamate receptors contributes to neuro...
Role of calcium ion (Ca2+) in the functioning of neurons from their naive state to mature state is o...
The pathogenesis of various acute and chronic neurodegenerative disorders has been linked to excitot...
t is widely accepted that a critical factor in determining neuronal death during cerebral ischemia i...
Excitotoxicity resulting from excessive Ca(2+) influx through glutamate receptors contributes to neu...
The ubiquitous, Ca2+-dependent, neutral proteases mu-calpain and m-calpain are heterodimeric regulat...
Physiological Ca2+ signals are essential for cell function and survival. On the other hand, perturba...
The molecular mechanisms responsible for A1-42-peptide induced intracellular Ca2+ homeostasis dysre...