There is considerable interest in understanding long-term potentiation (LTP) of glutamatergic synaptic transmission because the molecular mechanisms involved in its induction and expression are believed to be critical for learning and memory. There are two distinct forms of LTP. One type is triggered by synaptic activation of NMDA receptors and the other is NMDA receptor-independent. The latter type of LTP has been mostly studied at mossy fiber/CA3 synapses. Here we summarise some of our recent studies concerning the mechanisms of the induction of the NMDA receptor-independent form of LTP at these CA3 synapses. This form of LTP is triggered by the synaptic activation of kainate receptors. We also address the importance of Ca2+ availability ...
It is currently unknown why glutamatergic presynaptic terminals express multiple types of glutamate ...
AbstractThe mechanisms involved in mossy fiber LTP in the hippocampus are not well established. In t...
It is currently unknown why glutamatergic presynaptic terminals express multiple types of glutamate ...
There is considerable interest in understanding long-term potentiation (LTP) of glutamatergic synapt...
There is considerable interest in understanding long-term potentiation (LTP) of glutamatergic synapt...
There is considerable interest in understanding long-term potentiation (LTP) of glutamatergic synapt...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
AbstractCompared with NMDA receptor-dependent LTP, much less is known about the mechanism of inducti...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
SummaryThe mossy fiber to CA3 pyramidal cell synapse (mf-CA3) provides a major source of excitation ...
Hippocampal mossy fiber synapses show an unusual form of long-term potentiation (LTP) that is indepe...
AbstractKainate receptors alter the excitability of mossy fiber axons and have been reported to play...
It is currently unknown why glutamatergic presynaptic terminals express multiple types of glutamate ...
AbstractThe mechanisms involved in mossy fiber LTP in the hippocampus are not well established. In t...
It is currently unknown why glutamatergic presynaptic terminals express multiple types of glutamate ...
There is considerable interest in understanding long-term potentiation (LTP) of glutamatergic synapt...
There is considerable interest in understanding long-term potentiation (LTP) of glutamatergic synapt...
There is considerable interest in understanding long-term potentiation (LTP) of glutamatergic synapt...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
AbstractCompared with NMDA receptor-dependent LTP, much less is known about the mechanism of inducti...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
Compared with NMDA receptor-dependent LTP, much less is known about the mechanism of induction of NM...
SummaryThe mossy fiber to CA3 pyramidal cell synapse (mf-CA3) provides a major source of excitation ...
Hippocampal mossy fiber synapses show an unusual form of long-term potentiation (LTP) that is indepe...
AbstractKainate receptors alter the excitability of mossy fiber axons and have been reported to play...
It is currently unknown why glutamatergic presynaptic terminals express multiple types of glutamate ...
AbstractThe mechanisms involved in mossy fiber LTP in the hippocampus are not well established. In t...
It is currently unknown why glutamatergic presynaptic terminals express multiple types of glutamate ...