Asynchronous GABA Release Is a Key Determinant of Tonic Inhibition and Controls Neuronal Excitability: A Study in the Synapsin II−/−Mouse

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Epileptogenic Q555X SYN1 mutant triggers imbalances in release dynamics and short-term plasticity

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Methods for recording and measuring tonic GABAA receptor-mediated inhibition

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Synapsin II desynchronizes neurotransmitter release at inhibitory synapses by interacting with presynaptic calcium channels

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Increased asynchronous GABA release causes more inhibition in human epileptic brain?

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Synaptic and Extrasynaptic Origin of the Excitation/Inhibition Imbalance in the Hippocampus of Synapsin I/II/III Knockout Mice

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GABAAreceptor modulation by neurosteroids in models of temporal lobe epilepsies

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Neuroethologically delineated differences in the seizure behavior of Synapsin 1 and Synapsin 2 knock-out mice

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Tonic GABAA receptor-mediated signalling in temporal lobe epilepsy

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Enhancement of Asynchronous Release from Fast-Spiking Interneuron in Human and Rat Epileptic Neocortex

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Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters

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SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

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STXBP1 mutations cause not only Ohtahara syndrome but also West syndrome-Result of Japanese cohort study

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Cortico-hippocampal hyperexcitability in synapsin I/II/III knockout mice: age-dependency and response to the antiepileptic drug levetiracetam

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Distinct roles for two synaptotagmin isoforms in synchronous and asynchronous transmitter release at zebrafish neuromuscular junction

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Desynchronization of Neocortical Networks by Asynchronous Release of GABA at Autaptic and Synaptic Contacts from Fast-Spiking Interneurons

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Shunting Inhibition Controls the Gain Modulation Mediated by Asynchronous Neurotransmitter Release in Early Development

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Down-regulation Synaptic Vesicle Protein 2A in the Anterior Temporal Neocortex of Patients with Intractable Epilepsy

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Association of intronic polymorphism rs3773364 A>G in synapsin-2 gene with idiopathic epilepsy

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De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

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Synapsin-dependent development of glutamatergic synaptic vesicles and presynaptic plasticity in postnatal mouse brain

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Conformational Switch of Syntaxin-1 Controls Synaptic Vesicle Fusion

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