Distinct roles for two synaptotagmin isoforms in synchronous and asynchronous transmitter release at zebrafish neuromuscular junction.
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Architecture of the synaptotagmin-SNARE machinery for neuronal exocytosisSynaptotagmin-7 Is Essential for Ca2+-Triggered Delayed Asynchronous Release But Not for Ca2+-Dependent Vesicle Priming in Retinal Ribbon SynapsesSynaptotagmin-1 and -7 Are Redundantly Essential for Maintaining the Capacity of the Readily-Releasable Pool of Synaptic VesiclesSynaptotagmin-1 and synaptotagmin-7 trigger synchronous and asynchronous phases of neurotransmitter releaseThe functional significance of synaptotagmin diversity in neuroendocrine secretionThe calcium sensor synaptotagmin 7 is required for synaptic facilitationSynaptotagmin 7 functions as a Ca2+-sensor for synaptic vesicle replenishmentDifferent types of retinal inhibition have distinct neurotransmitter release properties.Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathyVesicles derived via AP-3-dependent recycling contribute to asynchronous release and influence information transferSynaptotagmin-7 is an asynchronous calcium sensor for synaptic transmission in neurons expressing SNAP-23Altered active zones, vesicle pools, nerve terminal conductivity, and morphology during experimental MuSK myasthenia gravisZebrafish CaV2.1 calcium channels are tailored for fast synchronous neuromuscular transmission.A sequential vesicle pool model with a single release sensor and a Ca(2+)-dependent priming catalyst effectively explains Ca(2+)-dependent properties of neurosecretion.Transmembrane tethering of synaptotagmin to synaptic vesicles controls multiple modes of neurotransmitter releaseDoc2 is a Ca2+ sensor required for asynchronous neurotransmitter release.Molecular underpinnings of synaptic vesicle pool heterogeneity.A Phenomenological Synapse Model for Asynchronous Neurotransmitter Release.Slow changes in Ca2(+) cause prolonged release from GABAergic retinal amacrine cells.N-terminal domain of complexin independently activates calcium-triggered fusion.Fatigue in Rapsyn-Deficient Zebrafish Reflects Defective Transmitter ReleaseSynchronous and asynchronous modes of synaptic transmission utilize different calcium sources.Molecular mechanisms for synchronous, asynchronous, and spontaneous neurotransmitter release.Exocytosis and synaptic vesicle function.The molecular machinery of neurotransmitter release (Nobel lecture).Translating neuronal activity at the synapse: presynaptic calcium sensors in short-term plasticity.Molecular mechanisms governing Ca(2+) regulation of evoked and spontaneous release.Functionally heterogeneous synaptic vesicle pools support diverse synaptic signalling.C2-domain containing calcium sensors in neuroendocrine secretion.Synaptic Vesicle-Recycling Machinery Components as Potential Therapeutic Targets.The Mechanisms and Functions of Synaptic Facilitation.Zebrafish calls for reinterpretation for the roles of P/Q calcium channels in neuromuscular transmission.Synapsin II desynchronizes neurotransmitter release at inhibitory synapses by interacting with presynaptic calcium channels.A synaptotagmin suppressor screen indicates SNARE binding controls the timing and Ca2+ cooperativity of vesicle fusion.Postsynaptic synaptotagmins mediate AMPA receptor exocytosis during LTP.Asynchronous GABA Release Is a Key Determinant of Tonic Inhibition and Controls Neuronal Excitability: A Study in the Synapsin II-/- Mouse.Heterogeneity of presynaptic proteins: do not forget isoforms.A Gradient in Synaptic Strength and Plasticity among Motoneurons Provides a Peripheral Mechanism for Locomotor Control.The primed SNARE-complexin-synaptotagmin complex for neuronal exocytosis.An asymptomatic mutation complicating severe chemotherapy-induced peripheral neuropathy (CIPN): a case for personalised medicine and a zebrafish model of CIPN.
P2860
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P2860
Distinct roles for two synaptotagmin isoforms in synchronous and asynchronous transmitter release at zebrafish neuromuscular junction.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Distinct roles for two synapto ...... rafish neuromuscular junction.
@ast
Distinct roles for two synapto ...... rafish neuromuscular junction.
@en
Distinct roles for two synapto ...... rafish neuromuscular junction.
@nl
type
label
Distinct roles for two synapto ...... rafish neuromuscular junction.
@ast
Distinct roles for two synapto ...... rafish neuromuscular junction.
@en
Distinct roles for two synapto ...... rafish neuromuscular junction.
@nl
prefLabel
Distinct roles for two synapto ...... rafish neuromuscular junction.
@ast
Distinct roles for two synapto ...... rafish neuromuscular junction.
@en
Distinct roles for two synapto ...... rafish neuromuscular junction.
@nl
P2093
P2860
P921
P356
P1476
Distinct roles for two synapto ...... rafish neuromuscular junction.
@en
P2093
Gail Mandel
Glen M Corson
Matthew J McGinley
Michael W Linhoff
Paul Brehm
P2860
P304
13906-13911
P356
10.1073/PNAS.1008598107
P407
P50
P577
2010-07-19T00:00:00Z