Pages that link to "Q52648212"

The following pages link to Neurotransmitter release and its facilitation in crayfish. VIII. Modulation of release by hyperpolarizing pulses. (Q52648212):

Displaying 29 items.

• Autoreceptors, membrane potential and the regulation of transmitter release (Q33826757) (← links)
• The timing of phasic transmitter release is Ca2 -dependent and lacks a direct influence of presynaptic membrane potential (Q34393072) (← links)
• Amount and time-course of release. The calcium hypothesis and the calcium-voltage hypothesis (Q36534563) (← links)
• Neurotransmitter release at fast synapses (Q40500928) (← links)
• Theoretical models for describing neural signal transduction (Q40556134) (← links)
• Action potentials must admit calcium to evoke transmitter release (Q41133814) (← links)
• The calcium hypothesis and modulation of transmitter release by hyperpolarizing pulses (Q41172609) (← links)
• Effect of Ca2 diffusion on the time course of neurotransmitter release (Q41195994) (← links)
• Neurotransmitter release: development of a theory for total release based on kinetics (Q41277355) (← links)
• Membrane depolarization evokes neurotransmitter release in the absence of calcium entry (Q41278024) (← links)
• Effect of an intracellular calcium chelator on the regulation of electrically evoked [3H]-noradrenaline release from rat hippocampal slices (Q42187963) (← links)
• Calcium dependence of quantal release triggered by graded depolarization pulses to nerve terminals on crayfish and frog muscle (Q43416596) (← links)
• Twin pulse facilitation in dependence on pulse duration and calcium concentration at motor nerve terminals of crayfish and frogs (Q43796247) (← links)
• Activation and inactivation of oxytocin and vasopressin release from isolated nerve endings (neurosecretosomes) of the rat neurohypophysis (Q43923081) (← links)
• Blockage of synaptic release by brief hyperpolarizing pulses in the neuromuscular junction of the crayfish (Q44999896) (← links)
• Parallel computation enables precise description of Ca2 distribution in nerve terminals (Q51649172) (← links)
• Energy requirements for diphtheria toxin translocation are coupled to the maintenance of a plasma membrane potential and a proton gradient (Q52070548) (← links)
• The magnitude and significance of Ca2 domains for release of neurotransmitter. (Q52367705) (← links)
• Release kinetics as a tool to describe drug effects on neurotransmitter release. (Q52483781) (← links)
• Dependence of double-pulse facilitation on amplitude and duration of the depolarization pulses at frog's motor nerve terminals. (Q52642297) (← links)
• Neurotransmitter release and its facilitation in crayfish. VII. Another voltage dependent process beside Ca entry controls the time course of phasic release. (Q52648234) (← links)
• Membrane potential has no direct role in evoking neurotransmitter release (Q59095719) (← links)
• Contribution of Ca2 inflow to quantal, phasic transmitter release from nerve terminals of frog muscle (Q67525738) (← links)
• Inhibition of Ca2 inflow at nerve terminals of frog muscle blocks facilitation while phasic transmitter release is still considerable (Q68086120) (← links)
• Evoked phasic release in frog nerve terminals obtained after block of Ca2 entry by Cd2 (Q68264885) (← links)
• Shifts in the voltage dependence of synaptic release due to changes in the extracellular calcium concentration at nerve terminals on muscle of crayfish and frogs (Q69378632) (← links)
• Transmitter release from nerve terminals evoked by depolarization pulses contains a short phase of repression (Q69886407) (← links)
• Spatial facilitation and depression within one motor nerve terminal of frogs (Q72876923) (← links)
• Effects of replacing extracellular chloride with formate on the inhibitory neuromuscular junction of the crayfish opener muscle (Q77386872) (← links)