A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
about
Manipulating neuronal circuits with endogenous and recombinant cell-surface tethered modulatorsA rapidly diverging superfamily of peptide toxins in venomous Gemmula speciesZiconotide: a review of its pharmacology and use in the treatment of painThe Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic PotentialFrom foe to friend: using animal toxins to investigate ion channel functionStructure-function of proteins interacting with the α1 pore-forming subunit of high-voltage-activated calcium channelsNMR solution structures of delta-conotoxin EVIA from Conus ermineus that selectively acts on vertebrate neuronal Na+ channelsPharmacological discrimination between effects of carbamazepine on hippocampal basal, Ca(2+)- and K(+)-evoked serotonin releaseNovel omega-conotoxins from Conus catus discriminate among neuronal calcium channel subtypesIsolation and characterization of a novel conus peptide with apparent antinociceptive activity.A new conotoxin isolated from Conus consors venom acting selectively on axons and motor nerve terminals through a Na+-dependent mechanism.Phoneutria nigriventer omega-phonetoxin IIA blocks the Cav2 family of calcium channels and interacts with omega-conotoxin-binding sites.Systemic effects induced by intralesional injection of ω-conotoxin MVIIC after spinal cord injury in rats.Speciation of cone snails and interspecific hyperdivergence of their venom peptides. Potential evolutionary significance of introns.Glycine-rich conotoxins from the Virgiconus clade.Membrane-tethered ligands: tools for cell-autonomous pharmacological manipulation of biological circuits.Chemical synthesis and characterization of maurocalcine, a scorpion toxin that activates Ca(2+) release channel/ryanodine receptors.Structure-activity relationships of omega-conotoxins at N-type voltage-sensitive calcium channels.Alteration of P-type calcium channel gating by the spider toxin omega-Aga-IVA.Novel peptides from assassin bugs (Hemiptera: Reduviidae): isolation, chemical and biological characterization.Omega-conotoxin MVIIC attenuates neuronal apoptosis in vitro and improves significant recovery after spinal cord injury in vivo in ratsNatural products and ion channel pharmacologySlowed N-type calcium channel (CaV2.2) deactivation by the cyclin-dependent kinase inhibitor roscovitine.Neurotensin and substance P inhibit low- and high-voltage-activated Ca2+ channels in cultured newborn rat nucleus basalis neurons.An improved diagnostic assay for Lambert-Eaton myasthenic syndrome.Conantokin-P, an unusual conantokin with a long disulfide loopSpontaneous glutamate release is independent of calcium influx and tonically activated by the calcium-sensing receptor.Role of N-type calcium channels in autonomic neurotransmission in guinea-pig isolated left atriaSO-3, a new O-superfamily conopeptide derived from Conus striatus, selectively inhibits N-type calcium currents in cultured hippocampal neurons.Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channelsCalcium channel subtypes for the sympathetic and parasympathetic nerves of guinea-pig atria.Factors involved in the relaxation of female pig urethra evoked by electrical field stimulation.NANC neurotransmission in lamina propria of the rabbit urethra: regulation by different subsets of calcium channels.Inhibition of neuromuscular transmission in the myenteric plexus of guinea-pig ileum by omega-conotoxins GVIA, MVIIA, MVIIC and SVIB.Neuronal activity regulates remyelination via glutamate signalling to oligodendrocyte progenitorsAnalgesic conotoxins: block and G protein-coupled receptor modulation of N-type (Ca(V) 2.2) calcium channels.Ziconotide, an intrathecally administered N-type calcium channel antagonist for the treatment of chronic pain.Calcium influx is required for endocytotic membrane retrieval.R-type Ca2+ currents evoke transmitter release at a rat central synapse.A selective N-type calcium channel antagonist protects against neuronal loss after global cerebral ischemia.
P2860
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P2860
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
description
1992 nî lūn-bûn
@nan
1992 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@ast
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@en
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@nl
type
label
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@ast
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@en
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@nl
prefLabel
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@ast
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@en
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@nl
P2093
P3181
P1433
P1476
A new Conus peptide ligand for mammalian presynaptic Ca2+ channels
@en
P2093
A Azimi-Zoonooz
D R Hillyard
G Miljanich
J M McIntosh
J Ramachandran
P3181
P356
10.1016/0896-6273(92)90221-X
P407
P577
1992-07-01T00:00:00Z