Results 31 to 40 of about 24,889 (220)

High conopeptide diversity in Conus striatus: Revealed by integration of two transcriptome sequencing platforms

open access: yesFrontiers in Marine Science, 2022
Marine cone snail venoms represent a vast library of bioactive peptides with proven potential as research tools, drug leads, and therapeutics. In this study, a transcriptome library of four different organs, namely radular sheath, venom duct, venom gland,
Yanling Liao   +8 more
doaj   +1 more source

Graph-Directed Approach for Downselecting Toxins for Experimental Structure Determination

open access: yesMarine Drugs, 2020
Conotoxins are short, cysteine-rich peptides of great interest as novel therapeutic leads and of great concern as lethal biological agents due to their high affinity and specificity for various receptors involved in neuromuscular transmission. Currently,
Rachael A. Mansbach   +3 more
doaj   +1 more source

Calcium regulation of muscle spindle mechanosensory afferent function. [PDF]

open access: yesExp Physiol
Abstract Extracellular calcium is crucial for the normal function of muscle spindle sensory afferents. They express multiple calcium buffering proteins. Extracellular calcium is essential for recycling of synaptic‐like vesicles (SLVs) in the terminals and for the stretch‐evoked inward calcium current of the receptor potential.
Simon A   +5 more
europepmc   +2 more sources

Nonspecific, Reversible Inhibition of Voltage-Gated Calcium Channels by CaMKII Inhibitor CK59 [PDF]

open access: yes, 2013
Investigation of kinase-related processes often uses pharmacological inhibition to reveal pathways in which kinases are involved. However, one concern about using such kinase inhibitors is their potential lack of specificity.
Kahrls, Andrew S., Mynlieff, Michelle
core   +2 more sources

mGluR5 antagonism inhibits cocaine reinforcement and relapse by elevation of extracellular glutamate in the nucleus accumbens via a CB1 receptor mechanism. [PDF]

open access: yes, 2018
Metabotropic glutamate receptor 5 (mGluR5) antagonism inhibits cocaine self-administration and reinstatement of drug-seeking behavior. However, the cellular and molecular mechanisms underlying this action are poorly understood.
Bi, Guo-Hua   +9 more
core   +2 more sources

Structural studies of conotoxins [PDF]

open access: yesIUBMB Life, 2009
AbstractConotoxins are small disulfide‐rich peptides from the venoms of marine cone snails. They target a variety of ion channels, transporters, and receptors besides the interest in their natural functions in venoms and they are of much interest as drug leads.
Daly, Norelle L., Craik, David J.
openaire   +3 more sources

Principal Component and Structural Element Analysis Provide Insights into the Evolutionary Divergence of Conotoxins

open access: yesBiology, 2022
Predatory cone snails (Conus) developed a sophisticated neuropharmacological mechanism to capture prey, escape against other predators, and deter competitors.
Akira Kio V. Kikuchi, Lemmuel L. Tayo
doaj   +1 more source

Lavender oil-potent anxiolytic properties via modulating voltage dependent calcium channels [PDF]

open access: yes, 2013
Recent clinical data support the clinical use of oral lavender oil in patients suffering from subsyndromal anxiety. We identified the molecular mechanism of action that will alter the perception of lavender oil as a nonspecific ingredient of aromatherapy
Klugbauer, Norbert   +5 more
core   +4 more sources

Activity-dependent plasticity of transmitter release from nerve terminals in rat fast and slow muscles [PDF]

open access: yes, 2018
Available under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported license.Peer reviewedPublisher ...
Bewick, Guy Smith   +4 more
core   +1 more source

Chemical Synthesis and NMR Solution Structure of Conotoxin GXIA from Conus geographus

open access: yesMarine Drugs, 2021
Conotoxins are disulfide-rich peptides found in the venom of cone snails. Due to their exquisite potency and high selectivity for a wide range of voltage and ligand gated ion channels they are attractive drug leads in neuropharmacology.
David A. Armstrong   +5 more
doaj   +1 more source

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