Reference health

Designer receptor technology for the treatment of epilepsy

https://doi.org/10.1016/j.ebiom.2019.04.059
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72/72 checkable references clean · checked 2026-07-22

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

6 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 72 checked references that resolve
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Adeno-associated viral vector-induced overexpression of neuropeptide Y Y2 receptors in the hippocampus suppresses seizures
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Optogenetic and Potassium Channel Gene Therapy in a Rodent Model of Focal Neocortical Epilepsy
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Changing channels in pain and epilepsy: Exploiting ion channel gene therapy for disorders of neuronal hyperexcitability
resolves10.1038/ncomms2376
On-demand optogenetic control of spontaneous seizures in temporal lobe epilepsy
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Closed-loop optogenetic control of thalamus as a tool for interrupting seizures after cortical injury
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KCC2 overexpression prevents the paradoxical seizure-promoting action of somatic inhibition
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Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand
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An Engineered Glutamate-gated Chloride (GluCl) Channel for Sensitive, Consistent Neuronal Silencing by Ivermectin
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Biochemical autoregulatory gene therapy for focal epilepsy
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An Improved Ivermectin-activated Chloride Channel Receptor for Inhibiting Electrical Activity in Defined Neuronal Populations
resolves10.1126/science.1206606
Chemical and Genetic Engineering of Selective Ion Channel–Ligand Interactions
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Ultrapotent chemogenetics for research and potential clinical applications
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Controlling signaling with a specifically designed G <sub>i</sub> -coupled receptor
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DREADDs for Neuroscientists
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Selective and Quickly Reversible Inactivation of Mammalian Neurons In Vivo Using the Drosophila Allatostatin Receptor
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Chemogenetic Synaptic Silencing of Neural Circuits Localizes a Hypothalamus→Midbrain Pathway for Feeding Behavior
resolves10.1038/ncomms4847
Chemical–genetic attenuation of focal neocortical seizures
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A chemical-genetic approach to study G protein regulation of β cell function in vivo
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Design and Functional Characterization of a Novel, Arrestin-Biased Designer G Protein-Coupled Receptor
resolves10.1016/j.neuron.2015.03.065
A New DREADD Facilitates the Multiplexed Chemogenetic Interrogation of Behavior
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Chemogenetic Tools to Interrogate Brain Functions
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DREADDs (Designer Receptors Exclusively Activated by Designer Drugs): Chemogenetic Tools with Therapeutic Utility
resolves10.1038/gt.2016.56
DREADDs suppress seizure-like activity in a mouse model of pharmacoresistant epileptic brain tissue
resolves10.1016/j.expneurol.2016.07.003
Chemogenetic silencing of the midline and intralaminar thalamus blocks amygdala-kindled seizures
resolves10.1038/s41598-018-23659-x
Dynamic interaction of local and transhemispheric networks is necessary for progressive intensification of hippocampal seizures
resolves10.1523/JNEUROSCI.3456-16.2017
Selective Silencing of Hippocampal Parvalbumin Interneurons Induces Development of Recurrent Spontaneous Limbic Seizures in Mice
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Chemogenetic silencing of hippocampal neurons suppresses epileptic neural circuits
resolves10.3389/fncel.2018.00293
Chemogenetic Recruitment of Specific Interneurons Suppresses Seizure Activity
resolves10.1016/j.nbd.2018.06.006
Pharmaco-genetic therapeutics targeting parvalbumin neurons attenuate temporal lobe epilepsy
resolves10.1126/science.aan2475
Chemogenetics revealed: DREADD occupancy and activation via converted clozapine
resolves10.1016/j.biopsych.2006.09.023
Seizure Incidence in Psychopharmacological Clinical Trials: An Analysis of Food and Drug Administration (FDA) Summary Basis of Approval Reports
resolves10.1021/cn500325v
The First Structure–Activity Relationship Studies for Designer Receptors Exclusively Activated by Designer Drugs
resolves10.1021/acsptsci.8b00012
DREADD Agonist 21 Is an Effective Agonist for Muscarinic-Based DREADDs<i>in Vitro</i>and<i>in Vivo</i>
resolves10.1038/s41598-019-41088-2
Pharmacokinetic and pharmacodynamic actions of clozapine-N-oxide, clozapine, and compound 21 in DREADD-based chemogenetics in mice
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Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogenetics
resolves10.1016/S0140-6736(14)60456-6
Epilepsy: new advances
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Structural insights into Cys-loop receptor function and ligand recognition
resolves10.1111/epi.12797
Tonic glutamate in <scp>CA</scp>1 of aging rats correlates with phasic glutamate dysregulation during seizure
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Extracellular hippocampal glutamate and spontaneous seizure in the conscious human brain
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Selective Electrical Silencing of Mammalian Neurons<i>In Vitro</i>by the Use of Invertebrate Ligand-Gated Chloride Channels
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Ivermectin and its target molecules: shared and unique modulation mechanisms of ion channels and receptors by ivermectin
resolves10.1016/S0165-0270(02)00362-X
Codon optimization of Caenorhabditis elegans GluCl ion channel genes for mammalian cells dramatically improves expression levels
resolves10.1093/brain/awx201
Using an engineered glutamate-gated chloride channel to silence sensory neurons and treat neuropathic pain at the source
resolves10.1074/jbc.M011264200
Ivermectin, an Unconventional Agonist of the Glycine Receptor Chloride Channel
resolves10.3389/fnmol.2015.00055
Functional characterization of ivermectin binding sites in α1β2γ2L GABA(A) receptors
resolves10.1016/S0022-3565(24)39005-6
Anticonvulsant and Adverse Effects of Avermectin Analogs in Mice Are Mediated through the γ-Aminobutyric AcidA Receptor
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Serious Neurological Adverse Events after Ivermectin—Do They Occur beyond the Indication of Onchocerciasis?
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Blood-Brain Barrier: From Physiology to Disease and Back
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Cas9 immunity creates challenges for CRISPR gene editing therapies
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Injection parameters and virus dependent choice of promoters to improve neuron targeting in the nonhuman primate brain
resolves10.3389/fnmol.2018.00291
Impaired Glycine Receptor Trafficking in Neurological Diseases
resolves10.3389/fncel.2013.00184
Glycine receptors and brain development
resolves10.1016/j.neuron.2017.04.016
Homeostatic Plasticity Shapes Cell-Type-Specific Wiring in the Retina
resolves10.1038/nrd4609
An analysis of the attrition of drug candidates from four major pharmaceutical companies
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Deconstruction of a neural circuit for hunger
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A double-blind study evaluating the long-term safety of varenicline for smoking cessation
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Pre‐clinical properties of the α4β2 nicotinic acetylcholine receptor partial agonists varenicline, cytisine and dianicline translate to clinical efficacy for nicotine dependence
resolves10.1016/j.bbamem.2014.11.003
Pharmacological and molecular studies on the interaction of varenicline with different nicotinic acetylcholine receptor subtypes. Potential mechanism underlying partial agonism at human α4β2 and α3β4 subtypes
resolves10.1089/humc.2017.010
Persistent Expression of Dopamine-Synthesizing Enzymes 15 Years After Gene Transfer in a Primate Model of Parkinson's Disease
resolves10.1002/ana.25450
Magnetic resonance imaging–guided phase 1 trial of putaminal <i>AADC</i> gene therapy for Parkinson's disease
resolves10.1038/d41586-018-07644-y
Gene therapy targets epilepsy
resolves10.1038/nature17188
Crystal structures of the M1 and M4 muscarinic acetylcholine receptors
resolves10.1038/nature10939
Structure of the human κ-opioid receptor in complex with JDTic
resolves10.1038/nature10139
Principles of activation and permeation in an anion-selective Cys-loop receptor
resolves10.1038/nature14853
Glycine receptor mechanism elucidated by electron cryo-microscopy
The 6 references without a DOI — listed, not checked
no DOI — not checkedChemogenetic silencing of excitatory hippocampal neurons prevents spontaneous seizures in a mosue model for temporal lobe epilepsy
no DOI — not checkedSelective elimination of glutamate activation and introduction of fluorescent proteins into a Caenorhabditis elegans chloride channel
no DOI — not checkedNicotine receptor partial agonists for smoking cessation
no DOI — not checked10.1016/j.ebiom.2019.04.059_bb0345
no DOI — not checked10.1016/j.ebiom.2019.04.059_bb0350
no DOI — not checked10.1016/j.ebiom.2019.04.059_bb0355
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