Glycine receptor mutants of the mouse: what are possible routes of inhibitory compensation? - Wikidata - awgldk - TriplyDB

Glycine receptor mutants of the mouse: what are possible routes of inhibitory compensation?

Glycine receptor mutants of the mouse: what are possible routes of inhibitory compensation?

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The Intracellular Loop of the Glycine Receptor: It's not all about the Size Voltage-Dependent Inhibition of Glycine Receptor Channels by Niflumic Acid Glycine receptor mouse mutants: model systems for human hyperekplexia Adeno-associated virus-RNAi of GlyRα1 and characterization of its synapse-specific inhibition in OFF alpha transient retinal ganglion cells.Investigating the Mechanism by Which Gain-of-function Mutations to the α1 Glycine Receptor Cause Hyperekplexia.Molecular probes and switches for functional analysis of receptors, ion channels and synaptic networks.Disruption of a Structurally Important Extracellular Element in the Glycine Receptor Leads to Decreased Synaptic Integration and Signaling Resulting in Severe Startle Disease.Functional Consequences of the Postnatal Switch From Neonatal to Mutant Adult Glycine Receptor α1 Subunits in the Shaky Mouse Model of Startle Disease.Impaired Glycine Receptor Trafficking in Neurological Diseases

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Glycine receptor mutants of the mouse: what are possible routes of inhibitory compensation?

http://www.wikidata.org/entity/Q30461478

description

2012 nî lūn-bûn

@nan

2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Glycine receptor mutants of th ...... es of inhibitory compensation?

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Glycine receptor mutants of th ...... es of inhibitory compensation?

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FNMOL.2012.00098

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Frontiers in molecular neuroscience

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Glycine receptor mutants of th ...... es of inhibitory compensation?

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Carmen Villmann

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Natascha Schaefer

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Nicolas Vogel

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P2860

The beta subunit determines the ligand binding properties of synaptic glycine receptors

A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

Decreased agonist affinity and chloride conductance of mutant glycine receptors associated with human hereditary hyperekplexia

Differential agonist sensitivity of glycine receptor alpha2 subunit splice variants

A novel mutation (Gln266-->His) in the alpha 1 subunit of the inhibitory glycine-receptor gene (GLRA1) in hereditary hyperekplexia

Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors

X-ray structure of a prokaryotic pentameric ligand-gated ion channel

Structure of a potentially open state of a proton-activated pentameric ligand-gated ion channel

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