Glycine receptor mouse mutants: model systems for human hyperekplexia - Wikidata - wikimedia - TriplyDB

Glycine receptor mouse mutants: model systems for human hyperekplexia

Glycine receptor mouse mutants: model systems for human hyperekplexia

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The Intracellular Loop of the Glycine Receptor: It's not all about the Size The impact of human hyperekplexia mutations on glycine receptor structure and function Murine startle mutant Nmf11 affects the structural stability of the glycine receptor and increases deactivation.The Concise Guide to PHARMACOLOGY 2013/14: ligand-gated ion channels.Disturbed neuronal ER-Golgi sorting of unassembled glycine receptors suggests altered subcellular processing is a cause of human hyperekplexia.Disruption of a Structurally Important Extracellular Element in the Glycine Receptor Leads to Decreased Synaptic Integration and Signaling Resulting in Severe Startle Disease.GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder.Trapping of ivermectin by a pentameric ligand-gated ion channel upon open-to-closed isomerization.Single expressed glycine receptor domains reconstitute functional ion channels without subunit-specific desensitization behavior.Disturbances of Ligand Potency and Enhanced Degradation of the Human Glycine Receptor at Affected Positions G160 and T162 Originally Identified in Patients Suffering from Hyperekplexia.Modulation of defensive reactivity by GLRB allelic variation: converging evidence from an intermediate phenotype approach.Mutational Analysis at Intersubunit Interfaces of an Anionic Glutamate Receptor Reveals a Key Interaction Important for Channel Gating by Ivermectin.Activation and modulation of recombinant glycine and GABAA receptors by 4-halogenated analogues of propofol.

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Glycine receptor mouse mutants: model systems for human hyperekplexia

http://www.wikidata.org/entity/Q30426940

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2013 nî lūn-bûn

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2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Glycine receptor mouse mutants: model systems for human hyperekplexia

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Glycine receptor mouse mutants: model systems for human hyperekplexia

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Glycine receptor mouse mutants: model systems for human hyperekplexia

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Glycine receptor mouse mutants: model systems for human hyperekplexia

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Glycine receptor mouse mutants: model systems for human hyperekplexia

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British Journal of Pharmacology

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Glycine receptor mouse mutants: model systems for human hyperekplexia

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P2093

Carmen Villmann

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Christoph J Kluck

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Georg Langlhofer

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Natascha Schaefer

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P2860

A structural and mutagenic blueprint for molecular recognition of strychnine and d-tubocurarine by different cys-loop receptors

Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)

A novel recessive hyperekplexia allele GLRA1 (S231R): genotyping by MALDI-TOF mass spectrometry and functional characterisation as a determinant of cellular glycine receptor trafficking

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

Alpha subunit variants of the human glycine receptor: primary structures, functional expression and chromosomal localization of the corresponding genes

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

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

Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis

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

From ab initio quantum mechanics to molecular neurobiology: a cation-pi binding site in the nicotinic receptor

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933-952

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10.1111/BPH.12335

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23941355

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