Disruption of a Structurally Important Extracellular Element in the Glycine Receptor Leads to Decreased Synaptic Integration and Signaling Resulting in Severe Startle Disease
Natascha Schaefer(University of Würzburg), Carmen Villmann(University of Würzburg)
Cited by 17
Related Papers
<scp>Glycine Receptor</scp> Autoantibodies Impair Receptor Function and Induce Motor Dysfunction
|Annals of Neurology|2020|48
A Novel Glycine Receptor Variant with Startle Disease Affects Syndapin I and Glycinergic Inhibition
|Journal of Neuroscience|2020|14
Novel Functional Properties of Missense Mutations in the Glycine Receptor β Subunit in Startle Disease
|Frontiers in Molecular Neuroscience|2021|11
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
|Frontiers in Molecular Neuroscience|2015|10
The GlyR Extracellular β8–β9 Loop – A Functional Determinant of Agonist Potency
|Frontiers in Molecular Neuroscience|2017|5