Functional recovery of glycine receptors in spastic murine model of startle disease
- 28 February 2006
- journal article
- Published by Elsevier in Neurobiology of Disease
- Vol. 21 (2) , 291-304
- https://doi.org/10.1016/j.nbd.2005.05.030
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Hydrophobic Interactions Mediate Binding of the Glycine Receptor β-Subunit to GephyrinJournal of Neurochemistry, 2008
- Interactively optimizing signal-to-noise ratios in expression profiling: project-specific algorithm selection and detection p-value weighting in Affymetrix microarraysBioinformatics, 2004
- Expression profiling — best practices for data generation and interpretation in clinical trialsNature Reviews Genetics, 2004
- The Activation Mechanism of α1 Homomeric Glycine ReceptorsJournal of Neuroscience, 2004
- Altered inhibitory synaptic transmission in superficial dorsal horn neurones in spastic and oscillator miceThe Journal of Physiology, 2003
- Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexiaHuman Genetics, 2001
- Phenotypic heterogeneity and disease course in three murine strains with mutations in genes encoding for α1 and β glycine receptor subunitsMovement Disorders, 1997
- Hyperekplexia: abnormal startle response due to glycine receptor mutationsThe British Journal of Psychiatry, 1997
- The inhibitory glycine receptor: architecture, synaptic localization and molecular pathology of a postsynaptic ion-channel complexCurrent Opinion in Neurobiology, 1995
- An additional family with Startle disease and a G1192A mutation at the α1 subunit of the inhibitory glycine receptor geneHuman Molecular Genetics, 1994