Differential protein structural disturbances and suppression of assembly partners produced by nonsense GABRG2 epilepsy mutations: implications for disease phenotypic heterogeneity. [electronic resource]
- Scientific reports 10 2016
- 35294 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
2045-2322
10.1038/srep35294 doi
Binding Sites Cell Membrane--metabolism Codon, Nonsense Epilepsies, Myoclonic--genetics Epilepsy, Absence--genetics Evoked Potentials--physiology Gene Expression HEK293 Cells Humans Hydrophobic and Hydrophilic Interactions Molecular Docking Simulation Patch-Clamp Techniques Phenotype Protein Binding Protein Conformation, alpha-Helical Protein Conformation, beta-Strand Protein Interaction Domains and Motifs Protein Multimerization Protein Subunits--chemistry Receptors, GABA-A--chemistry Seizures--genetics Severity of Illness Index Structural Homology, Protein Transfection